Ignite Creation Date:
2024-05-06 @ 2:34 PM
Last Modification Date:
2024-10-26 @ 1:33 PM
Study NCT ID:
NCT04353180
Status:
UNKNOWN
Last Update Posted:
2021-08-05
First Post:
2020-04-10
Brief Title:
Assessment the Activity Value of Isotretinoin 13- Cis-Retinoic Acid in the Treatment of COVID-19 Isotretinoin in Treatment of COVID-19 Randomized
Sponsor:
Kafrelsheikh University
Organization:
Kafrelsheikh University
Study Overview
Official Title:
Isotretinoin in Treatment of COVID-19 Randomized
Status:
UNKNOWN
Status Verified Date:
2021-07
Last Known Status:
NOT_YET_RECRUITING
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
Isotretinoin
Brief Summary:
Assessment the Activity Value of Isotretinoin 13- Cis-Retinoic Acid in the Treatment of COVID-19
Mahmoud ELkazzaz1Tamer Haydara2 Mohamed Abdelaal3 Abedelaziz Elsayed4 Yousry Abo-amer5 Hesham Attia6 Quan Liu7 Tim Duong8 and Heba Sahyon9
1 Department of chemistry and biochemistry Faculty of Science Damietta University Egypt
2 Department of Internal Medicine Faculty of Medicine Kafrelsheikh University Egypt
3 Department of Cardiothoracic Surgery Faculty of Medicine Kafrelsheikh University Egypt
4 Department of Pharmaceutical Biotechnology Faculty of Pharmacy Tanta University Egypt
5 HepatologyGastroenterology and Infectious Diseases Department Mahala Hepatology Teaching Hospital Egypt
6 Department of Immunology and Parasitology Faculty of Science Cairo University Egypt
7 School of Life Sciences and Engineering Foshan University Laboratory of Emerging Infectious Disease Institute of Translational Medicine The First Hospital of Jilin University Changchun China
8 Montefiore Health System and Albert Einstein College of Medicine New York United States of America
9 Chemistry Department Faculty of Science Kafrelsheikh University Egypt
This clinical study is the first clinical study in literature submitted on 20 April 2020 which demonstrated that Isotretinoin will provide complete protection against COVID-19
Abstract
The COVID-19 pandemic caused by severe acute respiratory syndrome coronavirus 2 SARS-CoV-2 has infected over 100 million people causing over 24 million deaths over the world and it is still expanding There is an urgent need for targeted and effective COVID-19 treatments which has put great pressure on researchers across the world for developing effective drugs In this clinical study we attempt to demonstrate Isotretinoin could be an effective and promising treatment for SARS-CoV-2 based on the intracellular mechanism of SARS-CoV-2 transmission and consequences caused Isotretinoin could strongly inhibit both inflammation and viral entry in severe acute respiratory syndrome coronavirus 2 infection via decreasing the overproduction of early response proinflammatory cytokines interleukin-6 which are over expressed in COVID-19 and contributed to disease progression poor outcomes vascular hyper permeability and multiorgan failure in patients infected with COVID-19 It could also block the entry of COVID-19 by inhibiting androgenic factors that induce serine 2 transmembrane protease TMPRSS2 expressions In addition to inhibiting of Angiotensin-converting enzyme-2 ACE2 Angiotensin T1 protein and Angiotensin II-mediated intracellular calcium release pathway which is responsible for COVID-19 cell fusion and entry ACE2-expressing cells are prone to SARS-CoV-2 infection as ACE2 receptor facilitates cellular viral entry and invasion Moreover isotretinoin is a potential repressor and inhibitor of papain-like protease PLpro which is a lethal protein expressed by COVID-19 genes and is an enzyme of dubiquitination which facilitates virus replication in patients with COVID-19The genome of Middle East Respiratory Syndrome Coronavirus is recognized by melanoma differentiation-associated protein-5 MDA5 retinoic acid inducible gene-1 RIG-1 and endosomal toll-like receptor 3 TLR3 as pathogen-associated molecular patterns This recognition resulted in the formation of type-1 interferon IFN1 As an evasion mechanism virus synthesize proteins that hinder the production IFN1 in the pathway 13-cis retinoic acid induced significant upregulation of toll-like receptor 3 TLR3 mitochondrial antiviral-signaling protein MAVS and IFN regulatory factor 1 expression in a time-dependent Furthermore 13 cis Retinoic Acid 13 cis RA could be an effective and promising treatment for SARS-CoV-2 owing to its ability to increase CD4 cells and induce mucosal IgA antibodies that are less prone to Antibody Dependent Enhancement process ADE and responsible for passive mucosal immunity in the respiratory tract ADE is a phenomenon in which antiviral antibodies facilitate viral infection of target immune cells and in some cases make a second infection worse such as dengue fever dengue virus By inducing IgA antibodies 13 cis retinoic acid enhances mucosal immunity and is known to be a potent IgA isotype13 Cis retinoic acid induced significant upregulation of toll-like receptor 3 an immune boosting action that may result in an immune response to dsRNA intermediate leading to the production of type I IFNs which is important to enhance the release of antiviral proteins for the protection of uninfected cells Isotretinoin therapy has furthermore proven anti-platelet and fibrinolytic activities which may protect patients infected with covid-19 from widespread blood clots From this point we suggest that isotretinon will be the Immunity passport in the context of COVID-19
Mahmoud ELkazzaz1Tamer Haydara2 Mohamed Abdelaal3 Abedelaziz Elsayed4 Yousry Abo-amer5 Hesham Attia6 Quan Liu7 Tim Duong8 and Heba Sahyon9
1 Department of chemistry and biochemistry Faculty of Science Damietta University Egypt
2 Department of Internal Medicine Faculty of Medicine Kafrelsheikh University Egypt
3 Department of Cardiothoracic Surgery Faculty of Medicine Kafrelsheikh University Egypt
4 Department of Pharmaceutical Biotechnology Faculty of Pharmacy Tanta University Egypt
5 HepatologyGastroenterology and Infectious Diseases Department Mahala Hepatology Teaching Hospital Egypt
6 Department of Immunology and Parasitology Faculty of Science Cairo University Egypt
7 School of Life Sciences and Engineering Foshan University Laboratory of Emerging Infectious Disease Institute of Translational Medicine The First Hospital of Jilin University Changchun China
8 Montefiore Health System and Albert Einstein College of Medicine New York United States of America
9 Chemistry Department Faculty of Science Kafrelsheikh University Egypt
This clinical study is the first clinical study in literature submitted on 20 April 2020 which demonstrated that Isotretinoin will provide complete protection against COVID-19
Abstract
The COVID-19 pandemic caused by severe acute respiratory syndrome coronavirus 2 SARS-CoV-2 has infected over 100 million people causing over 24 million deaths over the world and it is still expanding There is an urgent need for targeted and effective COVID-19 treatments which has put great pressure on researchers across the world for developing effective drugs In this clinical study we attempt to demonstrate Isotretinoin could be an effective and promising treatment for SARS-CoV-2 based on the intracellular mechanism of SARS-CoV-2 transmission and consequences caused Isotretinoin could strongly inhibit both inflammation and viral entry in severe acute respiratory syndrome coronavirus 2 infection via decreasing the overproduction of early response proinflammatory cytokines interleukin-6 which are over expressed in COVID-19 and contributed to disease progression poor outcomes vascular hyper permeability and multiorgan failure in patients infected with COVID-19 It could also block the entry of COVID-19 by inhibiting androgenic factors that induce serine 2 transmembrane protease TMPRSS2 expressions In addition to inhibiting of Angiotensin-converting enzyme-2 ACE2 Angiotensin T1 protein and Angiotensin II-mediated intracellular calcium release pathway which is responsible for COVID-19 cell fusion and entry ACE2-expressing cells are prone to SARS-CoV-2 infection as ACE2 receptor facilitates cellular viral entry and invasion Moreover isotretinoin is a potential repressor and inhibitor of papain-like protease PLpro which is a lethal protein expressed by COVID-19 genes and is an enzyme of dubiquitination which facilitates virus replication in patients with COVID-19The genome of Middle East Respiratory Syndrome Coronavirus is recognized by melanoma differentiation-associated protein-5 MDA5 retinoic acid inducible gene-1 RIG-1 and endosomal toll-like receptor 3 TLR3 as pathogen-associated molecular patterns This recognition resulted in the formation of type-1 interferon IFN1 As an evasion mechanism virus synthesize proteins that hinder the production IFN1 in the pathway 13-cis retinoic acid induced significant upregulation of toll-like receptor 3 TLR3 mitochondrial antiviral-signaling protein MAVS and IFN regulatory factor 1 expression in a time-dependent Furthermore 13 cis Retinoic Acid 13 cis RA could be an effective and promising treatment for SARS-CoV-2 owing to its ability to increase CD4 cells and induce mucosal IgA antibodies that are less prone to Antibody Dependent Enhancement process ADE and responsible for passive mucosal immunity in the respiratory tract ADE is a phenomenon in which antiviral antibodies facilitate viral infection of target immune cells and in some cases make a second infection worse such as dengue fever dengue virus By inducing IgA antibodies 13 cis retinoic acid enhances mucosal immunity and is known to be a potent IgA isotype13 Cis retinoic acid induced significant upregulation of toll-like receptor 3 an immune boosting action that may result in an immune response to dsRNA intermediate leading to the production of type I IFNs which is important to enhance the release of antiviral proteins for the protection of uninfected cells Isotretinoin therapy has furthermore proven anti-platelet and fibrinolytic activities which may protect patients infected with covid-19 from widespread blood clots From this point we suggest that isotretinon will be the Immunity passport in the context of COVID-19
Detailed Description:
The study is a randomized interventional comparative Phase III trial 10000 adult male and female patients with positive COVID-19 diagnosis and fulfilling the below outlined inclusion criteria will be enrolled into the study
Isotretinoin13cis RA may be able to inhibit COVID 2019 entry via down regulation of ACE2 AT1 protein and Ang II-mediated intracellular calcium release rather than inhibition of interleukin-6 IL-6 and this is discussed as follow
The COVID-19 pandemic caused by SARS-COV-2 has infected over 2000000 people causing over 150000 deaths A key host cellular protein required for the virus entry is angiotensin-converting enzyme 2 ACE2 whose expression has been demonstrated in many tissues including alveolar epithelial type II cells in lungs oral mucosa intestine heart kidney endothelium and skin ACE2-expressing cells can act as home cells and are prone to SARS-CoV-2 infection as ACE2 receptor facilitates cellular viral entry and replication A study demonestrated that patients with hypertension and diabetes mellitus may be at higher risk of SARS-CoV-2 infection as these patients are often treated with ACE inhibitors ACEIs or angiotensin II type-I receptor blockers ARBs which have been previously suggested to increase ACE2 expression In another study by Sinha et al who analyzed a publicly available Connectivity Map CMAP dataset of prepost transcriptomic profiles for drug treatment in cell lines for over 20000 small molecules isotretinoin was the strongest down-regulator of ACE 2 receptors On the other hand they found 6 drugs in CMAP that are currently being investigated in clinical trials for treating COVID-19 chloroquine thalidomide methylprednisolone losartan lopinavir and ritonavir from clinicaltrialsgov none of which was found to significantly alter ACE2 expression P01 Moreover another study demonstrated that isotretinoin is a potential papain like protease PLpro inhibitor which is a protein encoded by SARS-CoV-2 genes and considered one of the proteins that should be targeted in COVID-19 treatment by performing target-based virtual ligand screening
Previous studies on the related severe acute respiratory syndrome coronavirus SARS-CoV and SARS-CoV FP FP have shown that calcium Ca2 plays an important role for fusogenic activity via a Ca2 binding pocket with conserved glutamic acid E and aspartic acid D residuesdemonstrated that intracellular Ca2 enhances MERS-CoV WT PPs infection by approximately two-fold and that E891 is a crucial residue for Ca2interaction Electron spin resonance revealed that this enhancement could be attributed to Ca2 increasing MERS-CoV FP fusion-relevant membrane ordering Intriguingly isothermal calorimetry titration showed that MERS-CoV FP binds one Ca2 as opposed to SARS-CoV FP which binds to two Ca2 ion
Angiotensin II increases the intracellular calcium activity in podocytes of the intact glomerulus The L-type Ca2 channel blocker nicardipine did not influence the Ang II-mediated Ca2 increase and it has been postulated that SARS-CoV-2 binding to ACE2 may attenuate residual ACE2 activity skewing the ACEACE2 balance to a state of heightened angiotensin II activity leading to pulmonary vasoconstriction and inflammatory and oxidative organ damage which increases the risk for acute lung injury ALI AngII via AT1 receptors upregulates many proinflammatory genes such as vascular cell adhesion molecule-1 VCAM-1 intercellular adhesion molecule-1 ICAM-1 interleukin-6 IL-630 but 13cis RA specifically down-regulated the AT1 protein in a dose- and time-dependent manner Down-regulation of the AT1 expression leads to reduced AngII-mediated intracellular calcium release Similarly with receptor down-regulation Treatment with 13cRA resulted in a significant reduction in AT1 mRNA 13cRA has a glucose- and RARRXR independent mechanism for transcriptional inhibition of AT1
Isotretinoin13cis RA and ATRA may be able to inhibit COVID 2019 infection via inducing the antiviral immunity and this is discussed as follow
Since effective immune response against viral infections depends on the activation of cytotoxic T cells that can clear infection by killing virus-infected cells boosting the numbers and function of T cells in COVID-19 patients is critical for successful recovery A recent study reported that the 821 of COVID-19 cases displayed low circulating lymphocyte counts A CoV infects macrophages and then macrophages present CoV antigens to T cells This process leads to T cell activation and differentiation including the production of cytokines associated with the different T cell subsets Th17 followed by a massive release of cytokines for immune response amplification The continued production of these mediators due to viral persistence has a negative effect on NK and CD8 T cell activation However CD8 T cells produce very effective mediators to clear CoV However the factors which might cause the reduction in count and the activation status of T cells in COVID-19 patients remain uninvestigated
Recent study of 522 COVID patients and 40 healthy controls from two hospitals in Wuhan China demonstrated that T cell numbers are negatively correlated to serum IL-6 IL-10 and TNF-α concentration with patients in decline period showing reduced IL-6 IL-10 and TNF-α concentrations and restored T cell counts T cells from COVID-19 patients have significantly higher levels of the exhausted marker programmed cell death proteinPD-1 as compared to health controls Moreover increasing PD-1 and Tim-3 expression on T cells could be seen as patients progressed from prodromal to overtly symptomatic stages further indicative of T cell exhaustion T cell exhaustion is a progressive loss of effector function due to prolonged antigen stimulation characteristic of chronic infections Dendritic cell inhibition is connected to exhaustion of CD8 T cell polyfunctionality during chronic hepatitis C virus infection CD8 T cells produce very effective mediators to clear nCoV2019
Dendritic cells DCs play a key role in innate immune and adaptive immune responses As the strongest antigen presenting cells in the organism they effectively stimulate the activation of T lymphocytes and B lymphocytes thus combining innate and adaptive immunity Immature DCs have strong migration ability and mature DCs can effectively activate T cells in the central link of startup regulation and maintenance of immune responses Thus once the maturation process of DCs is blocked it directly affects the initiation of subsequent adaptive immune response MERS-CoV-2 is able to affect human dendritic cells and macrophages in-vitro Productive replication of Middle East respiratory syndrome coronavirus in monocyte-derived dendritic cells modulates innate immune response
Another study proposed that C -C chemokine receptor type 4 CCR4 contributes to T cell lung homing imprinting It was found that lung DCs induce the expression of CCR4 on T cells Lung DCs-activated T cells traffic more efficiently into the lung and protect against influenza more effectively compared with T cells activated by DCs from other tissues Lim and colleagues suggested that CXCR4 plays a role in CD8 T cell migration to airway tissues
Dendritic cell inhibition is connected to exhaustion of CD8 T cell polyfunctionality during chronic hepatitis C virus infection CD8 T cells produce very effective mediators to clear nCoV2019
Presence of RA in different tissues is very imprtant for immune induction and fighting viral infection for example RA is present at high concentrations in the small intestine due to metabolizing dietary vitamin A by gut epithelial cells In this local environment RA activates and primes dendritic cells DCs to become CD103 DCs that produce RA3 4CD103 DCs are migratory cells that activate naive T cells in mesenteric lymph nodes to become effector T cells that contribute to both intestinal homeostasis and immunityand also RA is an important signal that induces IgA-producing B cells The gut homing T cells and B cells play essential roles in protecting the digestive tract from pathogens
Retinoic acid atRA can inhibit the spontaneous apoptosis of activated human T lymphocytes in vitro 13-cis RA activates Th2 cytokine production Enhanced circulating dendritic cell numbers
So according to this previous studies the principal investigator suggests that T cells lymphopenia and exhaustion may be resulted by Dendritic cells DCs infection and inhibition by MERS-CoV-2
Retinoic acid has profound effects on cellular proliferation and differentiation Moreover it has been reported that ATRA exhibits both anti-inflammatory and immunoregulatory effects Recent studies have shown that FOXP3 expression and the immune function of Regulatory T cells Tregs can be enhanced by ATRA in in both patients and mouse models 13Retinoic acid RA is produced by a number of cell types including macrophages and dendritic cells which express retinal dehydrogenases that convert vitamin A to its main biologically active metabolite all-trans RA All-trans RA binds to its nuclear retinoic acid receptors that are expressed in lymphoid cells and act as transcription factors to regulate cell homing and differentiation RA production by CD103 dendritic cells and alveolar macrophages functions with TGF-b to promote conversion of naive T cells into Foxp3 regulatory T cells and Thereby maintain mucosal tolerance
So principal investigator expects high inducing of Dendritic cells DCs by retinoic acid treatment which will lead to T cells activation and migration with less exhaustion phenomenon
According to this protocol treatment with retinoic acid will induce FOXP3 and CD8CD4CD25FOXP3 Tregs which their absence during acute infection alters the ability of the host to limit tissue damage and inducesT cells which were dramatically reduced in COVID-19 patients to exert its antiviral and anti-inflammatory effect protecting lung cells and neural cells from the inflammatory and the destructive effect of IL-6 IL-1 and TNF-α which are induced and highly expressed in COVID 2019 patients
Researchers from Wenzhou China looked at clinical laboratory features including lipid levels of patients with COVID 19 They found dramatic reductions in the cholesterol levels of patients infected with COVID 19 compared with healthy controls The study provides data to suggest that cholesterol levels decline quite rapidly during the early stages of infection and increase as the patient starts to recover Therefore indicating that cholesterol may have an important role to play in defending the body against such infections According to our protocol depending on previous studies the principal investigator demonstrated that there is a strong relation between immune system and cholesterol levels When the cholesterol level is low specifically in the case of viral infection like COVID 2019 infection the immune system is impaired and the antiviral immune cells will be declined and inhibited -
Cellular cholesterol is a component of the plasma membrane and is also essential in cell proliferation Regulation of intracellular cholesterol levels has been proposed as a mechanism to regulate T cell and macrophages proliferation Intracellular cholesterol level is regulated by two competing pathways cholesterol uptake and efflux and ABCA1 plays a major role in the cholesterol efflux pathway The ATRA induces ABCA1 expression and ABCA1-dependent cholesterol efflux in activated primary human CD4 T cells implying that RA could affect T cell functions by regulating the cellular cholesterol levels
ATRA upregulates ABCA1 expression only in activated CD4 T cells indicating that induction of ABCA1 by ATRA and 13 cis Retinoic Acid may play an important role in immune response
Retinoic acid and liver X receptor agonist synergistically inhibit HIV infection in CD4 T cells by up-regulating ABCA1-mediated cholesterol efflux
So the principal investigator expects that retinoic acid treatment will highly induce T cells and anti-inflammatory regulatory T cells T helper via cholesterol efflux and inducing ATP-binding cassette transporter ABCA1 and protect lung and neural cells and inhibit COVID 2019 infection
The genome of Middle East Respiratory Syndrome Coronavirus is recognized by melanoma differentiation-associated protein-5 MDA5 retinoic acid inducible gene-1 RIG-1 and endosomal toll-like receptor 3 TLR3 as pathogen-associated molecular patterns This recognition resulted in the formation of type-1 interferon IFN1 As an evasion mechanism virus synthesize proteins that hinder the production IFN1 in the pathway
RA also acts directly on macrophages at both mucosal sites and other immunological sites AtRA modulates peritoneal macrophage activation by endotoxin and IFN-γ by suppressing TNF production and nitric oxide NO synthesis In addition at RA inhibits the expression of PGE2 and COX-2 and the release of TNF which are induced by bacterial lipopolysaccharide LPS in murine peritoneal macrophages
A study reported recently that substance ATRA have preventive effects on pulmonary fibrosis by inhibiting IL-6-dependent proliferation and TGF-β1-dependent trans differentiation of lung fibroblasts Also another studies demonstrated that 13-cis-retinoic acid and other retinoid analogs inhibit IL-1-induced IL-6 production and that this effect is analog-specific and at least partially transcriptionally mediated This effect was dose-dependent with an IC50 of 10-7 M RA and significant inhibition being noted with doses of RA as low as 10-8 M IL-10 production was inhibited by ATRA administration
A study demonstrated that TLR3-- TLR4-- and TRAM-- mice are more susceptible to SARS-CoV than wild-type mice but experience only transient weight loss with no mortality in response to infection In contrast mice deficient in the TLR3TLR4 adaptor TRIF are highly susceptible to SARS-CoV infection showing increased weight loss mortality reduced lung function increased lung pathology and higher viral titers New studies showed that the high level of IFN-αβ produced from the TLR3-IRF3IRF7 pathway and IFN-β is the reason for inhibiting DENV replication 13Cis retinoic Acid induced significant upregulation of toll-like receptor 3 TLR3 resulting in an immune response to dsRNA intermediate which can be partially generated during CoV-2 replicationTLR3 sensitized by dsRNA and cascades of signaling pathways IRFs and NFκB activation respectively are activated to produce type I IFNs The production of type I IFNs is important to enhance the release of antiviral proteins for the protection of uninfected cells Sometimes accessory proteins of CoV can interfere with TLR3 signaling and bind the dsRNA of CoV during replication to prevent TLR3 activation and evade the immune response 13Cis retinoic Acid induced significant upregulation of toll-like receptor 3 TLR3 mitochondrial antiviral-signaling protein MAVS and retinoid-induced gene I RIG-I and IFN regulatory factor 1 expression in a time-dependent
In further research Tsai and Chen showed the high level of IFN-αβ produced from the TLR3-IRF3IRF7 pathway and IFN-β is the reason for inhibiting DENV replication In HUH-7 cells huTLR3 can recognize DENV-1 and induce the expression of IFN-β which can enhance the expression of huTLR3 on the contrary TLR3 also induces type I IFN during WNV
Doctors treating the sickest Covid-19 patients have zeroed in on a new phenomenon Some people have developed widespread blood clots their lungs peppered with tiny blockages that prevent oxygen from pumping into the bloodstream and bodyAs with so much else about the Covid-19 response health experts are learning about the symptom on the fly Blood clots are common in patients who are immobilized but they seem to be smaller and cause far more severe damage in some Covid-19 patients Doctors have said they see patients with blood clots forming not only in their lungs but also in blood vessels Autopsies have also revealed blood clots in kidneys and other organs which some experts say suggests an overwhelming immune system response to the virus that inflicts harm on the body
Retinoic acid is known to possess in vivo anti-inflammatory anti-platelet and fibrinolytic activities A study investigated the in vitro thrombin and platelet aggregation inhibitory activities of retinoic acid and retinaldehydeRetinoic acid retinaldehyde and retinol exhibited potent inhibition of thrombin with IC50 values of 67μgml 74μgml and 152μgml respectively for the inhibition of thrombin Sigma and 49μgml 74μgml and 178μgml respectively for the inhibition of thrombin plasma Amongst vitamin A and its derivatives retinoic acid showed the highest inhibition of both the forms of thrombin
Isotretinoin13cis RA may be able to inhibit COVID 2019 infection via reversIing the androgenic induction and activation effect of DHT on TMPRSS2 expression and helps to prevent cleaving and activating both the spike protein S of COVID 2019 and the viral receptor and this is discussed as follow
TMPRSS2 is both the most frequently altered gene in primary prostate cancer and a critical factor enabling cellular infection by coronaviruses including SARS-CoV-2 The modulation of its expression by steroids could contribute to the male predominance of severe infections and given that TMPRSS2 has no known indispensable functions and inhibitors are available it is an appealing target for prevention or treatment of respiratory viral infections
TMPRSS2 a key regulator in prostate cancerTMPRSS2 was first identified in prostate cancer shortly after the gene had been originally cloned Prostate cancer cell lines strongly upregulated TMPRSS2 expression in response to androgens TMPRSS2 is expressed on the luminal side of the prostate epithelium and its expression is increased in prostate cancer tissue compared to non-cancerous prostate tissue Notably the TMPRSS2 gene is a partner in one of the most common gene fusion eventsin solid tumors somatic gene rearrangements involving TMPRSS2 witha member of the ETS family of oncogenic transcription factors most commonly ERG This fusion occurs in approximately 50 of primary prostate cancers among men of European ancestryWhile ERG is not normally regulated by androgen the gene fusion juxtaposes the androgen receptor regulatory elements of TMPRSS2 with the ERG gene The ERG gene is consequently controlled by androgen receptor signaling and expressed highly in prostate cancers harboring the TMPRSS2 ERG fusion Intriguingly the prevalence of the TMPRSS2 ERG fusion is lower in prostate tumors of both black and Asian men The relevance of this to the current COVID-19 pandemic is unclearTMPRSS2 ERG fusion- cancers also have a distinct set of risk factors related to hormonal signaling For example men with higher genetically determined transcriptional activity of the androgen receptor have a higher risk of TMPRSS2 ERG fusion-positive prostate cancer but not of fusion-negative prostate cancer
TMPRSS2 is an androgen receptor signaling target gene and an androgen-regulated cell-surface serine protease expressed predominantly in prostate and lung epithelial cell TMPRSS2 is normally expressed several fold higher in the prostate relative to any other human tissue though the normal physiological functions remains unknown Importantly unlike other TTSPs TMPRSS2 transcription is regulated by androgenic ligands and the androgen receptor AR There is a positive correlation between AR and TMPRSS2 in microdissected primary tumor epithelium r2 039 p 0001
Dihydrotestosterone DHT significantly and dramatically induced the expression of TMPRSS2 protein with two molecular masses of 60 full-length and 38 kDa N-terminus in a dose responsive manner
Data from Chinese outbreak show death rates for men almost 50 per cent higher than for women show that Early research from China suggests women and children are less likely to die than men if they catch the coronavirus Death rates for Covid-19 the disease those infected with the coronavirus develop are low for everyone only 24 per cent of the 44672 people in the Chinese study died But although roughly even numbers of men and women catch the disease men are more likely to develop such a serious case of Covid-19 they die
More than 70 percent of Italys coronavirus deaths have been among men but scientists there admit they are mystified by the gender gap At least 3400 people in Italy have died of the devastating disease - it yesterday announced it had a higher death Toll than China - but less than 1000 of them have been women Men are also more likely to pick up the infection in the first place and account for 60 percent of confirmed cases according to Italys public health research agency An earlier analysis found that 80 per cent of the deaths were in men and just 20 per cent were in women - but the gap has narrowed over time
According to this data the principal investigator thinks that there is a strong relation between high mortality in males and androgenic effect specifically the effect of DHT on TMPRSS2 protein which is used by covid 2019 in cell invasion and entry and depending on this data related to six hormones specifically DHT The investigator was able to discover whey women and children less likely to die from illness than men So the investigator divided infected patients according to their six hormone because TMPRSS2 is an androgen-regulated cell-surface serine protease expressed predominantly in prostate and lung epithelial cell TMPRSS2
AndrogenDHT potential effect on TMPRSS2 expression in children is less than its effect in females and males followed by viral severity and vigrousity in men compared with children and women
Androgen DHT potential effect on TMPRSS2 expression in females is less than in males followed by viral severity and vigrousity in men compared with females
So the principal investigator thinks that when some researchers investigated the role of sex steroids in SARS-CoV pathogenesis by comparing gonadectomized and control counterparts after infection Gonadectomy or treatment with flutamide a non-steroidal anti-androgen did not affect morbidity and mortality in male mice following lethal MA15 infection They may be were wrong in their conclusions in suggesting that androgens do not play a role in SARS-CoV pathogenesis because Gonadectomy or treatment with flutamide will not completely affect or inhibit DHT and its derivatives5α-Androstan-3α17β-Diol concentration in tissues and blood because after inhibiting testosterone with flutamide the pathway of DHT formation will be activated to compensate the inhibited testosterone levels so the TMPRSS2 expression will be significantly induced by DHT and the treated animals will not be affected in case of flutamide treatment but in case of Gonadectomy the expression of TMPRSS2 will be decreased by DHT inhibition only if along time has passed on Gonadectomy in order to make sure that DHT and its derivatives completely declined in levels that will not allow it to affect on expression of TMPRSS2 and in female mice after blocking estrogen receptors it died because increasing formation of androgenic hormones
A study demonstrated that 13- cis -Retinoic acid competitively and reversibly inhibits Dihydrotestosterone So the principal investigator expects a significant modulation of TMPRSS2 expression after treating with 13- cis -Retinoic acid via temporary preventing the effect of dihydrotestosteroneDHT on TMPRSS2 promoting and expression And the type II transmembrane serine proteases TMPRSS2 which can cleave and activate the spike protein S of the severe acute respiratory syndrome coronavirus SARS-CoV for membrane fusion In addition these proteases cleave the viral receptor the carboxypeptidase angiotensin-converting enzyme 2 ACE2 and it was proposed that ACE2 cleavage augments viral infectivity
A study demonstrated that COVID-19 reduces testosterone levels in men by altering the functioning of the gonads So could the increased severity of the disease in men be due to lowered testosterone But according to the principal investigator explanation COVID-19 reduces testosterone levels because there is a dramatic reductions in the cholesterol levels of patients infected with COVID 19 compared with healthy controls Cholesterol levels decline quite rapidly during the early stages of infection and increase as the patient starts to recoverTherefore indicating that cholesterol may have an important role to play in defending the body against such infections and depending on the principal investigator explanation Testosterone is synthesized starting from cholesterol through a well-characterized steroid biosynthetic pathway involving the sequential action of multiple enzymes So when cholesterol levels are decreased this decrease will followed by decreasing in testosterone level and according to this explanation testosterone therapy in COVID 2019 is not recommended but temporary inhibitor of DHT is recommended such as Isotretinoin because this treatment by testosterone will inhibit cholesterol synthesis by feedback inhibition and decrease cholesterol uptake by Leydig cells in testis and this also will lead to over increase in DHT lvels and its derivatives in different tissues which will induce TMPRSS2 because DHT is a potent activator of TMPRSS2 and this will be followed by processing and activation of COVID2019 spike protein to bined its ACE2 receptors in lung and kidney leading to their damage specifically in testis because it contains high levels of proteases and ACE2 Serine proteases are emerging as important contributors to the production maturation and functional competence of spermatozoa
Depending on this data and according to this protocol The principal investigator expects and suggests that retinoic acid is specific modulator of androgens specifically DHT not testosterone and could reverse the androgenic induction and activation effect of DHT on TMPRSS2 expression and prevent cleaving and activating both the spike protein S of COVID 2019 and the viral receptor the carboxypeptidase angiotensin-converting enzyme 2 ACE2 All ideas and michanisms specifically role of Androgen in TMPRSS2 activation in COVID-19 Serendipity or opportunity for intervention and the inhibition of ACE2 AT1 protein and Ang II-mediated intracellular calcium release pathway which is responsible for SARS-CoV-2 cell fusion and entry included in the research protocol were submitted to Academy of scientific research and technology - Egypt- on 1 April 2020 in Call no 22019ASRT- Ideation Fund
________________________________________________________________________________________________________________________________________________________________________
Promising features of COVID 2019 treatment according Principal Investigator Protocol
1 This medication have the feature of Aerosolized Drug Delivery to increase its efficacy beside Oral administration Which makes it distinct from other medication in which should dose be only given orally A study demonstrated that treating with 13 cis retinoic acid aerosolized via inhalation rout did not cause any damage in lung cells Repeated high doses of 13 cis retinoic by inhalation resulted in moderate loss of body weight but microscopic investigation of ten tissues including lung and oesophagus did not detect any significant aerosol-induced damage The results suggest that administration of isotretinoin via powder aerosol inhalation is probably superior to its application via the oral route in terms of achieving efficacious drug concentrations in the lung
2 Inhaled isotretinoin might provide sufficient drug to the target cells for efficacy while avoiding systemic toxicity
3 A study demonstrated that 13 cis retinoic is used in treating Emphysema emphysema is a lung condition that causes shortness of breath
4 ATRA has been reported to induce formation of new alveoli and returns elastic recoil in the lung to approximately normal values in animal models of emphysema
5 Strong expectation of complete COVID 2019 blockade from cell entry and infection depending on strong ethics researches and references
6 Availability of our compounds
7 Ease of application
8 Expectation of COVID 2019 treating of by more than one distinct mechanism
9 Expectation of High induction of anti- inflammatory T cells and significant inhibition of IL-6 at low concentrations
10 Controlling Accompanying cytokine storm
11 No interactions with Egyptian protocol drugs were found
Isotretinoin13cis RA may be able to inhibit COVID 2019 entry via down regulation of ACE2 AT1 protein and Ang II-mediated intracellular calcium release rather than inhibition of interleukin-6 IL-6 and this is discussed as follow
The COVID-19 pandemic caused by SARS-COV-2 has infected over 2000000 people causing over 150000 deaths A key host cellular protein required for the virus entry is angiotensin-converting enzyme 2 ACE2 whose expression has been demonstrated in many tissues including alveolar epithelial type II cells in lungs oral mucosa intestine heart kidney endothelium and skin ACE2-expressing cells can act as home cells and are prone to SARS-CoV-2 infection as ACE2 receptor facilitates cellular viral entry and replication A study demonestrated that patients with hypertension and diabetes mellitus may be at higher risk of SARS-CoV-2 infection as these patients are often treated with ACE inhibitors ACEIs or angiotensin II type-I receptor blockers ARBs which have been previously suggested to increase ACE2 expression In another study by Sinha et al who analyzed a publicly available Connectivity Map CMAP dataset of prepost transcriptomic profiles for drug treatment in cell lines for over 20000 small molecules isotretinoin was the strongest down-regulator of ACE 2 receptors On the other hand they found 6 drugs in CMAP that are currently being investigated in clinical trials for treating COVID-19 chloroquine thalidomide methylprednisolone losartan lopinavir and ritonavir from clinicaltrialsgov none of which was found to significantly alter ACE2 expression P01 Moreover another study demonstrated that isotretinoin is a potential papain like protease PLpro inhibitor which is a protein encoded by SARS-CoV-2 genes and considered one of the proteins that should be targeted in COVID-19 treatment by performing target-based virtual ligand screening
Previous studies on the related severe acute respiratory syndrome coronavirus SARS-CoV and SARS-CoV FP FP have shown that calcium Ca2 plays an important role for fusogenic activity via a Ca2 binding pocket with conserved glutamic acid E and aspartic acid D residuesdemonstrated that intracellular Ca2 enhances MERS-CoV WT PPs infection by approximately two-fold and that E891 is a crucial residue for Ca2interaction Electron spin resonance revealed that this enhancement could be attributed to Ca2 increasing MERS-CoV FP fusion-relevant membrane ordering Intriguingly isothermal calorimetry titration showed that MERS-CoV FP binds one Ca2 as opposed to SARS-CoV FP which binds to two Ca2 ion
Angiotensin II increases the intracellular calcium activity in podocytes of the intact glomerulus The L-type Ca2 channel blocker nicardipine did not influence the Ang II-mediated Ca2 increase and it has been postulated that SARS-CoV-2 binding to ACE2 may attenuate residual ACE2 activity skewing the ACEACE2 balance to a state of heightened angiotensin II activity leading to pulmonary vasoconstriction and inflammatory and oxidative organ damage which increases the risk for acute lung injury ALI AngII via AT1 receptors upregulates many proinflammatory genes such as vascular cell adhesion molecule-1 VCAM-1 intercellular adhesion molecule-1 ICAM-1 interleukin-6 IL-630 but 13cis RA specifically down-regulated the AT1 protein in a dose- and time-dependent manner Down-regulation of the AT1 expression leads to reduced AngII-mediated intracellular calcium release Similarly with receptor down-regulation Treatment with 13cRA resulted in a significant reduction in AT1 mRNA 13cRA has a glucose- and RARRXR independent mechanism for transcriptional inhibition of AT1
Isotretinoin13cis RA and ATRA may be able to inhibit COVID 2019 infection via inducing the antiviral immunity and this is discussed as follow
Since effective immune response against viral infections depends on the activation of cytotoxic T cells that can clear infection by killing virus-infected cells boosting the numbers and function of T cells in COVID-19 patients is critical for successful recovery A recent study reported that the 821 of COVID-19 cases displayed low circulating lymphocyte counts A CoV infects macrophages and then macrophages present CoV antigens to T cells This process leads to T cell activation and differentiation including the production of cytokines associated with the different T cell subsets Th17 followed by a massive release of cytokines for immune response amplification The continued production of these mediators due to viral persistence has a negative effect on NK and CD8 T cell activation However CD8 T cells produce very effective mediators to clear CoV However the factors which might cause the reduction in count and the activation status of T cells in COVID-19 patients remain uninvestigated
Recent study of 522 COVID patients and 40 healthy controls from two hospitals in Wuhan China demonstrated that T cell numbers are negatively correlated to serum IL-6 IL-10 and TNF-α concentration with patients in decline period showing reduced IL-6 IL-10 and TNF-α concentrations and restored T cell counts T cells from COVID-19 patients have significantly higher levels of the exhausted marker programmed cell death proteinPD-1 as compared to health controls Moreover increasing PD-1 and Tim-3 expression on T cells could be seen as patients progressed from prodromal to overtly symptomatic stages further indicative of T cell exhaustion T cell exhaustion is a progressive loss of effector function due to prolonged antigen stimulation characteristic of chronic infections Dendritic cell inhibition is connected to exhaustion of CD8 T cell polyfunctionality during chronic hepatitis C virus infection CD8 T cells produce very effective mediators to clear nCoV2019
Dendritic cells DCs play a key role in innate immune and adaptive immune responses As the strongest antigen presenting cells in the organism they effectively stimulate the activation of T lymphocytes and B lymphocytes thus combining innate and adaptive immunity Immature DCs have strong migration ability and mature DCs can effectively activate T cells in the central link of startup regulation and maintenance of immune responses Thus once the maturation process of DCs is blocked it directly affects the initiation of subsequent adaptive immune response MERS-CoV-2 is able to affect human dendritic cells and macrophages in-vitro Productive replication of Middle East respiratory syndrome coronavirus in monocyte-derived dendritic cells modulates innate immune response
Another study proposed that C -C chemokine receptor type 4 CCR4 contributes to T cell lung homing imprinting It was found that lung DCs induce the expression of CCR4 on T cells Lung DCs-activated T cells traffic more efficiently into the lung and protect against influenza more effectively compared with T cells activated by DCs from other tissues Lim and colleagues suggested that CXCR4 plays a role in CD8 T cell migration to airway tissues
Dendritic cell inhibition is connected to exhaustion of CD8 T cell polyfunctionality during chronic hepatitis C virus infection CD8 T cells produce very effective mediators to clear nCoV2019
Presence of RA in different tissues is very imprtant for immune induction and fighting viral infection for example RA is present at high concentrations in the small intestine due to metabolizing dietary vitamin A by gut epithelial cells In this local environment RA activates and primes dendritic cells DCs to become CD103 DCs that produce RA3 4CD103 DCs are migratory cells that activate naive T cells in mesenteric lymph nodes to become effector T cells that contribute to both intestinal homeostasis and immunityand also RA is an important signal that induces IgA-producing B cells The gut homing T cells and B cells play essential roles in protecting the digestive tract from pathogens
Retinoic acid atRA can inhibit the spontaneous apoptosis of activated human T lymphocytes in vitro 13-cis RA activates Th2 cytokine production Enhanced circulating dendritic cell numbers
So according to this previous studies the principal investigator suggests that T cells lymphopenia and exhaustion may be resulted by Dendritic cells DCs infection and inhibition by MERS-CoV-2
Retinoic acid has profound effects on cellular proliferation and differentiation Moreover it has been reported that ATRA exhibits both anti-inflammatory and immunoregulatory effects Recent studies have shown that FOXP3 expression and the immune function of Regulatory T cells Tregs can be enhanced by ATRA in in both patients and mouse models 13Retinoic acid RA is produced by a number of cell types including macrophages and dendritic cells which express retinal dehydrogenases that convert vitamin A to its main biologically active metabolite all-trans RA All-trans RA binds to its nuclear retinoic acid receptors that are expressed in lymphoid cells and act as transcription factors to regulate cell homing and differentiation RA production by CD103 dendritic cells and alveolar macrophages functions with TGF-b to promote conversion of naive T cells into Foxp3 regulatory T cells and Thereby maintain mucosal tolerance
So principal investigator expects high inducing of Dendritic cells DCs by retinoic acid treatment which will lead to T cells activation and migration with less exhaustion phenomenon
According to this protocol treatment with retinoic acid will induce FOXP3 and CD8CD4CD25FOXP3 Tregs which their absence during acute infection alters the ability of the host to limit tissue damage and inducesT cells which were dramatically reduced in COVID-19 patients to exert its antiviral and anti-inflammatory effect protecting lung cells and neural cells from the inflammatory and the destructive effect of IL-6 IL-1 and TNF-α which are induced and highly expressed in COVID 2019 patients
Researchers from Wenzhou China looked at clinical laboratory features including lipid levels of patients with COVID 19 They found dramatic reductions in the cholesterol levels of patients infected with COVID 19 compared with healthy controls The study provides data to suggest that cholesterol levels decline quite rapidly during the early stages of infection and increase as the patient starts to recover Therefore indicating that cholesterol may have an important role to play in defending the body against such infections According to our protocol depending on previous studies the principal investigator demonstrated that there is a strong relation between immune system and cholesterol levels When the cholesterol level is low specifically in the case of viral infection like COVID 2019 infection the immune system is impaired and the antiviral immune cells will be declined and inhibited -
Cellular cholesterol is a component of the plasma membrane and is also essential in cell proliferation Regulation of intracellular cholesterol levels has been proposed as a mechanism to regulate T cell and macrophages proliferation Intracellular cholesterol level is regulated by two competing pathways cholesterol uptake and efflux and ABCA1 plays a major role in the cholesterol efflux pathway The ATRA induces ABCA1 expression and ABCA1-dependent cholesterol efflux in activated primary human CD4 T cells implying that RA could affect T cell functions by regulating the cellular cholesterol levels
ATRA upregulates ABCA1 expression only in activated CD4 T cells indicating that induction of ABCA1 by ATRA and 13 cis Retinoic Acid may play an important role in immune response
Retinoic acid and liver X receptor agonist synergistically inhibit HIV infection in CD4 T cells by up-regulating ABCA1-mediated cholesterol efflux
So the principal investigator expects that retinoic acid treatment will highly induce T cells and anti-inflammatory regulatory T cells T helper via cholesterol efflux and inducing ATP-binding cassette transporter ABCA1 and protect lung and neural cells and inhibit COVID 2019 infection
The genome of Middle East Respiratory Syndrome Coronavirus is recognized by melanoma differentiation-associated protein-5 MDA5 retinoic acid inducible gene-1 RIG-1 and endosomal toll-like receptor 3 TLR3 as pathogen-associated molecular patterns This recognition resulted in the formation of type-1 interferon IFN1 As an evasion mechanism virus synthesize proteins that hinder the production IFN1 in the pathway
RA also acts directly on macrophages at both mucosal sites and other immunological sites AtRA modulates peritoneal macrophage activation by endotoxin and IFN-γ by suppressing TNF production and nitric oxide NO synthesis In addition at RA inhibits the expression of PGE2 and COX-2 and the release of TNF which are induced by bacterial lipopolysaccharide LPS in murine peritoneal macrophages
A study reported recently that substance ATRA have preventive effects on pulmonary fibrosis by inhibiting IL-6-dependent proliferation and TGF-β1-dependent trans differentiation of lung fibroblasts Also another studies demonstrated that 13-cis-retinoic acid and other retinoid analogs inhibit IL-1-induced IL-6 production and that this effect is analog-specific and at least partially transcriptionally mediated This effect was dose-dependent with an IC50 of 10-7 M RA and significant inhibition being noted with doses of RA as low as 10-8 M IL-10 production was inhibited by ATRA administration
A study demonstrated that TLR3-- TLR4-- and TRAM-- mice are more susceptible to SARS-CoV than wild-type mice but experience only transient weight loss with no mortality in response to infection In contrast mice deficient in the TLR3TLR4 adaptor TRIF are highly susceptible to SARS-CoV infection showing increased weight loss mortality reduced lung function increased lung pathology and higher viral titers New studies showed that the high level of IFN-αβ produced from the TLR3-IRF3IRF7 pathway and IFN-β is the reason for inhibiting DENV replication 13Cis retinoic Acid induced significant upregulation of toll-like receptor 3 TLR3 resulting in an immune response to dsRNA intermediate which can be partially generated during CoV-2 replicationTLR3 sensitized by dsRNA and cascades of signaling pathways IRFs and NFκB activation respectively are activated to produce type I IFNs The production of type I IFNs is important to enhance the release of antiviral proteins for the protection of uninfected cells Sometimes accessory proteins of CoV can interfere with TLR3 signaling and bind the dsRNA of CoV during replication to prevent TLR3 activation and evade the immune response 13Cis retinoic Acid induced significant upregulation of toll-like receptor 3 TLR3 mitochondrial antiviral-signaling protein MAVS and retinoid-induced gene I RIG-I and IFN regulatory factor 1 expression in a time-dependent
In further research Tsai and Chen showed the high level of IFN-αβ produced from the TLR3-IRF3IRF7 pathway and IFN-β is the reason for inhibiting DENV replication In HUH-7 cells huTLR3 can recognize DENV-1 and induce the expression of IFN-β which can enhance the expression of huTLR3 on the contrary TLR3 also induces type I IFN during WNV
Doctors treating the sickest Covid-19 patients have zeroed in on a new phenomenon Some people have developed widespread blood clots their lungs peppered with tiny blockages that prevent oxygen from pumping into the bloodstream and bodyAs with so much else about the Covid-19 response health experts are learning about the symptom on the fly Blood clots are common in patients who are immobilized but they seem to be smaller and cause far more severe damage in some Covid-19 patients Doctors have said they see patients with blood clots forming not only in their lungs but also in blood vessels Autopsies have also revealed blood clots in kidneys and other organs which some experts say suggests an overwhelming immune system response to the virus that inflicts harm on the body
Retinoic acid is known to possess in vivo anti-inflammatory anti-platelet and fibrinolytic activities A study investigated the in vitro thrombin and platelet aggregation inhibitory activities of retinoic acid and retinaldehydeRetinoic acid retinaldehyde and retinol exhibited potent inhibition of thrombin with IC50 values of 67μgml 74μgml and 152μgml respectively for the inhibition of thrombin Sigma and 49μgml 74μgml and 178μgml respectively for the inhibition of thrombin plasma Amongst vitamin A and its derivatives retinoic acid showed the highest inhibition of both the forms of thrombin
Isotretinoin13cis RA may be able to inhibit COVID 2019 infection via reversIing the androgenic induction and activation effect of DHT on TMPRSS2 expression and helps to prevent cleaving and activating both the spike protein S of COVID 2019 and the viral receptor and this is discussed as follow
TMPRSS2 is both the most frequently altered gene in primary prostate cancer and a critical factor enabling cellular infection by coronaviruses including SARS-CoV-2 The modulation of its expression by steroids could contribute to the male predominance of severe infections and given that TMPRSS2 has no known indispensable functions and inhibitors are available it is an appealing target for prevention or treatment of respiratory viral infections
TMPRSS2 a key regulator in prostate cancerTMPRSS2 was first identified in prostate cancer shortly after the gene had been originally cloned Prostate cancer cell lines strongly upregulated TMPRSS2 expression in response to androgens TMPRSS2 is expressed on the luminal side of the prostate epithelium and its expression is increased in prostate cancer tissue compared to non-cancerous prostate tissue Notably the TMPRSS2 gene is a partner in one of the most common gene fusion eventsin solid tumors somatic gene rearrangements involving TMPRSS2 witha member of the ETS family of oncogenic transcription factors most commonly ERG This fusion occurs in approximately 50 of primary prostate cancers among men of European ancestryWhile ERG is not normally regulated by androgen the gene fusion juxtaposes the androgen receptor regulatory elements of TMPRSS2 with the ERG gene The ERG gene is consequently controlled by androgen receptor signaling and expressed highly in prostate cancers harboring the TMPRSS2 ERG fusion Intriguingly the prevalence of the TMPRSS2 ERG fusion is lower in prostate tumors of both black and Asian men The relevance of this to the current COVID-19 pandemic is unclearTMPRSS2 ERG fusion- cancers also have a distinct set of risk factors related to hormonal signaling For example men with higher genetically determined transcriptional activity of the androgen receptor have a higher risk of TMPRSS2 ERG fusion-positive prostate cancer but not of fusion-negative prostate cancer
TMPRSS2 is an androgen receptor signaling target gene and an androgen-regulated cell-surface serine protease expressed predominantly in prostate and lung epithelial cell TMPRSS2 is normally expressed several fold higher in the prostate relative to any other human tissue though the normal physiological functions remains unknown Importantly unlike other TTSPs TMPRSS2 transcription is regulated by androgenic ligands and the androgen receptor AR There is a positive correlation between AR and TMPRSS2 in microdissected primary tumor epithelium r2 039 p 0001
Dihydrotestosterone DHT significantly and dramatically induced the expression of TMPRSS2 protein with two molecular masses of 60 full-length and 38 kDa N-terminus in a dose responsive manner
Data from Chinese outbreak show death rates for men almost 50 per cent higher than for women show that Early research from China suggests women and children are less likely to die than men if they catch the coronavirus Death rates for Covid-19 the disease those infected with the coronavirus develop are low for everyone only 24 per cent of the 44672 people in the Chinese study died But although roughly even numbers of men and women catch the disease men are more likely to develop such a serious case of Covid-19 they die
More than 70 percent of Italys coronavirus deaths have been among men but scientists there admit they are mystified by the gender gap At least 3400 people in Italy have died of the devastating disease - it yesterday announced it had a higher death Toll than China - but less than 1000 of them have been women Men are also more likely to pick up the infection in the first place and account for 60 percent of confirmed cases according to Italys public health research agency An earlier analysis found that 80 per cent of the deaths were in men and just 20 per cent were in women - but the gap has narrowed over time
According to this data the principal investigator thinks that there is a strong relation between high mortality in males and androgenic effect specifically the effect of DHT on TMPRSS2 protein which is used by covid 2019 in cell invasion and entry and depending on this data related to six hormones specifically DHT The investigator was able to discover whey women and children less likely to die from illness than men So the investigator divided infected patients according to their six hormone because TMPRSS2 is an androgen-regulated cell-surface serine protease expressed predominantly in prostate and lung epithelial cell TMPRSS2
AndrogenDHT potential effect on TMPRSS2 expression in children is less than its effect in females and males followed by viral severity and vigrousity in men compared with children and women
Androgen DHT potential effect on TMPRSS2 expression in females is less than in males followed by viral severity and vigrousity in men compared with females
So the principal investigator thinks that when some researchers investigated the role of sex steroids in SARS-CoV pathogenesis by comparing gonadectomized and control counterparts after infection Gonadectomy or treatment with flutamide a non-steroidal anti-androgen did not affect morbidity and mortality in male mice following lethal MA15 infection They may be were wrong in their conclusions in suggesting that androgens do not play a role in SARS-CoV pathogenesis because Gonadectomy or treatment with flutamide will not completely affect or inhibit DHT and its derivatives5α-Androstan-3α17β-Diol concentration in tissues and blood because after inhibiting testosterone with flutamide the pathway of DHT formation will be activated to compensate the inhibited testosterone levels so the TMPRSS2 expression will be significantly induced by DHT and the treated animals will not be affected in case of flutamide treatment but in case of Gonadectomy the expression of TMPRSS2 will be decreased by DHT inhibition only if along time has passed on Gonadectomy in order to make sure that DHT and its derivatives completely declined in levels that will not allow it to affect on expression of TMPRSS2 and in female mice after blocking estrogen receptors it died because increasing formation of androgenic hormones
A study demonstrated that 13- cis -Retinoic acid competitively and reversibly inhibits Dihydrotestosterone So the principal investigator expects a significant modulation of TMPRSS2 expression after treating with 13- cis -Retinoic acid via temporary preventing the effect of dihydrotestosteroneDHT on TMPRSS2 promoting and expression And the type II transmembrane serine proteases TMPRSS2 which can cleave and activate the spike protein S of the severe acute respiratory syndrome coronavirus SARS-CoV for membrane fusion In addition these proteases cleave the viral receptor the carboxypeptidase angiotensin-converting enzyme 2 ACE2 and it was proposed that ACE2 cleavage augments viral infectivity
A study demonstrated that COVID-19 reduces testosterone levels in men by altering the functioning of the gonads So could the increased severity of the disease in men be due to lowered testosterone But according to the principal investigator explanation COVID-19 reduces testosterone levels because there is a dramatic reductions in the cholesterol levels of patients infected with COVID 19 compared with healthy controls Cholesterol levels decline quite rapidly during the early stages of infection and increase as the patient starts to recoverTherefore indicating that cholesterol may have an important role to play in defending the body against such infections and depending on the principal investigator explanation Testosterone is synthesized starting from cholesterol through a well-characterized steroid biosynthetic pathway involving the sequential action of multiple enzymes So when cholesterol levels are decreased this decrease will followed by decreasing in testosterone level and according to this explanation testosterone therapy in COVID 2019 is not recommended but temporary inhibitor of DHT is recommended such as Isotretinoin because this treatment by testosterone will inhibit cholesterol synthesis by feedback inhibition and decrease cholesterol uptake by Leydig cells in testis and this also will lead to over increase in DHT lvels and its derivatives in different tissues which will induce TMPRSS2 because DHT is a potent activator of TMPRSS2 and this will be followed by processing and activation of COVID2019 spike protein to bined its ACE2 receptors in lung and kidney leading to their damage specifically in testis because it contains high levels of proteases and ACE2 Serine proteases are emerging as important contributors to the production maturation and functional competence of spermatozoa
Depending on this data and according to this protocol The principal investigator expects and suggests that retinoic acid is specific modulator of androgens specifically DHT not testosterone and could reverse the androgenic induction and activation effect of DHT on TMPRSS2 expression and prevent cleaving and activating both the spike protein S of COVID 2019 and the viral receptor the carboxypeptidase angiotensin-converting enzyme 2 ACE2 All ideas and michanisms specifically role of Androgen in TMPRSS2 activation in COVID-19 Serendipity or opportunity for intervention and the inhibition of ACE2 AT1 protein and Ang II-mediated intracellular calcium release pathway which is responsible for SARS-CoV-2 cell fusion and entry included in the research protocol were submitted to Academy of scientific research and technology - Egypt- on 1 April 2020 in Call no 22019ASRT- Ideation Fund
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Promising features of COVID 2019 treatment according Principal Investigator Protocol
1 This medication have the feature of Aerosolized Drug Delivery to increase its efficacy beside Oral administration Which makes it distinct from other medication in which should dose be only given orally A study demonstrated that treating with 13 cis retinoic acid aerosolized via inhalation rout did not cause any damage in lung cells Repeated high doses of 13 cis retinoic by inhalation resulted in moderate loss of body weight but microscopic investigation of ten tissues including lung and oesophagus did not detect any significant aerosol-induced damage The results suggest that administration of isotretinoin via powder aerosol inhalation is probably superior to its application via the oral route in terms of achieving efficacious drug concentrations in the lung
2 Inhaled isotretinoin might provide sufficient drug to the target cells for efficacy while avoiding systemic toxicity
3 A study demonstrated that 13 cis retinoic is used in treating Emphysema emphysema is a lung condition that causes shortness of breath
4 ATRA has been reported to induce formation of new alveoli and returns elastic recoil in the lung to approximately normal values in animal models of emphysema
5 Strong expectation of complete COVID 2019 blockade from cell entry and infection depending on strong ethics researches and references
6 Availability of our compounds
7 Ease of application
8 Expectation of COVID 2019 treating of by more than one distinct mechanism
9 Expectation of High induction of anti- inflammatory T cells and significant inhibition of IL-6 at low concentrations
10 Controlling Accompanying cytokine storm
11 No interactions with Egyptian protocol drugs were found
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
True
Is an FDA AA801 Violation?:
None