Hospitalized patients with COVID-19 were found to have higher TMPRSS-2 and P450 aromatase levels and lower testosterone levels, suggesting that TMPRSS2, testosterone, and P450 aromatase can be used as markers of poor prognosis or increased disease severity in COVID-19.
Acute COVID-19, Long COVID, Post COVID-vaccination Syndrome & Other body systems-Clinical Studies
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SARS-CoV-2 antigens can persist in plasma for up to 14 months after acute infection
Analysis of temporal antigen profiles, performed by collecting blood samples at multiple time points, revealed that the prevalence of SARS-CoV-2 plasma antigens was 10.6% 3-6 months after the onset of COVID-19, 8.7% after 6-10 months and 5.4% after 10-14 months.
The persistence of residual SARS-CoV-2 RNA or proteins in different tissue samples four months after infection
This study showed the persistence of SARS-CoV-2 nucleic acid in solid tissue samples from various organs, including lung, liver, kidney, stomach, intestine, brain, breast, thyroid, blood vessels, and skin, in patients who had recovered from mild COVID-19 at one month, two months, and four months post-infection.
Other Entries
De novo onset or exacerbation of psoriasis following the SARS-CoV-2 infection or COVID-19 vaccination
This study described a case series of 28 patients who experienced de novo onset or flares of psoriasis following infection with the SARS-CoV-2 or vaccination. All of these patients were successfully managed with anti-IL-17 or anti-IL-23 medications.
Tuberculous pericarditis with tamponade in COVID-19
These case reports presented individuals who were diagnosed with COVID-19 and who developed tuberculous pericarditis with tamponade.
SARS-CoV-2 RNA and antigens were detected in the appendix and breast tissues of two post-COVID patients 426 and 175 days after the onset of acute SARS-CoV-2 infection
This study investigated the presence of residual SARS-CoV-2 RNA and antigens in tissues of two patients diagnosed with post-COVID syndrome.Â
Various time modes of proteomic recovery within two years after acute COVID-19Â
The results showed that different biological processes recovered in different time modes within two years after COVID-19, providing insights into the biological processes of the different long COVID syndrome phenotypes.
50% of vaccinated individuals were found to have circulating fragments of recombinant S protein 2–6 months after vaccination
50% of subjects who received mRNA-based vaccines had specific fragments of recombinant S protein in their blood samples 2–6 months after vaccination.
Circulating HERV-W envelope proteins and elevated levels of anti-SAR-CoV-2 IgE antibodies were detected in patients with post-COVID syndrome one year after the acute infection
HERV-W ENV protein was expressed in 58% of plasma samples of post-COVID patients, long after the acute SARS-CoV-2 infection was resolved .75% of post-COVID patients had elevated levels of anti-S and anti-N IgE antibodies compared to pre-pandemic controls.
Leprosy following COVID-19 vaccination
This study investigated leprosy or immune-mediated complications known as leprosy reactions diagnosed in the Leprosy Clinic at the Hospital for Tropical Diseases, London, within 12 weeks following COVID-19 vaccination.
HERV-W envelope proteins detected in plasma, blood cells and postmortem tissues of severe COVID-19 patients could serve as biomarkers of COVID-19 severity
SARS-CoV-2 can induce the expression of the HERV-W envelope proteins, suggesting their involvement in COVID-19-associated pathology.
A case series of Stevens-Johnson syndrome/toxic epidermal necrolysis associated with SARS-CoV-2 infection and COVID-19 vaccination
The largest case series of Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) associated with SARS-CoV-2 infection and COVID-19 vaccination.
129Xe MRI red blood cells-to-alveolar tissue barrier ratio shows abnormal gas exchange in long COVID patients
A lower 129Xe MRI RBC-to-barrier ratio in long COVID patients suggests that SARS-CoV-2 infection may have caused some microstructural abnormality to one or two volumes, such as pulmonary embolism, pulmonary blood flow alterations, or alveolar membrane thickening, which leads to decreased blood volume.