A new study aimed to determine if persistent inflammation and ongoing T-cell activation during convalescence were a contributing factor to the pathogenesis of #LongCovid 1/
Researchers followed 52 individuals with #LongCovid. They isolated peripheral blood mononuclear cells, and stained for multiple T cell activation markers. The activation states of participants’ CD4+ and CD8+ T-cells were also analyzed for each of the persistent symptoms 2/
Overall, the researchers found that participants with persistent symptoms had significantly higher levels of inflammation at multiple time points during convalescence when compared to those who fully recovered from COVID-19. 3/
They find CD8+ T-cell activation following SARS-CoV-2 infection in adults experiencing post-acute sequelae of COVID-19 and that the increase in T regulatory cells for a subset of these patients represents the ongoing attempt by the host to reduce inflammation. 4/
People w/ persistent dyspnea, forgetfulness, confusion & chest pain had significantly higher levels of effector T-cells (CD8+Ki67+) & those with chest pain, joint pain, difficulty concentrating, & forgetfulness had higher levels of regulatory T-cells (CD4+CD25+). 5/
Additionally, those with dyspnea had significantly higher levels of CD8+CD38+, CD8+ Granzyme B+, and CD8+IL10+ cells. 6/
A retrospective comparison of acute phase inflammatory markers in adults with & without #LongCovid showed that CD8+Ki67+ cells were significantly higher at the time of acute illness (up to 14 days post-diagnosis) in those who developed persistent dyspnea. 7/
Conclusions:
1-Persistently elevated inflammatory T cell markers may contribute to the development and progression of multiple #LongCovid symptoms. 8/
2-Continued CD8+ T-cell activation following SARS-CoV-2 infection in adults experiencing #LongCovid and that the increase in T regulatory cells for a subset of these patients represents the ongoing attempt by the host to reduce inflammation. 9/
3-Chronic inflammation is a risk factor for other chronic conditions, such as cardiovascular, cerebrovascular, or autoimmune disease, which heightens the significance of follow up investigation with this cohort 10/
4-The data from this study support a growing body of evidence associating PASC with persistent inflammation & immune dysregulation as early predictors of disease & warrant attention towards appropriate therapeutics and interventions for the prevention and treatment of PASC. 11/
Among all types of Covid19 vaccines, inactivated viral vaccines are the cheapest and have been used widely in India and China. Covid19 inactivated viral vaccines use the whole virus particle, which contains many non-capsid proteins that may cause adverse immune responses. 1/
Studies have shown that ADP-ribose-binding domains of #NSP3 protein of SARS-CoV-2 and human poly(ADP-ribose) polymerase family member 14 (#PARP14) share a significant degree of homology. 2/
In a new study, researchers further show that antibodies against NSP3 of SARS-CoV-2 can bind human PARP14 protein. These antibodies can cross-react with human skeletal muscle cells and astrocytes, but not human embryonic kidney 293T cells. 3/
A new study finds that human coronavirus OC43 infection can elicit polyfunctional CD8+ and CD4+ effector T cells that cross-react with SARS-CoV-2 peptides. Furthermore, pre-exposure to OC43 reduces subsequent SARS-CoV-2 infection and disease in the lung. 1/
Depletion of CD4+ T cells in transgenic mice with prior OC43 exposure results in increased viral burden in the lung but no change in virus-induced lung damage following infection with SARS-CoV-2 (versus CD4+ T cell-sufficient mice). 2/
This demonstrates that the OC43-elicited SARS-CoV-2 cross-reactive T cell-mediated cross-protection against SARS-CoV-2 is partially dependent on CD4+ T cells. 3/
There has been a lot of debate on the exact role of T cells in controlling Covid19 disease and their importance in halting virus replication within the respiratory tract during SARS-CoV-2 infection. 1/
In a new study, researchers used mice infected with a naturally occurring SARS-CoV-2 variant (B.1.351) and evaluated the role of T cells in the upper and lower respiratory tract. 2/
Following infection, SARS-CoV-2-specific CD4+ and CD8+ T cells are recruited to the respiratory tract and a vast proportion secrete the cytotoxic molecule Granzyme B. 3/
SARS-CoV-2 s developing a variety of strategies against the human immune system in a "molecular arms race."
Researchers have now discovered various "protective switches" in the coronavirus that shield it from attacks by the immune system. 1/
The researchers identified two previously unknown chemical protective switches in the virus's main "protease"—a crucial protein of the coronavirus. 2/
The most important drug against COVID-19, called Paxlovid, targets this protein. The virus uses its main protease to cut out the other virus proteins in our infected cells, thus driving its own replication. It uses the amino acid cysteine to do this. 3/
Previous studies have pointed to retinal involvement in COVID-19, such as central retinal artery/vein occlusion and acute macular neuroretinopathy, which can directly damage vision 1/
Retinal ganglion cells (RGCs) are particularly susceptible to SARS-CoV-2 infection, which can directly cause acute pathological changes and increase overall retinal thickness due to immune cells infiltration 2/
The viral infection induces a procoagulant state and endothelial inflammation with recruitment of inflammatory cells, resulting in micro-thrombosis and retinal thickening in the early stage. 3/
SARS-CoV-2 infection during pregnancy has been associated with adverse maternal and neonatal outcomes, including increased risk of prematurity, stillbirths, and severe maternal morbidity and mortality. 1/
While estimates of vertical transmission of SARS-CoV-2 from mother to child are low, there is growing concern for long-term neonatal consequences. Several experts have reported cases of infant respiratory distress (RD) among SARS-CoV-2-exposed uninfected (SEU) term neonates. 2/
Prior studies have attributed cases of RD among SEU neonates to maternal hypoxia & multiorgan failure, which increases the risk of premature delivery, a well-studied risk factor for neonatal RD. However, this does not explain the increased cases of RD among term infants 3/