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BREAKING NEWS
Source: Long-COVID Research  Dec 10, 2021  2 years, 3 months, 1 week, 1 day, 10 hours, 48 minutes ago

BREAKING! Ongoing U.S. Study Shows Persistence of SARS CoV-2 S1 Protein in CD16+ Monocytes in Post-Acute Sequelae of COVID-19 Up to 15 Months Post-Infection!

BREAKING! Ongoing U.S. Study Shows Persistence of SARS CoV-2 S1 Protein in CD16+ Monocytes in Post-Acute Sequelae of COVID-19 Up to 15 Months Post-Infection!
Source: Long-COVID Research  Dec 10, 2021  2 years, 3 months, 1 week, 1 day, 10 hours, 48 minutes ago
Long-COVID Research: An ongoing study by American researchers have alarmingly found the persistence of SARS CoV-2 spike 1 protein in CD16+ monocytes in Post-Acute Sequelae of COVID-19 (PASC) up to 15 Months post infection!

 
The study team from IncellDx Inc-USA, Lawrence General Hospital-Massachusetts, 3Bio-Rad-USA, Langone Medical Center-New York University-USA, Universidad de Costa Rica-Costa Rica, Avrok Laboratories Inc-USA and Oregon Health and Science University-USA published their preliminary findings as an abstract in the peer reviewed journal: Frontiers in Immunology. https://www.frontiersin.org/articles/10.3389/fimmu.2021.746021/abstract
 
The detailed study findings will shortly be published.
 
The ongoing COVID-19 pandemic is a treatment challenge in the acute infection stage but the recognition of chronic COVID-19 symptoms termed post-acute sequelae SARS-CoV-2 infection (PASC) or commonly referred to as Long COVID may affect up to 30% of all infected individuals.
 
The underlying mechanism and source of this distinct immunologic condition three months or more after initial infection remains elusive.
 
The study team investigated the presence of SARS-CoV-2 S1 protein in 46 individuals.
 
The Long-COVID Research study team analyzed T-cell, B-cell, and monocytic subsets in both severe COVID-19 patients and in patients with post-acute sequelae of COVID-19 (PASC).
 
Alarmingly the levels of both intermediate (CD14+, CD16+) and non-classical monocyte (CD14Lo, CD16+) were significantly elevated in PASC patients up to 15 months post-acute infection compared to healthy controls (P=0.002 and P=0.01, respectively).
 
More shockingly, a statistically significant number of non-classical monocytes contained SARS-CoV-2 S1 protein in both severe (P=0.004) and PASC patients (P=0.02) out to 15 months post-infection.
 
Non-classical monocytes were sorted from PASC patients using flow cytometric sorting and the SARS-CoV-2 S1 protein was confirmed by mass spectrometry. Cells from 4 out of 11 severe COVID-19 patients and 1 out of 26 PASC patients contained ddPCR+ peripheral blood mononuclear cells, however, only fragmented SARS-CoV-2 RNA was found in PASC patients. No full-length sequences were identified, and no sequences that could account for the observed S1 protein were identified in any patient.
 
It should be noted that non-classical monocytes are capable of causing inflammation throughout the body in response to fractalkine/CX3CL1 and RANTES/CCR5.
 
The study findings have alarming implications and more details are expected once the full study is published.
 
Thailand Medical News will provide further updates on the study findings.
 
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