- SARS-CoV-2 reservoir in post-acute sequelae of COVID-19 (PASC)
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SARS-CoV-2 reservoir in post-acute sequelae of COVID-19 (PASC)
Nature Immunology Sept 2023 https://doi.org/10.1038/s41590-023-01601-2
Amy D. Proal, Michael B. VanElzakker, Soo Aleman, Katie Bach, Brittany P. Boribong, Marcus Buggert, Sara Cherry, Daniel S. Chertow, Helen E. Davies, Christopher L. Dupont, Steven G. Deeks, William Eimer, E. Wesley Ely, Alessio Fasano, Marcelo Freire, Linda N. Geng, Diane E. Griffin, Timothy J. Henrich, Akiko Iwasaki, David Izquierdo-Garcia, Michela Locci, Saurabh Mehandru, Mark M. Painter, Michael J. Peluso, …E. John WherryTable of Contents
Millions of people are suffering from Long COVID or post-acute sequelae of COVID-19 (PASC). Several biological factors have emerged as potential drivers of PASC pathology. Some individuals with PASC may not fully clear the coronavirus SARS-CoV-2 after acute infection. Instead, replicating virus and/or viral RNA—potentially capable of being translated to produce viral proteins—persist in tissue as a ‘reservoir’. This reservoir could modulate host immune responses or release viral proteins into the circulation. Here we review studies that have identified SARS-CoV-2 RNA/protein or immune responses indicative of a SARS-CoV-2 reservoir in PASC samples. Mechanisms by which a SARS-CoV-2 reservoir may contribute to PASC pathology, including coagulation, microbiome and neuroimmune abnormalities, are delineated. We identify research priorities to guide the further study of a SARS-CoV-2 reservoir in PASC, with the goal that clinical trials of antivirals or other therapeutics with potential to clear a SARS-CoV-2 reservoir are accelerated.
Locations in the body
Research suggesions
Major areas of opportunity for research into a SARS-CoV-2 reservoir in PASC
- Which PASC cell and tissue types harbor SARS-CoV-2 RNA or protein?
- Is there a preference for persistence in certain cell or tissue types?
- Is SARS-CoV-2 RNA identified in PASC samples transcriptionally active, translating, replicating or infectious?
- Is the presence of a SARS-CoV-2 reservoir sufficient to drive PASC symptoms?
- Are SARS-CoV-2 RNA and proteins also identified in samples collected from post-COVID-19 individuals without PASC?
- If yes, what factors differentiate SARS-CoV-2 persistence in PASC from persistence in asymptomatic individuals?
- Do particular classes of symptoms tend to be driven by the location of the reservoir—for example, dyspnea from a lung reservoir or gastrointestinal symptoms from a gut reservoir?
- Do measurements of SARS-CoV-2 protein or antibody responses in body fluids correlate with SARS-COV-2 persistence in tissue?
- Can the transcriptional program of circulating immune cells be used as a biosensor of SARS-CoV-2 persistence in tissue?
- Does T cell exhaustion correlate with SARS-CoV-2 persistence in PASC?
- Are neutralizing antibody responses qualitatively different in patients with PASC?
- By what mechanisms can SARS-CoV-2 evade immune detection?
- Do such mechanisms differ by cell or tissue type, or by viral variant?
- Do viral mutations and selection contribute to persistence?
- Can the spike protein travel via EVs into the bloodstream?
- Does a SARS-CoV-2 reservoir or protein contribute to fibrin/ amyloid microclotting, platelet activation or related vasculature issues in PASC?
- Does a SARS-CoV-2 reservoir in PASC correlate with the reactivation of other pathogens such as herpesviruses?
- Does a SARS-CoV-2 reservoir in PASC correlate with changes in human endogenous retrovirus activity?
- Can a SARS-CoV-2 reservoir alter the local transcriptome or epigenome?
- Does a SARS-CoV-2 reservoir in PASC correlate with the disruption of microbiome composition or activity?
- If so, is disruption a cause or consequence of PASC?
- Is a SARS-CoV-2 reservoir associated with host epithelial barrier breakdown in PASC?
- Does this facilitate the translocation viral protein or bacterial/fungal organisms into blood?
- Can SARS-CoV-2 persistence or the reactivation of other latent pathogens lead to cross-reactive antibody responses in PASC blood or tissue?
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69+ VitaminDWiki pages have LONG-HAUL or LONG-COVID in the title
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VitaminDWiki comment: Virus protects itself by turning off the Vitamin D Receptor - which can be easily turned back on
VitaminDWiki -
37 studies in both categories Virus and Vitamin D Receptor This list is automatically updated
- Vitamin D preventing and treating COVID - 30,000 publications – Oct 2024
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- Long-COVID is now the biggest COVID concern - many studies
- COVID death 12X more likely if poor Vitamin D Receptor (less D gets to cells) - many studies
- COVID severity, ICU, and mortality all associated with poor vitamin D receptor (but not D, everyone had low D) -Dec 2021
- Different Vitamin D Receptor problems cause different COVID problems - Dec 2021
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- COVID-19 symptoms and comorbidities associated with the type of Vitamin D Receptor – Oct 2021
- Enveloped virus infection (RSV, coronavirus, HIV, etc.) 1.5X more likely if poor Vitamin D Receptor – meta-analysis Dec 2018
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- A virus that most adults have (Cytomegalovirus) decreases the amount of Vitamin D which gets to the cells – Jan 2017
- COVID virus alters the activation of 100 vitamin D related genes in the lung – April 2021
- Common sense COVID-19 risk reduction - masks, social distancing, vitamin D - Oct 2020
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- Vitamin D Receptor activation should reduce ARDS associated with COVID-19 - June 2020
- Dengue viral production decreased 1000X if activate Vitamin D Receptor (in lab) – July 2020
- Vitamin D, Quercetin, and Estradiol all increase vitamin D in cells and increase genes which reduce COVID-19 – May 21, 2020
- Quercetin and Vitamin D - Allies Against COVID-19
- Risk of enveloped virus infection is increased 50 percent if poor Vitamin D Receptor - meta-analysis Dec 2018
- Hand, foot, and Mouth disease is 14X more likely if poor Vitamin D Receptor – Oct 2019
- Treating herpes reduced incidence of senile dementia by 10 X (HSV1 reduces VDR by 8X) – 2018
- Severe hand, foot, and mouth virus is 2.9 X more likely if poor Vitamin D receptor – Oct 2018
- Hepatitis B virus reduced by 5X the Vitamin D getting to liver cells in the lab – Oct 2018
- Some enveloped virus are 1.2 X more likely if have a poor Vitamin D Receptor -Aug 2018
- Severe Pertussis is 1.5 times more likely if poor vitamin D receptor – Feb 2016
- Dengue Fever associated with poor vitamin D receptor – July 2002
- Dengue virus 2X to 4X more likely if vitamin D receptor gene problems
VitaminDWiki - Vitamin D Receptor activation can be increased in 14 ways
Resveratrol, Omega-3, Magnesium, Zinc, Quercetin, non-daily Vit D, Curcumin, intense exercise, Butyrate Ginger, Essential oils, etc Note: The founder of VitaminDWiki uses 10 of the 14 known VDR activators
Long-COVID can hide in the body for years in scores of locations – Sept 20237082 visitors, last modified 09 Sep, 2023, This page is in the following categories (# of items in each category)Attached files
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