A mathematical model of SARS‐CoV‐2 immunity predicts paxlovid rebound

Author:

Ranard Benjamin L.12ORCID,Chow Carson C.3,Megjhani Murad2,Asgari Shadnaz45,Park Soojin267,Vodovotz Yoram891011

Affiliation:

1. Division of Pulmonary, Allergy, and Critical Care Medicine, Department of Medicine, Columbia University Vagelos College of Physicians and Surgeons Columbia University/Columbia University Irving Medical Center/NewYork‐Presbyterian New York USA

2. Program for Hospital and Intensive Care Informatics, Department of Neurology Columbia University Vagelos College of Physicians and Surgeons New York USA

3. Mathematical Biology Section, Laboratory of Biological Modeling National Institute of Diabetes and Digestive and Kidney Diseases Bethesda Maryland USA

4. Department of Biomedical Engineering California State University Long Beach California USA

5. Department of Computer Engineering and Computer Science California State University Long Beach California USA

6. Department of Neurology & Division of Critical Care and Hospitalist Neurology, Columbia University Vagelos College of Physicians and Surgeons Columbia University/Columbia University Irving Medical Center/NewYork‐Presbyterian New York USA

7. Department of Biomedical Informatics, Columbia University Vagelos College of Physicians and Surgeons Columbia University/Columbia University Irving Medical Center/NewYork‐Presbyterian New York USA

8. Department of Surgery University of Pittsburgh Pittsburgh Pennsylvania USA

9. Department of Immunology University of Pittsburgh Pittsburgh Pennsylvania USA

10. Center for Inflammation and Regeneration Modeling, McGowan Institute for Regenerative Medicine University of Pittsburgh Pittsburgh Pennsylvania USA

11. Center for Systems Immunology University of Pittsburgh Pittsburgh Pennsylvania USA

Abstract

AbstractNirmatrelvir/ritonavir (Paxlovid), an oral antiviral medication targeting SARS‐CoV‐2, remains an important treatment for COVID‐19. Initial studies of nirmatrelvir/ritonavir were performed in SARS‐CoV‐2 unvaccinated patients without prior confirmed SARS‐CoV‐2 infection; however, most individuals have now either been vaccinated and/or have experienced SARS‐CoV‐2 infection. After nirmatrelvir/ritonavir became widely available, reports surfaced of “Paxlovid rebound,” a phenomenon in which symptoms (and SARS‐CoV‐2 test positivity) would initially resolve, but after finishing treatment, symptoms and test positivity would return. We used a previously described parsimonious mathematical model of immunity to SARS‐CoV‐2 infection to model the effect of nirmatrelvir/ritonavir treatment in unvaccinated and vaccinated patients. Model simulations show that viral rebound after treatment occurs only in vaccinated patients, while unvaccinated (SARS‐COV‐2 naïve) patients treated with nirmatrelvir/ritonavir do not experience any rebound in viral load. This work suggests that an approach combining parsimonious models of the immune system could be used to gain important insights in the context of emerging pathogens.

Funder

Agency for Healthcare Research and Quality

National Institute of Diabetes and Digestive and Kidney Diseases

Publisher

Wiley

Subject

Infectious Diseases,Virology

Reference18 articles.

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3. Covid-19: Pfizer’s paxlovid is 89% effective in patients at risk of serious illness, company reports

4. US Department of Health & Human Services. Biden Administration Secures 10 Million Courses of Pfizer's COVID‐19 Oral Antiviral Medicine as Additional Tool to Reduce Hospitalizations and Save Lives.2021. Accessed June 6 2022. https://www.hhs.gov/about/news/2021/11/18/biden-administration-secures-10-million-courses-pfizers-covid-19-oral-antiviral-medicine-as-additional-tool-reduce-hospitalizations-save-lives.html

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