Relationship of Heterologous Virus Responses and Outcomes in Hospitalized COVID-19 Patients.


Journal

Journal of immunology (Baltimore, Md. : 1950)
ISSN: 1550-6606
Titre abrégé: J Immunol
Pays: United States
ID NLM: 2985117R

Informations de publication

Date de publication:
15 10 2023
Historique:
received: 08 06 2023
accepted: 14 08 2023
pmc-release: 15 10 2024
medline: 29 9 2023
pubmed: 27 9 2023
entrez: 27 9 2023
Statut: ppublish

Résumé

The clinical trajectory of COVID-19 may be influenced by previous responses to heterologous viruses. We examined the relationship of Abs against different viruses to clinical trajectory groups from the National Institutes of Health IMPACC (Immunophenotyping Assessment in a COVID-19 Cohort) study of hospitalized COVID-19 patients. Whereas initial Ab titers to SARS-CoV-2 tended to be higher with increasing severity (excluding fatal disease), those to seasonal coronaviruses trended in the opposite direction. Initial Ab titers to influenza and parainfluenza viruses also tended to be lower with increasing severity. However, no significant relationship was observed for Abs to other viruses, including measles, CMV, EBV, and respiratory syncytial virus. We hypothesize that some individuals may produce lower or less durable Ab responses to respiratory viruses generally (reflected in lower baseline titers in our study), and that this may carry over into poorer outcomes for COVID-19 (despite high initial SARS-CoV-2 titers). We further looked at longitudinal changes in Ab responses to heterologous viruses, but found little change during the course of acute COVID-19 infection. We saw significant trends with age for Ab levels to many of these viruses, but no difference in longitudinal SARS-CoV-2 titers for those with high versus low seasonal coronavirus titers. We detected no difference in longitudinal SARS-CoV-2 titers for CMV seropositive versus seronegative patients, although there was an overrepresentation of CMV seropositives among the IMPACC cohort, compared with expected frequencies in the United States population. Our results both reinforce findings from other studies and suggest (to our knowledge) new relationships between the response to SARS-CoV-2 and Abs to heterologous viruses.

Identifiants

pubmed: 37756530
pii: 265884
doi: 10.4049/jimmunol.2300391
pmc: PMC10539027
mid: NIHMS1926113
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

1224-1231

Subventions

Organisme : NCI NIH HHS
ID : R33 CA094304
Pays : United States
Organisme : NIAID NIH HHS
ID : U19 AI057229
Pays : United States

Informations de copyright

Copyright © 2023 by The American Association of Immunologists, Inc.

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Auteurs

Yael Rosenberg-Hasson (Y)

Institute for Immunity, Transplantation, and Infection, Stanford University School of Medicine, Stanford, CA.

Tyson H Holmes (TH)

Institute for Immunity, Transplantation, and Infection, Stanford University School of Medicine, Stanford, CA.

Joann Diray-Arce (J)

Clinical & Data Coordinating Center, Precision Vaccines Program, Boston Children's Hospital, Boston, MA.

Jing Chen (J)

Clinical & Data Coordinating Center, Precision Vaccines Program, Boston Children's Hospital, Boston, MA.
Research Computing, Department of Information Technology, Boston Children's Hospital, Boston, MA.

Ryan Kellogg (R)

Department of Genetics, Stanford University School of Medicine, Stanford, CA.

Michael Snyder (M)

Department of Genetics, Stanford University School of Medicine, Stanford, CA.

Patrice M Becker (PM)

National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD.

Al Ozonoff (A)

Clinical & Data Coordinating Center, Precision Vaccines Program, Boston Children's Hospital, Boston, MA.

Nadine Rouphael (N)

Emory University, Atlanta, GA.

Elaine F Reed (EF)

University of California Los Angeles, Los Angeles, CA.

Holden T Maecker (HT)

Institute for Immunity, Transplantation, and Infection, Stanford University School of Medicine, Stanford, CA.

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