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Relationship of Heterologous Virus Responses and Outcomes in Hospitalized COVID-19 Patients.
Rosenberg-Hasson, Yael; Holmes, Tyson H; Diray-Arce, Joann; Chen, Jing; Kellogg, Ryan; Snyder, Michael; Becker, Patrice M; Ozonoff, Al; Rouphael, Nadine; Reed, Elaine F; Maecker, Holden T.
Afiliación
  • Rosenberg-Hasson Y; Institute for Immunity, Transplantation, and Infection, Stanford University School of Medicine, Stanford, CA.
  • Holmes TH; Institute for Immunity, Transplantation, and Infection, Stanford University School of Medicine, Stanford, CA.
  • Diray-Arce J; Clinical & Data Coordinating Center, Precision Vaccines Program, Boston Children's Hospital, Boston, MA.
  • Chen J; Clinical & Data Coordinating Center, Precision Vaccines Program, Boston Children's Hospital, Boston, MA.
  • Kellogg R; Research Computing, Department of Information Technology, Boston Children's Hospital, Boston, MA.
  • Snyder M; Department of Genetics, Stanford University School of Medicine, Stanford, CA.
  • Becker PM; Department of Genetics, Stanford University School of Medicine, Stanford, CA.
  • Ozonoff A; National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD.
  • Rouphael N; Clinical & Data Coordinating Center, Precision Vaccines Program, Boston Children's Hospital, Boston, MA.
  • Reed EF; Emory University, Atlanta, GA.
J Immunol ; 211(8): 1224-1231, 2023 10 15.
Article en En | MEDLINE | ID: mdl-37756530
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.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Virus Sincitial Respiratorio Humano / Infecciones por Citomegalovirus / Gripe Humana / COVID-19 Tipo de estudio: Observational_studies Límite: Humans Idioma: En Revista: J Immunol Año: 2023 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Virus Sincitial Respiratorio Humano / Infecciones por Citomegalovirus / Gripe Humana / COVID-19 Tipo de estudio: Observational_studies Límite: Humans Idioma: En Revista: J Immunol Año: 2023 Tipo del documento: Article
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