Evidence map›Paper›PMID 37756530›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2023

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

Yael Rosenberg-Hasson, Tyson H Holmes, Joann Diray-Arce, Jing Chen, Ryan Kellogg, Michael Snyder, Patrice M Becker, Al Ozonoff, Nadine Rouphael, Elaine F Reed and 2 more

Abstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Yael Rosenberg-HassonInstitute for Immunity, Transplantation, and Infection, Stanford University School of Medicine, Stanford, CA.
Tyson H HolmesInstitute for Immunity, Transplantation, and Infection, Stanford University School of Medicine, Stanford, CA.
Joann Diray-ArceClinical & Data Coordinating Center, Precision Vaccines Program, Boston Children's Hospital, Boston, MA.ORCID 0000-0003-2183-4269
Jing ChenClinical & Data Coordinating Center, Precision Vaccines Program, Boston Children's Hospital, Boston, MA.
Ryan KelloggDepartment of Genetics, Stanford University School of Medicine, Stanford, CA.
Michael SnyderDepartment of Genetics, Stanford University School of Medicine, Stanford, CA.
Patrice M BeckerNational Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD.ORCID 0000-0002-1170-8587
Al OzonoffClinical & Data Coordinating Center, Precision Vaccines Program, Boston Children's Hospital, Boston, MA.ORCID 0000-0003-4233-5899
Nadine RouphaelEmory University, Atlanta, GA.ORCID 0000-0002-2512-7919
Elaine F ReedUniversity of California Los Angeles, Los Angeles, CA.ORCID 0000-0002-3524-545X
IMPACC Network
Holden T MaeckerInstitute for Immunity, Transplantation, and Infection, Stanford University School of Medicine, Stanford, CA.ORCID 0000-0003-0795-9946

Funding

Using a tonsil organoid system to probe conditions for the induction of protective antibody and T cell responses to influenza.U19AI057229 · NIAID · STANFORD UNIVERSITY · PI Mark Morris Davis · 2003 to 2026
$88.5M
Transcriptomics to define biomarkers of neonatal vaccine immunogenicityU19AI118608 · NIAID · BOSTON CHILDREN'S HOSPITAL · PI OZONOFF, AL · 2017 to 2021
$24.7M
Detection/Dysplastic Epithelium/Gastrointestinal TractR33CA094304 · NCI · UNIVERSITY HOSPITALS OF CLEVELAND · PI SIVAK, MICHAEL V · 2002 to 2004
$1.5M
NCI NIH HHS R33 CA094304NIAID NIH HHS U19 AI057229NIAID NIH HHS U19 AI118608
6 · The paper itself

Abstract

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.

Indexed as

COVID-19Cytomegalovirus InfectionsInfluenza, HumanRespiratory Syncytial Virus, HumanHumansSARS-CoV-2

Identifiers

PMID37756530
PMCPMC10539027

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.