Evidence map›Paper›PMID 36134660›Full record

ArticleJCI insight2022

Cross-reactivity of SARS-CoV-2- and influenza A-specific T cells in individuals exposed to SARS-CoV-2.

Worarat Chaisawangwong, Hanzhi Wang, Theodore Kouo, Sebastian F Salathe, Ariel Isser, Joan Glick Bieler, Maya L Zhang, Natalie K Livingston, Shuyi Li, Joseph J Horowitz and 4 more

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.5field-weighted citation impact, top 9% of its field
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

21 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
  2. Review
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  7. HIV-1-specific CD8PNAS nexus · 2025
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  16. Review
  17. Article
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  19. Review
  20. Vaccine-induced CD8Nature immunology · 2023
    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

14 authors at 4 institutions in 3 countries.

Worarat ChaisawangwongDepartment of Pathology, School of Medicine.
Hanzhi WangDepartment of Biomedical Engineering, Whiting School of Engineering.
Theodore KouoDepartment of Pediatrics, Division of Emergency Medicine.
Sebastian F SalatheDepartment of Pathology, School of Medicine.
Ariel IsserDepartment of Biomedical Engineering, School of Medicine, and.
Joan Glick BielerDepartment of Pathology, School of Medicine.
Maya L ZhangDepartment of Biomedical Engineering, Whiting School of Engineering.
Natalie K LivingstonDepartment of Biomedical Engineering, School of Medicine, and.
Shuyi LiDepartment of Pathology, School of Medicine.
Joseph J HorowitzExpressCare Urgent Care, Bel Air, Maryland, USA.
Ron E SametDepartment of Anesthesiology, University of Maryland School of Medicine, Baltimore, Maryland, USA.
Israel ZyskindDepartment of Pediatrics, NYU Langone Medical Center, New York, New York, USA; Maimonides Medical Center, New York, New York, USA.
Avi Z RosenbergDepartment of Pathology, School of Medicine.
Jonathan P SchneckDepartment of Pathology, School of Medicine.
Johns Hopkins University · USCare International · CHMaimonides Medical Center · USUniversity of Maryland, Baltimore · US

Funding

Vaccine Response and Immunotherapeutics SWGP30AI094189 · NIAID · JOHNS HOPKINS UNIVERSITY · PI Richard E. Chaisson · 2012 to 2026
$67.0M
TR&D Project 3P41EB028239 · NIBIB · JOHNS HOPKINS UNIVERSITY · PI Jordan Green, JONATHAN P SCHNECK · 2019 to 2026
$11.5M
cGMP Manufacture, Fill-Finish, Release, Analytical and Stability Testing and Stability Program of a Nanoparticle Based HIV Envelope Vaccine75N93022D00005 · NIAID · INTERNATIONAL AIDS VACCINE INITIATIVE · PI HASSELL, THOMAS · 2022 to 2025
$8.0M
Task Area A shall encompass annual follow-up of cohort members, clinical events investigations, study operations, and data analysis and manuscript writing. If implemented, Task A.1 will provide fundin75N92020D00005 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI WATSON, KAROL E · 2020 to 2025
$5.1M
Institutional Training for PediatriciansT32HD044355 · NICHD · JOHNS HOPKINS UNIVERSITY · PI BRADY, TAMMY MCLOUGHLIN · 2003 to 2023
$4.1M
Use of aAPC for Melanoma Adoptive ImmunotherapyR01CA108835 · NCI · JOHNS HOPKINS UNIVERSITY · PI SCHNECK, JONATHAN P · 2004 to 2015
$3.3M
Biomimetic Matrix for Ex Vivo and In Vivo Activation of T CellsR01EB029341 · NIBIB · JOHNS HOPKINS UNIVERSITY · PI MAO, HAI-QUAN, SCHNECK, JONATHAN P · 2020 to 2023
$1.9M
A high-throughput nanoparticle assay to characterize cancer neoepitope-specific T cellsR33CA229042 · NCI · JOHNS HOPKINS UNIVERSITY · PI SCHNECK, JONATHAN P · 2019 to 2021
$1.4M
MoFlo to MoFlo XDP Upgrade for BSL3 SortingS10OD016315 · OD · JOHNS HOPKINS UNIVERSITY · PI MARGOLICK, JOSEPH B. · 2013 to 2013
$233k
Class II artificial antigen presenting cells for cancer immunotherapyF31CA254121 · NCI · JOHNS HOPKINS UNIVERSITY · PI ISSER, ARIEL YOSEF · 2021 to 2022
$75k
NCI NIH HHS F31 CA254121NCI NIH HHS R01 CA108835NCI NIH HHS R33 CA229042NHLBI NIH HHS 75N92020D00005NIAID NIH HHS 75N93022D00005NIAID NIH HHS 75N93023D00005NIAID NIH HHS P30 AI094189NIBIB NIH HHS P41 EB028239NIBIB NIH HHS R01 EB029341NICHD NIH HHS T32 HD044355NIDA NIH HHS 75N95020D00005NIH HHS S10 OD016315ORFDO NIH HHS 75N99020D00005
6 · The paper itself

Abstract

Cross-reactive immunity between SARS-CoV-2 and other related coronaviruses has been well-documented, and it may play a role in preventing severe COVID-19. Epidemiological studies early in the pandemic showed a geographical association between high influenza vaccination rates and lower incidence of SARS-CoV-2 infection. We, therefore, analyzed whether exposure to influenza A virus (IAV) antigens could influence the T cell repertoire in response to SARS-CoV-2, indicating a heterologous immune response between these 2 unrelated viruses. Using artificial antigen-presenting cells (aAPCs) combined with real-time reverse-transcription PCR (RT-qPCR), we developed a sensitive assay to quickly screen for antigen-specific T cell responses and detected a significant correlation between responses to SARS-CoV-2 epitopes and IAV dominant epitope (M158-66). Further analysis showed that some COVID-19 convalescent donors exhibited both T cell receptor (TCR) specificity and functional cytokine responses to multiple SARS-CoV-2 epitopes and M158-66. Utilizing an aAPC-based stimulation/expansion assay, we detected cross-reactive T cells with specificity to SARS-CoV-2 and IAV. In addition, TCR sequencing of the cross-reactive and IAV-specific T cells revealed similarities between the TCR repertoires of the two populations. These results indicate that heterologous immunity shaped by our exposure to other unrelated endemic viruses may affect our immune response to novel viruses such as SARS-CoV-2.

Indexed as

COVID-19Influenza, HumanAntigens, ViralCD8-Positive T-LymphocytesCytokinesEpitopesHumansReceptors, Antigen, T-CellSARS-CoV-2Antigens, ViralCytokinesEpitopesReceptors, Antigen, T-CellAdaptive immunityCOVID-19ImmunologyT cells

Identifiers

PMID36134660
PMCPMC9675569
OpenAlexW4296794950

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.