Evidence map›Paper›PMID 35561224›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2022

Vaccine-induced systemic and mucosal T cell immunity to SARS-CoV-2 viral variants.

Brock Kingstad-Bakke, Woojong Lee, Shaswath S Chandrasekar, David J Gasper, Cristhian Salas-Quinchucua, Thomas Cleven, Jeremy A Sullivan, Adel Talaat, Jorge E Osorio, M Suresh

Open access · hybridAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 97 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
97citing papers in PubMed, 1 pooled it
12.4field-weighted citation impact, top 1% 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

97 citing papers in PubMed, 1 synthesis or guideline pooled it, 126 citations in OpenAlex.

  1. Mucosal immune response in biology, disease prevention and treatment.Signal transduction and targeted therapy · 2025
    Pooled it
  2. Trial
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Intranasal measles virus- and mumps virus-based SARS-CoV-2 vaccine candidates prevent SARS-CoV-2 infection and transmission.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Upper respiratory tract immunization with PamFrontiers in immunology · 2025
    Article
  17. Review
  18. Article
  19. Article
  20. Article

37 more citing papers are in PubMed but not listed here.

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

10 authors at 1 institution in 1 country.

Brock Kingstad-BakkeDepartment of Pathobiological Sciences, University of Wisconsin-Madison, Madison, WI 53706.ORCID 0000-0002-3124-4484
Woojong LeeDepartment of Pathobiological Sciences, University of Wisconsin-Madison, Madison, WI 53706.ORCID 0000-0002-5906-7221
Shaswath S ChandrasekarDepartment of Pathobiological Sciences, University of Wisconsin-Madison, Madison, WI 53706.
David J GasperDepartment of Pathobiological Sciences, University of Wisconsin-Madison, Madison, WI 53706.ORCID 0000-0003-2069-7389
Cristhian Salas-QuinchucuaDepartment of Pathobiological Sciences, University of Wisconsin-Madison, Madison, WI 53706.ORCID 0000-0003-1571-5597
Thomas ClevenDepartment of Pathobiological Sciences, University of Wisconsin-Madison, Madison, WI 53706.ORCID 0000-0003-0796-5836
Jeremy A SullivanDepartment of Pathobiological Sciences, University of Wisconsin-Madison, Madison, WI 53706.ORCID 0000-0001-7290-0399
Adel TalaatDepartment of Pathobiological Sciences, University of Wisconsin-Madison, Madison, WI 53706.
Jorge E OsorioDepartment of Pathobiological Sciences, University of Wisconsin-Madison, Madison, WI 53706.ORCID 0000-0002-7474-6150
M SureshDepartment of Pathobiological Sciences, University of Wisconsin-Madison, Madison, WI 53706.ORCID 0000-0003-1794-3358
University of Wisconsin–Madison · US

Funding

Novel Combination Adjuvant for Eliciting Systemic and Mucosal CD8 T Cell MemoryU01AI124299 · NIAID · UNIVERSITY OF WISCONSIN-MADISON · PI KLEIN, BRUCE STEVEN, SURESH, MARULASIDDAPPA · 2016 to 2025
$6.2M
Mucosal Adjuvant to Induce Multipronged T Cell Immunity to TuberculosisR21AI149793 · NIAID · UNIVERSITY OF WISCONSIN-MADISON · PI SURESH, MARULASIDDAPPA · 2020 to 2021
$427k
NIAID NIH HHS R21 AI149793NIAID NIH HHS U01 AI124299
6 · The paper itself

Abstract

The first-generation COVID-19 vaccines have been effective in mitigating severe illness and hospitalization, but recurring waves of infections are associated with the emergence of SARS-CoV-2 variants that display progressive abilities to evade antibodies, leading to diminished vaccine effectiveness. The lack of clarity on the extent to which vaccine-elicited mucosal or systemic memory T cells protect against such antibody-evasive SARS-CoV-2 variants remains a critical knowledge gap in our quest for broadly protective vaccines. Using adjuvanted spike protein–based vaccines that elicit potent T cell responses, we assessed whether systemic or lung-resident CD4 and CD8 T cells protected against SARS-CoV-2 variants in the presence or absence of virus-neutralizing antibodies. We found that 1) mucosal or parenteral immunization led to effective viral control and protected against lung pathology with or without neutralizing antibodies, 2) protection afforded by mucosal memory CD8 T cells was largely redundant in the presence of antibodies that effectively neutralized the challenge virus, and 3) “unhelped” mucosal memory CD8 T cells provided no protection against the homologous SARS-CoV-2 without CD4 T cells and neutralizing antibodies. Significantly, however, in the absence of detectable virus-neutralizing antibodies, systemic or lung-resident memory CD4 and “helped” CD8 T cells provided effective protection against the relatively antibody-resistant B1.351 (β) variant, without lung immunopathology. Thus, induction of systemic and mucosal memory T cells directed against conserved epitopes might be an effective strategy to protect against SARS-CoV-2 variants that evade neutralizing antibodies. Mechanistic insights from this work have significant implications in the development of T cell–targeted immunomodulation or broadly protective SARS-CoV-2 vaccines.

Indexed as

CD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCOVID-19COVID-19 VaccinesIntraepithelial LymphocytesSARS-CoV-2Antibodies, NeutralizingAntibodies, ViralHumansImmune EvasionSpike Glycoprotein, CoronavirusAntibodies, NeutralizingAntibodies, ViralCOVID-19 VaccinesSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2antibodiesimmunitySARS-CoV-2T cellsvaccine

Identifiers

PMID35561224
PMCPMC9171754
OpenAlexW4280594901

What OpenQuestion holds

Textmetadata
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.