Evidence map›Paper›PMID 35857583›Full record

ArticleScience immunology2022

Respiratory mucosal immunity against SARS-CoV-2 after mRNA vaccination.

Jinyi Tang, Cong Zeng, Thomas M Cox, Chaofan Li, Young Min Son, In Su Cheon, Yue Wu, Supriya Behl, Justin J Taylor, Rana Chakaraborty and 17 more

Registry-linked trialOpen access · greenAbstract read
In one paragraph

Article in Science immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06142279 (Development and Qualification of Methods for Analyzing the Mucosal Immune Response to COVID-19), which is not on this map. Cited by 252 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
252citing papers in PubMed, 1 pooled it
34.2field-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.

NCT06142279 naunknown statusnot on this mapstarted 2023, after this paper: background citation

Development and Qualification of Methods for Analyzing the Mucosal Immune Response to COVID-19

TypeinterventionalSponsorUniversity Hospital, ToursRan2023 to 2024Enrolled240ConditionsCertain Disorders Involving the Immune MechanismArmsSampling, PCR (polymerase chain reaction) SARS-CoV-2
3 · Its place in the literature

Who cites it

252 citing papers in PubMed, 1 synthesis or guideline pooled it, 352 citations in OpenAlex.

  1. Mucosal immune response in biology, disease prevention and treatment.Signal transduction and targeted therapy · 2025
    Pooled it
  2. Review
  3. Monocyte-derived galectin-1Nature immunology · 2026
    Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
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  11. Review
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  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

27 authors at 10 institutions in 2 countries.

Jinyi TangCarter Immunology Center, University of Virginia, Charlottesville, VA 22908, USA.ORCID 0000-0003-3593-4324
Cong ZengCenter for Retrovirus Research, Ohio State University, Columbus, OH 43210, USA.ORCID 0000-0003-4423-3634
Thomas M CoxDivision of Pulmonary and Critical Medicine, Department of Medicine, Mayo Clinic, Rochester, MN 55905, USA.
Chaofan LiCarter Immunology Center, University of Virginia, Charlottesville, VA 22908, USA.ORCID 0000-0002-5426-1498
Young Min SonCarter Immunology Center, University of Virginia, Charlottesville, VA 22908, USA.ORCID 0000-0003-2978-8703
In Su CheonCarter Immunology Center, University of Virginia, Charlottesville, VA 22908, USA.ORCID 0000-0001-5160-7783
Yue WuDepartment of Immunology, Mayo Clinic, Rochester, MN 55905, USA.ORCID 0000-0003-3667-2960
Supriya BehlDepartment of Pediatrics and Adolescent Medicine, Mayo Clinic, Rochester, MN 55905, USA.
Justin J TaylorVaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.ORCID 0000-0001-9718-2901
Rana ChakarabortyDepartment of Pediatrics and Adolescent Medicine, Mayo Clinic, Rochester, MN 55905, USA.ORCID 0000-0002-6585-0087
Aaron J JohnsonDepartment of Immunology, Mayo Clinic, Rochester, MN 55905, USA.ORCID 0000-0002-7921-484X
Dante N ShiavoDivision of Pulmonary and Critical Medicine, Department of Medicine, Mayo Clinic, Rochester, MN 55905, USA.ORCID 0000-0002-5332-977X
James P UtzDivision of Pulmonary and Critical Medicine, Department of Medicine, Mayo Clinic, Rochester, MN 55905, USA.
Janani S ReisenauerDivision of Pulmonary and Critical Medicine, Department of Medicine, Mayo Clinic, Rochester, MN 55905, USA.ORCID 0000-0002-8824-6691
David E MidthunDivision of Pulmonary and Critical Medicine, Department of Medicine, Mayo Clinic, Rochester, MN 55905, USA.ORCID 0000-0002-4876-059X
John J MullonDivision of Pulmonary and Critical Medicine, Department of Medicine, Mayo Clinic, Rochester, MN 55905, USA.
Eric S EdellDivision of Pulmonary and Critical Medicine, Department of Medicine, Mayo Clinic, Rochester, MN 55905, USA.
Mohamad G AlamehDepartment of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Larry BorishDivision of Asthma, Allergy and Immunology, Department of Medicine, University of Virginia, Charlottesville, VA 22908, USA.
William G TeagueChild Health Research Center, Department of Pediatrics, University of Virginia, Charlottesville, VA 22908, USA.
Mark H KaplanDepartment of Microbiology and Immunology, Indiana University School of Medicine, Indianapolis, IN 46074, USA.ORCID 0000-0002-2923-8245
Drew WeissmanDepartment of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.ORCID 0000-0002-1501-6510
Ryan KernDivision of Pulmonary and Critical Medicine, Department of Medicine, Mayo Clinic, Rochester, MN 55905, USA.ORCID 0000-0002-6311-2881
Haitao HuDepartment of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX 77555, USA.ORCID 0000-0002-6964-2314
Robert VassalloDivision of Pulmonary and Critical Medicine, Department of Medicine, Mayo Clinic, Rochester, MN 55905, USA.ORCID 0000-0003-2328-0255
Shan-Lu LiuCenter for Retrovirus Research, Ohio State University, Columbus, OH 43210, USA.ORCID 0000-0003-4423-3634
Jie SunCarter Immunology Center, University of Virginia, Charlottesville, VA 22908, USA.ORCID 0000-0002-2347-4511
Mayo Clinic · USCarter Center · USMayo Clinic in Florida · USThe Ohio State University · USUniversity of Pennsylvania · USAsthma and Allergy Specialists · USFred Hutch Cancer Center · USIndiana University School of MedicineThe University of Texas Medical Branch at Galveston · USUniversity of Virginia Health System · US

Funding

Project 4: Computational panbetaCoV immunogen designP01AI158571 · NIAID · DUKE UNIVERSITY · PI HAYNES, BARTON F. · 2021 to 2023
$28.0M
Project 3: Responding to Changing Serological and Viral Information around COVID-19 (RESPOND)U54CA260582 · NCI · OHIO STATE UNIVERSITY · PI MCALEARNEY, ANN SCHECK, OLTZ, EUGENE M · 2020 to 2024
$10.4M
The role of PU.1 in T helper cell heterogeneityR01AI057459 · NIAID · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI KAPLAN, MARK H · 2005 to 2025
$8.2M
Host cellular network governing the development of post SARS-CoV-2 tissue sequelaeR01AI147394 · NIAID · UNIVERSITY OF VIRGINIA · PI Jie Sun · 2020 to 2026
$4.7M
CD8 T cell mediated disruption of Blood Brain Barrier Tight JunctionsR01NS103212 · NINDS · MAYO CLINIC ROCHESTER · PI Aaron J Johnson · 2017 to 2026
$4.6M
Elucidating the roles of alveolar macrophage inflammation and selfrenewal during influenza infectionR01AG069264 · NIA · UNIVERSITY OF VIRGINIA · PI Jie Sun · 2020 to 2026
$3.5M
Modulation of BRD4 to epigenetically suppress HIVR01AI157852 · NIAID · UNIVERSITY OF TEXAS MED BR GALVESTON · PI HU, HAITAO · 2021 to 2025
$3.0M
Defining MHC class I restricted antigen presentation to CD8 T cells in experimental AD and Tauopathy - SupplementRF1NS122174 · NINDS · MAYO CLINIC ROCHESTER · PI JOHNSON, AARON J · 2021 to 2023
$2.0M
Simultaneously boosting both humoral and cellular immunity following vaccinationR01AG047156 · NIA · MAYO CLINIC ROCHESTER · PI SUN, JIE · 2015 to 2019
$1.6M
Defining MHC class I restricted antigen presentation to CD8 T cells in experimental AD and TauopathyR01NS122174 · NINDS · MAYO CLINIC ROCHESTER · PI JOHNSON, AARON J · 2024 to 2025
$1.2M
TIM-mediated Inhibition of HIV Release: Cooperation with SERINC and Antagonism by NefR01AI150473 · NIAID · OHIO STATE UNIVERSITY · PI LIU, SHAN-LU · 2019 to 2021
$995k
In vitro and in vivo analysis of susceptibility of Ad26 vector-induced CD4 T cells to HIV/SIVR21AI147903 · NIAID · UNIVERSITY OF TEXAS MED BR GALVESTON · PI HU, HAITAO · 2020 to 2021
$435k
NCI NIH HHS U54 CA260582NIAID NIH HHS P01 AI158571NIAID NIH HHS R01 AI057459NIAID NIH HHS R01 AI147394NIAID NIH HHS R01 AI150473NIAID NIH HHS R01 AI157852NIAID NIH HHS R21 AI147903NIA NIH HHS R01 AG047156NIA NIH HHS R01 AG069264NINDS NIH HHS R01 NS103212NINDS NIH HHS R01 NS122174NINDS NIH HHS RF1 NS122174
6 · The paper itself

Abstract

SARS-CoV-2 mRNA vaccination induces robust humoral and cellular immunity in the circulation; however, it is currently unknown whether it elicits effective immune responses in the respiratory tract, particularly against variants of concern (VOCs), including Omicron. We compared the SARS-CoV-2 S-specific total and neutralizing antibody responses, and B and T cell immunity, in the bronchoalveolar lavage fluid (BAL) and blood of COVID-19-vaccinated individuals and hospitalized patients. Vaccinated individuals had significantly lower levels of neutralizing antibody against D614G, Delta (B.1.617.2), and Omicron BA.1.1 in the BAL compared with COVID-19 convalescents despite robust S-specific antibody responses in the blood. Furthermore, mRNA vaccination induced circulating S-specific B and T cell immunity, but in contrast to COVID-19 convalescents, these responses were absent in the BAL of vaccinated individuals. Using a mouse immunization model, we demonstrated that systemic mRNA vaccination alone induced weak respiratory mucosal neutralizing antibody responses, especially against SARS-CoV-2 Omicron BA.1.1 in mice; however, a combination of systemic mRNA vaccination plus mucosal adenovirus-S immunization induced strong neutralizing antibody responses not only against the ancestral virus but also the Omicron BA.1.1 variant. Together, our study supports the contention that the current COVID-19 vaccines are highly effective against severe disease development, likely through recruiting circulating B and T cell responses during reinfection, but offer limited protection against breakthrough infection, especially by the Omicron sublineage. Hence, mucosal booster vaccination is needed to establish robust sterilizing immunity in the respiratory tract against SARS-CoV-2, including infection by the Omicron sublineage and future VOCs.

Indexed as

COVID-19Viral VaccinesAntibodies, NeutralizingAntibodies, ViralCOVID-19 VaccinesHumansImmunity, MucosalRespiratory SystemRNA, MessengerSARS-CoV-2Spike Glycoprotein, CoronavirusVaccinationAntibodies, NeutralizingAntibodies, ViralCOVID-19 VaccinesRNA, MessengerSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2Viral Vaccines

Identifiers

PMID35857583
PMCPMC9348751
OpenAlexW4286217721

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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.