Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

MAIT cell compartment characteristics are associated with the immune response magnitude to the BNT162b2 mRNA anti-SARS-CoV-2 vaccine

13 May 2022

Abstract excerpt

Mucosa-associated invariant T (MAIT) cells are unconventional T cells with innate-like capacity to rapidly respond to microbial infection via MR1-restricted antigen recognition. Emerging evidence indicate that they can also act as rapid sensors of viral infection via innate cytokine activation. However, their possible role in the immune response to mRNA vaccination is unknown. Here, we evaluated the involvement...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to COVID-19 Clinical Research Studies
Share to Immunotherapy and Immune Responses
Share to SARS-CoV-2 and COVID-19 Research

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 35562666
DOI: 10.1186/s10020-022-00484-7

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

MAIT cell compartment characteristics are associated with the immune response magnitude to the BNT162b2 mRNA anti-SARS-CoV-2 vaccinePMID 35562666Read ↗

Immune defects associated with lower SARS-CoV-2 BNT162b2 mRNA vaccine response in aged peopleSemantic proximity Read ↗

The Robustness of Cellular Immunity Determines the Fate of SARS-CoV-2 InfectionSemantic proximity Read ↗

Discrete Immune Response Signature to SARS-CoV-2 mRNA Vaccination Versus InfectionSemantic proximity Read ↗

Systems biological assessment of human immunity to BNT162b2 mRNA vaccinationSemantic proximity Read ↗

The impact of BNT162b2 mRNA vaccine on adaptive and innate immune responsesSemantic proximity Read ↗

Impact of SARS-CoV-2 vaccination on systemic immune responses in people living with HIVSemantic proximity Read ↗

Multimodal characterization of antigen-specific CD8 <sup>+</sup> T cells across SARS-CoV-2 vaccination and infectionSemantic proximity Read ↗

Role of T cells in severe COVID-19 disease, protection, and long term immunitySemantic proximity Read ↗

Single-cell profiling of the antigen-specific response to BNT162b2 SARS-CoV-2 RNA vaccineSemantic proximity Read ↗

Serial vaccination expands and refines human CD4 <sup>+</sup> T cell memorySemantic proximity Read ↗

Insights into human CD8(+) T-cell memory using the yellow fever and smallpox vaccines.Semantic proximity Read ↗

Modulation of innate immune response to mRNA vaccination after SARS-CoV-2 infection or sequential vaccination in humansSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.