Evidence map›Paper›PMID 41400657›Full record

ArticleThe Journal of experimental medicine2026

Antibiotic use in early life impairs MAIT cell-mediated immunity in adulthood.

Gabrielle R LeBlanc, Adam L Sobel, Jonathan Melamed, Dominic Haas, Eduard Ansaldo, Aiko M Cirone, Elizabeth Murguia, Michael G Constantinides

Abstract read
In one paragraph

Article in The Journal of experimental medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

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

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Gabrielle R LeBlanc *Department of Immunology and Microbiology, Scripps Research, La Jolla, CA, USA.ORCID 0000-0001-9532-5235
Adam L Sobel *Department of Immunology and Microbiology, Scripps Research, La Jolla, CA, USA.ORCID 0000-0003-1915-6286
Jonathan MelamedDepartment of Immunology and Microbiology, Scripps Research, La Jolla, CA, USA.ORCID 0000-0002-5981-7766
Dominic HaasDepartment of Immunology and Microbiology, Scripps Research, La Jolla, CA, USA.ORCID 0000-0001-8833-1012
Eduard AnsaldoDepartment of Immunology and Microbiology, Scripps Research, La Jolla, CA, USA.ORCID 0000-0002-7128-3373
Aiko M CironeDepartment of Immunology and Microbiology, Scripps Research, La Jolla, CA, USA.ORCID 0009-0004-4350-2913
Elizabeth MurguiaDepartment of Immunology and Microbiology, Scripps Research, La Jolla, CA, USA.ORCID 0000-0003-4532-3041
Michael G ConstantinidesDepartment of Immunology and Microbiology, Scripps Research, La Jolla, CA, USA.ORCID 0000-0003-4770-7751

Funding

Innate lymphocyte responses to early-life infectionsR35GM151347 · NIGMS · SCRIPPS RESEARCH INSTITUTE, THE · PI Michael George Constantinides · 2023 to 2026
$1.8M
Modulation of in vivo MAIT cell responses with diverse MR1 ligandsR21AI171697 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI CONSTANTINIDES, MICHAEL GEORGE · 2022 to 2023
$488k
Crosstalk between MAIT cells and the microbiotaK22AI146217 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI CONSTANTINIDES, MICHAEL GEORGE · 2021 to 2022
$270k
National Science FoundationNatural Sciences and Engineering Research Council of CanadaNIAID NIH HHS K22 AI146217NIAID NIH HHS R21 AI171697NIGMS NIH HHS R35 GM151347NIH HHS K22AI146217NIH HHS R21AI171697NIH HHS R35GM151347Scripps Research
6 · The paper itself

Abstract

Mucosal-associated invariant T (MAIT) cells are predominantly located in barrier tissues where they rapidly respond to pathogens and commensals by recognizing microbial derivatives of riboflavin synthesis. Early-life exposure to these metabolites imprints the abundance of MAIT cells within tissues, so we hypothesized that antibiotic use during this period may abrogate their development. We identified antibiotics that deplete riboflavin-synthesizing commensals and revealed an early period of susceptibility during which antibiotic administration impaired MAIT cell development. The reduction in MAIT cell abundance rendered mice more susceptible to pneumonia, while MAIT cell-deficient mice were unaffected by early-life antibiotics. Concomitant administration of a riboflavin-synthesizing commensal during antibiotic treatment was sufficient to restore MAIT cell development and immunity. Our work demonstrates that transient depletion of riboflavin-synthesizing commensals in early life can adversely affect responses to subsequent infections.

Indexed as

Anti-Bacterial AgentsImmunity, CellularMucosal-Associated Invariant T CellsAnimalsFemaleMiceMice, Inbred C57BLMice, KnockoutPneumoniaRiboflavinAnti-Bacterial AgentsRiboflavin

Identifiers

PMID41400657
PMCPMC12893763

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.