Evidence map›Paper›PMID 36917674›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2023

Species-specific CD4

Matthew P Spindler, Ilaria Mogno, Prerna Suri, Graham J Britton, Jeremiah J Faith

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

6 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Untangling the CD4 T cell response to the microbiota.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  5. Review
  6. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Matthew P SpindlerPrecision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029.ORCID 0000-0002-1354-3499
Ilaria MognoPrecision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029.ORCID 0000-0002-8180-6609
Prerna SuriPrecision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029.
Graham J BrittonPrecision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029.ORCID 0000-0003-4630-1223
Jeremiah J FaithPrecision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029.
Icahn School of Medicine at Mount Sinai · US

Funding

Mount Sinai Medical Scientist Training ProgramT32GM146636 · NIGMS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Talia H Swartz · 2022 to 2026
$6.8M
The Influence Of Gut Microbiota Stability In Inflammatory Bowel DiseaseR01DK112978 · NIDDK · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Jeremiah James Faith · 2019 to 2026
$5.3M
Determination of mucosal immune responses to, and infection of the gastrointestinal tract by Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2)R01DK123749 · NIDDK · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI CERUTTI, ANDREA, FAITH, JEREMIAH JAMES · 2020 to 2024
$4.9M
Uncovering the rules of gut microbiome strain transmissionR01DK124133 · NIDDK · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Jeremiah James Faith · 2020 to 2026
$4.2M
Influence of gut microbiota strain variation on mucosal T-cell phenotypeF30DK124978 · NIDDK · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI SPINDLER, MATTHEW PAUL · 2021 to 2022
$85k
NIDDK NIH HHS F30 DK124978NIDDK NIH HHS R01 DK112978NIDDK NIH HHS R01 DK123749NIDDK NIH HHS R01 DK124133NIGMS NIH HHS T32 GM146636
6 · The paper itself

Abstract

How bacterial strains within a complex human microbiota collectively shape intestinal T cell homeostasis is not well understood. Methods that quickly identify effector strains or species that drive specific mucosal T cell phenotypes are needed to define general principles for how the microbiota modulates host immunity. We colonize germ-free mice with defined communities of cultured strains and profile antigen-specific responses directed toward individual strains ex vivo. We find that lamina propria T cells are specific to bacterial strains at the species level and can discriminate between strains of the same species. Ex vivo restimulations consistently identify the strains within complex communities that induce Th17 responses in vivo, providing the potential to shape baseline immune tone via community composition. Using an adoptive transfer model of colitis, we find that lamina propria T cells respond to different bacterial strains in conditions of inflammation versus homeostasis. Collectively, our approach represents a unique method for efficiently predicting the relative impact of individual bacterial strains within a complex community and for parsing microbiota-dependent phenotypes into component fractions.

Indexed as

IntestinesMicrobiotaAnimalsBacteriaCD4-Positive T-LymphocytesHumansIntestinal MucosaMiceMucous MembranePhenotypehost-microbemicrobiomemucosal T cell responsesT cells

Identifiers

PMID36917674
PMCPMC10041165
OpenAlexW4324132715

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.