Evidence map›Paper›PMID 34715017›Full record

ArticleImmunity2021

Commensal Cryptosporidium colonization elicits a cDC1-dependent Th1 response that promotes intestinal homeostasis and limits other infections.

Emilie V Russler-Germain, Jisun Jung, Aidan T Miller, Shannon Young, Jaeu Yi, Alec Wehmeier, Lindsey E Fox, Kristen J Monte, Jiani N Chai, Devesha H Kulkarni and 10 more

Open access · greenAbstract read
In one paragraph

Article in Immunity, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
6.2field-weighted citation impact, top 2% 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

36 citing papers in PubMed, 51 citations in OpenAlex.

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  16. The intersection of hostMicrobiology and molecular biology reviews : MMBR · 2024
    Review
  17. Review
  18. Genetic crosses within and between species ofProceedings of the National Academy of Sciences of the United States of America · 2024
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  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors at 1 institution in 1 country.

Emilie V Russler-GermainDepartment of Internal Medicine, Division of Rheumatology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Jisun JungDepartment of Internal Medicine, Division of Rheumatology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Aidan T MillerDepartment of Internal Medicine, Division of Rheumatology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Shannon YoungDepartment of Internal Medicine, Division of Rheumatology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Jaeu YiDepartment of Internal Medicine, Division of Rheumatology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Alec WehmeierDepartment of Internal Medicine, Division of Rheumatology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Lindsey E FoxDepartment of Internal Medicine, Division of Rheumatology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Kristen J MonteDepartment of Internal Medicine, Division of Rheumatology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Jiani N ChaiDepartment of Internal Medicine, Division of Rheumatology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Devesha H KulkarniDepartment of Internal Medicine, Division of Gastroenterology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Lisa J Funkhouser-JonesDepartment of Molecular Microbiology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Georgia WilkeDepartment of Molecular Microbiology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Vivek DuraiDepartment of Pathology, Division of Immunobiology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Bernd H ZinselmeyerDepartment of Pathology, Division of Immunobiology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Rafael S CzepielewskiDepartment of Pathology, Division of Immunobiology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Suellen GrecoDivision of Comparative Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA.
Kenneth M MurphyDepartment of Pathology, Division of Immunobiology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Rodney D NewberryDepartment of Internal Medicine, Division of Gastroenterology, Washington University School of Medicine, St. Louis, MO 63110, USA.
L David SibleyDepartment of Molecular Microbiology, Washington University School of Medicine, St. Louis, MO 63110, USA. Electronic address: sibley@wustl.edu.
Chyi-Song HsiehDepartment of Internal Medicine, Division of Rheumatology, Washington University School of Medicine, St. Louis, MO 63110, USA. Electronic address: chsieh@wustl.edu.
Washington University in St. Louis · US

Funding

NATIONAL RESEARCH SERVICE AWARD-MEDICAL SCIENTISTT32GM007200 · NIGMS · WASHINGTON UNIVERSITY · PI YOKOYAMA, WAYNE M. · 1985 to 2024
$59.8M
UNIQUE ROLES OF ANTIGEN PRESENTING CELLS ON T CELL TOLERANCE AND AUTOIMMUNITYR01AI079187 · NIAID · WASHINGTON UNIVERSITY · PI HSIEH, CHYI S · 2008 to 2021
$5.8M
The Role of Route of Entry by Bacterial Antigens on Colonic T Cell ResponsesR01AI136515 · NIAID · WASHINGTON UNIVERSITY · PI HSIEH, CHYI S, NEWBERRY, RODNEY D · 2018 to 2022
$2.8M
Effect of Microbial Metabolites on Growth of CryptosporidiumR01AI145496 · NIAID · WASHINGTON UNIVERSITY · PI SIBLEY, L. DAVID · 2020 to 2023
$2.7M
Evaluation of Antigen-Specific Immune Interactions with Commensal Bacteria in NeonatesU01AI131349 · NIAID · WASHINGTON UNIVERSITY · PI HSIEH, CHYI S · 2017 to 2021
$1.5M
The Role of CD101 in T Cell Tolerance in the GutF30DK111071 · NIDDK · WASHINGTON UNIVERSITY · PI RUSSLER-GERMAIN, EMILIE VERONICA · 2016 to 2018
$110k
NIAID NIH HHS R01 AI079187NIAID NIH HHS R01 AI136515NIAID NIH HHS R01 AI145496NIAID NIH HHS U01 AI131349NIDDK NIH HHS F30 DK111071NIGMS NIH HHS T32 GM007200
6 · The paper itself

Abstract

Cryptosporidium can cause severe diarrhea and morbidity, but many infections are asymptomatic. Here, we studied the immune response to a commensal strain of Cryptosporidium tyzzeri (Ct-STL) serendipitously discovered when conventional type 1 dendritic cell (cDC1)-deficient mice developed cryptosporidiosis. Ct-STL was vertically transmitted without negative health effects in wild-type mice. Yet, Ct-STL provoked profound changes in the intestinal immune system, including induction of an IFN-γ-producing Th1 response. TCR sequencing coupled with in vitro and in vivo analysis of common Th1 TCRs revealed that Ct-STL elicited a dominant antigen-specific Th1 response. In contrast, deficiency in cDC1s skewed the Ct-STL CD4 T cell response toward Th17 and regulatory T cells. Although Ct-STL predominantly colonized the small intestine, colon Th1 responses were enhanced and associated with protection against Citrobacter rodentium infection and exacerbation of dextran sodium sulfate and anti-IL10R-triggered colitis. Thus, Ct-STL represents a commensal pathobiont that elicits Th1-mediated intestinal homeostasis that may reflect asymptomatic human Cryptosporidium infection.

Indexed as

AnimalsCryptosporidiosisCryptosporidiumDendritic CellsDisease Models, AnimalHomeostasisHost-Parasite InteractionsIntestinal MucosaMiceMicrobiotaTh1 CellsT-Lymphocyte SubsetscDC1commensal protistcryptosporidiosiscryptosporidiumdendritic cellIFNγIL-12intestinemicrobiomeT cell differentiationTCR sequencingTh1

Identifiers

PMID34715017
PMCPMC8716016
OpenAlexW3208225263

What OpenQuestion holds

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Registered trials

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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.