Evidence map›Paper›PMID 35030033›Full record

ArticleScience immunology2022

BATF promotes group 2 innate lymphoid cell-mediated lung tissue protection during acute respiratory virus infection.

Xiaopeng Wu, Moujtaba Y Kasmani, Shikan Zheng, Achia Khatun, Yao Chen, Wendy Winkler, Ryan Zander, Robert Burns, Elizabeth J Taparowsky, Jie Sun and 1 more

Open 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. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.1field-weighted citation impact, top 7% 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

34 citing papers in PubMed, 40 citations in OpenAlex.

  1. Review
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  8. Review
  9. Advances in Single-Cell Sequencing for Infectious Diseases: Progress and Perspectives.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Review
  10. Review
  11. Article
  12. Article
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  14. The mCell death and differentiation · 2025
    Article
  15. Article
  16. Article
  17. Review
  18. Progesterone amplifies allergic inflammation and airway pathology in association with higher lung ILC2 responses.American journal of physiology. Lung cellular and molecular physiology · 2024
    Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 4 institutions in 1 country.

Xiaopeng WuBlood Research Institute, Versiti Wisconsin, Milwaukee, WI 53213, USA.ORCID 0000-0002-9449-0818
Moujtaba Y KasmaniBlood Research Institute, Versiti Wisconsin, Milwaukee, WI 53213, USA.ORCID 0000-0002-5753-5335
Shikan ZhengBlood Research Institute, Versiti Wisconsin, Milwaukee, WI 53213, USA.
Achia KhatunBlood Research Institute, Versiti Wisconsin, Milwaukee, WI 53213, USA.
Yao ChenBlood Research Institute, Versiti Wisconsin, Milwaukee, WI 53213, USA.
Wendy WinklerBlood Research Institute, Versiti Wisconsin, Milwaukee, WI 53213, USA.ORCID 0000-0001-7283-0490
Ryan ZanderBlood Research Institute, Versiti Wisconsin, Milwaukee, WI 53213, USA.ORCID 0000-0002-7431-8535
Robert BurnsBlood Research Institute, Versiti Wisconsin, Milwaukee, WI 53213, USA.
Elizabeth J TaparowskyDepartment of Biological Sciences, Purdue University Center for Cancer Research, Purdue University, West Lafayette, IN 47907, USA.
Jie SunDepartment of Medicine, Mayo Clinic, Rochester, MN 55905, USA.ORCID 0000-0002-2347-4511
Weiguo CuiBlood Research Institute, Versiti Wisconsin, Milwaukee, WI 53213, USA.ORCID 0000-0003-1562-9218
Versiti Blood Center of Wisconsin · USMedical College of Wisconsin · USMayo Clinic · USPurdue University West Lafayette · US

Funding

Medical Scientist Training ProgramT32GM080202 · NIGMS · MEDICAL COLLEGE OF WISCONSIN · PI BARBIERI, JOSEPH T, SALZMAN, NITA H · 2010 to 2024
$5.7M
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
Molecular regulation of protective CD8 immunity against influenza infectionR01AI112844 · NIAID · UNIVERSITY OF VIRGINIA · PI SUN, JIE · 2015 to 2024
$4.5M
Phenotypic, Functional and Transcriptional Heterogeneity in T Cell ExhaustionR01AI148403 · NIAID · VERSITI WISCONSIN, INC. · PI WEIGUO CUI · 2020 to 2026
$3.1M
The Cellular and Transcriptional Control of CD8 T Cell Functional Adaptation to Chronic VirusesR01AI125741 · NIAID · VERSITI WISCONSIN, INC. · PI CUI, WEIGUO · 2016 to 2020
$2.1M
Simultaneously boosting both humoral and cellular immunity following vaccinationR01AG047156 · NIA · MAYO CLINIC ROCHESTER · PI SUN, JIE · 2015 to 2019
$1.6M
Defining the transcriptional, phenotypic, and functional heterogeneity of virus-specific CD4 T cells during chronic viral infectionR00AI153537 · NIAID · UNIVERSITY OF IOWA · PI ZANDER, RYAN · 2022 to 2023
$498k
Defining the transcriptional, phenotypic, and functional heterogeneity of virus-specific CD4 T cells during chronic viral infectionK99AI153537 · NIAID · VERSITI WISCONSIN, INC. · PI ZANDER, RYAN · 2020 to 2021
$224k
Mechanistic study of TCR signaling strength in CD8 T cell differentiation during pathogenesis of T1DMF30DK127526 · NIDDK · MEDICAL COLLEGE OF WISCONSIN · PI KASMANI, MOUJTABA Y · 2020 to 2023
$198k
NIAID NIH HHS K99 AI153537NIAID NIH HHS R00 AI153537NIAID NIH HHS R01 AI112844NIAID NIH HHS R01 AI125741NIAID NIH HHS R01 AI147394NIAID NIH HHS R01 AI148403NIA NIH HHS R01 AG047156NIDDK NIH HHS F30 DK127526NIGMS NIH HHS T32 GM080202
6 · The paper itself

Abstract

Activated group 2 innate lymphoid cells (ILC2s) accumulate and promote inflammatory resolution and tissue repair in host defense against acute respiratory viral infections. However, the heterogeneity of ILC2s in the lung and the mechanisms by which ILC2 cells contribute to tissue repair remain elusive. Using single-cell RNA sequencing, we identify a transcriptionally distinct ILC2 subset that showed enrichment for wound healing signature genes and the transcription factor BATF. BATF promotes the proliferation and function of ILC2s and restricts their plasticity during infection with influenza virus. In the absence of BATF, ILC2s lose their immune protective properties and acquire pathogenic ILC3-like functions, leading to persistent neutrophil infiltration, tissue damage, and respiratory failure. Mechanistically, BATF directly binds to the cis-regulatory elements of wound healing genes, maintains their chromatin accessibility, and promotes their expression. Last, BATF plays an important role in an IL-33–ST2 feed-forward loop that supports ILC2 cell identity and function. Collectively, our findings shed light on a BATF-dependent ILC2 program, thereby providing a potential therapeutic target for terminating detrimental inflammation during acute viral infection.

Indexed as

AnimalsBasic-Leucine Zipper Transcription FactorsFemaleHumansImmunity, InnateInfluenza, HumanLungLymphocytesMiceMice, Inbred C57BLMice, KnockoutMice, TransgenicOrthomyxoviridae InfectionsBasic-Leucine Zipper Transcription FactorsBatf protein, mouse

Identifiers

PMID35030033
PMCPMC9005262
OpenAlexW4205837570

What OpenQuestion holds

Textmetadata
LicenceTDM
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.