Evidence map›Paper›PMID 32931481›Full record

ArticleThe Journal of clinical investigation2021

Tissue-resident PSGL1loCD4+ T cells promote B cell differentiation and chronic graft-versus-host disease-associated autoimmunity.

Xiaohui Kong, Deye Zeng, Xiwei Wu, Bixin Wang, Shijie Yang, Qingxiao Song, Yongping Zhu, Martha Salas, Hanjun Qin, Ubaydah Nasri and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
1.8field-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

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 33 citations in OpenAlex.

  1. Tissue-Resident Memory T Cells in Skin Diseases: A Systematic Review.International journal of molecular sciences · 2021
    Pooled it
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  10. Targeting PRMT1 prevents acute and chronic graft-versus-host disease.Molecular therapy : the journal of the American Society of Gene Therapy · 2023
    Article
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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

16 authors at 5 institutions in 2 countries.

Xiaohui KongDiabetes and Metabolism Research Institute, the Beckman Research Institute of City of Hope, Duarte, California, USA.
Deye ZengDiabetes and Metabolism Research Institute, the Beckman Research Institute of City of Hope, Duarte, California, USA.
Xiwei WuDepartment of Integrative Genomics Core, The Beckman Research Institute of City of Hope, Duarte, California, USA.
Bixin WangDiabetes and Metabolism Research Institute, the Beckman Research Institute of City of Hope, Duarte, California, USA.
Shijie YangDiabetes and Metabolism Research Institute, the Beckman Research Institute of City of Hope, Duarte, California, USA.
Qingxiao SongDiabetes and Metabolism Research Institute, the Beckman Research Institute of City of Hope, Duarte, California, USA.
Yongping ZhuDiabetes and Metabolism Research Institute, the Beckman Research Institute of City of Hope, Duarte, California, USA.
Martha SalasDiabetes and Metabolism Research Institute, the Beckman Research Institute of City of Hope, Duarte, California, USA.
Hanjun QinDepartment of Integrative Genomics Core, The Beckman Research Institute of City of Hope, Duarte, California, USA.
Ubaydah NasriDiabetes and Metabolism Research Institute, the Beckman Research Institute of City of Hope, Duarte, California, USA.
Karen M HaasDepartment of Microbiology and Immunology, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.
Arthur D RiggsDiabetes and Metabolism Research Institute, the Beckman Research Institute of City of Hope, Duarte, California, USA.
Ryotaro NakamuraHematologic Malignancies and Stem Cell Transplantation Institute, City of Hope National Medical Center, Duarte, California, USA.
Paul J MartinFred Hutchinson Cancer Research Center, Seattle, Washington, USA.
Aimin HuangDepartment of Pathology at School of Basic Medical Sciences, Institute of Oncology and Diagnostic Pathology Center, Fujian Medical University, Fuzhou, China.
Defu ZengDiabetes and Metabolism Research Institute, the Beckman Research Institute of City of Hope, Duarte, California, USA.
City Of Hope National Medical Center · USFujian Medical University · CNCity of Hope · USFred Hutch Cancer Center · USWake Forest University · US

Funding

Transgenic Mouse FacilityP30CA033572 · NCI · CITY OF HOPE/BECKMAN RESEARCH INSTITUTE · PI STANLEY R. HAMILTON · 1985 to 2026
$86.3M
Role of autoreactivity in the pathogenesis of chronic GVHDR01AI066008 · NIAID · CITY OF HOPE/BECKMAN RESEARCH INSTITUTE · PI ZENG, DEFU · 2005 to 2020
$6.1M
PD-L1 interacts with CD80 and PD-1 to regulate GVHD and GVL activityR01CA228465 · NCI · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI ZENG, DEFU · 2018 to 2022
$2.0M
NCI NIH HHS P30 CA033572NCI NIH HHS R01 CA228465NIAID NIH HHS R01 AI066008
6 · The paper itself

Abstract

CD4+ T cell interactions with B cells play a critical role in the pathogenesis of systemic autoimmune diseases such as systemic lupus and chronic graft-versus-host disease (cGVHD). Extrafollicular CD44hiCD62LloPSGL1loCD4+ T cells (PSGL1loCD4+ T cells) are associated with the pathogenesis of lupus and cGVHD, but their causal role has not been established. With murine and humanized MHC-/-HLA-A2+DR4+ murine models of cGVHD, we showed that murine and human PSGL1loCD4+ T cells from GVHD target tissues have features of B cell helpers with upregulated expression of programmed cell death protein 1 (PD1) and inducible T cell costimulator (ICOS) and production of IL-21. They reside in nonlymphoid tissues without circulating in the blood and have features of tissue-resident memory T cells with upregulated expression of CD69. Murine PSGL1loCD4+ T cells from GVHD target tissues augmented B cell differentiation into plasma cells and production of autoantibodies via their PD1 interaction with PD-L2 on B cells. Human PSGL1loCD4+ T cells were apposed with memory B cells in the liver tissues of humanized mice and cGVHD patients. Human PSGL1loCD4+ T cells from humanized GVHD target tissues also augmented autologous memory B cell differentiation into plasma cells and antibody production in a PD1/PD-L2-dependent manner. Further preclinical studies targeting tissue-resident T cells to treat antibody-mediated features of autoimmune diseases are warranted.

Indexed as

AutoimmunityAnimalsB-LymphocytesCD4-Positive T-LymphocytesCell DifferentiationChronic DiseaseDisease Models, AnimalFemaleGraft vs Host DiseaseHumansImmunologic MemoryMaleMembrane GlycoproteinsMiceMice, Inbred BALB CMice, KnockoutMembrane GlycoproteinsPDCD1 protein, humanPdcd1 protein, mouseProgrammed Cell Death 1 ReceptorP-selectin ligand proteinB cellsBone marrow transplantationT cellsTransplantation

Identifiers

PMID32931481
PMCPMC7773409
OpenAlexW3087623143

What OpenQuestion holds

Textmetadata
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.