Evidence map›Paper›PMID 40360528›Full record

ArticleNature communications2025

Blocking plasma cell fate enhances antigen-specific presentation by B cells to boost anti-tumor immunity.

Yunqiao Li, Raag Bhargava, Jenny Tuyet Tran, Tanya R Blane, Linghang Peng, Fangkun Luan, Zhe Huang, Zefan Zhang, Yunfan Sun, Changchun Xiao and 1 more

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
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  6. CIITA/PRMT5 promote CD4BMC medicine · 2026
    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

11 authors.

Yunqiao LiDepartment of Immunology and Microbiology, The Scripps Research Institute, La Jolla, CA, USA.ORCID http://orcid.org/0000-0001-9937-1634
Raag BhargavaDepartment of Immunology and Microbiology, The Scripps Research Institute, La Jolla, CA, USA.
Jenny Tuyet TranDepartment of Immunology and Microbiology, The Scripps Research Institute, La Jolla, CA, USA.
Tanya R BlaneDepartment of Immunology and Microbiology, The Scripps Research Institute, La Jolla, CA, USA.
Linghang PengDepartment of Immunology and Microbiology, The Scripps Research Institute, La Jolla, CA, USA.
Fangkun LuanDepartment of Immunology and Microbiology, The Scripps Research Institute, La Jolla, CA, USA.
Zhe HuangDepartment of Immunology and Microbiology, The Scripps Research Institute, La Jolla, CA, USA.
Zefan ZhangDepartment of Liver Surgery & Transplantation, Liver Cancer Institute, Zhongshan Hospital, Fudan University, Key Laboratory of Carcinogenesis and Cancer Invasion, Ministry of Education, Shanghai, China.
Yunfan SunDepartment of Liver Surgery & Transplantation, Liver Cancer Institute, Zhongshan Hospital, Fudan University, Key Laboratory of Carcinogenesis and Cancer Invasion, Ministry of Education, Shanghai, China.ORCID http://orcid.org/0000-0001-9790-2761
Changchun XiaoDepartment of Immunology and Microbiology, The Scripps Research Institute, La Jolla, CA, USA. cxiao@scripps.edu.ORCID http://orcid.org/0000-0001-8754-3208
David NemazeeDepartment of Immunology and Microbiology, The Scripps Research Institute, La Jolla, CA, USA. nemazee@scripps.edu.ORCID http://orcid.org/0000-0002-4769-6311

Funding

Functional Analysis of MicroRNAs and Target Genes in Immune ToleranceR01AI137252 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI NEMAZEE, DAVID · 2019 to 2024
$2.9M
NIAID NIH HHS R01 AI137252U.S. Department of Health & Human Services | NIH | National Institute of Allergy and Infectious Diseases (NIAID) R01AI137252
6 · The paper itself

Abstract

B cells engage in anti-tumor immunity but how they contribute to cancer suppression remains unclear. We report that inhibiting plasma cell differentiation either in IgMi mice lacking Igh elements needed for antibody secretion or in mice with B cell-specific knockout of Blimp-1 (Blimp-1 BcKO) promotes rather than inhibits antitumor immunity and increases numbers of activated B cells. Deficiency of Blimp-1 in tumor-infiltrating B cells generates a unique transcription profile associated with expansion of mutated clones targeting cognate tumor cells. Major histocompatibility complex class II (MHC II) is required for anti-tumor efficacy. Blimp-1-deficient B cells have increased expression of CD80 and CD86 costimulatory molecules that enhance effector T cell function. The Blimp-1 inhibitor valproic acid suppresses tumor growth in a B cell-dependent manner. Thus, inhibition of plasma cell differentiation results in enhanced tumor-specific antigen presentation by B cells and thereby tumor repression, suggesting a potential avenue of immunotherapy against cancer.

Indexed as

Antigen PresentationB-LymphocytesNeoplasmsPlasma CellsAnimalsB7-1 AntigenB7-2 AntigenCell DifferentiationCell Line, TumorHistocompatibility Antigens Class IILymphocyte ActivationMiceMice, Inbred C57BLMice, KnockoutPositive Regulatory Domain I-Binding Factor 1Valproic AcidB7-1 AntigenB7-2 AntigenHistocompatibility Antigens Class IIPositive Regulatory Domain I-Binding Factor 1Prdm1 protein, mouseValproic Acid

Identifiers

PMID40360528
PMCPMC12075458

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.