Evidence map›Paper›PMID 25545618›Full record

ArticleEuropean journal of immunology2015

Antitumor effector B cells directly kill tumor cells via the Fas/FasL pathway and are regulated by IL-10.

Huimin Tao, Lin Lu, Yang Xia, Fu Dai, Yi Wang, Yangyi Bao, Steven K Lundy, Fumito Ito, Qin Pan, Xiaolian Zhang and 8 more

Open access · bronzeAbstract read
In one paragraph

Article in European journal of immunology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 72 papers.

0numbers the graph read from it
0cells of the map it votes in
72citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

72 citing papers in PubMed, 107 citations in OpenAlex.

  1. B cells in cancer: functions, mechanisms and therapeutic advances.Signal transduction and targeted therapy · 2026
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  15. Advances in tumor-infiltrating B lymphocytes.Central-European journal of immunology · 2025
    Review
  16. Article
  17. Article
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  20. Review

12 more citing papers are in PubMed but not listed here.

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

18 authors at 9 institutions in 2 countries.

Huimin TaoDepartment of Surgery, University of Michigan, , Ann Arbor, MI, USA; Hubei Province Stem Cell Research and Appling Center, Institute of Hematology, , Union Hospital, , Tongji Medical College, , Huazhong University of Science and Technology, Wuhan, China.
Lin Lu
Yang Xia
Fu Dai
Yi Wang
Yangyi Bao
Steven K Lundy
Fumito Ito
Qin Pan
Xiaolian Zhang
Fang Zheng
Guoshun Shu
Bingmu Fang
Jinhong Jiang
Jianchuang Xia
Shiang Huang
Qiao Li
Alfred E Chang
University of Michigan–Ann Arbor · USAnhui Medical University · CNLishui City People's Hospital · CNWuhan University · CNCentral South University · CNHuazhong University of Science and Technology · CNSun Yat-sen University · CNSun Yat-sen University Cancer Center · CNUnion Hospital · CN

Funding

T CELL ACTIVATION FOR CANCER IMMUNOTHERAPYR01CA082529 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI CHANG, ALFRED E · 1999 to 2008
$2.8M
T and B cell Activation of Cancer ImmunotherapyR56CA082529 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI CHANG, ALFRED E · 2009 to 2009
$340k
NCI NIH HHS CA82529NCI NIH HHS R01 CA082529NCI NIH HHS R56 CA082529
6 · The paper itself

Abstract

We have previously reported that adoptive transfer of tumor-draining lymph node (TDLN) B cells confers tumor regression in a spontaneous pulmonary metastasis mouse model of breast cancer. In this study, we identified IL-10-producing cells within these B cells, and found that IL-10 removal, either by using IL-10(-/-) TDLN B cells or by systemic neutralization of IL-10, significantly augmented the therapeutic efficacy of adoptively transferred TDLN B cells. Depletion of IL-10 in B-cell adoptive transfers significantly increased CTLs and B-cell activity of PBMCs and splenic cells in the recipient. Activated TDLN B cells express Fas ligand, which was further enhanced by coculture of these TDLN B cells with 4T1 tumor cells. Effector B cells killed tumor cells directly in vitro in an antigen specific and Fas ligand-dependent manner. Trafficking of TDLN B cells in vivo suggested that they were recruited to the tumor and lung as well as secondary lymphoid organs. These findings further define the biological function of antitumor effector B cells, which may offer alternative cellular therapies to cancer.

Indexed as

Immunotherapy, AdoptiveAnimalsB-Lymphocyte SubsetsCell- and Tissue-Based TherapyCell Line, TumorCell MovementFas Ligand Proteinfas ReceptorFemaleInterleukin-10Lymph NodesLymphocyte ActivationMiceMice, Inbred BALB CMice, KnockoutNeoplasmsFas Ligand ProteinFasl protein, mousefas ReceptorInterleukin-10Adoptive ImmunotherapyB cellsCytotoxicityFasIL-10Tumor

Identifiers

PMID25545618
PMCPMC4414939
OpenAlexW1585132230

What OpenQuestion holds

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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.