Evidence map›Paper›PMID 39266726›Full record

ArticleNature cell biology2024

Solid tumour-induced systemic immunosuppression involves dichotomous myeloid-B cell interactions.

Xiaoxin Hao, Yichao Shen, Jun Liu, Angela Alexander, Ling Wu, Zhan Xu, Liqun Yu, Yang Gao, Fengshuo Liu, Hilda L Chan and 9 more

Abstract read
In one paragraph

Article in Nature cell biology, 2024. 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. B cells in cancer: functions, mechanisms and therapeutic advances.Signal transduction and targeted therapy · 2026
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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

19 authors.

Xiaoxin Hao *Lester and Sue Smith Breast Center, Baylor College of Medicine, Houston, TX, USA.ORCID 0000-0001-8763-3529
Yichao Shen *Lester and Sue Smith Breast Center, Baylor College of Medicine, Houston, TX, USA.
Jun LiuLester and Sue Smith Breast Center, Baylor College of Medicine, Houston, TX, USA.
Angela AlexanderDepartment of Breast Medical Oncology and Morgan Welch IBC Research Program and Clinic, University of Texas MD Anderson Cancer Center, Houston, TX, USA.ORCID 0000-0002-6649-7991
Ling WuLester and Sue Smith Breast Center, Baylor College of Medicine, Houston, TX, USA.ORCID 0000-0002-5786-4315
Zhan XuLester and Sue Smith Breast Center, Baylor College of Medicine, Houston, TX, USA.
Liqun YuLester and Sue Smith Breast Center, Baylor College of Medicine, Houston, TX, USA.
Yang GaoLester and Sue Smith Breast Center, Baylor College of Medicine, Houston, TX, USA.ORCID 0000-0003-1832-4380
Fengshuo LiuLester and Sue Smith Breast Center, Baylor College of Medicine, Houston, TX, USA.ORCID 0000-0003-4651-7710
Hilda L ChanLester and Sue Smith Breast Center, Baylor College of Medicine, Houston, TX, USA.ORCID 0000-0001-6882-4274
Che-Hsing LiGraduate Program in Immunology and Microbiology, Baylor College of Medicine, Houston, TX, USA.ORCID 0000-0003-0660-1125
Yunfeng DingLester and Sue Smith Breast Center, Baylor College of Medicine, Houston, TX, USA.
Weijie ZhangZhejiang Provincial Key Laboratory of Cancer Molecular Cell Biology, Life Sciences Institute, Zhejiang University, Hangzhou, China.ORCID 0000-0002-6462-6067
David G EdwardsLester and Sue Smith Breast Center, Baylor College of Medicine, Houston, TX, USA.
Nan ChenLester and Sue Smith Breast Center, Baylor College of Medicine, Houston, TX, USA.
Azadeh NasrazadaniDepartment of Breast Medical Oncology and Morgan Welch IBC Research Program and Clinic, University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Naoto T UenoDepartment of Breast Medical Oncology and Morgan Welch IBC Research Program and Clinic, University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Bora LimLester and Sue Smith Breast Center, Baylor College of Medicine, Houston, TX, USA.
Xiang H-F ZhangLester and Sue Smith Breast Center, Baylor College of Medicine, Houston, TX, USA. xiangz@bcm.edu.ORCID 0000-0002-5674-8670

Funding

Tumor BiologyP30CA125123 · NCI · BAYLOR COLLEGE OF MEDICINE · PI Michael M Ittmann · 2007 to 2026
$73.9M
Translational Research in Breast Cancer (SPORE)P50CA186784 · NCI · BAYLOR COLLEGE OF MEDICINE · PI MATTHEW J ELLIS · 2014 to 2026
$24.5M
Osteoclast-Independent Mechanisms of Early-Stage Bone Colonization of Breast CancerR01CA183878 · NCI · BAYLOR COLLEGE OF MEDICINE · PI ZHANG, XIANG · 2014 to 2024
$3.5M
Unveiling the mechanisms underlying secondary metastasis and possible therapeutic windowsR01CA251950 · NCI · BAYLOR COLLEGE OF MEDICINE · PI ZHANG, XIANG · 2020 to 2024
$2.6M
Osteogenic Niche Biology in Progression and Endocrine Resistance of Bone MetastasesR01CA221946 · NCI · BAYLOR COLLEGE OF MEDICINE · PI ROWLEY, DAVID R · 2018 to 2022
$2.4M
Rewired Metabolism Regulates Vessel Normalization and ImmunosuppressionR01CA227904 · NCI · BAYLOR COLLEGE OF MEDICINE · PI SREEKUMAR, ARUN, ZHANG, XIANG · 2019 to 2023
$2.3M
BD Biosciences Special Order LSRIIS10RR024574 · NCRR · BAYLOR COLLEGE OF MEDICINE · PI LUMPKIN, ELLEN A · 2009 to 2009
$430k
Harnessing neutrophils to improve the efficacy of immune checkpoint inhibitors in breast cancerK99CA279899 · NCI · BAYLOR COLLEGE OF MEDICINE · PI GAO, YANG · 2023 to 2024
$238k
Acquisition of 10X Genomics Chromium Instrument to Accelerate Genomic and Single Cell Transcriptomic ResearchS10OD025240 · OD · BAYLOR COLLEGE OF MEDICINE · PI DODDAPANENI, HARSHA VARDHAN · 2018 to 2018
$125k
NCI NIH HHS K99 CA279899NCI NIH HHS P30 CA125123NCI NIH HHS P50 CA186784NCI NIH HHS R01 CA183878NCI NIH HHS R01 CA221946NCI NIH HHS R01 CA227904NCI NIH HHS R01 CA251950NCRR NIH HHS S10 RR024574NIH HHS S10 OD025240U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI) NCI CA183878, NCI CA251950, NCI CA221946, NCI CA227904,NCI CA253533U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI) NCI K99CA279899
6 · The paper itself

Abstract

Solid tumours induce systemic immunosuppression that involves myeloid and T cells. B cell-related mechanisms remain relatively understudied. Here we discover two distinct patterns of tumour-induced B cell abnormality (TiBA; TiBA-1 and TiBA-2), both associated with abnormal myelopoiesis in the bone marrow. TiBA-1 probably results from the niche competition between pre-progenitor-B cells and myeloid progenitors, leading to a global reduction in downstream B cells. TiBA-2 is characterized by systemic accumulation of a unique early B cell population, driven by interaction with excessive neutrophils. Importantly, TiBA-2-associated early B cells foster the systemic accumulation of exhaustion-like T cells. Myeloid and B cells from the peripheral blood of patients with triple-negative breast cancer recapitulate the TiBA subtypes, and the distinct TiBA profile correlates with pathologic complete responses to standard-of-care immunotherapy. This study underscores the inter-patient diversity of tumour-induced systemic changes and emphasizes the need for treatments tailored to different B and myeloid cell abnormalities.

Indexed as

B-LymphocytesImmune ToleranceMyeloid CellsAnimalsCell CommunicationFemaleHumansMiceMiddle AgedMyelopoiesisNeutrophilsT-LymphocytesTriple Negative Breast NeoplasmsTumor Microenvironment

Identifiers

PMID39266726
PMCPMC12228142

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.