Evidence map›Paper›PMID 35393541›Full record

ReviewNature reviews. Cancer2022

Tumour-infiltrating B cells: immunological mechanisms, clinical impact and therapeutic opportunities.

Céline M Laumont, Allyson C Banville, Mara Gilardi, Daniel P Hollern, Brad H Nelson

Open access · greenAbstract readReview
In one paragraph

Review in Nature reviews. Cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 345 papers.

0numbers the graph read from it
0cells of the map it votes in
345citing papers in PubMed
50.4field-weighted citation impact, top 1% 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

345 citing papers in PubMed, 482 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Article
  6. IgM promotes antitumor immunity to a Tn-expressing solid tumor.Journal for immunotherapy of cancer · 2026
    Article
  7. Review
  8. Article
  9. B cells in cancer: functions, mechanisms and therapeutic advances.Signal transduction and targeted therapy · 2026
    Review
  10. Review
  11. Review
  12. Review
  13. Review
  14. Article
  15. Article
  16. Humoral immunity in cancer.Signal transduction and targeted therapy · 2026
    Review
  17. Article
  18. Article
  19. Article
  20. Review

285 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

5 authors at 2 institutions in 2 countries.

Céline M LaumontDeeley Research Centre, BC Cancer, Victoria, British Columbia, Canada.ORCID 0000-0002-9067-4054
Allyson C BanvilleDeeley Research Centre, BC Cancer, Victoria, British Columbia, Canada.ORCID 0000-0002-9289-4157
Mara GilardiNOMIS Center for Immunobiology and Microbial Pathogenesis, Salk Institute, San Diego, CA, USA.ORCID 0000-0001-8730-3642
Daniel P HollernNOMIS Center for Immunobiology and Microbial Pathogenesis, Salk Institute, San Diego, CA, USA.
Brad H NelsonDeeley Research Centre, BC Cancer, Victoria, British Columbia, Canada. bnelson@bccrc.ca.ORCID 0000-0002-4445-5539
University of British Columbia · CASalk Institute for Biological Studies · US

Funding

Viral Vector Core (VVC)P30CA014195 · NCI · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI Reuben Shaw · 1985 to 2026
$82.8M
CIHR 429161CIHR FBD-177882NCI NIH HHS P30 CA014195
6 · The paper itself

Abstract

Although immunotherapy research to date has focused largely on T cells, there is mounting evidence that tumour-infiltrating B cells and plasma cells (collectively referred to as tumour-infiltrating B lymphocytes (TIL-Bs)) have a crucial, synergistic role in tumour control. In many cancers, TIL-Bs have demonstrated strong predictive and prognostic significance in the context of both standard treatments and immune checkpoint blockade, offering the prospect of new therapeutic opportunities that leverage their unique immunological properties. Drawing insights from autoimmunity, we review the molecular phenotypes, architectural contexts, antigen specificities, effector mechanisms and regulatory pathways relevant to TIL-Bs in human cancer. Although the field is young, the emerging picture is that TIL-Bs promote antitumour immunity through their unique mode of antigen presentation to T cells; their role in assembling and perpetuating immunologically 'hot' tumour microenvironments involving T cells, myeloid cells and natural killer cells; and their potential to combat immune editing and tumour heterogeneity through the easing of self-tolerance mechanisms. We end by discussing the most promising approaches to enhance TIL-B responses in concert with other immune cell subsets to extend the reach, potency and durability of cancer immunotherapy.

Indexed as

Lymphocytes, Tumor-InfiltratingNeoplasmsB-LymphocytesHumansImmunotherapyTumor Microenvironment

Identifiers

PMID35393541
PMCPMC9678336
OpenAlexW4226068368

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.