Evidence map›Paper›PMID 35392082›Full record

ArticleFrontiers in immunology2022

Human B Cells Mediate Innate Anti-Cancer Cytotoxicity Through Concurrent Engagement of Multiple TNF Superfamily Ligands.

Bratislav M Janjic, Aditi Kulkarni, Robert L Ferris, Lazar Vujanovic, Nikola L Vujanovic

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.9field-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

14 citing papers in PubMed, 22 citations in OpenAlex.

  1. Trial
  2. 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

5 authors at 2 institutions in 1 country.

Bratislav M JanjicUPMC Hillman Cancer Center, University of Pittsburgh, Pittsburgh, PA, United States.
Aditi KulkarniUPMC Hillman Cancer Center, University of Pittsburgh, Pittsburgh, PA, United States.
Robert L FerrisUPMC Hillman Cancer Center, University of Pittsburgh, Pittsburgh, PA, United States.
Lazar VujanovicUPMC Hillman Cancer Center, University of Pittsburgh, Pittsburgh, PA, United States.
Nikola L VujanovicUPMC Hillman Cancer Center, University of Pittsburgh, Pittsburgh, PA, United States.
UPMC Hillman Cancer Center · USUniversity of Pittsburgh · US

Funding

VECTOR CORE FACILITYP30CA047904 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Jessie Nedrow · 1988 to 2026
$158.0M
WILD TYPE P53-BASED ADJUVANT IMMUNOTHERAPY FOR SCCHNP50CA097190 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI CHRISTOPHER J. BAKKENIST · 2004 to 2026
$49.6M
Therapuetic Immune Targeting of EphA2 Expressed by Melanoma & Its Tumor-AssociateP50CA121973 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI KIRKWOOD, JOHN MUNN · 2008 to 2018
$22.9M
Impaired Tumoricidal Activity Of DCs in HNC PatientsR01DE014775 · NIDCR · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI VUJANOVIC, NIKOLA LAZAR · 2002 to 2006
$1.6M
NCI NIH HHS P30 CA047904NCI NIH HHS P50 CA121973NIDCR NIH HHS R01 DE014775
6 · The paper itself

Abstract

The essential innate immunity effector cells, natural killer and dendritic cells, express multiple plasma membrane-associated tumor necrosis factor (TNF) superfamily (TNFSF) ligands that, through simultaneous and synergistic engagement, mediate anti-cancer cytotoxicity. Here, we report that circulating B cells, mediators of adaptive humoral immunity, also mediate this innate anti-cancer immune mechanism. We show that resting human B cells isolated from peripheral blood induce apoptosis of, and efficiently kill a large variety of leukemia and solid tumor cell types. Single-cell RNA sequencing analyses indicate, and flow cytometry data confirm that B cells from circulation express transmembrane TNF, Fas ligand (FasL), lymphotoxin (LT) α1β2 and TNF-related apoptosis-inducing ligand (TRAIL). The cytotoxic activity can be inhibited by individual and, especially, combined blockade of the four transmembrane TNFSF ligands. B cells from tumor-bearing head and neck squamous cell carcinoma patients express lower levels of TNFSF ligands and are less cytotoxic than those isolated from healthy individuals. In conclusion, we demonstrate that B cells have the innate capacity to mediate anti-cancer cytotoxicity through concurrent activity of multiple plasma membrane-associated TNFSF ligands, that this mechanism is deficient in cancer patients and that it may be part of a general cancer immunosurveillance mechanism.

Indexed as

B-LymphocytesNeoplasmsTNF-Related Apoptosis-Inducing LigandApoptosis Regulatory ProteinsHumansLigandsTumor Necrosis Factor-alphaApoptosis Regulatory ProteinsLigandsTNF-Related Apoptosis-Inducing LigandTumor Necrosis Factor-alphaB cellscancercytotoxichead and neck squamous cell carcinomainnate immunitysingle-cell RNA sequencing (scRNAseq)TNF superfamily ligands

Identifiers

PMID35392082
PMCPMC8983021
OpenAlexW4220750658

What OpenQuestion holds

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LicenceCC BY
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.