Evidence map›Paper›PMID 31855578›Full record

ArticleJCI insight2020

Multipanel mass cytometry reveals anti-PD-1 therapy-mediated B and T cell compartment remodeling in tumor-draining lymph nodes.

Won Jin Ho, Mark Yarchoan, Soren Charmsaz, Rebecca M Munday, Ludmila Danilova, Marcelo B Sztein, Elana J Fertig, Elizabeth M Jaffee

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 22% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

  1. Pooled it
  2. Lymph node fine-tuning FcγR signaling boosts anti-PD-1 therapy.Journal for immunotherapy of cancer · 2026
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  15. Systemic inhibition of PTPN22 augments anticancer immunity.The Journal of clinical investigation · 2021
    Article
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  18. Review
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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

8 authors at 2 institutions in 2 countries.

Won Jin HoSidney Kimmel Comprehensive Cancer Center.
Mark YarchoanSidney Kimmel Comprehensive Cancer Center.
Soren CharmsazSidney Kimmel Comprehensive Cancer Center.
Rebecca M MundayMcKusick-Nathans Institute for Genetic Medicine, and.
Ludmila DanilovaSidney Kimmel Comprehensive Cancer Center.
Marcelo B SzteinCenter for Vaccine Development and Global Health.
Elana J FertigSidney Kimmel Comprehensive Cancer Center.
Elizabeth M JaffeeSidney Kimmel Comprehensive Cancer Center.
Bloomberg (United States) · USUniversity of Maryland, Baltimore · US

Funding

Tumor Antigens for Individual Signatures and TherapyP50CA062924 · NCI · JOHNS HOPKINS UNIVERSITY · PI JAFFEE, ELIZABETH M. · 1993 to 2022
$54.6M
ONCOLOGY: CHEMOTHERAPY, IMMUNOLOGY, BIOLOGYT32CA009071 · NCI · JOHNS HOPKINS UNIVERSITY · PI Mary Y Armanios, Nilofer S. Azad · 1985 to 2026
$12.8M
Comprehensive Analysis and Multi-Omics Data Integration for Cancer-Related StudiesR50CA243627 · NCI · JOHNS HOPKINS UNIVERSITY · PI Ludmila Danilova · 2019 to 2026
$975k
NCI NIH HHS P50 CA062924NCI NIH HHS R50 CA243627NCI NIH HHS T32 CA009071
6 · The paper itself

Abstract

Anti-programmed cell death protein 1 (anti-PD-1) therapy has become an immunotherapeutic backbone for treating many cancer types. Although many studies have aimed to characterize the immune response to anti-PD-1 therapy in the tumor and in the peripheral blood, relatively less is known about the changes in the tumor-draining lymph nodes (TDLNs). TDLNs are primary sites of tumor antigen exposure that are critical to both regulation and cross-priming of the antitumor immune response. We used multipanel mass cytometry to obtain a high-parameter proteomic (39 total unique markers) immune profile of the TDLNs in a well-studied PD-1-responsive, immunocompetent mouse model. Based on combined hierarchal gating and unsupervised clustering analyses, we found that anti-PD-1 therapy enhances remodeling of both B and T cell compartments toward memory phenotypes. Functionally, expression of checkpoint markers was increased in conjunction with production of IFN-γ, TNF-α, or IL-2 in key cell types, including B and T cell subtypes, and rarer subsets, such as Tregs and NKT cells. A deeper profiling of the immunologic changes that occur in the TDLN milieu during effective anti-PD-1 therapy may lead to the discovery of novel biomarkers for monitoring response and provide key insights toward developing combination immunotherapeutic strategies.

Indexed as

AnimalsAntibodies, NeoplasmB-LymphocytesFemaleInterferon-gammaInterleukin-2Lymph NodesMiceMice, Inbred C57BLNatural Killer T-CellsNeoplasmsProgrammed Cell Death 1 ReceptorProteomicsT-LymphocytesTumor Necrosis Factor-alphaAntibodies, NeoplasmInterferon-gammaInterleukin-2Pdcd1 protein, mouseProgrammed Cell Death 1 ReceptorTumor Necrosis Factor-alphaB cellsImmunologyLymphOncologyT cells

Identifiers

PMID31855578
PMCPMC7098715
OpenAlexW2996268273

What OpenQuestion holds

Textmetadata
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.