Evidence map›Paper›PMID 32767371›Full record

ArticleBioEssays : news and reviews in molecular, cellular and developmental biology2020

Why the Outcome of Anti-Tumor Immune Responses is Heterogeneous: A Novel Idea in the Context of Immunological Heterogeneity in Cancers.

Jing H Wang

Abstract read
In one paragraph

Article in BioEssays : news and reviews in molecular, cellular and developmental biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
–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

11 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Preexisting TCR Clones Drive Major Pathologic Responses in Patients with HNSCC Treated with Dual Immune Checkpoint Inhibitors.Clinical cancer research : an official journal of the American Association for Cancer Research · 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

1 author.

Jing H WangDepartment of Immunology and Microbiology, School of Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO, 80045, USA.ORCID 0000-0003-4343-2527

Funding

Elucidating Mechanism of Immune Evasion in Head and Neck CancersR01DE027329 · NIDCR · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI WANG, JING HONG, WANG, XIAO-JING · 2018 to 2022
$2.8M
Mechanisms of Dual Inhibition of TGFbeta/PD-L1 in HNSCCR01DE028420 · NIDCR · UNIVERSITY OF COLORADO DENVER · PI WANG, JING HONG, WANG, XIAO-JING · 2019 to 2023
$2.7M
Developing newly combined therapeutic strategies for mature B cell lymphomaR01CA229174 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI WANG, JING HONG · 2019 to 2023
$2.5M
B cell antigen receptor (BCR)-driven mechanistic connection between B cell lymphomagenesis and autoimmunityR01CA249940 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI WANG, JING HONG · 2020 to 2024
$1.8M
Mechanisms promoting translocations and mature B cell lymphomasR01CA166325 · NCI · UNIVERSITY OF COLORADO DENVER · PI WANG, JING HONG · 2012 to 2016
$1.7M
A Novel Approach to Evaluate Genetic Variants in Primary Antibody DeficiencyR21AI133110 · NIAID · UNIVERSITY OF COLORADO DENVER · PI WANG, JING HONG · 2018 to 2019
$428k
Role of Target DNA sequences in mutation and DNA Break GenerationR21AI110777 · NIAID · UNIVERSITY OF COLORADO DENVER · PI WANG, JING HONG · 2015 to 2016
$427k
Genomic instability mediated via differential DNA repair mechanisms in B cellsR21CA184707 · NCI · UNIVERSITY OF COLORADO DENVER · PI WANG, JING HONG · 2015 to 2016
$372k
NCI NIH HHS R01 CA166325NCI NIH HHS R01 CA229174NCI NIH HHS R01 CA249940NCI NIH HHS R21 CA184707NIAID NIH HHS R21 AI110777NIAID NIH HHS R21 AI133110NIDCR NIH HHS R01 DE027329NIDCR NIH HHS R01 DE028420
6 · The paper itself

Abstract

The question as to why some hosts can eradicate their tumors while others succumb to tumor-progression remains unanswered. Here, a provocative concept is proposed that intrinsic differences in the T cell receptor (TCR) repertoire of individuals may influence the outcome of anti-tumor immunity by affecting the frequency and/or variety of tumor-reactive CD8 and/or CD4 tumor-infiltrating lymphocytes. This idea implicates that the TCR repertoire in a given patient might not provide sufficiently different TCR clones that can recognize tumor antigens, namely, "a hole in the TCR repertoire" might exist. This idea may provide a novel perspective to further dissect the mechanisms underlying heterogeneous anti-tumor immune responses in different hosts. Besides tumor-intrinsic heterogeneity and host microbiome, the various factors that may constantly shape the dynamic TCR repertoire are also discussed. Elucidating mechanistic differences in different individuals' immune systems will allow to better harness immune system to design new personalized cancer immunotherapy.

Indexed as

NeoplasmsReceptors, Antigen, T-CellCD8-Positive T-LymphocytesHumansImmunityLymphocytes, Tumor-InfiltratingReceptors, Antigen, T-Cellcancer immunologyheterogeneity of anti-tumor immunityTCR repertoiretumor immunogenicity

Identifiers

PMID32767371
PMCPMC7546576

What OpenQuestion holds

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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.