Evidence map›Paper›PMID 30995949›Full record

ReviewJournal for immunotherapy of cancer2019

Exploring the emerging role of the microbiome in cancer immunotherapy.

Jessica Fessler, Vyara Matson, Thomas F Gajewski

Abstract readReview
In one paragraph

Review in Journal for immunotherapy of cancer, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 177 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
177citing papers in PubMed, 4 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

177 citing papers in PubMed, 4 syntheses or guidelines pooled it.

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117 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

3 authors.

Jessica FesslerDepartment of Pathology, The University of Chicago, Chicago, IL, USA.
Vyara MatsonDepartment of Pathology, The University of Chicago, Chicago, IL, USA.
Thomas F GajewskiDepartment of Pathology, The University of Chicago, Chicago, IL, USA. tgajewsk@medicine.bsd.uchicago.edu.

Funding

Multi-Disciplinary Training Grant in Cancer ResearchT32CA009594 · NCI · UNIVERSITY OF CHICAGO · PI KAY F MACLEOD, Scott A. Oakes · 1989 to 2026
$11.5M
Overcoming resistance to anti-PD1 immunotherapyR35CA210098 · NCI · UNIVERSITY OF CHICAGO · PI THOMAS F GAJEWSKI · 2017 to 2026
$10.4M
Role of the gut microbiome in modulating the efficacy of checkpoint blockade therapyF32CA236296 · NCI · UNIVERSITY OF CHICAGO · PI MATSON, VYARA · 2019 to 2021
$206k
Identifying mechanisms of microbiota-dependent anti-tumor immune modulation and metabolically manipulating bacteria to improve treatment efficacyF99CA234946 · NCI · UNIVERSITY OF CHICAGO · PI FESSLER, JESSICA LYNN · 2018 to 2019
$91k
NCI NIH HHS F32 CA236296NCI NIH HHS F99 CA234946NCI NIH HHS R35 CA210098NCI NIH HHS T32 CA009594
6 · The paper itself

Abstract

The activity of the commensal microbiota significantly impacts human health and has been linked to the development of many diseases, including cancer. Gnotobiotic animal models have shown that the microbiota has many effects on host physiology, including on the development and regulation of immune responses. More recently, evidence has indicated that the microbiota can more specifically influence the outcome of cancer immunotherapy. Therapeutic interventions to optimize microbiota composition to improve immunotherapy outcomes have shown promise in mouse studies. Ongoing endeavors are translating these pre-clinical findings to early stage clinical testing. In this review we summarize 1) basic methodologies and considerations for studies of host-microbiota interactions; 2) experimental evidence towards a causal link between gut microbiota composition and immunotherapeutic efficacy; 3) possible mechanisms governing the microbiota-mediated impact on immunotherapy efficacy. Moving forward, there is need for a deeper understanding of the underlying biological mechanisms that link specific bacterial strains to host immunity. Integrating microbiome effects with other tumor and host factors regulating immunotherapy responsiveness versus resistance could facilitate optimization of therapeutic outcomes.

Indexed as

AnimalsAnti-Bacterial AgentsAntineoplastic Agents, ImmunologicalDisease Models, AnimalDrug Resistance, NeoplasmGastrointestinal MicrobiomeHumansImmunotherapyMiceNeoplasmsProgression-Free SurvivalAnti-Bacterial AgentsAntineoplastic Agents, Immunological16S rRNA gene sequencingAnti-PD-1Germ-free miceGut microbiomeImmune checkpoint blockadeImmunotherapyMetagenomicsMicrobiome-based therapy

Identifiers

PMID30995949
PMCPMC6471869

What OpenQuestion holds

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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.