Evidence map›Paper›PMID 38923991›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2024

Post-immunotherapy CTLA-4 Ig treatment improves antitumor efficacy.

Stephen Mok, Didem Ağaç Çobanoğlu, Huey Liu, James J Mancuso, James P Allison

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
–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

20 citing papers in PubMed.

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  6. Regulatory T cells in cancer and inflammation.Signal transduction and targeted therapy · 2026
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  16. B cell-derived acetylcholine mitigates skin inflammation in mice through α9 nicotinic acetylcholine receptor-mediated signaling.Proceedings of the National Academy of Sciences of the United States of America · 2025
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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.

Stephen MokDepartment of Immunology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030.
Didem Ağaç ÇobanoğluDepartment of Immunology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030.
Huey LiuDepartment of Immunology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030.
James J MancusoDepartment of Immunology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030.ORCID 0000-0001-5776-8617
James P AllisonDepartment of Immunology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immune checkpoint therapies (ICT) improve overall survival of patients with cancer but may cause immune-related adverse events (irAEs) such as myocarditis. Cytotoxic T lymphocyte-associated antigen 4 immunoglobulin fusion protein (CTLA-4 Ig), an inhibitor of T cell costimulation through CD28, reverses irAEs in animal models. However, concerns exist about potentially compromising antitumor response of ICT. In mouse tumor models, we administered CTLA-4 Ig 1) concomitantly with ICT or 2) after ICT completion. Concomitant treatment reduced antitumor efficacy, while post-ICT administration improved efficacy without affecting frequency and function of CD8 T cells. The improved response was independent of the ICT used, whether CTLA-4 or PD-1 blockade. The frequency of Tregs was significantly decreased with CTLA-4 Ig. The resulting increased CD8/Treg ratio potentially underlies the enhanced efficacy of ICT followed by CTLA-4 Ig. This paradoxical mechanism shows that a CTLA-4 Ig regimen shown to reduce irAE severity does not compromise antitumor efficacy.

Indexed as

CTLA-4 AntigenImmunotherapyAbataceptAnimalsCD8-Positive T-LymphocytesCell Line, TumorFemaleHumansImmune Checkpoint InhibitorsMiceMice, Inbred C57BLNeoplasmsProgrammed Cell Death 1 ReceptorT-Lymphocytes, RegulatoryAbataceptCTLA-4 AntigenImmune Checkpoint InhibitorsProgrammed Cell Death 1 Receptoranti-CTLA-4anti-PD-1immune checkpoint therapiesirAEsmyocarditis

Identifiers

PMID38923991
PMCPMC11228532

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.