Evidence map›Paper›PMID 41415427›Full record

ArticlebioRxiv : the preprint server for biology2025

Phenotypic and functional characterization of tumor-reactive T cells in malignant pleural effusions.

Noam S Gaiger, Jack Coburn, Mark N Lee, Lin Zhang, Heng-Le Chen, Gavitt A Woodard, Harriet M Kluger, David A Schoenfeld, Benjamin Y Lu

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Noam S GaigerDepartment of Medicine (Section of Medical Oncology and Hematology), Yale School of Medicine, New Haven, CT, USA.ORCID 0000-0002-5638-1151
Jack CoburnDepartment of Medicine (Section of Medical Oncology and Hematology), Yale School of Medicine, New Haven, CT, USA.
Mark N LeeDepartment of Laboratory Medicine, Yale School of Medicine, New Haven, CT, USA.ORCID 0000-0002-9576-9589
Lin ZhangDepartment of Medicine (Section of Medical Oncology and Hematology), Yale School of Medicine, New Haven, CT, USA.
Heng-Le ChenDepartment of Medicine (Section of Medical Oncology and Hematology), Yale School of Medicine, New Haven, CT, USA.
Gavitt A WoodardDepartment of Surgery (Section of Thoracic Surgery), Yale School of Medicine, New Haven, CT, USA.
Harriet M KlugerDepartment of Medicine (Section of Medical Oncology and Hematology), Yale School of Medicine, New Haven, CT, USA.ORCID 0000-0002-4932-9873
David A SchoenfeldDepartment of Medicine (Section of Medical Oncology and Hematology), Yale School of Medicine, New Haven, CT, USA.ORCID 0000-0003-1948-3711
Benjamin Y LuDepartment of Medicine (Section of Medical Oncology and Hematology), Yale School of Medicine, New Haven, CT, USA.ORCID 0000-0001-8764-8384

Funding

Yale Pathology Tissue Services Shared ResourceP30CA016359 · NCI · YALE UNIVERSITY · PI MEGAN C KING · 1985 to 2026
$85.0M
Yale SPORE in Lung Cancer (YSILC): The Biology and Personalized Treatment of Lung CancerP50CA196530 · NCI · YALE UNIVERSITY · PI Kurt A Schalper · 2015 to 2026
$31.1M
YALE CANCER CENTER CALABRESI IMMUNO-ONCOLOGY TRAINING PROGRAMK12CA215110 · NCI · YALE UNIVERSITY · PI Harriet M. Kluger · 2018 to 2026
$6.1M
High Performance Computing Instrumentation for the Yale Center for Genome AnalysisS10OD030363 · OD · YALE UNIVERSITY · PI MANE, SHRIKANT M · 2022 to 2022
$1.2M
The antigen specificity of tumor-targeting T cells in non-small cell lung cancerK08CA270191 · NCI · YALE UNIVERSITY · PI Mark N. Lee · 2023 to 2026
$1.1M
NCI NIH HHS K08 CA270191NCI NIH HHS K12 CA215110NCI NIH HHS P30 CA016359NCI NIH HHS P50 CA196530NIH HHS S10 OD030363
6 · The paper itself

Abstract

Background: Adoptive cell therapy using tumor-infiltrating lymphocytes (TIL) is approved for the treatment of advanced melanoma but is limited by the need for patients to undergo surgical tumor resection. Malignant pleural effusions (MPE) may represent a more accessible source of tumor-reactive T cells. Here, we characterize the cellular composition as well as the transcriptional and functional properties of T cells from MPE compared with pulmonary metastasis and blood from a patient with melanoma. Methods: The immune cellular composition was immunophenotyped by high-dimensional flow cytometry from synchronously collected MPE, a lung metastasis, and blood from a patient with metastatic melanoma. Sorted CD3 Results: MPE had higher proportions of CD45 Conclusions: MPE harbors polyclonal, tumor-reactive T cells with lower features of terminal exhaustion and higher cytotoxic potential relative to tumor T cells. MPE may therefore serve as a more accessible source for TIL therapy.

Indexed as

adoptive cell therapyimmunotherapymalignant pleural effusionmelanomatumor-infiltrating lymphocytes

Identifiers

PMID41415427
PMCPMC12709480

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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.