Response to Chemoimmunotherapy Is Associated With Expansion of Systemic Antitumor CD4 + Th1 Response in Metastatic Non-Small Cell Lung Cancer.


Journal

Journal of immunotherapy (Hagerstown, Md. : 1997)
ISSN: 1537-4513
Titre abrégé: J Immunother
Pays: United States
ID NLM: 9706083

Informations de publication

Date de publication:
01 09 2023
Historique:
received: 30 12 2022
accepted: 23 01 2023
medline: 10 8 2023
pubmed: 18 2 2023
entrez: 17 2 2023
Statut: ppublish

Résumé

Limited data have reported the evolution of antitumor immune responses under chemoimmunotherapy (chemo-IO) in patients with metastatic non-small cell lung cancer. In this concise study, we performed dynamic monitoring of antitumor CD4 + T helper 1 (Th1) response in peripheral blood from 12 patients receiving a first-line chemo-IO. Tumor-reactive CD4 + Th1 cells were assessed within blood lymphocytes using interferon-gamma enzyme-linked immunospot assay to detect telomerase (TERT)-specific T cells at baseline, 3 and 12 months after treatment. An induction of circulating anti-TERT CD4 + Th1 response were found in 6 of 12 patients at 3 months after chemo-IO. In contrast, 3 patients had a substantial decrease in their preexisting response and 3 remained nonimmune responders. Among patients with chemo-IO-induced immune response, half achieved an objective clinical response and had long-lasting circulating anti-TERT CD4 + Th1 cells detected for at least 1 year. In contrast, no objective response was documented in nonimmune responders and a link between the loss of anti-TERT CD4 + Th1 responses were observed in patients with progressive disease. This preliminary work supports a relationship between the efficacy of combinatorial chemo-IO and circulating anti-TERT CD4 + Th1 responses and highlights the interest to implement blood-based monitoring of tumor-reactive CD4 + T cells that could be additional help for patient management.

Identifiants

pubmed: 36799899
doi: 10.1097/CJI.0000000000000454
pii: 00002371-990000000-00039
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

279-283

Informations de copyright

Copyright © 2023 Wolters Kluwer Health, Inc. All rights reserved.

Références

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Auteurs

Mylène Wespiser (M)

INSERM, EFS, UMR1098, RIGHT, Host-Graft-Tumor Interactions & Cellular and Genetic Engineering, University of Bourgogne Franche-Comté, Besançon, France.
Department of Medical Oncology, University Hospital of Besançon, Besançon, France.

Amélie Marguier (A)

INSERM, EFS, UMR1098, RIGHT, Host-Graft-Tumor Interactions & Cellular and Genetic Engineering, University of Bourgogne Franche-Comté, Besançon, France.

Benoît Lecoester (B)

INSERM, EFS, UMR1098, RIGHT, Host-Graft-Tumor Interactions & Cellular and Genetic Engineering, University of Bourgogne Franche-Comté, Besançon, France.

Thibault Richard (T)

INSERM, EFS, UMR1098, RIGHT, Host-Graft-Tumor Interactions & Cellular and Genetic Engineering, University of Bourgogne Franche-Comté, Besançon, France.

Laura Boullerot (L)

INSERM, EFS, UMR1098, RIGHT, Host-Graft-Tumor Interactions & Cellular and Genetic Engineering, University of Bourgogne Franche-Comté, Besançon, France.
INSERM CIC-1431, EFS, Biomonitoring Platform, Besançon, France.

Marine Malfroy (M)

INSERM, EFS, UMR1098, RIGHT, Host-Graft-Tumor Interactions & Cellular and Genetic Engineering, University of Bourgogne Franche-Comté, Besançon, France.

Abhishek Kumar (A)

INSERM, EFS, UMR1098, RIGHT, Host-Graft-Tumor Interactions & Cellular and Genetic Engineering, University of Bourgogne Franche-Comté, Besançon, France.

Caroline Laheurte (C)

INSERM, EFS, UMR1098, RIGHT, Host-Graft-Tumor Interactions & Cellular and Genetic Engineering, University of Bourgogne Franche-Comté, Besançon, France.
INSERM CIC-1431, EFS, Biomonitoring Platform, Besançon, France.

Olivier Adotévi (O)

INSERM, EFS, UMR1098, RIGHT, Host-Graft-Tumor Interactions & Cellular and Genetic Engineering, University of Bourgogne Franche-Comté, Besançon, France.
Department of Medical Oncology, University Hospital of Besançon, Besançon, France.
INSERM CIC-1431, EFS, Biomonitoring Platform, Besançon, France.

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