Prevalence and Cellular Distribution of Novel Immune Checkpoint Targets Across Longitudinal Specimens in Treatment-naïve Melanoma Patients: Implications for Clinical Trials
Autor: | Robyn P. M. Saw, Richard A. Scolyer, Angela Ferguson, John F. Thompson, Ines Pires da Silva, Annie Tasker, Jarem Edwards, Ruth Allen, James S. Wilmott, Alexander M. Menzies, Benjamin M. Allanson, Marcel Batten, Umaimainthan Palendira, Georgina V. Long, Camelia Quek |
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Rok vydání: | 2019 |
Předmět: |
0301 basic medicine
Cancer Research business.industry medicine.medical_treatment Melanoma Receptor expression Cancer Immunotherapy medicine.disease Immune checkpoint 03 medical and health sciences 030104 developmental biology 0302 clinical medicine Immune system medicine.anatomical_structure Oncology 030220 oncology & carcinogenesis Cancer research medicine Receptor business Lymph node |
Zdroj: | Clinical Cancer Research. 25:3247-3258 |
ISSN: | 1557-3265 1078-0432 |
DOI: | 10.1158/1078-0432.ccr-18-4011 |
Popis: | Purpose: Immunotherapies targeting costimulating and coinhibitory checkpoint receptors beyond PD-1 and CTLA-4 have entered clinical trials. Little is known about the relative abundance, coexpression, and immune cells enriched for each specific drug target, limiting understanding of the biological basis of potential treatment outcomes and development of predictive biomarkers for personalized immunotherapy. We sought to assess the abundance of checkpoint receptors during melanoma disease progression and identify immune cells enriched for them. Experimental Design: Multiplex immunofluorescence staining for immune checkpoint receptors (ICOS, GITR, OX40, PD-1, TIM-3, VISTA) was performed on 96 melanoma biopsies from 41 treatment-naïve patients, including patient-matched primary tumors, nodal metastases, and distant metastases. Mass cytometry was conducted on tumor dissociates from 18 treatment-naïve melanoma metastases to explore immune subsets enriched for checkpoint receptors. Results: A small subset of tumor-infiltrating leukocytes expressed checkpoint receptors at any stage of melanoma disease. GITR and OX40 were the least abundant checkpoint receptors, with 70%) and other coinhibitory but not costimulatory receptors. The proportion of GITR+ T cells decreased from primary melanoma (>5%) to lymph node ( Conclusions: This study provides the first comprehensive assessment of immune checkpoint receptor expression in any cancer and provides important data for rational selection of targets for trials and predictive biomarker development. |
Databáze: | OpenAIRE |
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