Influence of ipilimumab on expanded tumour derived T cells from patients with metastatic melanoma

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INTRODUCTION: Tumour infiltrating lymphocyte (TIL) based adoptive cell therapy (ACT) is a promising treatment for patients with advanced melanoma. Retrospective studies suggested an association between previous treatment with anti-CTLA-4 antibodies and long term survival after subsequent ACT. Thus, we hypothesized that treatment with anti-CTLA-4 antibodies can induce favourable changes to be detected in TILs.

RESULTS: Expanded T cells from Ipilimumab treated patients had a higher proportion of cells expressing CD27, intracellular CTLA-4, TIM-3 and LAG-3. In addition, broader and more frequent T cell responses against common tumour antigens were detected in patients treated with Ipilimumab as compared to anti-CTLA-4 naïve patients.

MATERIALS AND METHODS: Expanded TILs were obtained from patients with advanced melanoma who had received Ipilimumab in the previous six months, or had not received any type of anti-CTLA-4 antibody. T cell specificity and expression of phenotypic and exhaustion markers were scrutinized as well as functional properties.

CONCLUSIONS: Ipilimumab may induce tumor-infiltration of T cells of a more naïve phenotype expressing markers related to activation or exhaustion. Additionally, Ipilimumab may increase the frequency of T cells recognizing common tumour associated antigens.

Original languageEnglish
JournalOncoTarget
Volume8
Issue number16
Pages (from-to)27062-27074
ISSN1949-2553
DOIs
Publication statusPublished - 2017

    Research areas

  • Adult, Aged, Antineoplastic Agents, Immunological/pharmacology, Antineoplastic Combined Chemotherapy Protocols/adverse effects, Biomarkers, CTLA-4 Antigen/antagonists & inhibitors, Female, Humans, Immunomodulation/drug effects, Ipilimumab/pharmacology, Lymphocyte Activation/drug effects, Lymphocytes, Tumor-Infiltrating/drug effects, Male, Melanoma/drug therapy, Middle Aged, Neoplasm Grading, Neoplasm Staging, Phenotype, T-Cell Antigen Receptor Specificity/immunology

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