Detection of ABCB5 tumour antigen-specific CD8+ T cells in melanoma patients and implications for immunotherapy
Autor: | A. Tahedl, C. Maβlo, Markus H. Frank, Christoph Ganss, Sylvia Borchers, Jasmina Esterlechner, Y. Nowak, J. Volkind, Mark A. Kluth, V Umansky, Carola A. Müller, Jochen Utikal |
---|---|
Rok vydání: | 2017 |
Předmět: |
0301 basic medicine
business.industry medicine.medical_treatment T cell Immunology ABCB5 Immunotherapy 03 medical and health sciences Interleukin 21 030104 developmental biology 0302 clinical medicine medicine.anatomical_structure Immune system Cancer immunotherapy 030220 oncology & carcinogenesis medicine Cancer research Immunology and Allergy Cytotoxic T cell business CD8 |
Zdroj: | Clinical and Experimental Immunology. 191:74-83 |
ISSN: | 1365-2249 0009-9104 |
Popis: | Summary ATP binding cassette subfamily B member 5 (ABCB5) has been identified as a tumour-initiating cell marker and is expressed in various malignancies, including melanoma. Moreover, treatment with anti-ABCB5 monoclonal antibodies has been shown to inhibit tumour growth in xenotransplantation models. Therefore, ABCB5 represents a potential target for cancer immunotherapy. However, cellular immune responses against ABCB5 in humans have not been described so far. Here, we investigated whether ABCB5-reactive T cells are present in human melanoma patients and tested the applicability of ABCB5-derived peptides for experimental induction of human T cell responses. Peripheral blood mononuclear cells (PBMNC) isolated from blood samples of melanoma patients (n = 40) were stimulated with ABCB5 peptides, followed by intracellular cytokine staining (ICS) for interferon (IFN)-γ and tumour necrosis factor (TNF)-α. To evaluate immunogenicity of ABCB5 peptides in naive healthy donors, CD8 T cells were co-cultured with ABCB5 antigen-loaded autologous dendritic cells (DC). ABCB5 reactivity in expanded T cells was assessed similarly by ICS. ABCB5-reactive CD8+ T cells were detected ex vivo in 19 of 29 patients, melanoma antigen recognised by T cells (MART-1)-reactive CD8+ T cells in six of 21 patients. In this small, heterogeneous cohort, reactivity against ABCB5 was significantly higher than against MART-1. It occurred significantly more often and independently of clinical characteristics. Reactivity against ABCB5 could be induced in 14 of 16 healthy donors in vitro by repeated stimulation with peptide-loaded autologous DC. As ABCB5-reactive CD8 T cells can be found in the peripheral blood of melanoma patients and an ABCB5-specific response can be induced in vitro in naive donors, ABCB5 could be a new target for immunotherapies in melanoma. |
Databáze: | OpenAIRE |
Externí odkaz: |