In vivoanti-melanoma activities of the Melan-A/MART-1101-115T CD4+ cell peptide

Malignant melanoma causes significant health problems. The identification of tumour-associated antigens has led to novel approaches to increase T cell mediated anti-tumour immune response. Melan-A/MART-1 has been use as target antigen for several T cell based immunotherapeutic treatments. More recen...

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Veröffentlicht in:Vaccine 2009-10, Vol.27 (44), p.6107
Hauptverfasser: Balasse, Emilie, Gatouillat, Gregory, Patigny, Dominique, Andry, Marie Christine, Madoulet, Claudie
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container_issue 44
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container_title Vaccine
container_volume 27
creator Balasse, Emilie
Gatouillat, Gregory
Patigny, Dominique
Andry, Marie Christine
Madoulet, Claudie
description Malignant melanoma causes significant health problems. The identification of tumour-associated antigens has led to novel approaches to increase T cell mediated anti-tumour immune response. Melan-A/MART-1 has been use as target antigen for several T cell based immunotherapeutic treatments. More recently, the critical role of CD4+ T cells in inducing and maintaining anti-tumour immunity has been increasingly recognized. In order to optimize tumour immunotherapy, greater efforts have been concentrated on the identification of tumour antigens presented by MHC class II molecules to CD4+ T cells. In a publication, Tiwari et al. (2004)[1]have identified by a computational approach the 15-mer amino-acid sequence 101-115 (PPAYEKLSAEQSPPP) of the Melan-A/MART-1 as a good target for a vigorous and safe immunotherapy. Therefore, we have investigated thein vivoanti-tumour activity of this peptide in a murine melanoma model. For the prophylactic treatment, 20μg or 50μg peptide was subcutaneously injected in mice once a week during 3 weeks before tumour induction. Treatment with 50μg peptide significantly affected tumour development. Thus, our preliminary data demonstrate potentialin vivoprophylactic activity of the 101-115 peptide-based vaccine to control melanoma growth.
doi_str_mv 10.1016/j.vaccine.2009.07.109
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The identification of tumour-associated antigens has led to novel approaches to increase T cell mediated anti-tumour immune response. Melan-A/MART-1 has been use as target antigen for several T cell based immunotherapeutic treatments. More recently, the critical role of CD4+ T cells in inducing and maintaining anti-tumour immunity has been increasingly recognized. In order to optimize tumour immunotherapy, greater efforts have been concentrated on the identification of tumour antigens presented by MHC class II molecules to CD4+ T cells. In a publication, Tiwari et al. (2004)[1]have identified by a computational approach the 15-mer amino-acid sequence 101-115 (PPAYEKLSAEQSPPP) of the Melan-A/MART-1 as a good target for a vigorous and safe immunotherapy. Therefore, we have investigated thein vivoanti-tumour activity of this peptide in a murine melanoma model. 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source Elsevier ScienceDirect Journals
subjects Antigens
Cytotoxicity
Health problems
Immune response
Immune system
Immunotherapy
Lymphocytes
Melanoma
Peptides
Proteins
Skin cancer
Tumors
Vaccines
title In vivoanti-melanoma activities of the Melan-A/MART-1101-115T CD4+ cell peptide
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