MELOE-1 is a new antigen overexpressed in melanomas and involved in adoptive T cell transfer efficiency - Archive ouverte HAL Access content directly
Journal Articles Journal of Experimental Medicine Year : 2008

MELOE-1 is a new antigen overexpressed in melanomas and involved in adoptive T cell transfer efficiency

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Abstract

A cytotoxic T lymphocyte (CTL) clone was derived from a tumor-infiltrating lymphocyte (TIL) population infused to a melanoma patient who remained relapse free for 10 yr after this adoptive transfer. This clone recognized all melanoma cell lines tested and, to a lower extent, melanocytes, in the context of human histocompatibility leukocyte antigen A2 (HLA-A2), but it did not recognize other tumor cell types. The gene coding for the antigen recognized by this clone was identified by the screening of a melanoma complementary DNA expression library. This antigen is overexpressed in melanomas, compared with other cancer cell lines and healthy tissues, and was thus called melanoma-overexpressed antigen (meloe). Remarkably, the structure of meloe was unusual, with multiple short open reading frames (ORFs). The peptide recognized by the CTL clone was encoded by one of these ORFs, called MELOE-1. Using a specific HLA-A2/peptide tetramer, we showed a correlation between the infusion of TILs containing MELOE-1-specific T cells and relapse prevention in HLA-A2 patients. Indeed, 5 out of 9 patients who did not relapse were infused with TILs that contained MELOE-1-specific T cells, whereas 0 out of the 21 patients who relapsed was infused with such TIL-containing lymphocytes. Overall, our results suggest that this new antigen is involved in immunosurveillance and, thus, represents an attractive target for immunotherapy protocols of melanoma.
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inserm-02482029 , version 1 (17-02-2020)

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Yann Godet, Agnès Moreau-Aubry, Yannick Guilloux, Virginie Vignard, Amir Khammari, et al.. MELOE-1 is a new antigen overexpressed in melanomas and involved in adoptive T cell transfer efficiency. Journal of Experimental Medicine, 2008, 205 (11), pp.2673-2682. ⟨10.1084/jem.20081356⟩. ⟨inserm-02482029⟩
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