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Immunology

NY-ESO-1 119–143 Is a Promiscuous Major Histocompatibility Complex Class II T-Helper Epitope Recognized by Th1- and Th2-Type Tumor-reactive CD4+ T Cells

Hassane M. Zarour, Bernard Maillere, Vladimir Brusic, Kara Coval, Eileen Williams, Sandra Pouvelle-Moratille, Florence Castelli, Stephanie Land, Jaafar Bennouna, Theodore Logan and John M. Kirkwood
Hassane M. Zarour
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Bernard Maillere
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Vladimir Brusic
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Kara Coval
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Eileen Williams
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Sandra Pouvelle-Moratille
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Florence Castelli
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Stephanie Land
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Jaafar Bennouna
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Theodore Logan
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John M. Kirkwood
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DOI:  Published January 2002
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Abstract

The NY-ESO-1 gene product is expressed by a range of human tumors and is recognized by antibodies from sera of cancer patients with NY-ESO-1-expressing tumors. The NY-ESO-1 gene also encodes several MHC class I- and MHC class II-restricted tumor epitopes recognized by T lymphocytes. In particular, we previously reported that the NY-ESO-1 119–143 peptide contains at least two HLA-DRB1*0401-presented epitopes that are recognized by melanoma-reactive CD4+ T cells. Here we report that the NY-ESO-1 119–143 peptide can be presented in the context of multiple HLA-DR alleles to stimulate tumor-reactive CD4+ T cells. The NY-ESO-1 119–143 peptide is able to bind to several DR molecules. The NY-ESO-1 119–143 peptide is also capable of inducing specific CD4+ T cells in vitro from peripheral blood lymphocytes of normal donors and patients with melanoma who express these HLA-DR alleles. These CD4+ T cells recognize NY-ESO-1+, HLA-matched or autologous melanoma cell lines, as well as autologous antigen-presenting cells fed with the NY-ESO-1 protein. We also demonstrate that the NY-ESO-1 119–143 peptide stimulates in vitro both Th1-type and Th2-type CD4+ T-cell responses from peripheral blood lymphocytes of normal donors and melanoma patients. Taken together, these data suggest a key role of the NY-ESO-1 119–143 peptide sequence in the induction of cellular and humoral responses against NY-ESO-1-expressing tumors. They support the relevance of cancer vaccine trials with the NY-ESO-1 119–143 peptide in the large number of cancer patients with NY-ESO-1-expressing tumors.

Footnotes

  • The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked advertisement in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

  • ↵1 This work was supported by NIH Grant CA 56774 (to J. M. K.), a Clinical Trial Grant/Melanoma Initiative from the Cancer Research Institute (to J. M. K.), the Competitive Medical Research Fund of the University of Pittsburgh Medical Center, and a Cancer Research Institute/Elaine R. Shepard Memorial Fellowship (to H. M. Z.).

  • ↵2 To whom requests for reprints should be addressed, at the University of Pittsburgh Cancer Institute, Biomedical Science Tower, E 1051, 211 Lothrop Street, Pittsburgh, PA 15213-2582. Phone: (412) 648-9119; Fax: (412) 624-7794; E-mail: zarourhm{at}msx.upmc.edu

  • Received July 30, 2001.
  • Accepted November 1, 2001.
  • ©2002 American Association for Cancer Research.
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Cancer Research: 62 (1)
January 2002
Volume 62, Issue 1
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NY-ESO-1 119–143 Is a Promiscuous Major Histocompatibility Complex Class II T-Helper Epitope Recognized by Th1- and Th2-Type Tumor-reactive CD4+ T Cells
Hassane M. Zarour, Bernard Maillere, Vladimir Brusic, Kara Coval, Eileen Williams, Sandra Pouvelle-Moratille, Florence Castelli, Stephanie Land, Jaafar Bennouna, Theodore Logan and John M. Kirkwood
Cancer Res January 1 2002 (62) (1) 213-218;

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NY-ESO-1 119–143 Is a Promiscuous Major Histocompatibility Complex Class II T-Helper Epitope Recognized by Th1- and Th2-Type Tumor-reactive CD4+ T Cells
Hassane M. Zarour, Bernard Maillere, Vladimir Brusic, Kara Coval, Eileen Williams, Sandra Pouvelle-Moratille, Florence Castelli, Stephanie Land, Jaafar Bennouna, Theodore Logan and John M. Kirkwood
Cancer Res January 1 2002 (62) (1) 213-218;
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