TY - JOUR
T1 - Identification of CD4+ T cell epitopes from NY-ESO-1 presented by HLA- DR molecules
AU - Zeng, Gang
AU - Touloukian, Christopher E.
AU - Wang, Xiang
AU - Restifo, Nicholas P.
AU - Rosenberg, Steven A.
AU - Wang, Rong Fu
N1 - Copyright:
Copyright 2017 Elsevier B.V., All rights reserved.
PY - 2000/7/15
Y1 - 2000/7/15
N2 - In previous studies, the shared cancer-testis Ag, NY-ESO-1, was demonstrated to be recognized by both Abs and CD8+ T cells. Gene expression of NY-ESO-1 was detected in many tumor types, including melanoma, breast, and lung cancers, but was not found in normal tissues, with the exception of testis. In this study, we describe the identification of MHC class II- restricted T cell epitopes from NY-ESO-1. Candidate CD4+ T cell peptides were first identified using HLA-DR4 transgenic mice immunized with the NY- ESO-1 protein. NY-ESO-1-specific CD4+ T cells were then generated from PBMC of a patient with melanoma stimulated with the candidate peptides in vitro. These CD4+ T cells recognized NY-ESO-1 peptides or protein pulsed on HLA- DR4+ EBV B cells, and also recognized tumor cells expressing HLA-DR4 and NY- ESO-1. A 10-mer peptide (VLLKEFTVSG) was recognized by CD4+ T cells. These studies provide new opportunities for developing more effective vaccine strategies by using tumor-specific CD4+ T cells. This approach may be applicable to the identification of CD4+ T cell epitopes from many known tumor Ags recognized by CD8+ T cells.
AB - In previous studies, the shared cancer-testis Ag, NY-ESO-1, was demonstrated to be recognized by both Abs and CD8+ T cells. Gene expression of NY-ESO-1 was detected in many tumor types, including melanoma, breast, and lung cancers, but was not found in normal tissues, with the exception of testis. In this study, we describe the identification of MHC class II- restricted T cell epitopes from NY-ESO-1. Candidate CD4+ T cell peptides were first identified using HLA-DR4 transgenic mice immunized with the NY- ESO-1 protein. NY-ESO-1-specific CD4+ T cells were then generated from PBMC of a patient with melanoma stimulated with the candidate peptides in vitro. These CD4+ T cells recognized NY-ESO-1 peptides or protein pulsed on HLA- DR4+ EBV B cells, and also recognized tumor cells expressing HLA-DR4 and NY- ESO-1. A 10-mer peptide (VLLKEFTVSG) was recognized by CD4+ T cells. These studies provide new opportunities for developing more effective vaccine strategies by using tumor-specific CD4+ T cells. This approach may be applicable to the identification of CD4+ T cell epitopes from many known tumor Ags recognized by CD8+ T cells.
UR - http://www.scopus.com/inward/record.url?scp=0034662263&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0034662263&partnerID=8YFLogxK
U2 - 10.4049/jimmunol.165.2.1153
DO - 10.4049/jimmunol.165.2.1153
M3 - Article
C2 - 10878395
AN - SCOPUS:0034662263
SN - 0022-1767
VL - 165
SP - 1153
EP - 1159
JO - Journal of Immunology
JF - Journal of Immunology
IS - 2
ER -