抗原
细胞毒性T细胞
CD8型
免疫学
外周血单个核细胞
黑色素瘤
生物
医学
癌症研究
体外
生物化学
作者
Danila Valmori,Valérie Dutoit,Danielle Líénard,Donata Rimoldi,Mikaël J. Pittet,Patrick Champagne,Kim Ellefsen,Uğur Şahin,Daniel E. Speiser,Ferdy J. Lejeune,Jean‐Charles Cerottini,Pedro Romero
出处
期刊:PubMed
日期:2000-08-15
卷期号:60 (16): 4499-506
被引量:192
摘要
Cancer testis (CT) antigens are particularly interesting candidates for cancer vaccines. However, T-cell reactivity to CT antigens has been detected only occasionally in cancer patients, even after vaccination. A new group of CT antigens has been recently identified using the SEREX technique based on immunoscreening of tumor cDNA expression libraries with autologous sera. We have used fluorescent HLA-A2/peptide tetramers containing an optimized antigenic peptide to directly identify HLA-A2-restricted CD8+ T cells specific for the SEREX-defined CT antigen NY-ESO-1 in melanoma patients. High frequencies of NY-ESO-1-specific CD8+ T cells were readily detected in peptide-stimulated peripheral blood mononuclear cells as well as in lymphocytes infiltrating melanoma lesions from patients with measurable antibody responses to NY-ESO-1. NY-ESO-1-specific CD8+ T cells were also detectable in peptide-stimulated peripheral blood mononuclear cells from some seronegative patients. Whereas the frequencies of NY-ESO-1-specific CD8+ T cells in circulating lymphocytes were usually below the limit of detection by tetramer staining, the presence of NY-ESO-1 CD8+ T cells displaying a memory phenotype was clearly detectable ex vivo in blood from a seropositive patient over an extended period of time. These results indicate that sustained CD8+ T-cell responses to CT antigens can naturally occur both locally and systemically in melanoma patients.
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