Ayyoub Maha, Stevanovic Stefan, Sahin Ugur, Guillaume Philippe, Servis Catherine, Rimoldi Donata, Valmori Danila, Romero Pedro, Cerottini Jean-Charles, Rammensee Hans-Georg, Pfreundschuh Michael, Speiser Daniel, Lévy Frédéric
Division of Clinical Onco-Immunology, Ludwig Institute for Cancer Research, University Hospital, Lausanne, Switzerland.
J Immunol. 2002 Feb 15;168(4):1717-22. doi: 10.4049/jimmunol.168.4.1717.
The tumor Ag SSX-2 (HOM-MEL-40) was found by serological identification of Ags by recombinant expression cloning and was shown to be a cancer/testis Ag expressed in a wide variety of tumors. It may therefore represent a source of CD8(+) T cell epitopes useful for specific immunotherapy of cancer. To identify potential SSX-2-derived epitopes that can be recognized by CD8(+) T cells, we used an approach that combined: 1) the in vitro proteasomal digestion of precursor peptides overlapping the complete SSX-2 sequence; 2) the prediction of SSX-2-derived peptides with an appropriate HLA-A2 binding score; and 3) the analysis of a tumor-infiltrated lymph node cell population from an HLA-A2(+) melanoma patient with detectable anti-SSX-2 serum Abs. This strategy allowed us to identify peptide SSX-2(41-49) as an HLA-A2-restricted epitope. SSX2(41-49)-specific CD8(+) T cells were readily detectable in the tumor-infiltrated lymph node population by multimer staining, and CTL clones isolated by multimer-guided cell sorting were able to lyse HLA-A2(+) tumor cells expressing SSX-2.
通过重组表达克隆对肿瘤抗原进行血清学鉴定,发现了肿瘤抗原SSX-2(HOM-MEL-40),并证明它是一种在多种肿瘤中表达的癌胚抗原。因此,它可能是用于癌症特异性免疫治疗的CD8(+) T细胞表位的来源。为了鉴定可被CD8(+) T细胞识别的潜在SSX-2衍生表位,我们采用了一种组合方法:1)对与完整SSX-2序列重叠的前体肽进行体外蛋白酶体消化;2)预测具有适当HLA-A2结合评分的SSX-2衍生肽;3)分析来自一名具有可检测抗SSX-2血清抗体的HLA-A2(+)黑色素瘤患者的肿瘤浸润淋巴结细胞群体。该策略使我们能够鉴定出肽SSX-2(41-49)作为一种HLA-A2限制性表位。通过多聚体染色在肿瘤浸润淋巴结群体中很容易检测到SSX2(41-49)特异性CD8(+) T细胞,并且通过多聚体引导的细胞分选分离出的CTL克隆能够裂解表达SSX-2的HLA-A2(+)肿瘤细胞。
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