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鉴定一种源自癌睾丸抗原HOM-MEL-40/SSX2的HLA-A*02限制性免疫原性肽。

Identification of an HLA-A*02 restricted immunogenic peptide derived from the cancer testis antigen HOM-MEL-40/SSX2.

作者信息

Wagner Claudia, Neumann Frank, Kubuschok Boris, Regitz Evi, Mischo Axel, Stevanovic Stefan, Friedrich Michael, Schmidt Werner, Rammensee Hans-Georg, Pfreundschuh Michael

机构信息

Med. Klinik I, Saarland University Medical School, D-66424 Homburg, Germany.

出版信息

Cancer Immun. 2003 Dec 17;3:18.

Abstract

HOM-MEL-40/SSX2 is a SEREX-defined cancer testis antigen with frequent expression in various human neoplasms. To search for HLA-A0201 restricted peptides that induce HOM-MEL-40/SSX2-specific CD8+ responses in breast cancer patients, we used the SYFPEITHI algorithm to identify three HOM-MEL-40/SSX2-derived nonamers with high binding affinity for HLA-A0201, which has a prevalence of 40% in the Caucasian population. Of the three peptides, p41-49 and p103-111 but not p167-175 had been shown to be processed by the proteasome. Only stimulation with p103-111 induced HOM-MEL-40-specific CTLs in 5/7 patients with HOM-MEL-40/SSX2 positive breast cancers and in 6/11 healthy controls. HLA-A*0201 restriction of p103-111 was demonstrated by blocking with specific antibodies. The natural processing and presentation of p103-111 was demonstrated by the recognition of the HOM-MEL-40/SSX2 positive cell line SK-MEL-37 and of COS7/A2 cells transfected with HOM-MEL-40/SSX2 by p103-111 specific CD8+ cells. No correlation was found between CD8+ T-cell responses against p103-111 and anti-HOM-MEL-40/SSX2 antibody titers in the serum of patients, suggesting that CD8+ and B-cell responses against HOM-MEL-40/SSX2 are regulated independently. p103-111 holds promise as a broadly applicable peptide vaccine for patients with HOM-MEL-40/SSX2 positive neoplasms.

摘要

HOM-MEL-40/SSX2是一种通过血清学鉴定的肿瘤睾丸抗原,在多种人类肿瘤中频繁表达。为了寻找能在乳腺癌患者中诱导HOM-MEL-40/SSX2特异性CD8+反应的HLA-A0201限制性肽段,我们使用SYFPEITHI算法鉴定出三条与HLA-A0201具有高结合亲和力的HOM-MEL-40/SSX2来源的九肽,该等位基因在白种人群中的频率为40%。在这三条肽段中,p41-49和p103-111而非p167-175已被证明可被蛋白酶体加工处理。仅用p103-111刺激可在5/7例HOM-MEL-40/SSX2阳性乳腺癌患者及6/11例健康对照中诱导出HOM-MEL-40特异性CTL。用特异性抗体阻断证明了p103-111的HLA-A*0201限制性。p103-111特异性CD8+细胞对HOM-MEL-40/SSX2阳性细胞系SK-MEL-37及转染了HOM-MEL-40/SSX2的COS7/A2细胞的识别证明了p103-111的天然加工和呈递。在患者血清中,针对p103-111的CD8+ T细胞反应与抗HOM-MEL-40/SSX2抗体滴度之间未发现相关性,提示针对HOM-MEL-40/SSX2的CD8+和B细胞反应是独立调节的。p103-111有望成为一种广泛适用于HOM-MEL-40/SSX2阳性肿瘤患者的肽疫苗。

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