Immune Responses to the Cancer Testis Antigen XAGE-1b in Non Small Cell Lung Cancer Caucasian Patients

被引:3
作者
Saito, Kanako [1 ]
Nakayama, Eiichi [2 ]
Valmori, Danila [1 ,3 ]
机构
[1] Inst Cancerol Ouest, INSERM, Equipe Labellisee Ligue Canc, U1102, Nantes, France
[2] Kawasaki Univ Med Welf, Fac Hlth & Welf, Kurashiki, Okayama, Japan
[3] Univ Nantes, Fac Med, Nantes, France
来源
PLOS ONE | 2016年 / 11卷 / 03期
关键词
CD4; T-CELLS; EWINGS-SARCOMA; THERAPY; EXPRESSION; NY-ESO-1; ANTIBODY; GENE; IDENTIFICATION; MUTATIONS; FEATURES;
D O I
10.1371/journal.pone.0150623
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Immunotherapy approaches using checkpoint blockade, alone, or in combination with tumor antigen vaccination, or adoptive cell transfer, are emerging as promising approaches for the treatment of non-small cell lung cancer (NSCLC). In preparation for upcoming combined immunotherapy approaches in NSCLC, here, we have assessed spontaneous immune responses to XAGE-1b, a tumor specific antigen of the Cancer Testis Antigen group that has been previously reported to be spontaneously immunogenic in the Japanese population, in a cohort of Caucasian patients with NSCLC. We found spontaneous serological responses to XAGE-1b in 9% of the patients. Importantly, these responses were limited to, and represented 13% of, patients with adenocarcinoma tumors, the most frequent histological subtype, for which immunotherapy approaches are under development. Using a set of overlapping peptides spanning the entire XAGE-1b protein, and in support of the serological data, we detected significant XAGE-1b specific CD4(+) T cell responses in all XAGE-1b seropositive patients and identified several CD4(+) T cell epitopes. Altogether, our results support the relevance of the XAGE-1b antigen in Caucasians NSCLC patients with adenocarcinoma, and the implementation of future immunotherapies exploiting the high immunogenicity of the antigen in this patient population.
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页数:11
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