Viral antigen mismatch affects antiviral T-cell response and may impair immunotherapeutic efficacy against adult T-cell leukemia/lymphoma

Kenji Sugata, Mitsuyoshi Takatori, Omnia Reda, Benjy Jek Yang Tan, Masahito Tokunaga, Tomoo Sato, Mitsuharu Ueda, Yoshihisa Yamano, Atae Utsunomiya, Yorifumi Satou
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Abstract

HTLV-1 transforms primary CD4+ T cells in vitro within a short time; however, majority of infected individuals maintain an asymptomatic condition, suggesting there is an equilibrium between the infected cells and the host immunity. In this study, we identified a variation in a major viral antigen epitope, HTLV-1 Tax301-309, in HLA-A24-positive individuals. Mismatch in A24/Tax301-309 multimers impaired detection of anti-Tax CTLs. Notably, over half of the TCRs of the anti-Tax CTLs did not recognize mismatched Tax301-309 peptides. These findings highlighted the importance of matching the viral antigen epitope type in T-cell-based immunotherapy against ATL by using viral antigen Tax.
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病毒抗原错配会影响抗病毒 T 细胞反应,并可能损害针对成人 T 细胞白血病/淋巴瘤的免疫治疗效果
HTLV-1 可在体外短时间内转化初级 CD4+ T 细胞,但大多数感染者仍保持无症状状态,这表明感染细胞与宿主免疫之间存在平衡。在这项研究中,我们在 HLA-A24 阳性个体中发现了主要病毒抗原表位 HTLV-1 Tax301-309 的变异。A24/Tax301-309多聚体中的错配损害了抗Tax CTL的检测。值得注意的是,超过一半的抗泰克CTL的TCR不能识别不匹配的Tax301-309多肽。这些发现强调了在使用病毒抗原Tax的基于T细胞的ATL免疫疗法中匹配病毒抗原表位类型的重要性。
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