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人类白细胞抗原I类等位基因与黑色素瘤对α干扰素(IFN-α)和白细胞介素-2(IL-2)免疫治疗的反应性。

HLA class I alleles and responsiveness of melanoma to immunotherapy with interferon-alpha (IFN-alpha) and interleukin-2 (IL-2).

作者信息

Scheibenbogen C, Keilholz U, Mytilineos J, Suciu S, Manasterski M, Hunstein W

机构信息

Department of Medicine V (Hematology/Oncology), University of Heidelberg, Germany.

出版信息

Melanoma Res. 1994 Jun;4(3):191-4. doi: 10.1097/00008390-199406000-00008.

Abstract

MHC-restricted recognition of melanoma cells by cytotoxic T lymphocytes is an important mechanism in vitro. Several HLA alleles can function as restriction elements for melanoma cell recognition. In this study we investigated whether there is a correlation between responsiveness of patients with metastatic melanoma (MM) to immunotherapy and the HLA type of the patient. Seventy-two patients received immunotherapy with IFN-alpha and IL-2 according to two different schedules with an overall response rate of 24%. In 54 patients, including 16 responders and 16 patients with stable disease, in whom peripheral blood lymphocytes were available, we determined HLA haplotypes. As a control group we prospectively determined HLA types in 67 melanoma patients of all stages who underwent surgery or received chemotherapy and of 126 healthy donors from our blood bank. Two HLA alleles that have been shown to function as restriction elements in vitro were observed more frequently in responding patients, namely Cw7 (p = 0.014) and A1 (p = 0.19). No association was found for A2 and B44. These observations provide evidence that the responsiveness of MM to immunotherapy with IL-2 is associated with certain HLA types, suggesting an important role of HLA-restricted T lymphocytes for IL-2-induced tumour regression.

摘要

在体外,细胞毒性T淋巴细胞对黑色素瘤细胞的MHC限制性识别是一种重要机制。几种HLA等位基因可作为黑色素瘤细胞识别的限制元件。在本研究中,我们调查了转移性黑色素瘤(MM)患者对免疫治疗的反应性与患者的HLA类型之间是否存在相关性。72例患者根据两种不同方案接受了干扰素-α和白细胞介素-2免疫治疗,总缓解率为24%。在54例患者中,包括16例缓解者和16例病情稳定患者,其外周血淋巴细胞可用,我们确定了HLA单倍型。作为对照组,我们前瞻性地确定了67例接受手术或化疗的各期黑色素瘤患者以及我们血库中126名健康供者的HLA类型。在缓解患者中更频繁地观察到两种在体外已被证明可作为限制元件的HLA等位基因,即Cw7(p = 0.014)和A1(p = 0.19)。未发现A2和B44有相关性。这些观察结果提供了证据,表明MM对白细胞介素-2免疫治疗的反应性与某些HLA类型相关,提示HLA限制性T淋巴细胞对白细胞介素-2诱导的肿瘤消退起重要作用。

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