Tsuda N, Nonaka Y, Shichijo S, Yamada A, Ito M, Maeda Y, Harada M, Kamura T, Itoh K
Department of Immunology, Kurume University School of Medicine, 67 Asohi-machi, Kurume, Fukuoka 830-0011, Japan.
Br J Cancer. 2002 Oct 21;87(9):1006-12. doi: 10.1038/sj.bjc.6600593.
Patient prognosis in the case of malignant brain tumours is generally poor, despite significant improvements in the early detection of the tumours, and thus the development of new treatment modalities is needed. One of the most prominent modalities is specific immunotherapy, for which the elucidation of antigenic molecules of malignant brain tumours recognized by T cells is essential. We report here a gene, UDP-Gal: betaGlcNAc beta1, 3-galactosyltransferase, polypeptide 3, encoding three epitope peptides recognised by tumor-reactive cytotoxic T lymphocytes in an HLA-A2-restricted manner. Two of the three peptides possessed an ability to induce HLA-A2-restricted and tumour-reactive cytotoxic T lymphocytes from peripheral blood mononuclear cells of patients with brain tumours. These peptides may be useful in the peptide-based specific immunotherapy for patients with malignant brain tumours.
尽管恶性脑肿瘤的早期检测有了显著改善,但患者的预后通常较差,因此需要开发新的治疗方法。最突出的方法之一是特异性免疫疗法,为此,阐明T细胞识别的恶性脑肿瘤抗原分子至关重要。我们在此报告一个基因,UDP-半乳糖:β-葡萄糖胺β1,3-半乳糖基转移酶,多肽3,其编码三种以HLA-A2限制性方式被肿瘤反应性细胞毒性T淋巴细胞识别的表位肽。这三种肽中的两种具有从脑肿瘤患者外周血单核细胞诱导HLA-A2限制性和肿瘤反应性细胞毒性T淋巴细胞的能力。这些肽可能对恶性脑肿瘤患者的基于肽的特异性免疫疗法有用。