Chang Chien-Chung, Campoli Michael, Ferrone Soldano
Department of Immunology, Roswell Park Cancer Institute, Buffalo, New York 14263, USA.
Curr Opin Immunol. 2004 Oct;16(5):644-50. doi: 10.1016/j.coi.2004.07.015.
HLA class I antigen defects are frequently found in malignant cells. They appear to play a role in the clinical course of the disease, probably because they provide tumor cells with a mechanism to escape cytotoxic T lymphocyte (CTL) recognition and destruction. Expression of HLA class I antigens, however, is not always associated with the susceptibility of tumor cells to CTL lysis. Many mechanisms may underlie this finding, including the lack of tumor antigen (TA)-derived peptide presentation by a given HLA class I allospecificity, and/or the expression of immunosuppressive molecules such as HLA-G. These findings emphasize the need to develop probes to measure HLA class I allospecificity-TA peptide complex expression in malignant cells. Furthermore, the evaluation of the role of HLA class I antigens in the interaction of malignant cells with host immune cells should take into account the potential interference of tumor-derived immunomodulators.
HLA I类抗原缺陷在恶性细胞中经常被发现。它们似乎在疾病的临床进程中发挥作用,可能是因为它们为肿瘤细胞提供了一种逃避细胞毒性T淋巴细胞(CTL)识别和破坏的机制。然而,HLA I类抗原的表达并不总是与肿瘤细胞对CTL裂解的敏感性相关。这一发现可能有多种机制,包括特定HLA I类同种特异性缺乏肿瘤抗原(TA)衍生肽的呈递,和/或免疫抑制分子如HLA-G的表达。这些发现强调了开发探针以测量恶性细胞中HLA I类同种特异性-TA肽复合物表达的必要性。此外,在评估HLA I类抗原在恶性细胞与宿主免疫细胞相互作用中的作用时,应考虑肿瘤衍生免疫调节剂的潜在干扰。