Nitta T, Ebato M, Sato K
Department of Neurosurgery, Juntendo University School of Medicine, Tokyo, Japan.
Neurosurg Rev. 1994;17(3):211-5. doi: 10.1007/BF00418435.
Many immune responses are controlled by genes of the major histocompatibility complex (MHC). In humans these include the loci encoding the HLA-A, -B, -C, -DR, -DQ, and -DP antigens, and many diseases have been linked with these. However, little information is available about any connection between malignant tumors and HLA. In this study the possible association of HLA-A, -B, -C and -DR specificities with susceptibilities to malignant glioma was investigated in 42 patients with malignant glioma and 42 controls with non-glial intracranial tumors using the Terasaki-NIH standard method. The data were also compared with those of the 11th International HLA Workshop. The result showed that a high frequency of HLA-24(9) was observed in patients with intracranial malignant gliomas, which was not common in other, non-glial patient groups. In animals the MHC acts in defense against virally induced tumors, but until now there has been no evidence that they do so in human gliomas. Our discovery of its association with an HLA antigen is important for understanding the immunogenetic basis of susceptibility to glioma.
许多免疫反应受主要组织相容性复合体(MHC)基因的控制。在人类中,这些基因包括编码HLA - A、- B、- C、- DR、- DQ和 - DP抗原的基因座,并且许多疾病都与这些基因座有关。然而,关于恶性肿瘤与HLA之间的任何联系,目前所知甚少。在本研究中,采用Terasaki - NIH标准方法,对42例恶性胶质瘤患者和42例非胶质细胞性颅内肿瘤患者进行研究,探讨HLA - A、- B、- C和 - DR特异性与恶性胶质瘤易感性之间的可能关联。还将这些数据与第11届国际HLA研讨会的数据进行了比较。结果显示,颅内恶性胶质瘤患者中观察到HLA - 24(9)的高频率,这在其他非胶质细胞性患者组中并不常见。在动物中,MHC可抵御病毒诱导的肿瘤,但迄今为止,尚无证据表明其在人类胶质瘤中也有此作用。我们发现其与一种HLA抗原相关,这对于理解胶质瘤易感性的免疫遗传基础具有重要意义。