Pesando J M, Graf L
J Immunol. 1986 Jun 1;136(11):4311-8.
HLA class II antigens mediate interactions among cells involved in the immune response and play an important role in the process of self recognition. We made use of conventional alloantisera and six well-characterized monoclonal antibodies (MoAb) to study the HLA class II antigens on CALLA-positive malignant B cell populations and autologous normal B cell lines. Forty additional HLA class II-specific MoAb were also tested for their ability to bind to these cells. By using indirect immunofluorescence and immune precipitation assays, we find that malignant B cells often fail to express one or more of the three known types of HLA class II antigens. Cell lines with the following five phenotypes have been identified: HLA-DR+, -DQ+, -DP+; HLA-DR+, -DQ-, -DP+; HLA-DR-, -DQ+, -DP+; HLA-DR-, -DQ-, -DP+; and HLA-DR-, -DQ-, -DP-. These cell lines have been used to characterize the subregion specificity of MoAb that react with HLA class II antigens. This work confirms the existence of complicated patterns of serologic cross-reactivity between the three different types of HLA class II molecules. It also increases our understanding of the specificity of individual MoAb, thereby facilitating future investigation of the distribution and function of individual antigens. Our studies are consistent with the proposal that altered expression of HLA antigens on tumors might impair recognition of these cells by the immune system of the host, thereby contributing to the proliferation of a malignant clone.
人类白细胞抗原II类抗原介导免疫反应中细胞间的相互作用,并在自身识别过程中发挥重要作用。我们利用传统的同种抗血清和六种特征明确的单克隆抗体(MoAb)来研究CALLA阳性恶性B细胞群体和自体正常B细胞系上的人类白细胞抗原II类抗原。还检测了另外40种人类白细胞抗原II类特异性单克隆抗体与这些细胞结合的能力。通过间接免疫荧光和免疫沉淀试验,我们发现恶性B细胞常常无法表达三种已知类型的人类白细胞抗原II类抗原中的一种或多种。已鉴定出具有以下五种表型的细胞系:人类白细胞抗原-DR +、-DQ +、-DP +;人类白细胞抗原-DR +、-DQ -、-DP +;人类白细胞抗原-DR -、-DQ +、-DP +;人类白细胞抗原-DR -、-DQ -、-DP +;以及人类白细胞抗原-DR -、-DQ -、-DP -。这些细胞系已用于表征与人类白细胞抗原II类抗原反应的单克隆抗体的亚区域特异性。这项工作证实了三种不同类型的人类白细胞抗原II类分子之间存在复杂的血清学交叉反应模式。它还增进了我们对单个单克隆抗体特异性的理解,从而有助于未来对单个抗原的分布和功能进行研究。我们的研究与以下观点一致,即肿瘤上人类白细胞抗原表达的改变可能会损害宿主免疫系统对这些细胞的识别,从而导致恶性克隆的增殖。