Posnett D N, Duggan A, McGrath H
Department of Medicine, Cornell University Medical College, New York, NY 10021.
J Immunol. 1990 Feb 1;144(3):929-33.
The HC2 Ag is defined by a mAb raised against leukemic B lymphocytes from a patient with hairy cell leukemia (HCL). This 60 to 70-kDa Ag was immunoprecipitated from EBV-transformed B lymphoblastoid cell lines, from HCL-B cells, from the HUT-102 T cell line infected with HTLVI, and from activated monocytes. A binding assay with radioiodinated Fab' anti-HC2 confirmed this cellular distribution of the Ag and demonstrated 500 to 3000 binding sites on resting T cells, 300 to 11,000 binding sites on non-T cells, less than 3000 binding sites on chronic lymphocytic leukemia B cells, and 29,000 to 223,000 binding sites on HCL-B cells. PMA plus anti-CD3 up-regulated HC2 expression on T cells and IFN-gamma up-regulated expression on monocytes. On B cells, EBV transformation may result in HC2 expression, and antibody to HC2 has been found to inhibit B cell differentiation and proliferation. The combined results suggest an important role for the HC2 membrane-associated Ag on cells responsible for the immune response.
HC2抗原是由一种单克隆抗体所定义的,该单克隆抗体是针对一名毛细胞白血病(HCL)患者的白血病B淋巴细胞产生的。这种60至70千道尔顿的抗原可从EB病毒转化的B淋巴母细胞系、HCL - B细胞、感染HTLV - I的HUT - 102 T细胞系以及活化的单核细胞中通过免疫沉淀获得。用放射性碘化的抗HC2 Fab'进行的结合试验证实了该抗原的这种细胞分布,并显示静息T细胞上有500至3000个结合位点,非T细胞上有300至11,000个结合位点,慢性淋巴细胞白血病B细胞上少于3000个结合位点,而HCL - B细胞上有29,000至223,000个结合位点。佛波酯(PMA)加抗CD3可上调T细胞上的HC2表达,干扰素 - γ可上调单核细胞上的表达。在B细胞上,EB病毒转化可能导致HC2表达,并且已发现抗HC2抗体可抑制B细胞的分化和增殖。综合结果表明,HC2膜相关抗原在负责免疫反应的细胞上具有重要作用。