Orgad S, Yang S Y, Gazit E, Relias V, Zaizov R, Lyson S, Yunis E J
Hum Immunol. 1985 Mar;12(3):133-41. doi: 10.1016/0198-8859(85)90331-3.
The presence of extra HLA antigens has been demonstrated, serologically and biochemically, on the surface of lymphoblasts from a patient with acute lymphoblastic leukemia of the T-cell subtype (T-ALL). Family analysis of this patient revealed the presence of the expected antigens, plus an additional HLA antigen (A24) which could be demonstrated by cytotoxicity on the lymphoblasts. Absorption studies revealed that the lymphoblasts had the ability to remove cytotoxic antibodies from alloantisera; similarly, absorption of these alloantisera with normal cells removed the reaction against the extra antigen from the lymphoblasts. The extra HLA molecules were also demonstrated by one-dimensional IEF. Two heavy chain-like molecules, together with the beta 2m subunit, were obtained after removal of appropriate antigens from externally labeled leukemia cells by the use of monoclonal antibody W6/32, which detects a class I specific determinant. The pI of the one heavy chain was shown to be very similar to that of the serologically detected A24. Our data thus suggest that the extra antigens detected by serological reagents may have been due to activation of silent class I MHC gene(s) at the protein level.
在一名T细胞亚型急性淋巴细胞白血病(T-ALL)患者的淋巴母细胞表面,已通过血清学和生化方法证实存在额外的HLA抗原。对该患者的家族分析显示存在预期的抗原,以及一种额外的HLA抗原(A24),可通过对淋巴母细胞的细胞毒性检测到。吸收研究表明,淋巴母细胞有能力从同种异体抗血清中去除细胞毒性抗体;同样,用正常细胞吸收这些同种异体抗血清可消除淋巴母细胞对额外抗原的反应。通过一维IEF也证实了额外的HLA分子。使用检测I类特异性决定簇的单克隆抗体W6/32从外部标记的白血病细胞中去除适当抗原后,获得了两条重链样分子以及β2m亚基。其中一条重链的pI显示与血清学检测到的A24非常相似。因此,我们的数据表明,血清学试剂检测到的额外抗原可能是由于沉默的I类MHC基因在蛋白质水平上的激活所致。