Billing R J, Clark B, Terasaki P I
Hum Immunol. 1980 Sep;1(2):141-50. doi: 10.1016/0198-8859(80)90101-9.
Heteroantisera were raised in rabbits to thymocytes, HSB2 cells, and Sezary cells. Following absorption with Ia-positive leukemia cells, these sera appeared to be specific for different T cell antigens. Both the anti-HSB2 and the anti-Sezary sera reacted with approximately 50% and the antithymocyte serum with 100% of normal peripheral blood T lymphocytes. None of the sera reacted with B cells. The apparent molecular weights of the antigens being detected were determined by immunoprecipitation followed by SDS polyacrylamide gel electrophoresis. A dimer of 170,000 daltons consisting of two similar 85,000-dalton polypeptide chains was immunoprecipitated by the anti-HSB2 serum whereas single polypeptides of 53,000 and 64,000 daltons were immunoprecipitated by the anti-Sezary and antithymocyte sera, respectively.
用兔制备针对胸腺细胞、HSB2细胞和Sezary细胞的异种抗血清。在用Ia阳性白血病细胞吸收后,这些血清似乎对不同的T细胞抗原具有特异性。抗HSB2血清和抗Sezary血清与大约50%的正常外周血T淋巴细胞发生反应,抗胸腺细胞血清与100%的正常外周血T淋巴细胞发生反应。这些血清均不与B细胞发生反应。通过免疫沉淀后进行SDS聚丙烯酰胺凝胶电泳来确定所检测抗原的表观分子量。抗HSB2血清免疫沉淀出由两条相似的85,000道尔顿多肽链组成的170,000道尔顿二聚体,而抗Sezary血清和抗胸腺细胞血清分别免疫沉淀出53,000道尔顿和64,000道尔顿的单一多肽。