Collavo D, Biasi G, Colombatti A, Chieco-Bianchi L
Eur J Immunol. 1976 Sep;6(9):612-8. doi: 10.1002/eji.1830060904.
Primary virus-induced murine leukemias and transplantable leukemic cell lines, originally induced by virus, chemical or physical agents, failed to stimulate normal spleen cells differing at the H-2 complex or at Mls locus in the one-way mixed leukocyte culture. Lack of stimulation seems at least partially due to a nonspecific inhibitory effect since in a "three-party" culture system the leukemic cells interfered with the mixed leukocyte reaction (MLR) of normal allogeneic cells. Characterization of the leukemic cell populations used, according to their T or B cell origin, disclosed that in most cases T cell markers were present. Also, no Ia antigens were detected on leukemic cells. Furthermore, using a 51Cr release assay, leukemic cells could sensitize allogeneic normal lymphocytes to kill specifically normal as well as leukemic targets, even when no MLR was detected in parallel cultures.
原发性病毒诱导的鼠白血病以及最初由病毒、化学或物理因素诱导产生的可移植白血病细胞系,在单向混合淋巴细胞培养中无法刺激在H-2复合体或Mls位点存在差异的正常脾细胞。缺乏刺激作用似乎至少部分归因于非特异性抑制效应,因为在“三方”培养系统中,白血病细胞干扰了正常同种异体细胞的混合淋巴细胞反应(MLR)。根据白血病细胞群体的T或B细胞起源对其进行表征,结果显示在大多数情况下存在T细胞标志物。此外,在白血病细胞上未检测到Ia抗原。此外,使用51Cr释放试验,白血病细胞可以使同种异体正常淋巴细胞致敏,从而特异性杀伤正常以及白血病靶细胞,即使在平行培养中未检测到MLR。