Abehsira O, Edwards A, Simpson E
Eur J Immunol. 1981 Apr;11(4):275-81. doi: 10.1002/eji.1830110402.
Monoclonal anti-Thy-1.1 and anti-Thy-1.2 antisera selected for complement-dependent cytotoxicity have high cytotoxic and binding titers on thymocytes and peripheral T cells of mouse strains bearing the appropriate Thy-1 allele. The effect of both anti-Thy=1.1 and anti-Thy-1.2 monoclonal antisera plus complement on cytoxic T cell effectors is to abrogate their activity. On the functional activity of precursor cytotoxic T cells, monoclonal antisera against the two alleles have different effects: anti-Thy1.2 plus complement removes precursor activity of Thy-1.2-bearing strains, including (Thy-1.1 X Thy-1.2) F heterozygotes, In contrast, six different anti-Thy-1.1 monoclonals, including four of the IgM class and two of the IgG class, failed to remove cytotoxic precursor activity from the splenic T cells of AKR, A. Thy-1.1 or (CBA X AKR) F1 mice. Analysis by florescence-activated cell sorting of in vitro cultured AKR spleen cells shows that Thy-1.1 antigen appears on the cel surface during the five-day culture period.
经选择用于补体依赖细胞毒性的抗Thy-1.1和抗Thy-1.2单克隆抗血清,对携带相应Thy-1等位基因的小鼠品系的胸腺细胞和外周T细胞具有高细胞毒性和结合效价。抗Thy-1.1和抗Thy-1.2单克隆抗血清加补体对细胞毒性T细胞效应器的作用是消除其活性。对于前体细胞毒性T细胞的功能活性,针对这两个等位基因的单克隆抗血清具有不同的作用:抗Thy1.2加补体可消除携带Thy-1.2品系的前体活性,包括(Thy-1.1×Thy-1.2)F杂合子。相比之下,六种不同的抗Thy-1.1单克隆抗体,包括四种IgM类和两种IgG类,未能从AKR、A.Thy-1.1或(CBA×AKR)F1小鼠的脾T细胞中去除细胞毒性前体活性。通过对体外培养的AKR脾细胞进行荧光激活细胞分选分析表明,在为期五天的培养期内,Thy-1.1抗原出现在细胞表面。