Snodgrass H R, Bosma M J, Wilson D B
J Exp Med. 1981 Aug 1;154(2):491-500. doi: 10.1084/jem.154.2.491.
This study describes long-term-cultured lines and clones of cytotoxic T cells (Tc) with specificity for determinants of the Igh-1(b) immunoglobulin allotype. These Tc clones were initiated by repeated stimulation of immune spleen cells from BALB/c mice with an Igh-1(b)-producing myeloma, and then they were maintained in medium supplemented with mitogen-induced growth factors in the absence offurther antigenic stimulation . The lytic potency of these clones was 30-100-fold greater than the primary cultures from which they were derived, and specificity studies showed them to be lytic for Igh-1(b) targets and not for targets expressing Igh-1(a) or Igh-4(b), nor the lipopolysaccharide blasts . Finally, soluble preparations of Ig were tested for their ability to block lysis of labeled Igh-1(b)-expressing targets. The results showed that Igh-1(b) and not other immunoglobulin allotypes or isotypes could block lysis, and that the mechanism of lytic inhibition is due to Igh-1(b)-induced autolysis of the killer cells.
本研究描述了对Igh-1(b)免疫球蛋白同种异型决定簇具有特异性的细胞毒性T细胞(Tc)的长期培养系和克隆。这些Tc克隆是通过用产生Igh-1(b)的骨髓瘤反复刺激BALB/c小鼠的免疫脾细胞而启动的,然后在没有进一步抗原刺激的情况下,在补充有丝裂原诱导生长因子的培养基中进行培养。这些克隆的裂解效力比其来源的原代培养物高30至100倍,特异性研究表明它们对Igh-1(b)靶细胞具有裂解作用,而对表达Igh-1(a)或Igh-4(b)的靶细胞以及脂多糖刺激的胚细胞无裂解作用。最后,测试了Ig的可溶性制剂阻断标记的表达Igh-1(b)靶细胞裂解的能力。结果表明,Igh-1(b)而非其他免疫球蛋白同种异型或同型可以阻断裂解,并且裂解抑制机制是由于Igh-1(b)诱导杀伤细胞自溶。