Teh H S, Phillips R A, Miller R G
J Immunol. 1978 Feb;120(2):425-8.
Murine cytotoxic lymphocyte precursor cells (CLP) appear to be specificity restricted, yet 2 to 4% of the total pool appears to be activated in a response against a single foreign H-2 alloantigen. The simplest model that provides enough CLP for all possible reactions is that H-2 antigens have cross-reacting determinants. Experimentally, we observed that activation of RNC-nu/+ (H-2k) LN cells with H-2b spleen cells activated 1200 to 1800 CLP per 10(6) LN cells capable of lysing H-2b target cells. Of these, 3 to 4% could also lyse H-2d target cells. In addition, a small number of clones (approximately 25/10(6) LN cells) were activated which could lyse H-2d but not H-2b target cells. However, the total number of such apparent nonspecifically activated clones is small since greater than 80% of all the CLP activated on culturing with H-2b alloantigens will lyse H-2b targets. The results are discussed in terms of specificity restriction and possible subpopulations of CLP.
小鼠细胞毒性淋巴细胞前体细胞(CLP)似乎具有特异性限制,但在针对单一外来H-2同种异体抗原的反应中,总库中2%至4%的细胞似乎被激活。能为所有可能反应提供足够CLP的最简单模型是H-2抗原具有交叉反应决定簇。在实验中,我们观察到用H-2b脾细胞激活RNC-nu/+(H-2k)淋巴结细胞,每10⁶个淋巴结细胞中可激活1200至1800个能够裂解H-2b靶细胞的CLP。其中,3%至4%的CLP也能裂解H-2d靶细胞。此外,还激活了少量克隆(约25/10⁶个淋巴结细胞),这些克隆能裂解H-2d靶细胞,但不能裂解H-2b靶细胞。然而,这种明显非特异性激活的克隆总数较少,因为在用H-2b同种异体抗原培养时激活的所有CLP中,超过80%会裂解H-2b靶细胞。将根据特异性限制和CLP可能的亚群对结果进行讨论。