Golding H, Singer A
J Immunol. 1985 Sep;135(3):1610-5.
Most cytolytic T lymphocytes (CTL) recognize class I rather than class II MHC determinants, and relatively little is known about those CTL that do recognize class II MHC determinants. The present study was undertaken to document the specificity, phenotype, and precursor frequency of primary class II allospecific CTL. It was found that class II-allospecific CTL could be consistently generated in vitro from unprimed spleen or thymus populations in the presence of exogenously added helper factors. The class II MHC specificity of both the precursor and CTL effectors activated in primary cultures by Ia-disparate stimulator cells was documented both by blocking experiments with anti-Ia mAb and by the use of L cell transfectants. The mechanism by which primary allospecific CTL effectors lysed their targets appeared to involve direct cell-cell contact, because they failed to lyse bystander target cells. The frequency in unprimed spleen populations of precursor CTL specific for class II alloantigens was examined by limiting dilution analysis and was found to be as high as 1/15,000 splenocytes and approximately 10% of the frequency reported for primary class I allospecific CTL. Finally, the Lyt phenotype of primary class II allospecific CTL precursors and effectors was determined. It was found that anti-class II CTL derive from at least two distinct precursor subpopulations that are either L3T4+Lyt-2- or L3T4-Lyt-2+, and that the Lyt phenotype expressed by the CTL effectors are concordant with that of their precursors. No correlation was found between the I subregion gene products recognized by CTL effectors and the Lyt phenotype they expressed in that both I-A- and I-E-specific CTL were both L3T4+Lyt-2- and L3T4-Lyt-2+.
大多数细胞溶解性T淋巴细胞(CTL)识别I类而非II类主要组织相容性复合体(MHC)决定簇,而对于那些确实识别II类MHC决定簇的CTL了解相对较少。本研究旨在记录原发性II类同种特异性CTL的特异性、表型和前体细胞频率。结果发现,在存在外源性添加的辅助因子的情况下,可从未经致敏的脾或胸腺细胞群体中在体外持续产生II类同种特异性CTL。通过用抗Ia单克隆抗体进行阻断实验以及使用L细胞转染体,证明了在原发性培养物中由Ia不同的刺激细胞激活的前体和CTL效应细胞的II类MHC特异性。原发性同种特异性CTL效应细胞裂解其靶标的机制似乎涉及直接的细胞间接触,因为它们不能裂解旁观者靶细胞。通过有限稀释分析检测了未经致敏的脾细胞群体中对II类同种抗原特异的前体CTL的频率,发现其高达1/15,000脾细胞,约为报道的原发性I类同种特异性CTL频率的10%。最后,确定了原发性II类同种特异性CTL前体和效应细胞的Lyt表型。发现抗II类CTL源自至少两个不同的前体亚群,即L3T4 + Lyt-2-或L3T4 - Lyt-2 +,并且CTL效应细胞表达的Lyt表型与其前体一致。未发现CTL效应细胞识别的I亚区基因产物与其表达的Lyt表型之间存在相关性,因为I-A特异性和I-E特异性CTL均为L3T4 + Lyt-2-和L3T4 - Lyt-2 +。