Friedman A, Lider O, Beraud E, Cohen I R
Department of Animal Science, Faculty of Agriculture, Hebrew University of Jerusalem, Israel.
Scand J Immunol. 1989 Jun;29(6):747-50.
Antigen fragments, biologically degraded by antigen-presenting cells (APC), combine with Ia positive moieties (IPM) to stimulate antigen-specific T lymphocyte lines. The main objective of this study was to evaluate whether this interaction was determined by the major histocompatibility complex (MHC) genotype of the APC, thus genetically restricting antigen-specific T lymphocyte proliferative responses. To do so, we assayed the capacity of processed basic protein, associated with IPM, to stimulate basic protein specific T lymphocyte lines derived from the Lewis (LW), Brown Norway (BN), and (LW x BN)F1 rat strains. Our findings are that: (a) IPM replaced the requirement for intact APC in proliferative responses of T lymphocytes to processed basic protein; (b) processed basic protein, irrespective of the genotype of APC from which it was prepared, was fully reconstituted by all IPM genotypes tested. Hence, the interaction between processed antigen and IPM was not found to be MHC-restricted. The possible implication of this conclusion is discussed.
抗原呈递细胞(APC)对其进行生物学降解后的抗原片段,会与Ia阳性部分(IPM)结合,以刺激抗原特异性T淋巴细胞系。本研究的主要目的是评估这种相互作用是否由APC的主要组织相容性复合体(MHC)基因型所决定,从而在遗传上限制抗原特异性T淋巴细胞的增殖反应。为此,我们检测了与IPM相关的经处理的碱性蛋白刺激来自Lewis(LW)、Brown Norway(BN)和(LW×BN)F1大鼠品系的碱性蛋白特异性T淋巴细胞系的能力。我们的研究结果如下:(a)在T淋巴细胞对经处理的碱性蛋白的增殖反应中,IPM取代了对完整APC的需求;(b)无论制备经处理的碱性蛋白的APC基因型如何,所有测试的IPM基因型都能使其完全重组。因此,未发现经处理的抗原与IPM之间的相互作用受MHC限制。本文讨论了这一结论的可能影响。