Rich S S, David C S, Rich R R
J Exp Med. 1979 Jan 1;149(1):114-26. doi: 10.1084/jem.149.1.114.
The presence of H-2 gene products on mixed leukocyte reaction (MLR) supressor factor was investigated by passage of MLR-suppressor factor (SF) over solid immunoadsorbents prepared with various anti-H-2 subregion sera. Antisera with specificity for all or certain I subregion determinants removed or significantly reduced suppressor activity; adsorption was not consistent with K or D region specificity. The single I subregion specificity common to all adsorbing preparations was I-C. Serologic differentiation of I-C products of k and d haplotypes expressed on MLR-SF was established with antisera prepared in I-Cd/I-Ck disparate strain combinations. These sera define allelic T cell restricted Lad determinants encoded by I-C genes. MLR-SF prepared from (BALB/c X CBA)F1 mice and exposed to the I-Cd and I-Ck specific adsorbents demonstrated d and k haplotype specific adsorption respectively. F1 suppressor activity adsorbed on an anti-I-Cd column was eluted by glycine-HCl buffer and suppressed only BALB/c (H-2d) responses. B10.A suppressor activity was removed by anti-I-Cd sera, but was unaffected by anti-I-Ck sera, indicating that B10.A suppressor activity is encoded by an I-C subregion derived from the d haplotype. Antisera with anti-I-Jk specificity did not remove suppressor activity of various H-2k factors. Finally, adsorption with antisera directed against H-2-associated determinants of the allogeneic cell used to stimulate suppressor factor generation demonstrated that sensitizing alloantigens are not components of MLR suppressor factor. Thus among the major histocompatibility complex (MHC)-controlled suppressor factors, MLR suppressor factor is uniquely determined by the I-C subregion.
通过将混合淋巴细胞反应(MLR)抑制因子(SF)通过用各种抗H-2亚区血清制备的固体免疫吸附剂,研究了H-2基因产物在MLR抑制因子上的存在情况。对所有或某些I亚区决定簇具有特异性的抗血清去除或显著降低了抑制活性;吸附与K或D区特异性不一致。所有吸附制剂共有的单一I亚区特异性是I-C。用在I-Cd/I-Ck不同品系组合中制备的抗血清建立了在MLR-SF上表达的k和d单倍型的I-C产物的血清学区分。这些血清定义了由I-C基因编码的等位基因T细胞限制性Lad决定簇。从(BALB/c×CBA)F1小鼠制备并暴露于I-Cd和I-Ck特异性吸附剂的MLR-SF分别表现出d和k单倍型特异性吸附。吸附在抗I-Cd柱上的F1抑制活性用甘氨酸-HCl缓冲液洗脱,并且仅抑制BALB/c(H-2d)反应。B10.A抑制活性被抗I-Cd血清去除,但不受抗I-Ck血清影响,表明B10.A抑制活性由源自d单倍型的I-C亚区编码。具有抗I-Jk特异性的抗血清没有去除各种H-2k因子的抑制活性。最后,用针对用于刺激抑制因子产生的同种异体细胞的H-2相关决定簇的抗血清进行吸附表明,致敏同种异体抗原不是MLR抑制因子的成分。因此,在主要组织相容性复合体(MHC)控制的抑制因子中,MLR抑制因子由I-C亚区独特地决定。