Warner C M, Berntson T J, Eakley L, McIvor J L, Newton R C
J Exp Med. 1978 Jun 1;147(6):1849-53. doi: 10.1084/jem.147.6.1849.
The question of whether or not lymphoid cells can cooperate across a histocompatibility difference barrier has been studied in several laboratories. Using an adoptive transfer system, Katz et al. (1) first showed that T cells from (low responder x high responder) F(1) mice, primed to the terpolymer L-glutamic acid, L-lysine, L-tyrosine (GLT), could collaborate with 2,4-dinitrophenyl (DNP)-primed B cells from a high responder, but not a low responder strain, in response to DNP-GLT. The response to GLT is under H- 2-1inked Ir gene control. In contrast, studies with mouse bone marrow chimeras have shown that T cells can interact with H-2-histoincompatible B cells in response to antigens not under Ir gene control (2-4). Another type of chimera, the allophenic mouse, has been used to study possible histoincompatible cell interactions to a number of antigens, including DNP-L- glutamic acid, L-lysine, L-alanine; L-glutamic acid, L-alanine, L-tyrosine; L-glutamic acid, L-lysine, L-phenylalanine; and poly-L (Tyr, Glu)-poly D,L- Ala-poly-L-Lys[T,G)-A-L] (5-9). The response to each of these antigens is under H-2-1inked Ir gene control. It was initially reported (8, 9) that in allophenic mice containing both high and low responder cells, the antibody to (T,G)-A-L was of both the high and low responder allotype. This was interpreted to mean that high responder T cells had cooperated with low responder B cells across a histocompatibility difference barrier in the environment of the allophenic mice. However, Press and McDevitt (10) have recently reported that additional and more accurate analyses of these allophenic mouse sera failed to detect any anti-(T,G)-A-L antibody of the low responder allotype. Moreover, in an experiment using bone marrow chimeras, there was no low responder allotype antibody produced in response to (T,G)-A- L(10). The present study was undertaken to test the immune response of allophonic mice to an antigen, DNP-bovine gamma globulin (DNP(56)BGG), known to be controlled by genes both inside and outside the H-2 complex (11, 12).(1) When high and low responder cells to DNP(56)BGG are present in allophenic mice, only antibody of the high responder allotype is produced. The results suggest that cell cooperation in allophenic mice cannot occur across a histocompatibility difference barrier in response to an antigen whose genetic control is at least partially within the H-2 complex.
淋巴细胞能否跨越组织相容性差异屏障进行协作这一问题已在多个实验室展开研究。Katz等人(1)利用过继转移系统首先表明,来自(低反应者×高反应者)F1小鼠、经三元聚合物L-谷氨酸、L-赖氨酸、L-酪氨酸(GLT)致敏的T细胞,在对二硝基苯基(DNP)-GLT的反应中,能够与来自高反应者而非低反应者品系、经DNP致敏的B细胞协作。对GLT的反应受H-2连锁Ir基因控制。相比之下,对小鼠骨髓嵌合体的研究表明,T细胞能够与H-2组织不相容的B细胞相互作用,以应对不受Ir基因控制的抗原(2-4)。另一种嵌合体,即异表型小鼠,已被用于研究对多种抗原可能存在的组织不相容细胞相互作用,这些抗原包括DNP-L-谷氨酸、L-赖氨酸、L-丙氨酸;L-谷氨酸、L-丙氨酸、L-酪氨酸;L-谷氨酸、L-赖氨酸、L-苯丙氨酸;以及聚-L(酪氨酸,谷氨酸)-聚D,L-丙氨酸-聚-L-赖氨酸[T,G)-A-L](5-9)。对这些抗原中的每一种的反应都受H-2连锁Ir基因控制。最初有报道称(8,9),在同时含有高反应者和低反应者细胞的异表型小鼠中,针对(T,G)-A-L的抗体具有高反应者和低反应者两种同种异型。这被解释为意味着高反应者T细胞在异表型小鼠的环境中跨越了组织相容性差异屏障与低反应者B细胞进行了协作。然而,Press和McDevitt(10)最近报道,对这些异表型小鼠血清进行的进一步且更精确的分析未能检测到任何低反应者同种异型的抗(T,G)-A-L抗体。此外,在一项使用骨髓嵌合体的实验中,未产生针对(T,G)-A-L的低反应者同种异型抗体(10)。本研究旨在测试异表型小鼠对一种抗原,即二硝基苯基牛γ球蛋白(DNP(56)BGG)的免疫反应,已知该抗原受H-2复合体内部和外部的基因控制(11,12)。(1)当异表型小鼠中存在对DNP(56)BGG的高反应者和低反应者细胞时,仅产生高反应者同种异型的抗体。结果表明,在异表型小鼠中,针对其遗传控制至少部分在H-2复合体内的抗原,细胞协作无法跨越组织相容性差异屏障发生。