Sůla K, Sobotková E, Svobodová M, Nouza K
Institute of Experimental Medicine, Czechoslovak Academy of Sciences, Prague.
Immunobiology. 1988 Jul;177(3):305-16. doi: 10.1016/S0171-2985(88)80049-4.
Monoclonal mouse anti-Thy-1.2 antibody of IgG3 isotype (MTA) inhibits in a significant and long-term manner the regional graft-versus-host reaction (GVHR) when administered to donors as well as to recipients. The process of sensitization in the reaction of delayed type hypersensitivity to SRBC (DTH) is, on the other hand, suppressed only if MTA is administered immediately prior to sensitization. If the time interval between the injection of MTA and of SRBC is extended, the resulting DTH is stimulated. Similarly, the titers of total Ig against SRBC are decreased only if MTA is administered shortly before immunization. Contrasting effects of MTA on the production of IgM and IgG were observed. While the production of IgG was inhibited even after the time interval between the administration of MTA and immunization had been increased, the production of IgM antibodies was stimulated. In recipients of allogeneic Sarcoma I treated with MTA, the primary growth of the tumor is enhanced and the percentage of permanent progressors is increased. Mechanisms of MTA activity are discussed.
IgG3 同种型的单克隆小鼠抗 Thy-1.2 抗体(MTA)在给予供体以及受体时,能以显著且长期的方式抑制局部移植物抗宿主反应(GVHR)。另一方面,只有在致敏前立即给予 MTA,对 SRBC 的迟发型超敏反应(DTH)中的致敏过程才会受到抑制。如果 MTA 注射与 SRBC 注射之间的时间间隔延长,则会刺激产生 DTH。同样,只有在免疫前不久给予 MTA,针对 SRBC 的总 Ig 滴度才会降低。观察到 MTA 对 IgM 和 IgG 产生的对比效应。尽管在 MTA 给药与免疫之间的时间间隔增加后,IgG 的产生仍受到抑制,但 IgM 抗体的产生却受到刺激。在用 MTA 治疗的同种异体肉瘤 I 受体中,肿瘤的原发性生长增强,永久性进展者的百分比增加。本文讨论了 MTA 的作用机制。