McDevitt H O, Sela M
J Exp Med. 1965 Sep 1;122(3):517-31. doi: 10.1084/jem.122.3.517.
Immunization of CBA and C57 mice with a branched, multichain synthetic polypeptide, poly (tyr,glu)-poly DL-ala--poly lys, ((T,G)-A--L), in Freund's complete adjuvant results in a tenfold or more difference in the antigen-binding capacity of sera from the two strains, although they respond equally to bovine serum albumin. Immunization of CBA x C57 F(1), F(1) x CBA, and F(1) x C57 mice reveals definite genetic control of the response to (T,G)-A--L, which appears to be due to a single major genetic factor, with perhaps one or more modifying factors. Immunization of CBA and C57 mice with (H,G)-A--L, a synthetic polypeptide in which histidine replaces tyrosine, gives the opposite result, CBA's respond and C57's do not. From this, it appears that the genetic control of the response to (T,G)-A--L is specific for the antigenic determinant. The implications of these results are discussed.
在弗氏完全佐剂中,用一种分支多链合成多肽聚(酪氨酰、谷氨酸)-聚DL-丙氨酸-聚赖氨酸((T,G)-A-L)对CBA和C57小鼠进行免疫,结果发现,尽管这两种品系的小鼠对牛血清白蛋白的反应相同,但它们血清的抗原结合能力相差10倍或更多。对CBA×C57 F(1)、F(1)×CBA和F(1)×C57小鼠进行免疫,结果显示对(T,G)-A-L的反应存在明确的遗传控制,这似乎是由一个主要遗传因素导致的,可能还有一个或多个修饰因素。用组氨酸取代酪氨酸的合成多肽(H,G)-A-L对CBA和C57小鼠进行免疫,结果相反,CBA小鼠有反应而C57小鼠没有。由此看来,对(T,G)-A-L反应的遗传控制对抗原决定簇具有特异性。文中讨论了这些结果的意义。