Seman M, Zilberfarb V
Immunogenetics. 1981;12(1-2):89-99. doi: 10.1007/BF01561653.
A low level of IgG2a antibodies is observed in B10 mice after primary immunization with SRBC. Analysis of the response in different H-2b mice and among B10 animals with different H-2 haplotypes reveals that this selective isotype deficiency is under the control of at least two genes: a background gene and an H-2-linked gene. Responses of H-2 recombinant B10 strains map the H-2-linked gene to the 1-E subregion. Evidence is presented for complementation between H-2 and non-H-2 genes in the determination of the low responder phenotype. Low responsiveness appears to be inherited as a dominant trait. Possible functions of the two series of genes are discussed in relation to suppressor mechanisms.
用绵羊红细胞对B10小鼠进行初次免疫后,观察到其IgG2a抗体水平较低。对不同H-2b小鼠以及具有不同H-2单倍型的B10动物的反应分析表明,这种选择性同种型缺陷受至少两个基因的控制:一个背景基因和一个H-2连锁基因。H-2重组B10品系的反应将H-2连锁基因定位到1-E亚区。有证据表明,在低反应表型的决定中,H-2基因和非H-2基因之间存在互补作用。低反应性似乎作为显性性状遗传。结合抑制机制讨论了这两类基因的可能功能。