Kontianen S, Howie S, Maurer P H, Feldmann M
J Immunol. 1979 Jan;122(1):253-9.
The capacity of responder and nonresponder strains of mice to generate suppressor cells and factors to two antigens under MHC linked Ir gene control was investigated. Eight different H-2 types (H-2b,d,f,k,p,q,r,s) as well as seven independently derived strains (B10, BALB/c, CBA/Ca, A/St, DBA/2, P/J, SJL) were tested, and all yielded suppressor factor (SF) to (T,G)-A--L and GAT. This indicated that the genetic control of SF production was different from that of helper cell induction. Unlike previous reports of GAT suppressor extracts that GAT-specific supressor factors acted equally on both responder and nonresponder strains. As reported earlier with in vitro induced protein- (KLH) specific suppressor factors, GAT and (T,G)-A--L specific suppressor factors failed to show any genetic restriction in their function. The implications of these results for the general mechanism of Ir gene control are discussed.
研究了应答和不应答品系小鼠在MHC连锁Ir基因控制下产生针对两种抗原的抑制细胞和因子的能力。测试了八种不同的H-2类型(H-2b、d、f、k、p、q、r、s)以及七个独立衍生的品系(B10、BALB/c、CBA/Ca、A/St、DBA/2、P/J、SJL),所有品系都产生了针对(T,G)-A--L和GAT的抑制因子(SF)。这表明SF产生的遗传控制与辅助细胞诱导的遗传控制不同。与先前关于GAT抑制提取物的报道不同,GAT特异性抑制因子对等应答和不应答品系均有作用。如先前关于体外诱导的蛋白质(KLH)特异性抑制因子的报道,GAT和(T,G)-A--L特异性抑制因子在其功能上未显示任何遗传限制。讨论了这些结果对Ir基因控制一般机制的意义。