Geczy A F, Coulits N
Immunology. 1982 Jan;45(1):139-45.
The in vivo effects of alloantisera, on the production of mixed leucocyte culture (MLC)-suppressor cells and suppressor factor (MLC-SF) as well as on the adoptive transfer of MLC suppression, were investigated. Intravenously administered anti-B.2 serum specifically eliminates B.2-associated MLC unresponsiveness and prevents the production of MLC-SF. By contrast, antisera directed against other B locus (homologous to the mouse H-2D or H-2K regions) or I region determinants do not appear to interfere with suppressor cell or factor production. Peritoneal exudate cells (PEC) from B.2-positive guinea-pigs can transfer MLC unresponsiveness to "normal' B.1-positive recipients; treatment of donor animals with anti-B.2 serum specifically prevents the transfer of MLC suppression. the results of this study support our earlier in vitro demonstration of B.2-bearing suppressor T cells which are sensitive to lysis by anti-B.2 sera in the presence of complement.
研究了同种抗血清对混合淋巴细胞培养(MLC)抑制细胞和抑制因子(MLC-SF)产生以及对MLC抑制的过继转移的体内作用。静脉注射抗B.2血清可特异性消除与B.2相关的MLC无反应性,并阻止MLC-SF的产生。相比之下,针对其他B位点(与小鼠H-2D或H-2K区域同源)或I区域决定簇的抗血清似乎不会干扰抑制细胞或因子的产生。来自B.2阳性豚鼠的腹腔渗出细胞(PEC)可将MLC无反应性转移至“正常”B.1阳性受体;用抗B.2血清处理供体动物可特异性阻止MLC抑制的转移。本研究结果支持我们早期在体外证明的携带B.2的抑制性T细胞,其在补体存在下对抗B.2血清的裂解敏感。