Herzenberg L A, Okumura K, Cantor H, Sato V L, Shen F W, Boyse E A, Herzenberg L A
J Exp Med. 1976 Aug 1;144(2):330-44. doi: 10.1084/jem.144.2.330.
Allotype suppressor T cells (Ts) generated in SJL X BALB/c mice specifically suppress production of antibodies marked with the Ig-1a allotype. The studies presented here show that allotypes Ts suppress by specifically removing helper T cell (Th) activity required to facilitate differentiation and expansion of B cells to Ig-1b antibody-forming cells. We show first that Ts and Th belong to different T-cell subclasses as defined by Ly surface antigens. Ts are Ly2+Lyl- and thus belong to the same subclass as cytotoxic precursor and effector cells; Th are Lyl+Ly2- cells and thus belong to the subclass containing cells which can exert helper functions and initiate delayed hypersensitivity reactions. Placing these cells in these two subclasses shows that Th are different from Ts and suggests that they play different roles in regulating antibody responses. The difference in these roles is defined by the evidence presented here showing that Ts attack Th and regulate the antibody response by specifically regulating the availability of Th activity. We show that in allotype suppressed mice, Ts which suppress Ig-1b antibody production have completely removed the Th activity of helping Ig-1b cells without impairing Th activity which helps other IgB B cells. These findings imply the existence of allotype-specific Th for Ig-1b cells (Ig-1b Th). We directly establish that Ig-1b cells require such help by showing that carrier-primed spleen cells from Iga/Iga congenic hybrids help Ig-1a B cells from hapten-primed Igb/Iga donors but do not help Ig-1b B cells from the same donor in the same adoptive recipient.
在SJL×BALB/c小鼠中产生的同种异型抑制性T细胞(Ts)特异性抑制带有Ig-1a同种异型标记的抗体的产生。此处呈现的研究表明,同种异型Ts通过特异性去除促进B细胞分化和扩增为Ig-1b抗体形成细胞所需的辅助性T细胞(Th)活性来发挥抑制作用。我们首先表明,根据Ly表面抗原定义,Ts和Th属于不同的T细胞亚类。Ts是Ly2⁺Lyl⁻,因此与细胞毒性前体和效应细胞属于同一亚类;Th是Lyl⁺Ly2⁻细胞,因此属于包含能够发挥辅助功能并引发迟发型超敏反应的细胞的亚类。将这些细胞归为这两个亚类表明Th与Ts不同,并表明它们在调节抗体反应中发挥不同作用。这些作用的差异由此处呈现的证据界定,该证据表明Ts攻击Th并通过特异性调节Th活性的可用性来调节抗体反应。我们表明,在同种异型抑制的小鼠中,抑制Ig-1b抗体产生的Ts已完全消除了帮助Ig-1b细胞的Th活性,而未损害帮助其他IgB B细胞的Th活性。这些发现意味着存在针对Ig-1b细胞的同种异型特异性Th(Ig-1b Th)。我们通过证明来自Iga/Iga同基因杂种的载体致敏脾细胞可帮助来自半抗原致敏的Igb/Iga供体的Ig-1a B细胞,但在同一过继受体中却不能帮助来自同一供体的Ig-1b B细胞,直接证实了Ig-1b细胞需要这种帮助。