首页> 外文OA文献 >T cell development in B cell-deficient mice. II. Serological characterization of suppressor T cell factors (TsF1) produced in normal mice and in mice treated chronically with rabbit anti-mouse IgM antibodies
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T cell development in B cell-deficient mice. II. Serological characterization of suppressor T cell factors (TsF1) produced in normal mice and in mice treated chronically with rabbit anti-mouse IgM antibodies

机译:B细胞缺陷小鼠的T细胞发育。二。在正常小鼠和长期用兔抗小鼠IgM抗体治疗的小鼠中产生的抑制性T细胞因子(TsF1)的血清学表征

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摘要

Serological analysis of idiotypic specificities present in azobenzenearsonate (ABA)-specific first-order suppressor T cell factors (TsF1) from C.AL-20 and BALB/c mice revealed a significant difference between TsF from these two strains of mice. The idiotypic composition of TsF1 from BALB/c mice appears to be more heterogeneous, and at least two different fractions can be readily identified. One bears the characteristic BALB/c-associated CRI(C) (crossreactive idiotype) determinants, and the other is non-CRI(C)-bearing. Analysis of ABA- specific TsF1 from animals lacking B cells uncovered a fundamental change in the expression of their idiotypic specificities. TsF from rabbit anti-mouse IgM (anti-mu)-treated C.AL-20 mice failed to express the characteristic CRI(A) determinants. Instead, they express CRI(C) specificities. Similarly, TsF1 from anti-mu-treated BALB/c mice did not express their characteristic CRI(C) specificities, but rather express CRI(A) determinants. These experiments provide strong evidence that the Igh restriction specificity of TsF is dictated by the particular idiotypic specificities expressed. They also clearly demonstrate that B cells and their products play an important role in establishing the idiotypic composition and repertoire of suppressor T cells.
机译:对来自C.AL-20和BALB / c小鼠的偶氮苯磺酸盐(ABA)特异性一级抑制性T细胞因子(TsF1)中存在的独特型进行血清学分析,发现这两种小鼠的TsF之间存在显着差异。来自BALB / c小鼠的TsF1的独特型组成似乎更具异质性,并且可以容易地识别出至少两个不同的部分。一个带有特征性的与BALB / c相关的CRI(C)(交叉反应独特型)的决定因素,另一个带有非CRI(C)的特征。对缺乏B细胞的动物进行的ABA特异性TsF1分析发现,其独特型特异性表达发生了根本性变化。来自兔抗小鼠IgM(抗μ)处理的C.AL-20小鼠的TsF无法表达特征性CRI(A)决定簇。相反,它们表示CRI(C)特异性。同样,来自抗mu处理的BALB / c小鼠的TsF1不表达其特征性CRI(C)特异性,而是表达CRI(A)决定簇。这些实验提供了有力的证据,表明TsF的Igh限制性特异性是由表达的特定独特型特异性决定的。他们还清楚地表明,B细胞及其产物在建立抑制T细胞的独特型组成和库中起着重要作用。

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