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抗独特型抗体对体外人单克隆类风湿因子合成的抑制作用。靶细胞和分子要求。

Suppression of in vitro monoclonal human rheumatoid factor synthesis by antiidiotypic antibody. Target cells and molecular requirements.

作者信息

Koopman W J, Schrohenloher R E, Barton J C, Greenleaf E C

出版信息

J Clin Invest. 1983 Oct;72(4):1410-9. doi: 10.1172/JCI111097.

Abstract

Previous studies have indicated that antiidiotypic antibody can modulate expression of idiotype both in vivo and in vitro. Although the precise mechanisms underlying modulation of idiotype expression by antiidiotype remains unclear, a requirement for intact IgG antiidiotypic antibody has been suggested and T cells appear to play a role in some systems. We have studied peripheral blood mononuclear leukocytes (MNL) from a patient with a B cell lymphoma and a circulating IgMK rheumatoid factor (RF) paraprotein in an effort to delineate mechanisms involved in regulation of idiotype expression by antiidiotypic antibody. 1-10% of MNL from this patient could be cytoplasmically stained with specific F(ab')2 antiidiotypic antibody. MNL from the patient spontaneously synthesized IgM RF in culture that possessed the same idiotype as the circulating IgM RF paraprotein. Production of RF by MNL was suppressed by pretreatment with either intact IgG or the F(ab')2 fragments of antiidiotypic antibody (50% inhibitory concentration was 0.2 and 1.1 micrograms/culture, respectively). In contrast, the Fab' fragment of antiidiotypic antibody was not inhibitory (up to 57 micrograms/culture) despite retaining demonstrable antiidiotype activity. Suppression of RF production was not observed over the same concentration range with the IgG or F(ab')2 fractions of a non-cross-reactive antiidiotypic antibody prepared against another monoclonal IgMK RF paraprotein or with IgG or F(ab')2 fractions prepared from normal rabbit serum. Inhibition of RF production by antiidiotypic antibody did not require T cells. Antiidiotypic antibody decreased intracellular and extracellular levels of idiotype indicating diminished synthesis of idiotype by the patient's B cells. Synthesis of IgM RF by MNL obtained from unrelated donors was not suppressed by the antiidiotypic antibody specific for the patient's paraprotein. The results indicate that (a) antiidiotypic antibody is capable of directly suppressing human B cell release of idiotype, (b) the bivalent antigen-binding fragment (F[ab']2) of antiidiotypic antibody is sufficient for mediating such suppression, (c) an intact Fc portion of antiidiotypic antibody enhances suppression of idiotype, and (d) antiidiotypic antibody inhibits idiotype expression by suppressing synthesis of idiotype.

摘要

以往的研究表明,抗独特型抗体在体内和体外均可调节独特型的表达。尽管抗独特型抗体调节独特型表达的确切机制尚不清楚,但已有人提出完整的IgG抗独特型抗体是必需的,而且在某些系统中T细胞似乎发挥了作用。我们研究了一名B细胞淋巴瘤患者的外周血单个核白细胞(MNL)以及一种循环IgMκ类风湿因子(RF)副蛋白,以阐明抗独特型抗体调节独特型表达所涉及的机制。该患者1% - 10%的MNL可被特异性F(ab')2抗独特型抗体进行胞质染色。患者的MNL在培养中可自发合成与循环IgMκ RF副蛋白具有相同独特型的IgM RF。用完整的IgG或抗独特型抗体的F(ab')2片段预处理可抑制MNL产生RF(50%抑制浓度分别为0.2和1.1微克/培养物)。相比之下,尽管抗独特型抗体的Fab'片段保留了可证实的抗独特型活性,但却没有抑制作用(高达57微克/培养物)。针对另一种单克隆IgMκ RF副蛋白制备的非交叉反应性抗独特型抗体的IgG或F(ab')2片段,以及从正常兔血清制备的IgG或F(ab')2片段,在相同浓度范围内均未观察到对RF产生的抑制作用。抗独特型抗体抑制RF产生并不需要T细胞。抗独特型抗体降低了独特型的细胞内和细胞外水平,表明患者B细胞合成独特型的能力减弱。从无关供体获得的MNL合成IgM RF并未被针对该患者副蛋白的抗独特型抗体所抑制。结果表明:(a)抗独特型抗体能够直接抑制人B细胞释放独特型;(b)抗独特型抗体的二价抗原结合片段(F(ab')2)足以介导这种抑制作用;(c)抗独特型抗体完整的Fc部分可增强对独特型的抑制作用;(d)抗独特型抗体通过抑制独特型的合成来抑制独特型表达。

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