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抗IgD抗体增强小鼠体外体液免疫反应。

Augmentation of in vitro humoral immune responses in the mouse by an antibody to IgD.

作者信息

Finkelham F D, Woods V L, Wilburn S B, Mond J J, Stein K E, Berning A, Scher I

出版信息

J Exp Med. 1980 Sep 1;152(3):493-506. doi: 10.1084/jem.152.3.493.

Abstract

Heterologous anti-delta-chain antibodies have an adjuvant effect on specific in vivo humoral immune responses to simultaneously, or subsequently, injected antigens in the rat and rhesus monkey. We have used a hybridoma-secreted antibody that binds murine delta-chain of the allotype (4.22aM delta a) to study this phenomenon in the mouse and to investigate the mechanism of this effect. Injection of 4.22aM delta a into BALB/c mice removes almost all surface IgD (sIgD) from splenic B lymphocites. sIgD does not reappear until the serum level of 4.22aM delta a decreased 5-7 d after injection. 4.22aM delta a fails to induce detectable proliferation or to raise total serum Ig levels substantially above control values. However, 4.22aM dalta a injected 24 h before antigen elicits an approximately twofold enhancement of serum IgM and a 3- to 10-fold enhancement of serum IgG anti-trintriphenyl (TNP) antibodies in response to immunization with optimal doses of TNP-Ficoll or TNP-sheep red blood cells (TNP-SRBC). 4.22aM delta a injected 1 wk before or 3 d after TNP-SRBC, however, has no effect on IgG anti-TNP levels. The adjuvant effect of anti-delta-chain antibody was markedly decreased when suboptimal antigen doses were used. Furthermore, even in the case of TNP-Ficoll, a relatively T-independent antigen, the ability of 4.22aM dalta a to enhance the anti-TNP antibody response was T cell dependent. Our data suggest that the binding of anti-delta-chain antibody to cell sIgD may partially activate B lymphocytes and make them more capable of differentiating into antibody-secreting cells when stimulated by antigen-specific T cell help.

摘要

异源抗δ链抗体对大鼠和恒河猴体内针对同时或随后注射的抗原的特异性体液免疫反应具有佐剂效应。我们使用了一种杂交瘤分泌的抗体,它能结合同种异型(4.22aM δ a)的鼠δ链,以在小鼠中研究这一现象并探究这种效应的机制。向BALB/c小鼠注射4.22aM δ a可去除脾B淋巴细胞中几乎所有的表面IgD(sIgD)。直到注射后5 - 7天血清中4.22aM δ a水平下降,sIgD才会重新出现。4.22aM δ a未能诱导可检测到的增殖,也未能使总血清Ig水平大幅高于对照值。然而,在抗原注射前24小时注射4.22aM δ a,在使用最佳剂量的三硝基苯基 - 聚蔗糖(TNP - Ficoll)或三硝基苯基 - 绵羊红细胞(TNP - SRBC)进行免疫时,可使血清IgM增强约两倍,血清抗三硝基苯基(TNP)IgG抗体增强3至10倍。然而,在TNP - SRBC注射前1周或注射后3天注射4.22aM δ a,对IgG抗TNP水平没有影响。当使用次优抗原剂量时,抗δ链抗体的佐剂效应明显降低。此外,即使在TNP - Ficoll这种相对非T细胞依赖性抗原的情况下,4.22aM δ a增强抗TNP抗体反应的能力也是T细胞依赖性的。我们的数据表明,抗δ链抗体与细胞sIgD的结合可能部分激活B淋巴细胞,并使它们在受到抗原特异性T细胞辅助刺激时更有能力分化为抗体分泌细胞。

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