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抗CD4对CD4、45RA+与CD4、45RO+ T细胞辅助功能的影响。

The effect of anti-CD4 on helper function of CD4,45RA+ versus CD4,45RO+ T cells.

作者信息

Wang J, Yan T, Simmer B, Emmrich F

机构信息

Max-Planck-Gesellschaft, Klinische Arbeitsgruppe für Rheumatologie/Immunologie Universität Erlangen-Nürnberg, Germany.

出版信息

Clin Exp Immunol. 1994 Jan;95(1):128-34. doi: 10.1111/j.1365-2249.1994.tb06026.x.

DOI:10.1111/j.1365-2249.1994.tb06026.x
PMID:8287596
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1534612/
Abstract

Here we have investigated and compared the effects of anti-CD4 on helper function of CD4,45RA+ versus CD4,45RO+ T cells. Only CD4,45RO+ cells, but not CD4,45RA+ cells were able to promote B cell differentiation resulting in immunoglobulin production in vitro (IgM as well as IgG) which could be inhibited by anti-CD4 MoAbs (MAX.16H5 and T151). In pokeweed mitogen (PWM)-induced B cell proliferation a similar pattern of responsiveness was obtained. When we studied the anti-CD4 effects on cytokine production in T cells stimulated in mixed lymphocyte reaction (MLR) or by mitogens, we found that neither IL-2 nor IL-4 production was dramatically influenced by anti-CD4 in CD4,45RO+ cells. This led us to the conclusion that the inhibitory effect of anti-CD4 on B cell proliferation and immunoglobulin secretion was not due to inhibition of cytokine production. To clarify this point, we investigated the ability of anti-CD4 to inhibit conjugate formation between B and T cells. It was found that CD4,45RO+ T cells formed more conjugates than CD4,45RA+ cells, and that only the conjugate formation by CD4,45RO+ T cells was inhibited by anti-CD4. These results suggest that (i) anti-CD4 inhibits T helper functions primarily by affecting CD4,45RO+ cells, and (ii) this effect is probably mediated by contact inhibition in the early phase of T-B collaboration.

摘要

在此,我们研究并比较了抗CD4对CD4、45RA+与CD4、45RO+ T细胞辅助功能的影响。只有CD4、45RO+细胞,而非CD4、45RA+细胞能够促进B细胞分化,从而在体外产生免疫球蛋白(IgM以及IgG),而抗CD4单克隆抗体(MAX.16H5和T151)可抑制这种产生。在商陆丝裂原(PWM)诱导的B细胞增殖中,获得了类似的反应模式。当我们研究抗CD4对混合淋巴细胞反应(MLR)或有丝分裂原刺激的T细胞中细胞因子产生的影响时,我们发现抗CD4对CD4、45RO+细胞中的IL-2和IL-4产生均无显著影响。这使我们得出结论,抗CD4对B细胞增殖和免疫球蛋白分泌的抑制作用并非由于细胞因子产生受到抑制。为阐明这一点,我们研究了抗CD4抑制B细胞与T细胞之间共轭体形成的能力。发现CD4、45RO+ T细胞形成的共轭体比CD4、45RA+细胞更多,并且只有CD4、45RO+ T细胞形成的共轭体受到抗CD4的抑制。这些结果表明:(i)抗CD4主要通过影响CD4、45RO+细胞来抑制T辅助功能;(ii)这种作用可能在T - B协作的早期阶段通过接触抑制介导。

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