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抗原特异性人类B淋巴细胞反应的激活与免疫调节:单核细胞的多方面作用

Activation and immunoregulation of antigen-specific human b lymphocyte responses: multifaceted role of the monocyte.

作者信息

Gerrard T L, Fauci A S

出版信息

J Immunol. 1982 May;128(5):2367-72.

PMID:6174632
Abstract

The multifaceted role of the monocyte in the induction and modulation of antigen-specific antibody responses by human B cells was delineated. Monocytes were absolutely required for the induction of specific antibody responses to both TT and KLH in an antigen-induced in vitro assay. Monocytes were also required for the PWM induction of specific antibody in immunized subjects. Pulsing monocytes with specific antigen or with PWM consistently stimulated proliferation of T cells in absence of added antigen and could also stimulate specific antibody synthesis although less consistently. Stimulation of specific antibody responses with antigen required fewer numbers of monocytes than did stimulation of specific antibody responses with PWM. Polyclonal antibody synthesis induced by PWM was also dependent on monocytes. However, polyclonal antibody synthesis induced by supraoptimal concentrations of antigen was usually optimal in the absence of monocytes and was actually suppressed when increased numbers of monocytes were added to monocyte-depleted cultures. Monocyte supernatants could not replace the absolute requirements for monocytes in the induction of specific antibody synthesis. However, monocyte supernatants could profoundly modulate the antigen-specific as well as the polyclonal Ig response of lymphocytes to either antigen or PWM stimulation in a manner closely resembling monocytes themselves. Thus, we demonstrated that monocytes and their products play a critical role in the activation and immunoregulation of antigen-specific antibody responses of human B cells.

摘要

单核细胞在人B细胞诱导和调节抗原特异性抗体反应中的多方面作用已被阐明。在抗原诱导的体外试验中,诱导针对破伤风类毒素(TT)和钥孔戚血蓝蛋白(KLH)的特异性抗体反应绝对需要单核细胞。在免疫个体中,PWM诱导特异性抗体也需要单核细胞。用特异性抗原或PWM脉冲单核细胞,在无添加抗原的情况下持续刺激T细胞增殖,并且也能刺激特异性抗体合成,尽管不太稳定。与用PWM刺激特异性抗体反应相比,用抗原刺激特异性抗体反应所需的单核细胞数量更少。PWM诱导的多克隆抗体合成也依赖于单核细胞。然而,由超最佳浓度抗原诱导的多克隆抗体合成通常在无单核细胞时最佳,当向单核细胞耗尽的培养物中添加更多数量的单核细胞时,实际上会受到抑制。单核细胞上清液不能替代诱导特异性抗体合成时对单核细胞的绝对需求。然而,单核细胞上清液可以以与单核细胞本身非常相似的方式深刻调节淋巴细胞对抗原或PWM刺激的抗原特异性以及多克隆Ig反应。因此,我们证明单核细胞及其产物在人B细胞抗原特异性抗体反应的激活和免疫调节中起关键作用。

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