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B细胞在体外诱导针对单核细胞增生李斯特菌的产生γ干扰素的CD4+T细胞中的作用:正向和IL-10介导的负向调节

The role of B cells in in vitro induction of IFN-gamma-producing CD4+ T cells specific to Listeria monocytogens: positive and IL-10-mediated negative regulation.

作者信息

Song F, Matsuzaki G, Mitsuyama M, Nomoto K

机构信息

Department of Immunology, Medical Institute of Bioregulation, Kyushu University, Fukuoka, Japan.

出版信息

Cell Immunol. 1994 Sep;157(2):403-14. doi: 10.1006/cimm.1994.1237.

Abstract

We have reported that Listeria monocytogenes-specific IFN-gamma-producing CD4+ T cells are induced by in vitro 5-day culture of naive spleen cells with viable L. monocytogenes (VLM), but not induced by culture with heat-killed L. monocytogenes (HKLM). In the present study, the role of B cells in the regulation of induction of IFN-gamma-producing CD4+ T cells in the in vitro system was investigated. We found that L. monocytogenes-specific IFN-gamma-producing CD4+ T cells were not generated when B cells were depleted from spleen cells before culture with VLM although Ag-specific proliferative response was retained. IFN-gamma production by CD4+ T cells was restored by addition of B cells cultured with VLM to the culture of B cell-depleted spleen cells and VLM. In contrast, B cells cultured with HKLM could not restore the induction of IFN-gamma production when added in culture of B cell-depleted spleen cells and VLM. Analysis of cytokine gene expression by reverse transcription-polymerase chain reaction method revealed that expression of interleukin-10 (IL-10) was higher but TNF-alpha was lower in B cells cultured with HKLM when compared with that in B cells cultured with VLM. Furthermore, addition of neutralizing anti-IL-10 mAb into culture of naive spleen cells with HKLM resulted in appearance of IFN-gamma-producing cells. These results suggest that B cells have positive and negative roles in the induction of IFN-gamma-producing CD4+ T cells. The inhibition of induction of IFN-gamma-producing CD4+ T cells may depend on B cell-derived IL-10.

摘要

我们曾报道,用活的单核细胞增生李斯特菌(VLM)对未致敏的脾细胞进行体外5天培养可诱导产生单核细胞增生李斯特菌特异性分泌γ干扰素的CD4⁺T细胞,而用热灭活的单核细胞增生李斯特菌(HKLM)培养则不能诱导产生。在本研究中,我们调查了B细胞在该体外系统中对分泌γ干扰素的CD4⁺T细胞诱导调节中的作用。我们发现,在用VLM培养前从脾细胞中去除B细胞时,不会产生单核细胞增生李斯特菌特异性分泌γ干扰素的CD4⁺T细胞,尽管抗原特异性增殖反应得以保留。通过向去除B细胞的脾细胞与VLM的培养物中添加用VLM培养的B细胞,可恢复CD4⁺T细胞的γ干扰素产生。相反,在用HKLM培养的B细胞添加到去除B细胞的脾细胞与VLM的培养物中时,不能恢复γ干扰素产生的诱导。通过逆转录 - 聚合酶链反应方法分析细胞因子基因表达发现,与用VLM培养的B细胞相比,用HKLM培养的B细胞中白细胞介素 - 10(IL - 10)的表达较高,但肿瘤坏死因子 - α较低。此外,向用HKLM培养的未致敏脾细胞培养物中添加中和性抗IL - 10单克隆抗体导致出现分泌γ干扰素的细胞。这些结果表明,B细胞在分泌γ干扰素的CD4⁺T细胞的诱导中具有正负两方面的作用。分泌γ干扰素的CD4⁺T细胞诱导的抑制可能取决于B细胞衍生的IL - 10。

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