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CD8α⁺树突状细胞增强抗原特异性CD4⁺T细胞反应并加速胶原诱导性关节炎的发展。

CD8alpha+ dendritic cells enhance the antigen-specific CD4+ T-cell response and accelerate development of collagen-induced arthritis.

作者信息

Jung Young Ok, Min So-Youn, Cho Mi-La, Park Min-Jung, Jeon Ju-Youn, Lee Jae-Sun, Oh Hye-Joa, Kang Chang-Min, Park Hyun-Sil, Park Kyung-Soo, Cho Seok Goo, Park Sung-Hwan, Kim Ho-Youn

机构信息

Division of Rheumatology, Department of Internal Medicine, Kang-Nam Sacred Heart Hospital, Hallym University, Seoul, Republic of Korea.

出版信息

Immunol Lett. 2007 Aug 15;111(2):76-83. doi: 10.1016/j.imlet.2007.05.005. Epub 2007 Jun 18.

Abstract

To investigate the role of CD8alpha(+) DCs in the development of collagen-induced arthritis (CIA). The immunogenic properties of CD8alpha(+) and CD8alpha(-) DC subsets were investigated by mixed-lymphocyte reaction and cytokine enzyme-linked immunoassay. CII-pulsed CD8alpha(+) DCs or CD8alpha(-) DCs with CD4(+) T cells from CIA mice were adoptively transferred onto the hind footpad of DBA mice. The onset of arthritis and the arthritis index were examined for 14 weeks after adoptive transfer. Expression of MHC-II and CD80 but not CD86 and CD40 was higher in CD8alpha(+) DCs than in CD8alpha(-) DCs from the spleens of CIA mice. Culturing CD8alpha(+) DCs with CD4(+) T cells significantly increased the proliferative response of CD4(+) T cells in the presence of CII. The production of interleukin (IL)-12p70, IL-17, interferon (IFN)-gamma, and tumor necrosis factor (TNF)-alpha was slightly increased in CD8alpha(+) DCs than in CD8alpha(-) DCs. DBA/1 mice that were adoptively transferred with CII-pulsed CD8alpha(+) DCs and CD4(+) T cells into the footpads showed accelerated onset of CIA compared to control group. By contrast, CD8alpha(-) DCs showed a partial inhibitory effect on CIA. These findings show that CD8alpha(+) DCs accelerated the onset of CIA when aoptively transferred with CD4(+) T cells and that CD8alpha(+) DCs provoke the development of CIA probably by stimulating the immune responses of CII-reactive CD4(+) T cells and by increasing the production of inflammatory cytokines.

摘要

研究CD8α(+)树突状细胞(DCs)在胶原诱导性关节炎(CIA)发病过程中的作用。通过混合淋巴细胞反应和细胞因子酶联免疫测定法研究CD8α(+)和CD8α(-) DC亚群的免疫原性特性。将用Ⅱ型胶原(CII)脉冲处理的CD8α(+) DCs或CD8α(-) DCs与来自CIA小鼠的CD4(+) T细胞过继转移到DBA小鼠的后足垫。过继转移后14周观察关节炎的发病情况和关节炎指数。来自CIA小鼠脾脏的CD8α(+) DCs中MHC-II和CD80的表达高于CD8α(-) DCs,但CD86和CD40的表达并非如此。在CII存在的情况下,将CD8α(+) DCs与CD4(+) T细胞共培养可显著增加CD4(+) T细胞的增殖反应。CD8α(+) DCs中白细胞介素(IL)-12p70、IL-17、干扰素(IFN)-γ和肿瘤坏死因子(TNF)-α的产生比CD8α(-) DCs略有增加。与对照组相比,将用CII脉冲处理的CD8α(+) DCs和CD4(+) T细胞过继转移到足垫的DBA/1小鼠CIA发病加速。相比之下,CD8α(-) DCs对CIA显示出部分抑制作用。这些发现表明,当与CD4(+) T细胞过继转移时,CD8α(+) DCs加速了CIA的发病,并且CD8α(+) DCs可能通过刺激CII反应性CD4(+) T细胞的免疫反应和增加炎性细胞因子的产生来促进CIA的发展。

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