Brodskyn C I, DeKrey G K, Titus R G
Department of Pathology, College of Veterinary Medicine and Biomedical Sciences, Colorado State University, Fort Collins, Colorado 80523, USA.
Infect Immun. 2001 Feb;69(2):665-72. doi: 10.1128/IAI.69.2.665-672.2001.
The importance of CD40, CD80, and CD86 costimulatory molecules in anti-Leishmania immune responses has been established in murine models. A role for these costimulatory molecules in human anti-Leishmania immune responses was investigated in this study. Autologous macrophages and peripheral blood leukocytes (PBL) were prepared from peripheral blood mononuclear cells of Leishmania-naive donors and cultured with or without Leishmania major in various combinations. After 7 days of culture, high levels of CD40 and CD86 were expressed on macrophages in the presence or absence of L. major. When macrophages were cultured for an additional 7 days with PBL, expression of all three costimulatory molecules was detected. When L. major was present in these cultures, the expression of CD80, and to a lesser extent CD40, on macrophages was enhanced. Blockade of CD80, CD86, or both molecules (in the order of greatest effect) in cultures containing macrophages, PBL, and L. major significantly inhibited the production of gamma interferon, interleukin-5 (IL-5), and IL-12. Blockade of CD40-CD154 interactions also significantly inhibited production of these cytokines in response to L. major. Production of IL-10 was unaltered by the blockade of these costimulatory molecules. Thus, these data suggest that CD40, CD80, and CD86 expression and regulation may significantly impact anti-Leishmania immune responses in humans.
CD40、CD80和CD86共刺激分子在抗利什曼原虫免疫反应中的重要性已在小鼠模型中得到证实。本研究调查了这些共刺激分子在人类抗利什曼原虫免疫反应中的作用。从未感染利什曼原虫的供体的外周血单核细胞中制备自体巨噬细胞和外周血白细胞(PBL),并与或不与硕大利什曼原虫以各种组合进行培养。培养7天后,无论有无硕大利什曼原虫,巨噬细胞上均高水平表达CD40和CD86。当巨噬细胞与PBL再培养7天时,检测到所有三种共刺激分子的表达。当这些培养物中存在硕大利什曼原虫时,巨噬细胞上CD80的表达增强,CD40的表达也有一定程度的增强。在含有巨噬细胞、PBL和硕大利什曼原虫的培养物中,阻断CD80、CD86或这两种分子(按作用大小顺序)可显著抑制γ干扰素、白细胞介素-5(IL-5)和IL-12的产生。阻断CD40-CD154相互作用也可显著抑制对硕大利什曼原虫反应时这些细胞因子的产生。阻断这些共刺激分子对IL-10的产生没有影响。因此,这些数据表明,CD40、CD80和CD86的表达及调控可能对人类抗利什曼原虫免疫反应产生显著影响。