Lehman Tracy L, O'Halloran Kevin P, Fallon Samantha A, Habermann Lindsey M, Campbell Jennifer A, Nordone Shila, Dean Gregg A, Hoover Edward A, Avery Paul R
Departments of Microbiology, Immunology, and Pathology, Colorado State University, Fort Collins, 80523, USA.
Immunology. 2009 Mar;126(3):405-12. doi: 10.1111/j.1365-2567.2008.02907.x. Epub 2008 Sep 2.
Impaired dendritic cell (DC) function is thought to be central to human immunodeficiency virus-associated immunodeficiency. In this study, we examined the effect of chronic feline immunodeficiency virus (FIV) infection on DC cytokine production in response to microbial and T-cell stimulation. Cytokine production after either Toll-like receptor (TLR) or CD40 ligation in bone marrow-derived DCs (BM-DCs) was measured in naïve and chronically FIV-infected cats. The BM-DCs were stimulated with ligands to TLR-2, -3, -4, -7 and -9 or cocultured with 3T3 cells expressing feline CD40 ligand. Ligation of TLR-4 and TLR-9 in BM-DCs from infected cats resulted in a significant decrease in the ratio of interleukin-12 (IL-12) to IL-10. Conversely, TLR-7 ligation produced a significant increase in the IL-12 : IL-10 ratio in BM-DCs from infected cats. No difference was noted for TLR-3 ligation. RNA expression levels of TLR-2, -3, -4, -7 and -9 were not significantly altered by FIV infection. CD40 ligation significantly elevated both IL-10 and IL-12 messenger RNA production but did not alter the IL-12 : IL-10 ratio. Chronic FIV infection alters the ratio of immunoregulatory cytokines produced by BM-DCs in response to certain pathogen-derived signals, which is probably relevant to the increased risk of opportunistic infections seen in lentiviral infection.
树突状细胞(DC)功能受损被认为是人类免疫缺陷病毒相关免疫缺陷的核心。在本研究中,我们检测了慢性猫免疫缺陷病毒(FIV)感染对DC响应微生物和T细胞刺激产生细胞因子的影响。在未感染和慢性感染FIV的猫中,测量了骨髓来源的DC(BM-DC)在Toll样受体(TLR)或CD40连接后细胞因子的产生。用TLR-2、-3、-4、-7和-9的配体刺激BM-DC,或与表达猫CD40配体的3T3细胞共培养。感染猫的BM-DC中TLR-4和TLR-9的连接导致白细胞介素-12(IL-12)与IL-10的比例显著降低。相反,TLR-7连接使感染猫的BM-DC中IL-12:IL-10的比例显著增加。TLR-3连接未观察到差异。FIV感染未显著改变TLR-2、-3、-4、-7和-9的RNA表达水平。CD40连接显著提高了IL-10和IL-12信使RNA的产生,但未改变IL-12:IL-10的比例。慢性FIV感染改变了BM-DC响应某些病原体衍生信号产生的免疫调节细胞因子的比例,这可能与慢病毒感染中机会性感染风险增加有关。