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比较不同临床分期的猫免疫缺陷病毒感染猫的血浆球蛋白水平、CD21(-)B 细胞计数和 CD4(+)T 细胞中 FOXP3 mRNA 表达水平。

Comparative study of the plasma globulin level, CD21(-) B-cell counts and FOXP3 mRNA expression level in CD4(+) T-cells for different clinical stages of feline immunodeficiency virus infected cats.

机构信息

Kitasato University, Towada, Aomori, Japan.

出版信息

Res Vet Sci. 2012 Feb;92(1):157-61. doi: 10.1016/j.rvsc.2010.10.022. Epub 2010 Nov 11.

DOI:10.1016/j.rvsc.2010.10.022
PMID:21074227
Abstract

Feline immunodeficiency virus (FIV) infection leads to hypergammaglobulinemia through mechanisms that remain poorly understood. We investigated changes in plasma globulin level, B cells, and T cells with progression of the clinical stage of FIV-infected cats. We classified FIV-infected cats into the stage of Asymptomatic carrier (AC) and AIDS-related complex (ARC) based on the clinical symptoms, and measured the plasma globulin level, the CD4(+) T-cell counts, and analyzed surface markers of B cells. We investigated the relationship between the plasma globulin level and regulatory T cells (Tregs) using the Forkhead box P3 (FOXP3) mRNA expression level. In FIV-infected cats, the plasma globulin level and the surface immunoglobulin (sIg)(+) CD21(-) B-cell counts were increased, whereas the CD4(+) T-cell counts were decreased compared with specific-pathogen free (SPF) cats. The mRNA expression of Blimp-1 (master gene of plasma cells) was increased in peripheral blood, and the FOXP3 mRNA expression level was decreased in CD4(+) T-cells. These immunological changes were marked in the ARC stage. These data indicate that the decrease of Tregs and the increase of plasma cells lead to hypergammaglobulinemia.

摘要

猫免疫缺陷病毒(FIV)感染通过机制导致高球蛋白血症,但这些机制仍知之甚少。我们研究了随着 FIV 感染猫临床阶段的进展,血浆球蛋白水平、B 细胞和 T 细胞的变化。我们根据临床症状将 FIV 感染猫分为无症状携带者(AC)和 AIDS 相关复合征(ARC)阶段,并测量了血浆球蛋白水平、CD4(+) T 细胞计数,并分析了 B 细胞的表面标记物。我们使用叉头框 P3(FOXP3)mRNA 表达水平研究了血浆球蛋白水平与调节性 T 细胞(Tregs)之间的关系。在 FIV 感染猫中,与无特定病原体(SPF)猫相比,血浆球蛋白水平和表面免疫球蛋白(sIg)(+)CD21(-)B 细胞计数增加,而 CD4(+) T 细胞计数减少。外周血中 Blimp-1(浆细胞的主基因)的 mRNA 表达增加,而 CD4(+) T 细胞中的 FOXP3 mRNA 表达水平降低。这些免疫变化在 ARC 阶段更为明显。这些数据表明,Tregs 的减少和浆细胞的增加导致高球蛋白血症。

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