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猫免疫缺陷病毒的病毒抗原在感染早期猫淋巴结中的定位。

Localization of the viral antigen of feline immunodeficiency virus in the lymph nodes of cats at the early stage of infection.

作者信息

Toyosaki T, Miyazawa T, Furuya T, Tomonaga K, Shin Y S, Okita M, Kawaguchi Y, Kai C, Mori S, Mikami T

机构信息

Department of Veterinary Microbiology, Faculty of Agriculture, University of Tokyo, Japan.

出版信息

Arch Virol. 1993;131(3-4):335-47. doi: 10.1007/BF01378636.

Abstract

Immunohistochemical examinations of localization of feline immunodeficiency virus (FIV) Gag protein were performed on lymph nodes of cats experimentally inoculated with three different strains of FIV (infectious molecular clone of TM 1, Petaluma, and KYO-1 strains), using rabbit anti-FIV Gag serum. The FIV Gag antigens were observed in many follicular dendritic cells (FDCs) and sparsely in small lymphocytes of paracortical area in the lymph nodes of cats inoculated with Petaluma and KYO-1 strains. However, the antigens were present only in small lymphocytes, and not in FDCs of a cat inoculated with infectious molecular clone of the TM1 strain. The cell type differences in expression of the viral antigen in vivo might reflect on the cell tropisms of the FIV strains in vitro. By double immunohistochemical staining with rabbit anti-FIV Gag serum and monoclonal antibodies which recognize feline CD4, feline CD8 or feline pan-T molecules, the FIV Gag-positive lymphocytes were characterized as feline CD4-positive T cells. Since the distributions of FIV Gag antigens were mainly in the FDCs, the FDCs may play an important role as a major reservoir and may be a primary target of FIV at early stages of infection.

摘要

使用兔抗猫免疫缺陷病毒(FIV)Gag血清,对经三种不同FIV毒株(TM 1、Petaluma和KYO - 1毒株的感染性分子克隆)实验接种的猫的淋巴结进行FIV Gag蛋白定位的免疫组织化学检查。在接种Petaluma和KYO - 1毒株的猫的淋巴结中,在许多滤泡树突状细胞(FDC)中观察到FIV Gag抗原,在副皮质区的小淋巴细胞中则稀疏可见。然而,在接种TM1毒株感染性分子克隆的猫中,抗原仅存在于小淋巴细胞中,而不存在于FDC中。病毒抗原在体内表达的细胞类型差异可能反映了FIV毒株在体外的细胞嗜性。通过用兔抗FIV Gag血清和识别猫CD4、猫CD8或猫全T分子的单克隆抗体进行双重免疫组织化学染色,FIV Gag阳性淋巴细胞被鉴定为猫CD4阳性T细胞。由于FIV Gag抗原的分布主要在FDC中,FDC可能作为主要储存库发挥重要作用,并且可能是感染早期FIV的主要靶标。

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