Nagy-Oltvai Z, Jennings T A, Brady T G, Lucia H L, Armstrong J A, Hsiung G D
Department of Laboratory Medicine, Yale University School of Medicine, New Haven, Conn.
Intervirology. 1987;28(2):105-9. doi: 10.1159/000150002.
Female guinea pigs pretreated for 2 days with cyclosporin A (CsA), were then inoculated intranasally (IN) or intraperitoneally (IP) with a lymphotropic herpesvirus (GPHLV) and followed by 4 additional daily doses of CsA. Immunosuppressed animals did not show lymphocytosis and virus infectivity titers in their spleen, cervical lymph node and blood mononuclear cells were lower than those of oil-treated controls. While IN-inoculated CsA-treated animals expressed higher virus infectivity titer in their lungs compared to oil-treated controls, this difference was not seen in the IP-inoculated groups. At histopathology, lymphoid depletion was seen in all CsA-treated animals, but lymphocytic interstitial pneumonia was observed only in the lungs of IN-inoculated CsA-treated guinea pigs. Thus, CsA immunosuppression altered the pathogenesis of primary GPHLV infection with some notable differences attributed to the route of virus inoculation.
用环孢素A(CsA)预处理2天的雌性豚鼠,然后经鼻内(IN)或腹腔内(IP)接种嗜淋巴细胞疱疹病毒(GPHLV),随后每天再给予4剂CsA。免疫抑制的动物未出现淋巴细胞增多,其脾脏、颈淋巴结和血液单核细胞中的病毒感染性滴度低于用油处理的对照组。虽然与用油处理的对照组相比,经鼻内接种CsA处理的动物肺部的病毒感染性滴度更高,但在经腹腔内接种的组中未观察到这种差异。在组织病理学检查中,所有经CsA处理的动物均出现淋巴细胞减少,但仅在经鼻内接种CsA处理的豚鼠肺部观察到淋巴细胞间质性肺炎。因此,CsA免疫抑制改变了原发性GPHLV感染的发病机制,且因病毒接种途径不同而存在一些显著差异。