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CXCR4嗜性SHIVKU-1病毒静脉感染中国恒河猴初步研究
引用本文:丛喆,蒋虹,苏爱华,王卫,陈霆,薛婧,魏强. CXCR4嗜性SHIVKU-1病毒静脉感染中国恒河猴初步研究[J]. 中国实验动物学杂志, 2013, 0(6): 53-57,66
作者姓名:丛喆  蒋虹  苏爱华  王卫  陈霆  薛婧  魏强
作者单位:中国医学科学院医学实验动物研究所,卫生部人类疾病比较医学重点实验室,国家中医药管理局人类疾病动物模型三级实验室,北京100021
基金项目:国家十二五科技重大专项课题(编号:2012ZXl0004-501).
摘    要:目的了解SHIVKU一1静脉途径感染中国恒河猴的感染特点及进展规律。方法两只健康中国恒河猴,静脉感染SHIVKU-1病毒,定期采样检测血浆病毒载量、CD4+/CD8+比值、CD4+T细胞绝对数变化和血清中抗SHIVKU-1特异性IgG抗体水平。多色流式技术分析外周血、腹股沟淋巴结和十二指肠粘膜固有层CD4+T淋巴细胞记忆细胞亚群变化。结果两只实验猴成功感染SHIVKU-1病毒,一直到感染后3个月均保持稳定水平的病毒载量。外周血CD4+T淋巴细胞下降明显,CD4+/CD8+T细胞比值严重倒置。CD4+Tcm细胞比例在经历了感染早期的下降后,大幅升高,尤其是外周血和淋巴结。CD4+Tem则在粘膜固有层中增加明显。结论SHIVKU.1静脉途径成功感染了中国恒河猴,为SHIV/中国恒河猴疾病及评价模型的建立奠定了良好的基础,为今后使用此模型评价抗病毒药物或疫苗提供了条件。

关 键 词:SHIVKU-1  CXCR4  中国恒河猴  CD4+中心记忆性T细胞

Characterization of a Chinese-origin rhesus macaque model of X4-tropic pathogenic SHIVKU-I infection by intravenous injection
CONG Zhe,JIANG Hong,SU Ai-hua,WANG Wei,CHEN Ting,XUE Jing,WEI Qiang. Characterization of a Chinese-origin rhesus macaque model of X4-tropic pathogenic SHIVKU-I infection by intravenous injection[J]. Chinese Journal of Laboratory Animal Science, 2013, 0(6): 53-57,66
Authors:CONG Zhe  JIANG Hong  SU Ai-hua  WANG Wei  CHEN Ting  XUE Jing  WEI Qiang
Affiliation:( Key Laboratory of Human Diseases Comparative Medicine, Ministry of Health; Institute of Medical Laboratory Animal Science, Chinese Academy of Medical Sciences; Key Laboratory of Human Diseases Animal Models, State Administration of Traditional Chinese Medicine, Beijing 100021, China)
Abstract:Objective To study the characteristics of SHIVKU-1 infection in Chinese rhesus macaques and provide an animal platform in evaluation of the effectiveness of anti-HIV-1 drugs or vaccines with SHIVKU-1/rhesus animal model. Methods Two healthy Chinese-origin rhesus macaques, serum negative to SIV, SRV and STLV-1, were infected with SHIVKU-1 intravenously. CD4+ and CD8 + T cell subsets including memory CD4 + T cell subset in the peripheral blood (PBL), inguinal lymph nodes (ILN), and intestinal lamina propria (LP) were analyzed by flow cytometry. Viral load was detected by real time RT-PCR, so was the specific IgG antibody titer against SHIVKU-1 in the plasma using ELISA. Results Both of the two rhesus macaques established systemic infection, keeping steady viral load in 3 months after infection. The monkey G1302V died 457 days post-infection. Peripheral CD4 + T lymphocytes decreased significantlypost-infection, while the CD4+/CD8 + ratio went upside down. The proportion of CD4+ Tcm cells experienced a decline in the early stage of infection and rose sharply, especially in the peripheral blood and lymph nodes. CD4 + Tern increased significantly in the intestinal lamina propria. Conclusions A Chinese rhesus macaque model of SHIVKU-1 infection is successfully established by intravenous injection. It provides a choice to evaluate the efficiency of candidate vaccines or drugs aiming at the X4 tropic HIV, and for the pathogenesis studies as well.
Keywords:SHIVKU-1  CXCR4  Chinese-origin rhesus macaques  CD4+Tem
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