实验动物与比较医学 ›› 2011, Vol. 31 ›› Issue (1): 38-42.DOI: 10.3969/j.issn.1674-5817.2011.01.008

• 论著 • 上一篇    下一篇

SHIV1157ipd3N4小量多次阴道粘膜感染中国猕猴的初步研究

丛喆1, 蒋虹1, 金光1, 王卫1, 高虹1, 姚南1, 陶真1, 陈霆1, 杨志伟1, Sylvain.Fleury2, AnickChalifour2, Ruth.M.Ruprecht3, 魏强1, 秦川1   

  1. 1.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;
    2.Dana-Farber Cancer Institute, Boston, Massachusetts 021151;Harvard Medical School, Boston, Massachusetts 021152;
    3.Mymetics Corporation, CH 1066 Epalinges, Switzerland
  • 收稿日期:2010-07-26 出版日期:2011-02-25 发布日期:2011-02-25
  • 作者简介:丛喆, 硕士, 主管技师, 从事实验动物病毒分子生物学和模型研究工作。E-mail: zhengyihan@yahoo.com
  • 基金资助:
    国家十一五科技重大专项课题 (2009ZX10004- 402), 中央级公益性科研院所基本科研业务费专 项资金(DWS 201009)

Efficient Repeated Low-dose Intravaginal Infection with SHIV1157ipd3N4 in Rhesus Monkey

CONG Zhe1, JIANG Hong1, JIN Guang1, WANG Wei1, GAO Hong1, YAO Nan1, TAO Zhen1, CHEN Ting1, YANG Zhi-wei1, Sylvain. Fleury2, Anick Chalifour2, Ruth. M.Ruprecht3, WEI Qiang1, QIN Chuan1   

  1. 1. 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;
    2. Dana-Farber Cancer Institute, Boston, Massachusetts 021151; Harvard Medical School,Boston, Massachusetts 021152;
    3. Mymetics Corporation, CH 1066 Epalinges, Switzerland
  • Received:2010-07-26 Online:2011-02-25 Published:2011-02-25

摘要: 目的 建立R5-SHIV1157ipd3N4病毒中国猕猴阴道粘膜小剂量多次感染模型,为我国艾滋病疫苗有效性评价提供新的模型构建、应用策略。方法 选用10-20TCID50剂量的SHIV 1157ipd3N4病毒阴道黏膜途径感染6只雌性中国猕猴,共感染11次,每次攻毒间隔4~7 d。定期测定血浆病毒载量和外周血CD4+:CD8+结果 6只中国猕猴经11次病毒攻击后,均建立系统性感染, 血浆病毒载量呈阳性; CD4+:CD8+均有下降。结论 初步建立了R5-SHIV1157ipd3N4中国猕猴阴道黏膜小剂量多次感染模型,为艾滋病研究提供了更接近于自然感染状态的模型建立模式。

关键词: SHIV1157ipd3N4, 黏膜感染, 中国猕猴

Abstract: Objective To establish a CCR5-specific chimeric simian/human immunodeficiency virus, SHIV1157ipd3N4 repeated low-dose intravaginal infection model with rhesus monkeys. This new chimeric model could hopefully be more efficient model in AIDS vaccine development. Methods Six female Chinese rhesus monkeys were enrolled in this study. All animals were intra-vaginally challenged 11 times with 1 ml of a phosphate-buffer viral solution containing the heterologous SHIV1157ipd3N4, with 20 TCID50 for the first 3 challenges and 10 TCID50 for the remaining 8 challenges. Each challenge was accomplished at the interval of 4-7 days. Whole blood was collected and plasma virus was quantified by real-time SYBR Green RT-PCR and T cell subsets were determined by flow cytometry analysis. Results The systematic infection of six rhesus monkeys was established successfully after 11 challenges. The peaks of viral loads were between 106copies/ml to 108copies/ml.Conclusion The repeated low-dose technique was used for establishing a SHIV1157ipd3N4 infection model of Chinese rhesus monkey. This model aliking sexual route would be very useful for HIV-1 subtype C vaccine and pathogenesis studies.

Key words: SHIV1157ipd3N4, Vaginal transmission, Chinese rhesus monkey

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