In Vitro Infection of Human Umbilical Cord Blood CD34+ Hematopoietic Progenitor Cells by HIV-1 CRF07_BC Enveloped Pseudovirus

被引:1
|
作者
Li, Lin [1 ]
Qiu, Chao [2 ]
Li, Liangzhu [2 ]
Liu, Aiping [2 ]
Zhou, Mingzhe [2 ]
Han, Zhimin [3 ]
Qiu, Chenli [2 ]
Zhang, Xiaoyan [2 ,4 ,5 ,6 ]
Xu, Jianqing [2 ,4 ,5 ,6 ]
Zhu, Huanzhang [1 ]
机构
[1] Fudan Univ, Inst Genet, Sch Life Sci, State Key Lab Genet Engn, Shanghai 200433, Peoples R China
[2] Fudan Univ, Shanghai Publ Hlth Clin Ctr, Inst Biomed Sci, Res Ctr, Shanghai 201508, Peoples R China
[3] Fudan Univ, Shanghai Publ Hlth Clin Ctr, Dept Gynecol & Obstet, Shanghai 201508, Peoples R China
[4] Fudan Univ, Shanghai Med Coll, Minist Educ Hlth, Key Lab Med Mol Virol, Shanghai 200433, Peoples R China
[5] Fudan Univ, Shanghai Med Coll, Minist Educ Hlth, Inst Med Microbiol, Shanghai 200433, Peoples R China
[6] Chinese Ctr Dis Control & Prevent, State Key Lab Infect Dis Prevent & Control, Beijing 100050, Peoples R China
关键词
HIV-1; latency; hematopoietic progenitor cells; CRF07_BC; integration; IMMUNODEFICIENCY-VIRUS TYPE-1; BONE-MARROW; STEM-CELLS; PERIPHERAL-BLOOD; BETA-CHEMOKINES; R5; HIV; CHINA; AIDS; RECOMBINANT; INTEGRATION;
D O I
10.2174/157016212803305989
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
To determine whether CRF07_BC, one of the most predominant strains that accounts for one third HIV-1 prevalence in China, has the ability to infect hematopoietic progenitor cells (HPCs), human Umbilical Cord Blood (UCB) derived CD34(+) HPCs isolated with high purity were infected by HIV-1 pseudotyped with CRF07_BC envelope. After HIV-1 infection, similar to 0.86% CD34(+) HPCs were co-stained for CD34 and intracellular HIV Gag. HIV p24 antigen was detectable and reached maximal release between day 2-4 after HIV-1 infection. The data of nested Alu-LTR PCR proved the integration of HIV-1 genome into the host genome occurred in HIV-1-infected HPCs. These data demonstrated that the envelope of CRF07_BC from China has the capability of resulting in infection to CD34(+) HPCs, which may serve as a mechanism for long-term latency of HIV-1 infection in vivo.
引用
收藏
页码:572 / 577
页数:6
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