Journal of Capital Medical University ›› 2011, Vol. 32 ›› Issue (4): 449-452.doi: 10.3969/j.issn.1006-7795.2011.04.002

• 皮肤病与性病学专题 • Previous Articles     Next Articles

Optimization of Alu-LTR PCR approach to detect integrated HIV-1 DNA in variety of cell subsets at different stages after HAART

LI Juan, JIAO Yan-mei, GAO Yan-qing, KOU Bu-xin, ZHANG Tong, WU Hao   

  1. Clinical Center of STDS and AIDS, Beijing Youan Hospital, Capital Medical University, Beijing 100069, China
  • Received:2011-02-25 Revised:1900-01-01 Online:2011-08-21 Published:2011-08-21

Abstract: Objective To determine if there is integrated human immunodeficiency virus-1(HIV-1) DNA in variety of cell subsets at different stages after highly active antiretroviral therapy(HAART) through detecting HIV-1 DNA in CD4+T cell, CD8+T cell and B cell by Alu-long terminal repeat(LTR) polymerase chain reaction(PCR). Methods The genomic DNA from purified CD4+T, CD8+T, B cells of 20 HIV-1 patients after HAART 0, 4, 12 W and 10 healthy control subjects was obtained by Alu-LTR PCR. Results After Alu-LTR PCR, integrated HIV-1 was detected in each of the 20 cases of HIV/AIDS of CD4+T cells and CD8+T cells after HAART. The product of CD8+T cells were lower than that of the CD4+T cells. The product of HAART 4, 0, 12 W had no significant difference. Conclusion There exists integrated HIV-1 DNA in CD4+T cells and CD8+T cells, and HIV viral reservoir mainly exists in CD4+T cells. Integrated HIV-1 DNA do not exist in B cells. Integrated HIV-1 DNA still exist, and HAART do not eradicate HIV viral reservoir.

Key words: Alu-LTR PCR, integrated human immunodeficiency virus-1, CD4+T cell, CD8+T cell, B cell

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