Impaired replication of protease inhibitor-resistant HIV-1 in human thymus

被引:112
作者
Stoddart, CA [1 ]
Liegler, TJ
Mammano, F
Linquist-Stepps, VD
Hayden, MS
Deeks, SG
Grant, RM
Clavel, F
McCune, JM
机构
[1] San Francisco Gen Hosp, Gladstone Inst Virol & Immunol, San Francisco, CA 94110 USA
[2] San Francisco Gen Hosp, Dept Med, San Francisco, CA 94110 USA
[3] Univ Calif San Francisco, Dept Microbiol & Immunol, San Francisco, CA 94143 USA
[4] Hop Bichat Claude Bernard, IMEA, Rech Antivirale, INSERM,U552, F-75877 Paris 18, France
关键词
D O I
10.1038/89090
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Many HIV-1-infected patients treated with protease inhibitors (PI) develop PI-resistant HIV-1 variants and rebounds in viremia, but their CD4(+) T-cell counts often do not fall. We hypothesized that in these patients, T-cell counts remain elevated because PI-resistant virus spares intrathymic T-cell production. To test this, we studied recombinant HIV-1 clones containing wild-type or PI-resistant protease domains, as well as uncloned isolates from patients, in activated peripheral blood mononuclear cells, human thymic organ cultures and human thymus implants in SCID-hu Thy/Liv mice. In most cases, wild-type and PI-resistant HIV-1 isolates replicated to similar degrees in peripheral blood mononuclear cells. However, the replication of PI-resistant but not wild-type HIV-1 isolates was highly impaired in thymocytes. In addition, patients who had PI-resistant HIV-1 had abundant thymus tissue as assessed by computed tomography. We propose that the inability of PI-resistant HIV-1 to replicate efficiently in thymus contributes to the preservation of CD4(+) T-cell counts in patients showing virologic rebound on PI therapy.
引用
收藏
页码:712 / 718
页数:7
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