Expression of granzyme B mRNA is altered in human immunodeficiency virus infected patients

被引:3
作者
Jaspan, HB
Gaumer, HR
Garry, RF
机构
[1] Tulane Univ, Sch Med, Mol & Cellular Biol Program, New Orleans, LA 70112 USA
[2] Tulane Univ, Sch Med, Dept Microbiol & Immunol, New Orleans, LA 70112 USA
[3] Louisiana State Univ, Med Ctr, New Orleans, LA 70112 USA
关键词
HIV; granzyme B; cytotoxic T lymphocytes;
D O I
10.1016/S0014-4800(03)80003-5
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
CD8-positive cytotoxic T lymphocytes and natural killer cells are the major cytotoxic components of the antiviral immune response. The major pathway used by these cells in response to viral-infected cells involves granzymes, cytotoxic granule serine proteases involved in the pathway leading to target cell DNA fragmentation and apoptosis. The levels of granzyme B mRNA in peripheral blood cells of human immunodeficiency virus (HIV) type-1 infected patients in comparison to noninfected individuals were assessed by quantitative competitive reverse transcriptase polymerase chain reaction. Expression of granzyme B mRNA is altered in HIV-1 infected patients. Significantly fewer HIV patients had detectable granzyme B mRNA levels than controls. The one HIV-infected patient with detectable granzyme B mRNA displayed a much higher level of this mRNA than all healthy controls. Cell-mediated cytotoxicity during HIV-1 infection may be impaired due to a deficient quantity of active cytotoxic granules or to their abnormal regulation. (C) 2003 Elsevier Science (USA).
引用
收藏
页码:13 / 16
页数:4
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