Connectivity and HIV-1 infection:: Role of CD4+ T-cell counts and HIV-1 RNA copy number

被引:13
|
作者
Padierna-Olivos, L
Moreno-Altamirano, MMB
Sánchez-Colón, S
Massó-Rojas, F
Sánchez-García, FJ
机构
[1] Inst Politecn Nacl, Escuela Nacl Ciencias Biol, Dept Immunol, CINVESTAV, Mexico City 11340, DF, Mexico
[2] Inst Politecn Nacl, CINVESTAV, Lab Especialidades Inmunol, Mexico City 11340, DF, Mexico
[3] Inst Politecn Nacl, CINVESTAV, Dept Genet & Mol Biol, Mexico City 11340, DF, Mexico
[4] Inst Politecn Nacl, Escuela Nacl Ciencias Biol, Dept Bot, Mexico City 11340, DF, Mexico
[5] Inst Nacl Cardiol, Dept Biol Celular, Dept Bot, Mexico City, DF, Mexico
关键词
D O I
10.1046/j.1365-3083.2000.00812.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Following primary infection with human immundeficiency virus (HIV)-1, antibodies against specific HIV-1 epitopes are elicited. However, non-HIV-1 specific antibodies, including autoantibodies, also arise. In fact, it has been proposed that such autoantibodies have an important role in the pathogenesis of HIV-1 infection. Because an imbalance in connectivity has been associated with autoimmune processes, we investigated the connectivity status of HIV-1-infected individuals. Moreover, we tested the possible role of viral load and CD4(+) T-cell counts, in connectivity, because these parameters appear to be important in the prognosis of HIV-1 infection. Results show that indeed, there is an alteration in connectivity in these patients, both for immunoglobulin (Ig)G and IgM, which is an immune alteration not previously identified in HIV-1 infection. In addition, our results show that viral load and CD4(+) T-cell counts are both equally important in defining the characteristic pattern of connectivity in HIV-1-infected individuals, and that neither is independently responsible for alterations in patient connectivity status.
引用
收藏
页码:618 / 627
页数:10
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