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HIV感染的发病机制与自然史。

Pathogenesis and natural history of HIV infection.

作者信息

Sleasman J W, Goodenow M M

机构信息

Department of Pediatrics, University of Florida College of Medicine, Gainesville.

出版信息

J Fla Med Assoc. 1991 Oct;78(10):678-81.

PMID:1753233
Abstract

Acquired immune deficiency syndrome (AIDS) is caused by infection with the human immunodeficiency virus (HIV), a human retrovirus. The virus infects cells of the immune system by attachment of a glycoprotein viral envelope (gp 120) to a molecule expressed on human helper T cells called CD4. The fusion of the virus envelope protein to its specific receptor allows HIV to penetrate the T cell. Once inside the cell viral RNA is transcribed into double-stranded DNA by an enzyme unique to retroviruses, reverse transcriptase. The double-stranded, proviral DNA travels to the nucleus of the cell and is integrated into the infected cell's chromosomal DNA where it may remain latent for years. As a result of triggers that are poorly understood, viral replication becomes activated and proviral DNA is transcribed back into genomic RNA and RNA that is translated into viral proteins, both of which are packaged and bud from the infected T cell as infectious virus. The viral life cycle orchestrates the natural history of clinical HIV infection. Three to four weeks following exposure to HIV there is a phase of rapid viral replication, high levels of plasma viremia, and development of a "flue like" illness. Four to six weeks after exposure, during this stage of acute infection, antibodies to HIV core (p24) and envelope (gp 160, gp 120, gp41) proteins appear. Six to eight weeks after exposure symptoms disappear and plasma viremia subsides, presumably due to clearance by the immune system.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

获得性免疫缺陷综合征(艾滋病)由人类免疫缺陷病毒(HIV,一种人类逆转录病毒)感染引起。该病毒通过其糖蛋白病毒包膜(gp120)与人类辅助性T细胞表面表达的一种名为CD4的分子结合,从而感染免疫系统细胞。病毒包膜蛋白与其特异性受体融合,使HIV能够穿透T细胞。一旦进入细胞,病毒RNA会通过逆转录酶(一种逆转录病毒特有的酶)转录为双链DNA。双链的前病毒DNA进入细胞核,并整合到受感染细胞的染色体DNA中,在那里它可能潜伏数年。由于一些尚不清楚的触发因素,病毒复制被激活,前病毒DNA转录回基因组RNA,RNA被翻译成病毒蛋白,二者都会被包装并以感染性病毒的形式从受感染的T细胞中芽生出来。病毒生命周期主导着临床HIV感染的自然病程。接触HIV三到四周后,会进入一个病毒快速复制、血浆病毒血症水平高且出现“流感样”疾病的阶段。接触后四到六周,在急性感染阶段,会出现针对HIV核心(p24)和包膜(gp160、gp120、gp41)蛋白的抗体。接触后六到八周,症状消失,血浆病毒血症消退,这可能是由于免疫系统的清除作用。(摘要截选至250词)

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