The CD4-gp120 interaction and AIDS pathogenesis. NLM AIDSLINE Important note: Information in this article was accurate in 1992. The state of the art may have changed since the publication date.

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The CD4-gp120 interaction and AIDS pathogenesis.

Annu Rev Immunol. 1991;9:649-78. Unique Identifier : AIDSLINE MED/92000518
Capon DJ; Ward RH; Genentech Inc., South San Francisco, California 94080.


Abstract: Infection by the human immunodeficiency virus (HIV) leads to progressive destruction of the CD4+ subset of T lymphocytes, resulting in immunodeficiency and AIDS. The selectivity of CD4+ cell destruction is due to the specific binding of gp120, the external envelope glycoprotein of HIV, to CD4, initiating viral entry. Binding of gp120 to CD4 on the cell surface may also lead to CD4+ cell depletion by inappropriate immune targeting, and may interfere with CD4+ cell function and ontogeny by disrupting CD4-mediated cell signaling. The CD4-gp120 interaction is thus an obvious target for AIDS therapeutics.
Keywords: Acquired Immunodeficiency Syndrome/*ETIOLOGY/THERAPY Amino Acid Sequence Antigens, CD4/*METABOLISM Attachment Sites (Microbiology) Binding Sites Cell Fusion Human HIV Envelope Protein gp120/CHEMISTRY/*METABOLISM Molecular Sequence Data Protein Binding JOURNAL ARTICLE REVIEW REVIEW, ACADEMIC

KWDacquiredimmunodeficiencysyndrome/KWDetiology/therapyaminoacidsequenceantigens,cd4/KWDmetabolismattachmentsites(microbiology)bindingsitescellfusionhumanhivenvelopeproteingp120/chemistry/KWDmetabolismmolecularsequencedataproteinbindingjournalarticlereviewreview,academic
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M9210740


Copyright © 1992 - National Library of Medicine. Reproduced under license with the National Library of Medicine, Bethesda, MD.

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