Vasoactive intestinal peptide 1-12: a ligand for the CD4 (T4)/human immunodeficiency virus receptor. NLM AIDSLINE Important note: Information in this article was accurate in 1988. The state of the art may have changed since the publication date.

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Vasoactive intestinal peptide 1-12: a ligand for the CD4 (T4)/human immunodeficiency virus receptor.

J Neurosci Res. 1987;18(1):102-7. Unique Identifier : AIDSLINE MED/88062807
Sacerdote P; Ruff MR; Pert CB; Section on Brain Biochemistry, ADAMHA, Bethesda, MD 20892.


Abstract: A five-amino-acid (TDNYT) sequence of vasoactive intestinal polypeptide (VIP) shares homology with the proposed attachment sequences of the human immunodeficiency virus (HIV). Synthetic peptides with these sequences have previously been shown to block viral envelope (gp120) binding and HIV infectivity and to serve as agonists of the CD4 (or T4) receptor. Utilizing an in vitro human monocyte chemotaxis bioassay we examined novel synthetic VIP and gp120 sequences and characterized their pharmacological activities on monocyte chemotaxis. CD4 receptor activity is primarily specified by N-terminal (VIP [1-12]) amino acids. The profound immunosuppression of AIDS is not easily explained solely by virus infection. Recently described immunological functions of VIP are similar to some of the immunological abnormalities shown by patients with AIDS. An overproduction of a VIP-like molecule from viral sources (e.g. gp120) could explain some of the immune system impairments which have been described in AIDS.
Keywords: Acquired Immunodeficiency Syndrome/IMMUNOLOGY Chemotaxis, Leukocyte Human HIV/*PHYSIOLOGY In Vitro Ligands Monocytes Receptors, Virus/*PHYSIOLOGY Vasoactive Intestinal Peptide/*PHYSIOLOGY JOURNAL ARTICLE

KWDacquiredimmunodeficiencysyndrome/immunologychemotaxis,leukocytehumanhiv/KWDphysiologyinvitroligandsmonocytesreceptors,virus/KWDphysiologyvasoactiveintestinalpeptide/KWDphysiologyjournalarticle
880330
M8830352


Copyright © 1988 - National Library of Medicine. Reproduced under license with the National Library of Medicine, Bethesda, MD.

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