HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Prevention of HIV-1 IIIB infection in chimpanzees by CD4 immunoadhesin.

Abstract
The first step in infection by the human immunodeficiency virus (HIV) is the specific binding of gp120, the envelope glycoprotein of HIV, to its cellular receptor, CD4. To inhibit this interaction, soluble CD4 analogues that compete for gp120 binding and block HIV infection in vitro have been developed. To determine whether these analogues can protect an uninfected individual from challenge with HIV, we used the chimpanzee model system of cell-free HIV infection. Chimpanzees are readily infected with the IIIB strain of HIV-1, becoming viraemic within about 4-6 weeks of challenge, although they do not develop the profound CD4+ T-cell depletion and immunodeficiency characteristic of HIV infection in humans. CD4 immunoadhesin (CD4-IgG), a chimaeric molecule consisting of the N-terminal two immunoglobulin-like regions of CD4 joined to the Fc region of human IgG1, was selected as the CD4 analogue for testing because it has a longer half-life than CD4, contributed by the IgG Fc portion of the molecule. In humans, this difference results in a 25-fold increased concentration of CD4-IgG in the blood compared with recombinant CD4. Here we report that pretreatment with CD4-IgG can prevent the infection of chimpanzees with HIV-1. The need for a preventative agent is particularly acute in perinatal HIV transmission. As recombinant CD4-IgG, like the parent IgG molecule, efficiently crosses the primate placenta, it may be possible to set up an immune state in a fetus before HIV transfer occurs, thus preventing infection.
AuthorsR H Ward, D J Capon, C M Jett, K K Murthy, J Mordenti, C Lucas, S W Frie, A M Prince, J D Green, J W Eichberg
JournalNature (Nature) Vol. 352 Issue 6334 Pg. 434-6 (Aug 01 1991) ISSN: 0028-0836 [Print] England
PMID1907354 (Publication Type: Journal Article, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Antibodies, Anti-Idiotypic
  • Antigens, CD
  • CD4 Antigens
  • CD4 Immunoadhesins
  • Immunoglobulin Fc Fragments
  • Immunoglobulin G
  • Recombinant Proteins
Topics
  • Acquired Immunodeficiency Syndrome (prevention & control)
  • Animals
  • Antibodies, Anti-Idiotypic (administration & dosage, immunology, pharmacokinetics)
  • Antigens, CD (administration & dosage, immunology, pharmacokinetics)
  • CD4 Antigens (immunology)
  • CD4 Immunoadhesins
  • HIV-1
  • Immunization, Passive
  • Immunoglobulin Fc Fragments
  • Immunoglobulin G (administration & dosage, immunology, pharmacokinetics)
  • Pan troglodytes
  • Recombinant Proteins

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: