Scand J Immunol. 1995 Jan;41(1):18-22. Unique Identifier : AIDSLINE
Enhancement of virus infectivity after sCD4 treatment has been
documented for SIVagm and HIV-2. It has been suggested that a similar
phenomenon may play a role in HIV-1 infection. In the present study we
have analysed biological activities of virus neutralizing polyclonal and
monoclonal human antibodies and of sCD4, towards HIV-1 chimeras with
envelope proteins derived from one donor, which display different
biological phenotypes. The antibodies, which recognize the V3 and/or the
CD4 binding domains of the glycoproteins of these viruses and also sCD4
showed different levels of virus neutralizing activity toward the
syncytium inducing HIV-1 strains. In contrast, they all dramatically
enhanced the infectivity of an HIV-1 chimera with an envelope
glycoprotein displaying the non-syncytium-inducing phenotype. Given the
relatively conserved nature of non-syncytium-inducing HIV-1 surface
glycoproteins early after infection, these data suggest a major role for
antibody mediated enhancement of virus infectivity in the early
pathogenesis of HIV-1 infection.
Antibodies, Monoclonal/IMMUNOLOGY Antibody Affinity Antigens,
CD4/*METABOLISM Cell Fusion Gene Products, env/IMMUNOLOGY Human HIV
Antibodies/*IMMUNOLOGY HIV-1/IMMUNOLOGY/*PATHOGENICITY In Vitro
Neutralization Tests Support, Non-U.S. Gov't JOURNAL ARTICLE