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Journal of Virology, July 2001, p. 6700-6704, Vol. 75, No. 14
Department of Microbiology, Meharry Medical
College, Nashville, Tennessee 37208,1 and
Trimeris Inc., Durham, North Carolina
277072
Received 16 January 2001/Accepted 13 April 2001
Chimpanzees infected with the primary isolate DH012 mount potent
neutralizing antibodies. This DH012 neutralizing activity is highly
strain specific. Immune sera from guinea pigs immunized with
recombinant DH012 gp120 could also neutralize this primary isolate. The
neutralizing activity in chimpanzee and guinea pig sera against
wild-type DH012 appears to be independent of a linear epitope in
the V3 region of gp120. Interestingly, the neutralization escape
mutant derived from growing DH012 in the presence of the potent
neutralizing chimpanzee serum is at least 50-fold more sensitive than
wild-type DH012 to neutralization by guinea pig immune sera. The
unusually potent neutralizing activity against the DH012
neutralization-resistant virus is due to the presence of anti-V3
antibodies in guinea pig sera. These results suggested that recombinant
gp120 could induce neutralizing antibodies against primary isolate
DH012. The V3 of wild-type DH012 is poorly immunogenic in infected
chimpanzees and is not accessible to neutralizing V3 antibodies. It is
likely that this cryptic V3 region became exposed when the virus
escaped the neutralizing activity of the chimpanzee serum.
0022-538X/01/$04.00+0 DOI: 10.1128/JVI.75.14.6700-6704.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Induction and Characterization of Neutralizing Antibodies against
a Human Immunodeficiency Virus Type 1 Primary Isolate
*
Corresponding author. Mailing address: Department of
Microbiology, Meharry Medical College, 1005 D. B. Todd Blvd.,
Nashville, TN 37208. Phone: (615) 327-6672. Fax: (615) 327-6672. E-mail: cchen{at}mail.mmc.edu.
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