Protection of macaques against vaginal transmission of a pathogenic HIV-1/SIV chimeric virus by passive infusion of neutralizing antibodies (original) (raw)
- Article
- Published: February 2000
- Gabriela Stiegler3,
- Thomas C. VanCott1,
- Hermann Katinger3,
- Calvin B. Carpenter4,
- Chris E. Hanson4,
- Holly Beary1,
- Deborah Hayes1,
- Sarah S. Frankel1,
- Deborah L. Birx1 &
- …
- Mark G. Lewis1
Nature Medicine volume 6, pages 207–210 (2000)Cite this article
- 3032 Accesses
- 1099 Citations
- 9 Altmetric
- Metrics details
Abstract
The development of the human immunodeficiency virus-1 (HIV-1)/simian immunodeficiency virus (SIV) chimeric virus macaque model (SHIV) permits the in vivo evaluation of anti-HIV-1 envelope glycoprotein immune responses1,2,3. Using this model, others, and we have shown that passively infused antibody can protect against an intravenous challenge4,5. However, HIV-1 is most often transmitted across mucosal surfaces6,7,8,9 and the intravenous challenge model may not accurately predict the role of antibody in protection against mucosal exposure. After controlling the macaque estrous cycle with progesterone10, anti-HIV-1 neutralizing monoclonal antibodies 2F5 and 2G12, and HIV immune globulin were tested11,12,13. Whereas all five control monkeys displayed high plasma viremia and rapid CD4 cell decline, 14 antibody-treated macaques were either completely protected against infection or against pathogenic manifestations of SHIV-infection. Infusion of all three antibodies together provided the greatest amount of protection, but a single monoclonal antibody, with modest virus neutralizing activity, was also protective. Compared with our previous intravenous challenge study with the same virus and antibodies5, the data indicated that greater protection was achieved after vaginal challenge. This study demonstrates that antibodies can affect transmission and subsequent disease course after vaginal SHIV-challenge; the data begin to define the type of antibody response that could play a role in protection against mucosal transmission of HIV-1.
This is a preview of subscription content, access via your institution
Access options
Subscribe to this journal
Receive 12 print issues and online access
$209.00 per year
only $17.42 per issue
Buy this article
- Purchase on SpringerLink
- Instant access to full article PDF
Prices may be subject to local taxes which are calculated during checkout
Additional access options:
Figure 1: Plasma SHIV RNA (a) and peripheral CD4% (b) for four groups of monkeys after antibody infusion and vaginal SHIV89.6PD challenge.
Similar content being viewed by others
References
- Reimann, K.A. et al. A chimeric simian/human immunodeficiency virus expressing a primary patient human immunodeficiency virus type 1 isolate env causes an AIDS-Like disease after in vivo passage in rhesus monkeys. J. Virol. 70, 6922–6928 (1996).
CAS Google Scholar - Reimann, K.A. et al. An env gene derived from a primary human immunodeficiency virus type 1 isolate confers high in vivo replicative capacity to a chimeric simian human immunodeficiency virus in rhesus monkeys. J. Virol. 70, 3198–3206 ( 1996).
CAS Google Scholar - Shibata, R. et al. Infection and pathogenicity of chimeric simian-human immunodeficiency viruses in macaques: determinants of high virus loads and CD4 cell killing . J. Infect. Dis. 176, 362– 373 (1997).
Article CAS Google Scholar - Shibata, R. et al. Neutralizing antibody directed against the HIV-1 envelope glycoprotein can completely block HIV-1/SIV chimeric virus infections of macaque monkeys. Nature Med. 5, 204– 210 (1999).
Article CAS Google Scholar - Mascola, J.R. et al. Protection of macaques against pathogenic simian/human immunodeficiency virus 89.6PD by passive transfer of neutralizing antibodies. J. Virol. 73, 4009–4018 ( 1999).
CAS Google Scholar - Piot, P. The science of AIDS: A tale of two worlds. Science 280, 1844–1845 (1998).
Article CAS Google Scholar - Miller, C.J. & McGhee, J.R. Progress towards a vaccine to prevent sexual transmission of HIV. Nature Med. 2, 751–752 (1996).
Article CAS Google Scholar - Spira, A.I. et al. Cellular targets of infection and route of viral dissemination after an intravaginal inoculation of simian immunodeficiency virus into rhesus macaques. J. Exp. Med. 183, 215– 225 (1996).
Article CAS Google Scholar - Frankel, S.S. et al. Replication of HIV-1 in dendritic cell-derived syncytia at the mucosal surface of the adenoid. Science 272, 115–117 (1996).
Article CAS Google Scholar - Marx, P.A. et al. Progesterone implants enhance SIV vaginal transmission and early virus load. Nature Med. 2, 1084– 1089 (1996).
Article CAS Google Scholar - Burton, D.R. & Montefiori, D.C. The antibody response in HIV-1 infection. AIDS 11 Suppl. A, S87–S98 (1997).
Google Scholar - Lambert, J.S. et al. Safety and pharmacokinetics of hyperimmune anti-human immunodeficiency virus (HIV) immunoglobulin administered to HIV-infected pregnant women and their newborns. J. Infect. Dis. 175, 283 –291 (1997).
Article CAS Google Scholar - Mascola, J.R. et al. Potent and synergistic neutralization of human immunodeficiency virus (HIV) type 1 primary isolates by hyperimmune anti-HIV immunoglobulin combined with monoclonal antibodies 2F5 and 2G12. J. Virol. 71, 7198–7206 (1997).
CAS Google Scholar - Lu, Y.C., Pauza, C.D., Lu, X.S., Montefiori, D.C., & Miller, C.J. Rhesus macaques that become systemically infected with pathogenic SHIV 89.6-PD after intravenous, rectal, or vaginal inoculation and fail to make an antiviral antibody response rapidly develop AIDS. J. Acquir.Immune Defic. Syndr. Hum. Retrovirol. 19, 6–18 (1998).
Article CAS Google Scholar - Frankel, S.S. et al. Neutralizing monoclonal antibodies block human immunodeficiency virus type 1 infection of dendritic cells and transmission to T cells. J. Virol. 72, 9788–9794 (1998).
CAS Google Scholar - Kutteh, W.H., Moldoveanu, Z., & Mestecky, J. Mucosal immunity in the female reproductive tract: correlation of immunoglobulins, cytokines, and reproductive hormones in human cervical mucus around the time of ovulation. AIDS Res. Hum. Retroviruses 14 (Suppl. 1), 51–55 (1998).
Google Scholar - Lambert, G. et al. Effect of maternal CD4+ cell count, acquired immunodeficiency syndrome, and viral load on disease progression in infants with perinatally acquired human immunodeficiency virus type 1 infection. J. Pediatr. 130, 890–897 (1997).
Article CAS Google Scholar - Muster, T. et al. A conserved neutralizing epitope on gp41 of human immunodeficiency virus type 1. J. Virol. 67, 6642– 6647 (1993).
CAS Google Scholar - Trkola, A. et al. Human monoclonal antibody 2G12 defines a distinctive neutralization epitope on the gp120 glycoprotein of human immunodeficiency virus type 1. J. Virol. 70, 1100–1108 (1996).
CAS Google Scholar - Lewis, M.G. et al. Limited protection from a pathogenic chimeric simian-human immunodeficiency virus challenge following immunization with attenuated simian immunodeficiency virus. J.Virol. 73, 1262 –1270 (1999).
CAS Google Scholar - Vahey, M.T. & Wong, M.T. in PCR Primer: A Laboratory Manual 313–338. (Cold Spring Harbor Press, Plainview, NY, 1995).
Google Scholar - Artenstein, A.W. et al. Mucosal immune responses in four distinct compartments of women infected with human immunodeficiency virus type 1: a comparison by site and correlation with clinical information. J. Infect. Dis. 175, 265–271 (1997).
Article CAS Google Scholar
Acknowledgements
We thank Chris Sapan for supplying the HIVIG, Norman Letvin, Keith Reimann, and Yichen Lu for the SHIV89.6PD, Robin Garner for statistical advice, Dawn Harris for veterinary care and Francine McCutchan and Nelson Michael for manuscript reviews. We appreciate the excellent technical assistance from Mark Louder, Marcin Iwanicki, Jack Greenhouse, Mike Eller, and Jake Yalley-Ogunro. This work was supported in part by grants from the National Heart Lung and Blood Institute and by Cooperative Agreement between the U.S. Army Medical Research and Materiel Command and the Henry M. Jackson Foundation for the Advancement of Military Medicine.United States Department of Defense Disclaimer: The views and opinions expressed herein are those of the authors and do not purport to reflect the official policy or position of the U.S. Army, U.S. Navy or the Department of Defense.
Author information
Authors and Affiliations
- Division of Retrovirology, Walter Reed Army Institute of Research and Henry M. Jackson Foundation, 1 Taft Court, Suite 250, Rockville, 20850, Maryland, USA
John R. Mascola, Thomas C. VanCott, Holly Beary, Deborah Hayes, Sarah S. Frankel, Deborah L. Birx & Mark G. Lewis - Department of Infectious Diseases, Naval Medical Research Center, Forrest Glenn, 20910, Maryland, USA
John R. Mascola - Institute of Applied Microbiology, University of Agriculture, Vienna, Austria
Gabriela Stiegler & Hermann Katinger - Division of Veterinary Medicine, Walter Reed Army Institute of Research, Forrest Glenn, 20910 , Maryland, USA
Calvin B. Carpenter & Chris E. Hanson
Authors
- John R. Mascola
You can also search for this author inPubMed Google Scholar - Gabriela Stiegler
You can also search for this author inPubMed Google Scholar - Thomas C. VanCott
You can also search for this author inPubMed Google Scholar - Hermann Katinger
You can also search for this author inPubMed Google Scholar - Calvin B. Carpenter
You can also search for this author inPubMed Google Scholar - Chris E. Hanson
You can also search for this author inPubMed Google Scholar - Holly Beary
You can also search for this author inPubMed Google Scholar - Deborah Hayes
You can also search for this author inPubMed Google Scholar - Sarah S. Frankel
You can also search for this author inPubMed Google Scholar - Deborah L. Birx
You can also search for this author inPubMed Google Scholar - Mark G. Lewis
You can also search for this author inPubMed Google Scholar
Corresponding author
Correspondence toJohn R. Mascola.
Rights and permissions
About this article
Cite this article
Mascola, J., Stiegler, G., VanCott, T. et al. Protection of macaques against vaginal transmission of a pathogenic HIV-1/SIV chimeric virus by passive infusion of neutralizing antibodies.Nat Med 6, 207–210 (2000). https://doi.org/10.1038/72318
- Received: 07 November 1999
- Accepted: 01 December 1999
- Issue Date: February 2000
- DOI: https://doi.org/10.1038/72318