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Neutralizing Antibodies in Sera from Macaques Infected with Chimeric Simian-Human Immunodeficiency Virus Containing the Envelope Glycoproteins of either a Laboratory-Adapted Variant or a Primary Isolate of Human Immunodeficiency Virus Type 1
Authors:David C Montefiori  Keith A Reimann  Michael S Wyand  Kelledy Manson  Mark G Lewis  Ronald G Collman  Joseph G Sodroski  Dani P Bolognesi  and Norman L Letvin
Institution:Department of Surgery, Duke University Medical Center, Durham, North Carolina1.; Division of Viral Pathogenesis, Beth Israel Deaconess Medical Center,2. and Dana-Farber Cancer Institute,6. Harvard Medical School, Boston, and GTC Mason Laboratories, Worcester,3. Massachusetts; Henry M. Jackson Foundation, Rockville, Maryland4.; and Division of Pulmonary and Critical Care, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania5.
Abstract:The magnitude and breadth of neutralizing antibodies raised in response to infection with chimeric simian-human immunodeficiency virus (SHIV) in rhesus macaques were evaluated. Infection with either SHIV-HXB2, SHIV-89.6, or SHIV-89.6PD raised high-titer neutralizing antibodies to the homologous SHIV (SHIV-89.6P in the case of SHIV-89.6PD-infected animals) and significant titers of neutralizing antibodies to human immunodeficiency virus type 1 (HIV-1) strains MN and SF-2. With few exceptions, however, titers of neutralizing antibodies to heterologous SHIV were low or undetectable. The antibodies occasionally neutralized heterologous primary isolates of HIV-1; these antibodies required >40 weeks of infection to reach detectable levels. Notable was the potent neutralization of the HIV-1 89.6 primary isolate by serum samples from SHIV-89.6-infected macaques. These results demonstrate that SHIV-HXB2, SHIV-89.6, and SHIV-89.6P possess highly divergent, strain-specific neutralization epitopes. The results also provide insights into the requirements for raising neutralizing antibodies to primary isolates of HIV-1.
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