Use of recombinant cytokines for optimized induction of antiviral immunity against SIV in the nonhuman primate model of human AIDS
Identifieur interne : 000196 ( Istex/Corpus ); précédent : 000195; suivant : 000197Use of recombinant cytokines for optimized induction of antiviral immunity against SIV in the nonhuman primate model of human AIDS
Auteurs : Aftab A. Ansari ; Ann E. Mayne ; Nattawat Onlamoon ; Kovit Pattanapanyasat ; Kazuyasu Mori ; Francois VillingerSource :
- Immunologic Research [ 0257-277X ] ; 2004-06-01.
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- KwdEn :
Abstract
Abstract: Outbreaks of infectious diseases such as HIV and the much televised and attention-getting outbreaks of diseases such as Ebola, Hantaviruses, and the most recent outbreak of SARS have induced a significant new interest in the formulations and more importantly the science of vaccinology, which has previously to a large extent been conducted empirically. Our laboratory has focused on the use of recombinant nonhuman primate cytokines as adjunctive therapies for inducing antigen-specific immune responses in monkeys because most recombinant human cytokines appear to be immunogenic. This article provides a summary of our work with such cytokines, which includes attempts to define optimum dosing schedules that lead to optimal primary and lasting memory antigen-specific immune responses.
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DOI: 10.1385/IR:29:1-3:001
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<Para>Outbreaks of infectious diseases such as HIV and the much televised and attention-getting outbreaks of diseases such as Ebola, Hantaviruses, and the most recent outbreak of SARS have induced a significant new interest in the formulations and more importantly the science of vaccinology, which has previously to a large extent been conducted empirically. Our laboratory has focused on the use of recombinant nonhuman primate cytokines as adjunctive therapies for inducing antigen-specific immune responses in monkeys because most recombinant human cytokines appear to be immunogenic. This article provides a summary of our work with such cytokines, which includes attempts to define optimum dosing schedules that lead to optimal primary and lasting memory antigen-specific immune responses.</Para>
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<Keyword>Nonhuman primate</Keyword>
<Keyword>cytokines</Keyword>
<Keyword>antiviral immunity</Keyword>
<Keyword>SIV</Keyword>
<Keyword>AIDS</Keyword>
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<name type="personal"><namePart type="given">Aftab</namePart>
<namePart type="given">A.</namePart>
<namePart type="family">Ansari</namePart>
<affiliation>Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Room 2309 WMB, 1639 Pierce Drive, 30322, Atlanta, GA</affiliation>
<affiliation>E-mail: pathaaa@emory.edu</affiliation>
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<affiliation>Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Room 2309 WMB, 1639 Pierce Drive, 30322, Atlanta, GA</affiliation>
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<name type="personal"><namePart type="given">Nattawat</namePart>
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<affiliation>Division of Instrumentation, Mahidol University School of Medicine, Sriraj Hospital, Bangkok, Thailand</affiliation>
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<name type="personal"><namePart type="given">Kovit</namePart>
<namePart type="family">Pattanapanyasat</namePart>
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<name type="personal"><namePart type="given">Kazuyasu</namePart>
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<affiliation>Tsukuba Primate Research Center, National Center for AIDS Research, Tsukuba, Japan</affiliation>
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<name type="personal"><namePart type="given">Francois</namePart>
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<abstract lang="en">Abstract: Outbreaks of infectious diseases such as HIV and the much televised and attention-getting outbreaks of diseases such as Ebola, Hantaviruses, and the most recent outbreak of SARS have induced a significant new interest in the formulations and more importantly the science of vaccinology, which has previously to a large extent been conducted empirically. Our laboratory has focused on the use of recombinant nonhuman primate cytokines as adjunctive therapies for inducing antigen-specific immune responses in monkeys because most recombinant human cytokines appear to be immunogenic. This article provides a summary of our work with such cytokines, which includes attempts to define optimum dosing schedules that lead to optimal primary and lasting memory antigen-specific immune responses.</abstract>
<note>Immunology at Emory University</note>
<subject lang="en"><genre>Key Words</genre>
<topic>Nonhuman primate</topic>
<topic>cytokines</topic>
<topic>antiviral immunity</topic>
<topic>SIV</topic>
<topic>AIDS</topic>
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<subject><genre>Medicine & Public Health</genre>
<topic>Allergology</topic>
<topic>Immunology</topic>
<topic>Medicine/Public Health, general</topic>
<topic>Internal Medicine</topic>
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