Durable protection of rhesus macaques immunized with a replicating adenovirus-SIV multigene prime/protein boost vaccine regimen against a second SIVmac251 rectal challenge: role of SIV-specific CD8+ T cell responses

Previously, priming with replication-competent adenovirus-SIV multigenic vaccines and boosting with envelope subunits strongly protected 39% of rhesus macaques against rectal SIV(mac251) challenge. To evaluate protection durability, eleven of the protected and two SIV-infected unimmunized macaques t...

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Veröffentlicht in:Virology (New York, N.Y.) N.Y.), 2006-09, Vol.353 (1), p.83-98
Hauptverfasser: Malkevitch, Nina V, Patterson, L Jean, Aldrich, M Kristine, Wu, Yichen, Venzon, David, Florese, Ruth H, Kalyanaraman, V S, Pal, Ranajit, Lee, Eun Mi, Zhao, Jun, Cristillo, Anthony, Robert-Guroff, Marjorie
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container_title Virology (New York, N.Y.)
container_volume 353
creator Malkevitch, Nina V
Patterson, L Jean
Aldrich, M Kristine
Wu, Yichen
Venzon, David
Florese, Ruth H
Kalyanaraman, V S
Pal, Ranajit
Lee, Eun Mi
Zhao, Jun
Cristillo, Anthony
Robert-Guroff, Marjorie
description Previously, priming with replication-competent adenovirus-SIV multigenic vaccines and boosting with envelope subunits strongly protected 39% of rhesus macaques against rectal SIV(mac251) challenge. To evaluate protection durability, eleven of the protected and two SIV-infected unimmunized macaques that controlled viremia were re-challenged rectally with SIV(mac251). Strong protection was observed in 8/11 vaccinees, including two exhibiting
doi_str_mv 10.1016/j.virol.2006.05.012
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To evaluate protection durability, eleven of the protected and two SIV-infected unimmunized macaques that controlled viremia were re-challenged rectally with SIV(mac251). Strong protection was observed in 8/11 vaccinees, including two exhibiting &lt;50 SIV RNA copies. Decreased viremia compared to naïve controls was observed in the other three. The SIV-infected unimmunized macaques modestly controlled viremia but exhibited CD4 counts &lt; or =200, unlike the protected macaques. Durable protection was associated with significantly increased SIV-specific ELISPOT responses and lymphoproliferative responses to p27 at re-challenge. After CD8 depletion, 2 of 8 re-challenged, protected vaccinees maintained &lt;50 SIV RNA copies; SIV RNA emerged in 6. Re-appearance of CD8 cells and restoration of SIV-specific cellular immunity coincided with viremia suppression. 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source MEDLINE; Elsevier ScienceDirect Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals
subjects Adenoviridae - genetics
Adenoviridae - immunology
Administration, Rectal
Animals
CD8-Positive T-Lymphocytes - immunology
Immunity, Cellular
Immunization, Secondary
Macaca mulatta
Recombinant Fusion Proteins - immunology
RNA, Viral - analysis
SAIDS Vaccines - administration & dosage
SAIDS Vaccines - genetics
SAIDS Vaccines - immunology
Simian Acquired Immunodeficiency Syndrome - immunology
Simian Acquired Immunodeficiency Syndrome - prevention & control
Simian Acquired Immunodeficiency Syndrome - virology
Simian Immunodeficiency Virus - immunology
Simian Immunodeficiency Virus - isolation & purification
Time Factors
Vaccination
Vaccines, Synthetic - administration & dosage
Viremia
Virus Replication
title Durable protection of rhesus macaques immunized with a replicating adenovirus-SIV multigene prime/protein boost vaccine regimen against a second SIVmac251 rectal challenge: role of SIV-specific CD8+ T cell responses
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