Protection against Mucosal SHIV Challenge by Peptide and Helper-Dependent Adenovirus Vaccines 英文参考文献.docVIP
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Protection against Mucosal SHIV Challenge by Peptide and Helper-Dependent Adenovirus Vaccines 英文参考文献
Viruses 2009, 1, 920-938; doi:10.3390/v1030920
OPEN ACCESS
viruses
ISSN 1999-4915
/journal/viruses
Article
Protection against Mucosal SHIV Challenge by Peptide and
Helper-Dependent Adenovirus Vaccines
Eric A. Weaver 1,#, Pramod N. Nehete 2,#, Bharti P. Nehete 2, Stephanie J. Buchl 2,
Donna Palmer 3, David C. Montefiori 4, Philip Ng 3, K. Jagannadha Sastry 2,5 and
Michael A. Barry 1,6,7,
*
1
Department of Internal Medicine, Division of Infectious Diseases, Translational Immunovirology
Program, Mayo Clinic, Rochester, MN 55905, USA
2
3
Department of Veterinary Sciences, M.D. Anderson Cancer Center, The University of Texas,
Bastrop, TX 78602, USA
Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030,
USA
4
5
Duke University Medical Center, Durham, NC 27710, USA
Department of Immunology, M.D. Anderson Cancer Center, The University of Texas, Houston,
TX 77054, USA
6
7
Department of Immunology, Mayo Clinic, Rochester, MN 55905, USA
Department of Molecular Medicine, Mayo Clinic, Rochester, MN 55905, USA
* Author to whom correspondence should be addressed; E-mail: mab@;
Tel: +1-507-266-9090; Fax: +1-507-255-2811.
#
These authors contributed equally to this work.
Received: 5 October 2009; in revised form: 6 November 2009 / Accepted: 9 November 2009 /
Published: 10 November 2009
Abstract: Groups of rhesus macaques that had previously been immunized with HIV-1
envelope (env) peptides and first generation adenovirus serotype 5 (FG-Ad5) vaccines
expressing the same peptides were immunized intramuscularly three times with helper-
dependent adenovirus (HD-Ad) vaccines expressing only the HIV-1 envelope from JRFL.
No gag, pol, or other SHIV genes were used for vaccination. One group of the FG-Ad5-
immune animals was immunized three times with HD-Ad5 expressing env. One group was
immunized by serotype-switching with HD-Ad6, HD-Ad1, and HD-Ad2 expressing env.
Previous work demonstrated that seru
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