Effective induction of simian immunodeficiency virus-specific systemic and mucosal immune responses in primates by vaccination with proviral DNA producing intact but noninfectious virions

被引:55
作者
Wang, SW
Kozlowski, PA
Schmelz, G
Manson, K
Wyand, MS
Glickman, R
Montefiori, D
Lifson, JD
Johnson, RP
Neutra, MR
Aldovini, A
机构
[1] Childrens Hosp, Dept Med, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dept Pediat, Boston, MA 02115 USA
[3] Primedica, Worcester, MA USA
[4] Duke Univ, Durham, NC USA
[5] NCI, Frederick Canc Res & Dev Ctr, SAIC Frederick, AIDS Vaccine Program,Retroviral Pathogenesis Lab, Frederick, MD USA
[6] Harvard Univ, New England Reg Primate Res Ctr, Sch Med, Southborough, MA 01772 USA
[7] Massachusetts Gen Hosp, Partners AIDS Res Ctr, Charlestown, MA USA
[8] Massachusetts Gen Hosp, Infect Dis Unit, Charlestown, MA USA
关键词
D O I
10.1128/JVI.74.22.10514-10522.2000
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
We report a pilot evaluation of a DNA vaccine producing genetically inactivated simian immunodeficiency virus (SIV) particles in primates, with a focus on eliciting mucosal immunity. Our results demonstrate that DNA vaccines can be used to stimulate strong virus-specific mucosal immune responses in primates. The levels of immunoglobulin A (IgA) detected in rectal secretions of macaques that received the DNA vaccine intradermally and at the rectal mucosa were the most striking of all measured immune responses and were higher than usually achieved through natural infection. However, cytotoxic T lymphocyte responses were generally low and sporadically present in different animals. Upon rectal challenge with cloned SIVmac239, resistance to infection was observed, but some animals with high SIV-specific IgA levels in rectal secretions became infected. Our results suggest that high levels of IgA alone are not sufficient to prevent the establishment of chronic infection, although mucosal IgA responses may have a role in reducing the infectivity of the initial viral inoculum.
引用
收藏
页码:10514 / 10522
页数:9
相关论文
共 54 条
[1]   β-chemokine production in macaques vaccinated with live attenuated virus correlates with protection against simian immunodeficiency virus (SIVsm) challenge [J].
Ahmed, RKS ;
Nilsson, C ;
Wang, YF ;
Lehner, T ;
Biberfeld, G ;
Thorstensson, R .
JOURNAL OF GENERAL VIROLOGY, 1999, 80 :1569-1574
[2]   MUTATIONS OF RNA AND PROTEIN SEQUENCES INVOLVED IN HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 PACKAGING RESULT IN PRODUCTION OF NONINFECTIOUS VIRUS [J].
ALDOVINI, A ;
YOUNG, RA .
JOURNAL OF VIROLOGY, 1990, 64 (05) :1920-1926
[3]  
Ausubel FM, 1995, SHORT PROTOCOLS MOL
[4]  
BASBA TW, 2000, NAT MED, V6, P200
[5]   Epidemiologic and biologic characterization of a cohort of human immunodeficiency virus type I highly exposed, persistently seronegative female sex workers in northern Thailand [J].
Beyrer, C ;
Artenstein, AW ;
Rugpao, S ;
Stephens, H ;
VanCott, TC ;
Robb, ML ;
Rinkaew, M ;
Birx, DL ;
Khamboonruang, C ;
Zimmerman, PA ;
Nelson, KE ;
Natpratan, C .
JOURNAL OF INFECTIOUS DISEASES, 1999, 179 (01) :59-67
[6]   Cellular cytotoxic response induced by DNA vaccination in HIV-1-infected patients [J].
Calarota, S ;
Bratt, G ;
Nordlund, S ;
Hinkula, J ;
Leandersson, AC ;
Sandström, E ;
Wahren, B .
LANCET, 1998, 351 (9112) :1320-1325
[7]   A role for mucosal immunity in resistance to HIV infection [J].
Clerici, M ;
Salvi, A ;
Trabattoni, D ;
Lo Caputo, S ;
Semplici, F ;
Biasin, M ;
Ble, C ;
Meacci, F ;
Romeo, C ;
Piconi, S ;
Mazzotta, F ;
Villa, ML ;
Mazzoli, S .
IMMUNOLOGY LETTERS, 1999, 66 (1-3) :21-25
[8]   PROTECTIVE EFFECTS OF A LIVE ATTENUATED SIV VACCINE WITH A DELETION IN THE NEF GENE [J].
DANIEL, MD ;
KIRCHHOFF, F ;
CZAJAK, SC ;
SEHGAL, PK ;
DESROSIERS, RC .
SCIENCE, 1992, 258 (5090) :1938-1941
[9]   AN ESSENTIAL INTERACTION BETWEEN DISTINCT DOMAINS OF HIV-1 INTEGRASE MEDIATES ASSEMBLY OF THE ACTIVE MULTIMER [J].
ELLISON, V ;
GERTON, J ;
VINCENT, KA ;
BROWN, PO .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (07) :3320-3326
[10]   Priming of cytotoxic T lymphocytes by DNA vaccines: Requirement for professional antigen presenting cells and evidence for antigen transfer from myocytes [J].
Fu, TM ;
Ulmer, JB ;
Caulfield, MJ ;
Deck, RR ;
Friedman, A ;
Wang, S ;
Liu, X ;
Donnelly, JJ ;
Liu, MA .
MOLECULAR MEDICINE, 1997, 3 (06) :362-371