Use of vaxfectin adjuvant with DNA vaccine encoding the measles virus hemagglutinin and fusion proteins protects juvenile and infant rhesus macaques against measles virus

被引:33
作者
Pan, Chien-Hsiung [1 ]
Jimenez, Gretchen S. [4 ]
Nair, Nitya [1 ]
Wei, Qun [4 ]
Adams, Robert J. [2 ]
Polack, Fernando P. [1 ,3 ]
Rolland, Alain [4 ]
Vilalta, Adrian [4 ]
Griffin, Diane E. [1 ]
机构
[1] Johns Hopkins Bloomberg Sch Publ Hlth, W Harry Feinstone Dept Mol Microbiol & Immunol, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Dept Mol & Comparat Pathol, Baltimore, MD 21218 USA
[3] Johns Hopkins Univ, Sch Med, Dept Pediat, Baltimore, MD 21218 USA
[4] Vical Incorp, San Diego, CA 92121 USA
关键词
D O I
10.1128/CVI.00120-08
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
A measles virus vaccine for infants under 6 months of age would help control measles. DNA vaccines hold promise, but none has provided full protection from challenge. Codon-optimized plasmid DNAs encoding the measles virus hemagglutinin and fusion glycoproteins were formulated with the cationic lipid-based adjuvant Vaxfectin. In mice, antibody and gamma interferon (IFN-gamma) production were increased by two-to threefold. In macaques, juveniles vaccinated at 0 and 28 days with 500 mu g of DNA intradermally or with 1 mg intramuscularly developed sustained neutralizing antibody and H- and F-specific IFN-gamma responses. Infant monkeys developed sustained neutralizing antibody and T cells secreting IFN-gamma and interleukin-4. Twelve to 15 months after vaccination, vaccinated monkeys were protected from an intratracheal challenge: viremia was undetectable by cocultivation and rashes did not appear, while two naive monkeys developed viremia and rashes. The use of Vaxfectin-formulated DNA is a promising approach to the development of a measles vaccine for young infants.
引用
收藏
页码:1214 / 1221
页数:8
相关论文
共 50 条
[1]   PERSISTENCE OF MATERNAL ANTIBODY IN INFANTS BEYOND 12 MONTHS - MECHANISM OF MEASLES-VACCINE FAILURE [J].
ALBRECHT, P ;
ENNIS, FA ;
SALTZMAN, EJ ;
KRUGMAN, S .
JOURNAL OF PEDIATRICS, 1977, 91 (05) :715-718
[2]   LOSS OF MATERNALLY-ACQUIRED MEASLES ANTIBODY DURING INFANCY IN ILORIN, NIGERIA [J].
BABANIYI, OA ;
PARAKOYI, DB ;
AIYEDUN, BA ;
BELLO, MA .
JOURNAL OF TROPICAL PEDIATRICS, 1995, 41 (02) :115-117
[3]  
BLACK FL, 1989, PROG MED VIROL, V36, P1
[4]   Genetic immunization of neonates [J].
Bot, A ;
Bona, C .
MICROBES AND INFECTION, 2002, 4 (04) :511-520
[5]  
Centers for Disease Control and Prevention (CDC), 2007, MMWR Morb Mortal Wkly Rep, V56, P1237
[6]   MEASLES ANTIBODY - REEVALUATION OF PROTECTIVE TITERS [J].
CHEN, RT ;
MARKOWITZ, LE ;
ALBRECHT, P ;
STEWART, JA ;
MOFENSON, LM ;
PREBLUD, SR ;
ORENSTEIN, WA .
JOURNAL OF INFECTIOUS DISEASES, 1990, 162 (05) :1036-1042
[7]   Mechanisms of increased immunogenicity for DNA-based vaccines adsorbed onto cationic microparticles [J].
Denis-Mize, KS ;
Dupuis, M ;
Singh, M ;
Woo, C ;
Ugozzoli, M ;
O'Hagan, DT ;
Donnelly, JJ ;
Ott, G ;
McDonald, DM .
CELLULAR IMMUNOLOGY, 2003, 225 (01) :12-20
[8]   MEASLES-VIRUS FUSION PROTEIN PRESENTED IN AN IMMUNE-STIMULATING COMPLEX (ISCOM) INDUCES HEMOLYSIS-INHIBITING AND FUSION-INHIBITING ANTIBODIES, VIRUS-SPECIFIC T-CELLS AND PROTECTION IN MICE [J].
DEVRIES, P ;
VANBINNENDIJK, RS ;
VANDERMAREL, P ;
VANWEZEL, AL ;
VOORMA, HO ;
SUNDQUIST, B ;
UYTDEHAAG, FGCM ;
OSTERHAUS, ADME .
JOURNAL OF GENERAL VIROLOGY, 1988, 69 :549-559
[9]   DNA vaccines: Progress and challenges [J].
Donnelly, JJ ;
Wahren, B ;
Liu, MA .
JOURNAL OF IMMUNOLOGY, 2005, 175 (02) :633-639
[10]   Class I restricted CTL induction by mucosal immunization with naked DNA encoding measles virus haemagglutinin [J].
Etchart, N ;
Buckland, R ;
Liu, MA ;
Wild, TF ;
Kaiserlian, D .
JOURNAL OF GENERAL VIROLOGY, 1997, 78 :1577-1580