Oral or parenteral administration of replication-deficient adenoviruses expressing the measles virus haemagglutinin and fusion proteins: protective immune responses in rodents

被引:29
作者
Fooks, AR
Jeevarajah, D
Lee, J
Warnes, A
Niewiesk, S
ter Meulen, V
Stephenson, JR
Clegg, JCS
机构
[1] Publ Hlth Lab Serv, Ctr Appl Microbiol & Res, Salisbury SP4 0JG, Wilts, England
[2] Univ Wurzburg, Inst Virol & Immunobiol, D-97078 Wurzburg, Germany
关键词
D O I
10.1099/0022-1317-79-5-1027
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The genes encoding the measles virus (MV) haemagglutinin (H) and fusion (F) proteins were placed under the control of the human cytomegalovirus immediate early promoter in a replication-deficient adenovirus vector. Immunofluorescence and radioimmune precipitation demonstrated the synthesis of each protein and biological activity was confirmed by the detection of haemadsorption and fusion activities in infected cells. Oral as well as parenteral administration of the H-expressing recombinant adenovirus elicited a significant protective response in mice challenged with MV. While the F-expressing adenovirus failed to protect mice, cotton rats immunized with either the H- or F-expressing recombinant showed reduced MV replication in the lungs. Antibodies elicited in mice following immunization with either recombinant had no in vitro neutralizing activity, suggesting a protective mechanism involving a cell-mediated immune response. This study demonstrates the feasibility of using oral administration of adenovirus recombinants to induce protective responses to heterologous proteins.
引用
收藏
页码:1027 / 1031
页数:5
相关论文
共 23 条
[1]   ROLE OF VIRUS-STRAIN IN CONVENTIONAL AND ENHANCED MEASLES PLAQUE NEUTRALIZATION TEST [J].
ALBRECHT, P ;
HERRMANN, K ;
BURNS, GR .
JOURNAL OF VIROLOGICAL METHODS, 1981, 3 (05) :251-260
[2]   HIGH-LEVEL EUKARYOTIC INVIVO EXPRESSION OF BIOLOGICALLY-ACTIVE MEASLES-VIRUS HEMAGGLUTININ BY USING AN ADENOVIRUS TYPE-5 HELPER-FREE VECTOR SYSTEM [J].
ALKHATIB, G ;
BRIEDIS, DJ .
JOURNAL OF VIROLOGY, 1988, 62 (08) :2718-2727
[3]   INTRACELLULAR PROCESSING, GLYCOSYLATION, AND CELL-SURFACE EXPRESSION OF THE MEASLES-VIRUS FUSION PROTEIN (F) ENCODED BY A RECOMBINANT ADENOVIRUS [J].
ALKHATIB, G ;
RICHARDSON, C ;
SHEN, SH .
VIROLOGY, 1990, 175 (01) :262-270
[4]   IMMUNIZATION WITH A VACCINIA RECOMBINANT EXPRESSING THE F-PROTEIN PROTECTS RABBITS FROM CHALLENGE WITH A LETHAL DOSE OF RINDERPEST VIRUS [J].
BARRETT, T ;
BELSHAM, GJ ;
SUBBARAO, SM ;
EVANS, SA .
VIROLOGY, 1989, 170 (01) :11-18
[5]  
BETT AJ, 1995, VIRUS RES, V39, P75
[6]   EFFICACY OF INDIVIDUAL MEASLES-VIRUS STRUCTURAL PROTEINS IN THE PROTECTION OF RATS FROM MEASLES ENCEPHALITIS [J].
BRINCKMANN, UG ;
BANKAMP, B ;
REICH, A ;
TERMEULEN, V ;
LIEBERT, UG .
JOURNAL OF GENERAL VIROLOGY, 1991, 72 :2491-2500
[7]   PROTECTION OF MICE FROM FATAL MEASLES ENCEPHALITIS BY VACCINATION WITH VACCINIA VIRUS RECOMBINANTS ENCODING EITHER THE HEMAGGLUTININ OR THE FUSION PROTEIN [J].
DRILLIEN, R ;
SPEHNER, D ;
KIRN, A ;
GIRAUDON, P ;
BUCKLAND, R ;
WILD, F ;
LECOCQ, JP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (04) :1252-1256
[8]   A recombinant human adenovirus expressing the simian immunodeficiency virus Gag antigen can induce long-lived immune responses in mice [J].
Flanagan, B ;
Pringle, CR ;
Leppard, KN .
JOURNAL OF GENERAL VIROLOGY, 1997, 78 :991-997
[9]   HIGH-LEVEL EXPRESSION OF THE MEASLES-VIRUS NUCLEOCAPSID PROTEIN BY USING A REPLICATION-DEFICIENT ADENOVIRUS VECTOR - INDUCTION OF AN MHC-1-RESTRICTED CTL RESPONSE AND PROTECTION IN A MURINE MODEL [J].
FOOKS, AR ;
SCHADECK, E ;
LIEBERT, UG ;
DOWSETT, AB ;
RIMA, BK ;
STEWARD, M ;
STEPHENSON, JR ;
WILKINSON, GWG .
VIROLOGY, 1995, 210 (02) :456-465
[10]   IMMUNOGENICITY AND EFFICACY TESTING IN CHIMPANZEES OF AN ORAL HEPATITIS-B VACCINE BASED ON LIVE RECOMBINANT ADENOVIRUS [J].
LUBECK, MD ;
DAVIS, AR ;
CHENGALVALA, M ;
NATUK, RJ ;
MORIN, JE ;
MOLNARKIMBER, K ;
MASON, BB ;
BHAT, BM ;
MIZUTANI, S ;
HUNG, PP ;
PURCELL, RH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (17) :6763-6767