Vaccination with a cocktail of seven recombinantly expressed HSV-1 glycoproteins protects against ocular HSV-1 challenge more efficiently than vaccination with any individual glycoprotein

被引:45
作者
Ghiasi, H [1 ]
Nesburn, AB [1 ]
Wechsler, SL [1 ]
机构
[1] UNIV CALIF LOS ANGELES,SCH MED,DEPT OPHTHALMOL,LOS ANGELES,CA 90095
关键词
HSV-1; latency; glycoproteins; ocular; mice; vaccine;
D O I
10.1016/0264-410X(95)00169-2
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Our previous studies have shown that of seven HSV-1 glycoproteins (gB, gC, gD, gE, gG, gH and gI) individually expressed in baculovirus, vaccination with gD provides the best protection against HSV-1 challenge. To establish whether vaccination with a mixture of these seven expressed glycoproteins would provide better protection against HSV-1 challenge than vaccination with gD alone, we determined the level of protection afforded by vaccination with a cocktail of the seven expressed glycoproteins. The amount of each of the seven expressed glycoproteins in the mixture was equivalent to one-seventh the amount of gD used in the gD alone vaccination. Thus, the total amount of glycoprotein was the same for the cocktail and gD alone vaccine. For neutralizing antibody titer, delayed-type hypersensitivity (DTH), and survival following lethal challenge, no difference was observed between mice vaccinated with all seven glycoproteins and those vaccinated with gD. However, far other criteria, vaccination with all seven glycoproteins appeared to provide better protection than vaccination with gD. Following ocular challenge, virus was nor detected at any time in the tears of mice vaccinated with all seven glycoproteins. In contrast, virus was detected in the tears of gD vaccinated mice for up to 3 days post challenge. Mock vaccinated mice had virus in their tears for as long as 10 days. Mice vaccinated with all seven glycoproteins had no eye disease, while gD vaccinated mice had a significant amount of blepharitis. Finally, compared to gD vaccinated mice, the mice vaccinated with all seven glycoproteins were more efficiently protected against the establishment of HSV-1 latency following ocular infection. Our results therefore suggest that while for some protective criteria there was no significant difference between vaccination with gD or seven glycoproteins, vaccination with seven glycoproteins was move efficient in protecting challenged mice against some forms of eye disease, the duration of infection and the establishment of latency.
引用
收藏
页码:107 / 112
页数:6
相关论文
共 38 条
[1]   THE UL10 GENE OF HERPES-SIMPLEX VIRUS-1 ENCODES A NOVEL VIRAL GLYCOPROTEIN, GM, WHICH IS PRESENT IN THE VIRION AND IN THE PLASMA-MEMBRANE OF INFECTED-CELLS [J].
BAINES, JD ;
ROIZMAN, B .
JOURNAL OF VIROLOGY, 1993, 67 (03) :1441-1452
[2]   CHARACTERIZATION AND PHYSICAL MAPPING OF AN HSV-1 GLYCOPROTEIN OF APPROXIMATELY 115X10(3) MOLECULAR-WEIGHT [J].
BUCKMASTER, EA ;
GOMPELS, U ;
MINSON, A .
VIROLOGY, 1984, 139 (02) :408-413
[3]   CURRENT DEVELOPMENTS IN HERPES-SIMPLEX VIRUS-VACCINES [J].
BURKE, RL .
SEMINARS IN VIROLOGY, 1993, 4 (03) :187-197
[4]   EXPRESSION OF HERPES-SIMPLEX VIRUS-1 GLYCOPROTEIN-B BY A RECOMBINANT VACCINIA VIRUS AND PROTECTION OF MICE AGAINST LETHAL HERPES-SIMPLEX VIRUS-1 INFECTION [J].
CANTIN, EM ;
EBERLE, R ;
BALDICK, JL ;
MOSS, B ;
WILLEY, DE ;
NOTKINS, AL ;
OPENSHAW, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (16) :5908-5912
[5]  
CANTIN EM, 1988, TECHNOLOGICAL ADV VA, P215
[6]   SYNTHESIS AND PROCESSING OF GLYCOPROTEINS GD AND GC OF HERPES-SIMPLEX VIRUS TYPE-1 [J].
COHEN, GH ;
LONG, D ;
EISENBERG, RJ .
JOURNAL OF VIROLOGY, 1980, 36 (02) :429-439
[7]   VACCINIA VIRUS RECOMBINANT EXPRESSING HERPES-SIMPLEX VIRUS TYPE-1 GLYCOPROTEIN-D PREVENTS LATENT HERPES IN MICE [J].
CREMER, KJ ;
MACKETT, M ;
WOHLENBERG, C ;
NOTKINS, AL ;
MOSS, B .
SCIENCE, 1985, 228 (4700) :737-740
[8]  
DIX RD, 1987, PROG MED VIROL, V34, P89
[9]   SYNTHETIC GLYCOPROTEIN D-RELATED PEPTIDES PROTECT MICE AGAINST HERPES-SIMPLEX VIRUS CHALLENGE [J].
EISENBERG, RJ ;
CERINI, CP ;
HEILMAN, CJ ;
JOSEPH, AD ;
DIETZSCHOLD, B ;
GOLUB, E ;
LONG, D ;
DELEON, MP ;
COHEN, GH .
JOURNAL OF VIROLOGY, 1985, 56 (03) :1014-1017
[10]   NOVEL HERPES-SIMPLEX VIRUS TYPE-1 GLYCOPROTEINS IDENTIFIED BY ANTISERUM AGAINST A SYNTHETIC OLIGOPEPTIDE FROM THE PREDICTED PRODUCT OF GENE US4 [J].
FRAME, MC ;
MARSDEN, HS ;
MCGEOCH, DJ .
JOURNAL OF GENERAL VIROLOGY, 1986, 67 :745-751