Induction of protective immune responses against Venezuelan equine encephalitis (VEE) virus aerosol challenge with microencapsulated VEE virus vaccine

被引:33
作者
Greenway, TE
Eldridge, JH
Ludwig, G
Staas, JK
Smith, JF
Gilley, RM
Michalek, SM [1 ]
机构
[1] Univ Alabama Birmingham, Dept Microbiol, Birmingham, AL 35294 USA
[2] USA, Med Res Inst Infect Dis, Frederick, MD 21702 USA
[3] So Res Inst, Pharmaceut Formulat Dept, Birmingham, AL 35255 USA
关键词
oral immunization; intratracheal immunization; IgA antibodies; microspheres;
D O I
10.1016/S0264-410X(98)00008-5
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Venezuelan equine encephalomyelitis (VEE) virus, a member of the family Togaviridae, genus Alphavirus, causes disease in humans and equids. The virus is normally transmitted by the bite of an infected mosquito however; it can also be highly infectious by aerosol. The purpose of the present study was to determine the effectiveness of formalin-fixed, Co-60-irradiated VEE virus microencapsulated in poly DL-lactide-co-glycolide in inducing immune responses protective against aerosol challenge with virulent VEE virus. Balb/c mice were primed by subcutaneous injection of micro-encapsulated VEE virus vaccine followed 30 days later by a single immunization with the same vaccine given via the oral, intratracheal (i.t.) or subcutaneous (s.c.) route. Mice boosted by the i.t. or s.c. route had higher plasma IgG anti-VEE virus levels than orally immunized animals. The responses in the former groups were similar in magnitude to those seen in mice primed and boosted by the i.t. route. Antibody activity was detected in bronchial-alveolar and intestinal washes, fecal extracts and saliva fr om immunized animals. The levels of IgG and IgA antibody activity in bronchial-alveolar wash fluids from mice boosted by the i.t. route were higher than those seen in animals immunized by the oral or s.c. route with the microsphere vaccine. Mice immunized with the microencapsulated VEE virus vaccine were protected from lethal VEE virus infection following aerosol challenge at approximately three months after the initial immunization Mucosal immunization via the i.t. route appeared to be the most effective regimen, since 100% of the mice resisted aerosol challenge. (C) 1998 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1314 / 1323
页数:10
相关论文
共 47 条
[31]   BIODEGRADABLE MICROSPHERES FOR THE DELIVERY OF ORAL VACCINES [J].
MESTECKY, J ;
MOLDOVEANU, Z ;
NOVAK, M ;
HUANG, WQ ;
GILLEY, RM ;
STAAS, JK ;
SCHAFER, D ;
COMPANS, RW .
JOURNAL OF CONTROLLED RELEASE, 1994, 28 (1-3) :131-141
[32]   THE COMMON MUCOSAL IMMUNE-SYSTEM AND CURRENT STRATEGIES FOR INDUCTION OF IMMUNE-RESPONSES IN EXTERNAL SECRETIONS [J].
MESTECKY, J .
JOURNAL OF CLINICAL IMMUNOLOGY, 1987, 7 (04) :265-276
[33]   IMMUNOGLOBULIN-A (IGA) - MOLECULAR AND CELLULAR INTERACTIONS INVOLVED IN IGA BIOSYNTHESIS AND IMMUNE-RESPONSE [J].
MESTECKY, J ;
MCGHEE, JR .
ADVANCES IN IMMUNOLOGY, 1987, 40 :153-245
[34]  
Michalek S. M., 1994, HDB MUCOSAL IMMUNOLO, P373
[35]   ORAL IMMUNIZATION WITH INFLUENZA-VIRUS IN BIODEGRADABLE MICROSPHERES [J].
MOLDOVEANU, Z ;
NOVAK, M ;
HUANG, WQ ;
GILLEY, RM ;
STAAS, JK ;
SCHAFER, D ;
COMPANS, RW ;
MESTECKY, J .
JOURNAL OF INFECTIOUS DISEASES, 1993, 167 (01) :84-90
[36]   HUMAN IMMUNE-RESPONSES TO INFLUENZA-VIRUS VACCINES ADMINISTERED BY SYSTEMIC OR MUCOSAL ROUTES [J].
MOLDOVEANU, Z ;
CLEMENTS, ML ;
PRINCE, SJ ;
MURPHY, BR ;
MESTECKY, J .
VACCINE, 1995, 13 (11) :1006-1012
[37]  
NEDRUD JG, 1987, J IMMUNOL, V139, P3484
[38]  
OHAGAN DT, 1997, NEW GENERATION VACCI, P215
[39]  
PIERCE NF, 1981, J IMMUNOL, V127, P2461
[40]   SERUM ANTIBODY PREVENTS LETHAL MURINE INFLUENZA PNEUMONITIS BUT NOT TRACHEITIS [J].
RAMPHAL, R ;
COGLIANO, RC ;
SHANDS, JW ;
SMALL, PA .
INFECTION AND IMMUNITY, 1979, 25 (03) :992-997