PROTECTION OF MICE FROM BORDETELLA-PERTUSSIS RESPIRATORY-INFECTION USING MICROENCAPSULATED PERTUSSIS FIMBRIAE

被引:32
作者
JONES, DH [1 ]
MCBRIDE, BW [1 ]
JEFFERY, H [1 ]
OHAGAN, DT [1 ]
ROBINSON, A [1 ]
FARRAR, GH [1 ]
机构
[1] UNIV NOTTINGHAM, DEPT PHARMACEUT SCI, NOTTINGHAM NG7 2RD, ENGLAND
关键词
MICROENCAPSULATION; ACELLULAR PERTUSSIS VACCINE; PROTECTION;
D O I
10.1016/0264-410X(95)99876-J
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Conditions have been established which allow the efficient entrapment of Bordetella pertussis fimbriae in poly(lactide-co-glycolide) microspheres. Fimbriae released from the matrix were found to have retained some degree of conformational structure, as determined by assessing the capacity of fimbrial protein to bind to antibodies mapping to either conformational or denatured structures on the fimbriae. Following a single intraperitoneal injection, equivalent amounts of fimbriae, either encapsulated in microspheres with a mean diameter of 24 mu m and an estimated in vitro protein release rate of approximately 42 days, or conventionally adjuvanted with alhydrogel, elicited vigorous immune responses in mice. The encapsulated fimbriae appear to elicit marginally lower serum antibody levels than those induced by equivalent amounts of alhydrogel adjuvanted fimbriae. Mice immunised with both preparations were, however, protected against intranasal infection with live B. pertussis as evidenced by the significant reduction in levels of bacterial colonisation observed in the lungs and tracheas of immunised animals when compared to the immunologically naive controls.
引用
收藏
页码:675 / 681
页数:7
相关论文
共 29 条
[11]   EFFECT OF HEPTAKIS(2,6-O-DIMETHYL) BETA-CYCLODEXTRIN ON THE PRODUCTION OF PERTUSSIS TOXIN BY BORDETELLA-PERTUSSIS [J].
IMAIZUMI, A ;
SUZUKI, Y ;
ONO, S ;
SATO, H ;
SATO, Y .
INFECTION AND IMMUNITY, 1983, 41 (03) :1138-1143
[12]   THE PREPARATION AND CHARACTERIZATION OF POLY(LACTIDE-CO-GLYCOLIDE) MICROPARTICLES .2. THE ENTRAPMENT OF A MODEL PROTEIN USING A (WATER-IN-OIL)-IN-WATER EMULSION SOLVENT EVAPORATION TECHNIQUE [J].
JEFFERY, H ;
DAVIS, SS ;
OHAGAN, DT .
PHARMACEUTICAL RESEARCH, 1993, 10 (03) :362-368
[13]  
MALOY KJ, 1994, IMMUNOLOGY, V81, P661
[14]   PROTECTION AGAINST VAGINAL SIV TRANSMISSION WITH MICROENCAPSULATED VACCINE [J].
MARX, PA ;
COMPANS, RW ;
GETTIE, A ;
STAAS, JK ;
GILLEY, RM ;
MULLIGAN, MJ ;
YAMSHCHIKOV, GV ;
CHEN, DX ;
ELDRIDGE, JH .
SCIENCE, 1993, 260 (5112) :1323-1327
[15]   TARGETING AND CONTROLLED RELEASE OF ANTIGENS FOR THE EFFECTIVE INDUCTION OF SECRETORY ANTIBODY-RESPONSES [J].
MESTECKY, J ;
ELDRIDGE, JH .
CURRENT OPINION IN IMMUNOLOGY, 1991, 3 (04) :492-495
[16]  
MILLER CJ, 1992, CLIN EXP IMMUNOL, V88, P520, DOI 10.1111/j.1365-2249.1992.tb06481.x
[17]   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
[18]   POTENTIAL OF POLYMER MICROENCAPSULATION TECHNOLOGY FOR VACCINE INNOVATION [J].
MORRIS, W ;
STEINHOFF, MC ;
RUSSELL, PK .
VACCINE, 1994, 12 (01) :5-11
[19]   LONG-TERM ANTIBODY-RESPONSES IN MICE FOLLOWING SUBCUTANEOUS IMMUNIZATION WITH OVALBUMIN ENTRAPPED IN BIODEGRADABLE MICROPARTICLES [J].
OHAGAN, DT ;
JEFFERY, H ;
DAVIS, SS .
VACCINE, 1993, 11 (09) :965-969
[20]   BIODEGRADABLE MICROPARTICLES FOR ORAL IMMUNIZATION [J].
OHAGAN, DT ;
MCGEE, JP ;
HOLMGREN, J ;
MOWAT, AMCL ;
DONACHIE, AM ;
MILLS, KHG ;
GAISFORD, W ;
RAHMAN, D ;
CHALLACOMBE, SJ .
VACCINE, 1993, 11 (02) :149-154