Vaccination strategies for Francisella tularensis

被引:31
作者
Isherwood, KE
Titball, RW
Davies, DH
Felgner, PL
Morrow, WJW
机构
[1] Univ Washington, Washington Natl Primate Res Ctr, Seattle, WA 98121 USA
[2] Univ Washington, Dept Pathobiol, Seattle, WA 98121 USA
[3] Def Sci & Technol Lab, Salisbury, Wilts, England
[4] Univ Calif Irvine, Ctr Virus Res, Irvine, CA USA
关键词
tularemia; Francisella tularensis; live vaccine; LVS; TUL4;
D O I
10.1016/j.addr.2005.01.030
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Francisella tularensis is the etiologic agent of tularemia, a severe debilitating disease of humans and animals. The low infectious dose of F tularensis in humans and the relative ease of culture are probably the properties which originally attracted interest in this bacterium as a bioweapon. Even today, F tularensis is ranked as one of the pathogens most likely to be used as a biological warfare or bioterrorism agent. A live attenuated vaccine (LVS) has been available for over 50 years, but there are shortcomings associated with its use. This vaccine is not fully licensed and does not offer a high level of protection against respiratory challenge. Nevertheless, this vaccine does demonstrate the feasibility of vaccination against tularemia. Protection against tularemia is likely to be dependent on the induction of cellular and humoral immune responses. These types of responses are induced by the LVS vaccine and could also be induced by a rationally attenuated mutant of F tularensis. Evoking this range of responses with a sub-unit vaccine may be more difficult to achieve, and will be dependent on the use of suitable vaccine delivery systems.
引用
收藏
页码:1403 / 1414
页数:12
相关论文
共 79 条
[1]   GROWTH OF FRANCISELLA-SPP IN RODENT MACROPHAGES [J].
ANTHONY, LSD ;
BURKE, RD ;
NANO, FE .
INFECTION AND IMMUNITY, 1991, 59 (09) :3291-3296
[2]   Field investigations of tularemia in Norway [J].
Berdal, BP ;
Mehl, R ;
Meidell, NK ;
LorentzenStyr, AM ;
Scheel, O .
FEMS IMMUNOLOGY AND MEDICAL MICROBIOLOGY, 1996, 13 (03) :191-195
[3]   AGGLUTININS AND ANTIBODIES TO FRANCISELLA-TULARENSIS OUTER-MEMBRANE ANTIGENS IN THE EARLY DIAGNOSIS OF DISEASE DURING AN OUTBREAK OF TULAREMIA [J].
BEVANGER, L ;
MAELAND, JA ;
NAESS, AI .
JOURNAL OF CLINICAL MICROBIOLOGY, 1988, 26 (03) :433-437
[4]   Observations on the infection of chick embryos with Bacterium tularense, Brucella, and Pasteurella pestis [J].
Buddingh, GJ ;
Womack, FC .
JOURNAL OF EXPERIMENTAL MEDICINE, 1941, 74 (03) :213-U6
[5]  
Chakravarti D N, 2000, Dev Biol (Basel), V103, P81
[6]   Biological warfare - A historical perspective [J].
Christopher, GW ;
Cieslak, TJ ;
Pavlin, JA ;
Eitzen, EM .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1997, 278 (05) :412-417
[7]   Virulent and avirulent strains of Francisella tularensis prevent acidification and maturation of their phagosomes and escape into the cytoplasm in human macrophages [J].
Clemens, DL ;
Lee, BY ;
Horwitz, MA .
INFECTION AND IMMUNITY, 2004, 72 (06) :3204-3217
[9]   Mice vaccinated with the O-antigen of Francisella tularensis LVS lipopolysaccharide conjugated to bovine serum albumin develop varying degrees of protective immunity against systemic or aerosol challenge with virulent type A and type B strains of the pathogen [J].
Conlan, JW ;
Shen, H ;
Webb, A ;
Perry, MB .
VACCINE, 2002, 20 (29-30) :3465-3471
[10]   CD4(+) AND CD8(+) T-CELL-DEPENDENT AND T-CELL-INDEPENDENT HOST-DEFENSE MECHANISMS CAN OPERATE TO CONTROL AND RESOLVE PRIMARY AND SECONDARY FRANCISELLA-TULARENSIS LVS INFECTION IN MICE [J].
CONLAN, JW ;
SJOSTEDT, A ;
NORTH, RJ .
INFECTION AND IMMUNITY, 1994, 62 (12) :5603-5607