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
[21]   In vivo clearance of an intracellular bacterium, Francisella tularensis LVS, is dependent on the p40 subunit of interleukin-12 (IL-12) but not on IL-12 p70 [J].
Elkins, KL ;
Cooper, A ;
Colombini, SM ;
Cowley, SC ;
Kieffer, TL .
INFECTION AND IMMUNITY, 2002, 70 (04) :1936-1948
[22]   Minimal requirements for murine resistance to infection with Francisella tularesis LVS [J].
Elkins, KL ;
RhinehartJones, TR ;
Culkin, SJ ;
Yee, D ;
Winegar, RK .
INFECTION AND IMMUNITY, 1996, 64 (08) :3288-3293
[23]   Tularemia [J].
Ellis, J ;
Oyston, PCF ;
Green, M ;
Titball, RW .
CLINICAL MICROBIOLOGY REVIEWS, 2002, 15 (04) :631-+
[24]   Long-lasting recall response of CD4+ and CD8+ αβ T cells, but not γδ T cells, to heat shock proteins of Francisella tularensis [J].
Ericsson, M ;
Kroca, M ;
Johansson, T ;
Sjöstedt, A ;
Tärnvik, A .
SCANDINAVIAN JOURNAL OF INFECTIOUS DISEASES, 2001, 33 (02) :145-152
[25]   FRANCISELLA-TULARENSIS [J].
EVANS, ME .
INFECTION CONTROL AND HOSPITAL EPIDEMIOLOGY, 1985, 6 (09) :381-383
[26]  
Fortier A H, 1994, Immunol Ser, V60, P349
[27]   GROWTH OF FRANCISELLA-TULARENSIS LVS IN MACROPHAGES - THE ACIDIC INTRACELLULAR COMPARTMENT PROVIDES ESSENTIAL IRON REQUIRED FOR GROWTH [J].
FORTIER, AH ;
LEIBY, DA ;
NARAYANAN, RB ;
ASAFOADJEI, E ;
CRAWFORD, RM ;
NACY, CA ;
MELTZER, MS .
INFECTION AND IMMUNITY, 1995, 63 (04) :1478-1483
[29]   ANTITULAREMIC SERUM [J].
Francis, Edward ;
Felton, Lloyd D. .
PUBLIC HEALTH REPORTS, 1942, 57 (02) :44-55
[30]   ROLE OF LIPOPOLYSACCHARIDE AND A MAJOR OUTER-MEMBRANE PROTEIN FROM FRANCISELLA-TULARENSIS IN THE INDUCTION OF IMMUNITY AGAINST TULAREMIA [J].
FULOP, M ;
MANCHEE, R ;
TITBALL, R .
VACCINE, 1995, 13 (13) :1220-1225