Vaccine strategies against latent tuberculosis infection

被引:87
作者
Andersen, Peter [1 ]
机构
[1] State Serum Inst, Dept Infect Dis Immunol, DK-2300 Copenhagen, Denmark
关键词
D O I
10.1016/j.tim.2006.11.008
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The leading tuberculosis (TB) vaccines currently in clinical trials are all designed as prophylactic vaccines. Although these vaccines are highly active, they will most probably not result in sterilizing immunity and, therefore, will not solve the global problem of latent TB. An attractive strategy is to target the remaining dormant bacteria with vaccines based upon antigens induced as the bacteria change from active multiplication to nonreplicating dormancy (latency antigens) or during reactivation as dormant bacteria resume active metabolism (resuscitation antigens). These late-stage antigens might have potential as post-exposure vaccines or could form the basis for a multi-stage vaccine strategy, in which they are combined with prophylactic vaccines based on early antigens from replicating bacteria.
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页码:7 / 13
页数:7
相关论文
共 57 条
[1]   Protective immunity to tuberculosis with Ag85B-ESAT-6 in a synthetic cationic adjuvant system IC31 [J].
Agger, Else Marie ;
Rosenkrands, Ida ;
Olsen, Anja Weinreich ;
Hatch, Graham ;
Williams, Ann ;
Kritsch, Constantia ;
Lingnau, Karen ;
von Gabain, Alexander ;
Andersen, Claire Swetman ;
Korsholm, Karen Smith ;
Andersen, Peter .
VACCINE, 2006, 24 (26) :5452-5460
[2]   DOES THE PROTECTIVE EFFECT OF NEONATAL BCG CORRELATE WITH VACCINE-INDUCED TUBERCULIN REACTION [J].
ALKASSIMI, FA ;
ALHAJJAJ, MS ;
ALORAINEY, IO ;
BAMGBOYE, EA .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1995, 152 (05) :1575-1578
[3]  
[Anonymous], 2006, GLOBAL TUBERCULOSIS
[4]   Progress in tuberculosis vaccine development [J].
Baumann, Sven ;
Eddine, Ali Nasser ;
Kaufmann, Stefan H. E. .
CURRENT OPINION IN IMMUNOLOGY, 2006, 18 (04) :438-448
[5]   Evaluation of a nutrient starvation model of Mycobacterium tuberculosis persistence by gene and protein expression profiling [J].
Betts, JC ;
Lukey, PT ;
Robb, LC ;
McAdam, RA ;
Duncan, K .
MOLECULAR MICROBIOLOGY, 2002, 43 (03) :717-731
[6]   HUMAN T-CELL RESPONSES TO SECRETED ANTIGEN FRACTIONS OF MYCOBACTERIUM-TUBERCULOSIS [J].
BOESEN, H ;
JENSEN, BN ;
WILCKE, T ;
ANDERSEN, P .
INFECTION AND IMMUNITY, 1995, 63 (04) :1491-1497
[7]   The structure of a resuscitation-promoting factor domain from Mycobacterium tuberculosis shows homology to lysozymes [J].
Cohen-Gonsaud, M ;
Barthe, P ;
Bagnéris, C ;
Henderson, B ;
Ward, J ;
Roumestand, C ;
Keep, NH .
NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2005, 12 (03) :270-273
[8]  
COLDITZ GA, 1995, PEDIATRICS, V96, P29
[9]   Creating space: an antigen-independent, CpG-induced peripheral expansion of naive and memory T lymphocytes in a full T-cell compartment [J].
Davila, E ;
Velez, MG ;
Heppelmann, CJ ;
Celis, E .
BLOOD, 2002, 100 (07) :2537-2545
[10]   DNA vaccine combinations expressing either tissue plasminogen activator signal sequence fusion proteins or ubiquitin-conjugated antigens induce sustained protective immunity in a mouse model of pulmonary tuberculosis [J].
Delogu, G ;
Li, A ;
Repique, C ;
Collins, F ;
Morris, SL .
INFECTION AND IMMUNITY, 2002, 70 (01) :292-302