Comparative analysis of different vaccine constructs expressing defined antigens from Mycobacterium tuberculosis

被引:49
作者
Doherty, TM
Olsen, AW
Weischenfeldt, J
Huygen, K
D'Souza, S
Kondratieva, TK
Yeremeev, VV
Apt, AS
Raupach, BR
Grode, L
Kaufmann, S
Andersen, P
机构
[1] Statens Serum Inst, Dept Infect Dis Immunol, DK-2300 Copenhagen S, Denmark
[2] Pasteur Inst Brussels, Brussels, Belgium
[3] Cent Inst TB, Dept Immunol, Moscow, Russia
[4] Max Planck Inst Infect Biol, Dept Immunol, Berlin, Germany
关键词
D O I
10.1086/425931
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Studies of different vaccine constructs have demonstrated variable efficacy against Mycobacterium tuberculosis in animal models. Despite the fact that these vaccines have used one or another of a very small number of immunodominant antigens, a direct comparison of the relative efficacy of the antigens and delivery systems has been difficult, because the studies have used different parameters for assessment. Methods. We compared the efficacies of the most commonly used vaccine constructs - adjuvanted protein, plasmid DNA, and live bacterial vectors - bearing the immunodominant secreted antigens early secreted antigen target - 6 and antigen 85B, either alone or as a fusion protein. Mice were vaccinated with these constructs, and the effects of different delivery systems on protective efficacy ( as assessed by survival studies and by monitoring bacterial load) and antigen-specific responses ( including the contribution of CD4 and CD8 T cells to these responses) were assayed by various methods. Results. The relative efficacy of different vaccines is dependent on the delivery system, the antigen, and the animal model. Likewise, the relative immunodominance of individual antigens in the fusion molecule is altered by the choice of delivery system. Conclusion. These results clearly demonstrate the importance of assessing vaccine function by use of multiple parameters and indicate which parameters are most reliable for assessing vaccine efficacy.
引用
收藏
页码:2146 / 2153
页数:8
相关论文
共 35 条
[1]   Induction of a type 1 immune response to a recombinant antigen from Mycobacterium tuberculosis expressed in Mycobacterium vaccae [J].
AbouZeid, C ;
Gares, MP ;
Inwald, J ;
Janssen, R ;
Zhang, Y ;
Young, DB ;
Hetzel, C ;
Lamb, JR ;
Baldwin, SL ;
Orme, IM ;
Yeremeev, V ;
Nikonenko, BV ;
Apt, AS .
INFECTION AND IMMUNITY, 1997, 65 (05) :1856-1862
[2]   Tuberculosis subunit vaccine development:: on the role of interferon-γ [J].
Agger, EM ;
Andersen, P .
VACCINE, 2001, 19 (17-19) :2298-2302
[3]   TB vaccines: progress and problems [J].
Andersen, P .
TRENDS IN IMMUNOLOGY, 2001, 22 (03) :160-168
[4]   Failure of the Mycobacterium bovis BCG vaccine:: Some species of environmental mycobacteria block multiplication of BCG and induction of protective immunity to tuberculosis [J].
Brandt, L ;
Cunha, JF ;
Olsen, AW ;
Chilima, B ;
Hirsch, P ;
Appelberg, R ;
Andersen, P .
INFECTION AND IMMUNITY, 2002, 70 (02) :672-678
[5]   ESAT-6 subunit vaccination against Mycobacterium tuberculosis [J].
Brandt, L ;
Elhay, M ;
Rosenkrands, I ;
Lindblad, EB ;
Andersen, P .
INFECTION AND IMMUNITY, 2000, 68 (02) :791-795
[6]  
COLDITZ GA, 1995, PEDIATRICS, V96, P29
[7]   Vaccination with plasmid DNA encoding mycobacterial antigen 85A stimulates a CD4+ and CD8+ T-cell epitopic repertoire broader than that stimulated by Mycobacterium tuberculosis H37Rv infection [J].
Denis, O ;
Tanghe, A ;
Palfliet, K ;
Jurion, F ;
van den Berg, TP ;
Vanonckelen, A ;
Ooms, J ;
Saman, E ;
Ulmer, JB ;
Content, J ;
Huygen, K .
INFECTION AND IMMUNITY, 1998, 66 (04) :1527-1533
[8]   Tuberculosis vaccine development [J].
Doherty, TM ;
Andersen, P .
CURRENT OPINION IN PULMONARY MEDICINE, 2002, 8 (03) :183-187
[9]   VARIATION IN PROTECTION BY BCG - IMPLICATIONS OF AND FOR HETEROLOGOUS IMMUNITY [J].
FINE, PEM .
LANCET, 1995, 346 (8986) :1339-1345
[10]   B-cell epitopes and quantification of the ESAT-6 protein of Mycobacterium tuberculosis [J].
Harboe, M ;
Malin, AS ;
Dockrell, HS ;
Wiker, HG ;
Ulvund, G ;
Holm, A ;
Jorgensen, MC ;
Andersen, P .
INFECTION AND IMMUNITY, 1998, 66 (02) :717-723