Intradermal immunization improves protective efficacy of a novel TB vaccine candidate

被引:73
作者
Baldwin, Susan L. [1 ]
Bertholet, Sylvie [1 ]
Kahn, Maria [1 ]
Zharkikh, Irina [1 ]
Ireton, Gregory C. [1 ]
Vedvick, Thomas S. [1 ]
Reed, Steven G. [1 ]
Coler, Rhea N. [1 ]
机构
[1] Infect Dis Res Inst, Seattle, WA 98104 USA
关键词
Mycobacterium tuberculosis; Subunit vaccine; TLR agonists; MYCOBACTERIUM-TUBERCULOSIS INFECTION; TOLL-LIKE RECEPTORS; DENDRITIC CELLS; INTERFERON-GAMMA; IMMUNE-RESPONSES; LEISHMANIA-MAJOR; LANGERHANS CELLS; GUINEA-PIG; MICE; ALPHA;
D O I
10.1016/j.vaccine.2009.03.018
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We have developed the Mycobacterium tuberculosis (Mtb) fusion protein (11383), which contains the three Mtb proteins Rv1813, Rv3620 and Rv2608. We evaluated the immunogenicity and protective efficacy of ID83 in combination with several emulsion-formulated toll-like receptor agonists. The ID83 subunit vaccines containing synthetic TLR4 or TLR9 agonists generated a T helper-1 immune response and protected mice against challenge with Mtb regardless of route. The ID83 vaccine formulated with gardiquimod (a TLR7 agonist) also resulted in a protective response when administered intradermally, whereas the same vaccine given subcutaneously failed to provide protection. This highlights the need to explore different routes of immunization based on the adjuvant formulations used. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3063 / 3071
页数:9
相关论文
共 45 条
[31]   Who puts the tubercle in tuberculosis? [J].
Russell, David G. .
NATURE REVIEWS MICROBIOLOGY, 2007, 5 (01) :39-47
[32]   Translational mini-review series on vaccines: Development and evaluation of improved vaccines against tuberculosis [J].
Sander, C. ;
McShane, H. .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2007, 147 (03) :401-411
[33]   T-cell quality in memory and protection: implications for vaccine design [J].
Seder, Robert A. ;
Darrah, Patricia A. ;
Roederer, Mario .
NATURE REVIEWS IMMUNOLOGY, 2008, 8 (04) :247-258
[34]   Differential immune responses and protective efficacy induced by components of a tuberculosis polyprotein vaccine, Mtb72F, delivered as naked DNA or recombinant protein [J].
Skeiky, YAW ;
Alderson, MR ;
Ovendale, PJ ;
Guderian, JA ;
Brandt, L ;
Dillon, DC ;
Campos-Neto, A ;
Lobet, Y ;
Dalemans, W ;
Orme, IM ;
Reed, SG .
JOURNAL OF IMMUNOLOGY, 2004, 172 (12) :7618-7628
[35]   Characterisation of epidermal lipid composition and skin morphology of animal skin ex vivo [J].
Stahl, J. ;
Niedorf, F. ;
Kietzmann, M. .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2009, 72 (02) :310-316
[36]   TLR ligands can activate dendritic cells to provide a MyD88-dependent negative signal for Th2 cell development [J].
Sun, J ;
Walsh, M ;
Villarino, AV ;
Cervi, L ;
Hunter, CA ;
Choi, YW ;
Pearce, EJ .
JOURNAL OF IMMUNOLOGY, 2005, 174 (02) :742-751
[37]   Imiquimod, a topical immune response modifier, induces migration of Langerhans cells [J].
Suzuki, H ;
Wang, BH ;
Shivji, GM ;
Toto, P ;
Amerio, P ;
Tomai, MA ;
Miller, RL ;
Sauder, DN .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2000, 114 (01) :135-141
[38]  
Teloni R, 2004, INDIAN J MED RES, V119, P126
[39]   Immunopathogenesis of pulmonary granulomas in the guinea pig after infection with Mycobacterium tuberculosis [J].
Turner, OC ;
Basaraba, RJ ;
Orme, IM .
INFECTION AND IMMUNITY, 2003, 71 (02) :864-871
[40]   Cutaneous dendritic cells [J].
Valladeau, J ;
Saeland, S .
SEMINARS IN IMMUNOLOGY, 2005, 17 (04) :273-283