Immunogenicity and protective efficacy of recombinant Leptospira immunoglobulin-like protein B (rLigB) in a hamster challenge model

被引:71
作者
Yan, Weiwei
Faisal, Syed M.
McDonough, Sean P.
Divers, Thomas J.
Barr, Stephen C.
Chang, Chao-Fu [2 ]
Pan, Ming-Jeng [3 ]
Chang, Yung-Fu [1 ]
机构
[1] Cornell Univ, Dept Populat Med & Diagnost Sci, Coll Vet Med, Anim Hlth Diagnost Ctr, Ithaca, NY 14853 USA
[2] Cent Taiwan Univ Sci & Technol, Inst Med Biotechnol, Taichung, Taiwan
[3] Cent Taiwan Univ Sci & Technol, Inst Life Sci, Taichung, Taiwan
关键词
Leptospiral immunologlobublin-like protein (LigA; LigB); Subunit vaccine; Leptospira interrogans; Hamster; OUTER-MEMBRANE PROTEINS; IMMUNE-RESPONSE; INTERROGANS; LIGA; VACCINE; LIPL32; FIBRONECTIN; INDUCTION; BINDING; DOMAIN;
D O I
10.1016/j.micinf.2008.11.008
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Leptospiral immunoglobulin-like protein (LigB) was truncated into conserved (LigBcon) and variable (varB1, varB2) fragments and expressed as GST/His-tag fusion proteins. Four-week-old hamsters were immunized with equal amounts of each fragment individually or combined in alum adjuvant at days 0 and 21 and subsequently challenged three weeks after the booster with 2.5 LD50 live virulent Leptospira interrogans serovar Pomona. Our results demonstrate that immunization with LigB produced strong humoral immune responses as revealed by high titers against each fragment and significant enhancement in Th2 cytokines (IL-4, IL-10). A significant activation of CMI is revealed by enhanced proliferation of lymphocytes and up regulation of Th1 cytokines (IL-12p40, IFN-gamma) was also noted. Of the peptides studied, rLigBcon was able to impart maximum protection (71%), followed by rVarB1 (54%), whereas rVarB2 was not able to impart a significant level of protection (33%) against lethal infection as revealed by enhanced survival and reduced severity of histopathological lesions in vital organs (viz. kidney, liver, spleen) of the immunized animals. Moreover, concurrent administration of all three fragments significantly enhanced the protective efficacy of the vaccine (83%). Overall, our results clearly demonstrate that LigB has emerged as novel protective antigen that can be used in future subunit vaccines against leptospirosis. (C) 2008 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:230 / 237
页数:8
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