Encapsulation of chimeric protein rSAG1/2 into poly(lactide-co-glycolide) microparticles induces long-term protective immunity against Toxoplasma gondii in mice

被引:27
作者
Chuang, Shu-Chun [1 ]
Ko, Jing-Chun [2 ]
Chen, Chaio-Ping [2 ]
Du, Jia-Tze [2 ]
Yang, Chung-Da [2 ]
机构
[1] Kaohsiung Med Univ, Coll Med, Dept Physiol, Kaohsiung 807, Taiwan
[2] Natl Pingtung Univ Sci & Technol, Grad Inst Anim Vaccine Technol, Neipu 912, Pingtung, Taiwan
关键词
Toxoplasma gondii (T. gondii); rSAG1/2; Poly(lactide-co-glycolide) (PLG); PLG-rSAG1/2; microparticles; Long-term immunity; BIODEGRADABLE MICROSPHERES; BALB/C MICE; VACCINE; SURFACE; IMMUNIZATION; INDUCTION; RESPONSES; GAMMA;
D O I
10.1016/j.exppara.2013.04.002
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
090105 [作物生产系统与生态工程]; 100103 [病原生物学];
摘要
In the present study, the poly(lactide-co-glycolide) (PLG) polymer was used as an adjuvant to encapsulate the chimeric protein rSAG1/2 for preparing a microparticle vaccine against Toxoplasma gondii. The resulting PLG-encapsulated rSAG1/2 (PLG-rSAG1/2) microparticles, 1.27-1.65 mu m in diameter, showed 72-83% entrapment efficiency. The amount of released rSAG1/2 protein from microparticles gradually increased over a long 56-day period and the protein still retained its antigenicity. Intraperitoneal immunization with the microparticles in BALB/c mice elicited significant long-term (10 weeks) humoral and cell-mediated immune responses, accompanied by secretion of a large amount of IFN-gamma, to achieve strong protection (83%) against a lethal. subcutaneous tachyzoite challenge. In conclusion, we have successfully encapsulated rSAG1/2 with the PLG polymer to produce stable microparticles that can effectively induce not only long-term immunity but also high protection against T. gondii. These crucial data would be advantageous for developing long-term Toxoplasma vaccines for future use in humans and animals. (c) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:430 / 437
页数:8
相关论文
共 25 条
[1]
Development of a vaccine for toxoplasmosis: current status [J].
Bhopale, GM .
MICROBES AND INFECTION, 2003, 5 (05) :457-462
[2]
Intranasal immunization of BALB/c mice with enterotoxigenic Escherichia coli colonization factor CS6 encapsulated in biodegradable poly(DL-lactide-co-glycolide) microspheres [J].
Byrd, W ;
Cassels, FJ .
VACCINE, 2006, 24 (09) :1359-1366
[3]
Induction of long-lasting protective immunity against Toxoplasma gondii in BALB/c mice by recombinant surface antigen 1 protein encapsulated in poly (lactide-co-glycolide) microparticles [J].
Chuang, Shu-Chun ;
Ko, Jing-Chun ;
Chen, Chaio-Ping ;
Du, Jia-Tze ;
Yang, Chung-Da .
PARASITES & VECTORS, 2013, 6
[4]
SURFACE-ANTIGENS OF TOXOPLASMA-GONDII [J].
COUVREUR, G ;
SADAK, A ;
FORTIER, B ;
DUBREMETZ, JF .
PARASITOLOGY, 1988, 97 :1-10
[5]
Toxoplasma gondii: The role of parasite surface and secreted proteins in host cell invasion [J].
Grimwood, J ;
Smith, JE .
INTERNATIONAL JOURNAL FOR PARASITOLOGY, 1996, 26 (02) :169-173
[6]
Toxoplasma gondii:: transmission, diagnosis and prevention [J].
Hill, D ;
Dubey, JP .
CLINICAL MICROBIOLOGY AND INFECTION, 2002, 8 (10) :634-640
[7]
Veterinary vaccines against Toxoplasma gondii [J].
Innes, Elisabeth A. ;
Bartley, Paul M. ;
Maley, Stephen ;
Katzer, Frank ;
Buxton, David .
MEMORIAS DO INSTITUTO OSWALDO CRUZ, 2009, 104 (02) :246-251
[8]
Jain S, 2011, EXPERT REV VACCINES, V10, P1731, DOI [10.1586/erv.11.126, 10.1586/ERV.11.126]
[9]
THE PREPARATION AND CHARACTERIZATION OF POLY(LACTIDE-CO-GLYCOLIDE) MICROPARTICLES .2. THE ENTRAPMENT OF A MODEL PROTEIN USING A (WATER-IN-OIL)-IN-WATER EMULSION SOLVENT EVAPORATION TECHNIQUE [J].
JEFFERY, H ;
DAVIS, SS ;
OHAGAN, DT .
PHARMACEUTICAL RESEARCH, 1993, 10 (03) :362-368
[10]
Functional characterization of in vivo effector CD4+ and CD8+ T cell responses in acute Toxoplasmosis: An interplay of IFN-γ and cytolytic T cells [J].
Jongert, Erik ;
Lemiere, Arnaud ;
Van Ginderachter, Jo ;
De Craeye, Stephane ;
Huygen, Kris ;
D'Souza, Sushila .
VACCINE, 2010, 28 (13) :2556-2564