Enhancing immune responses to a DNA vaccine encoding Toxoplasma gondii GRA14 by calcium phosphate nanoparticles as an adjuvant

被引:40
作者
Ahmadpour, Ehsan [1 ]
Sarvi, Shahabeddin [2 ]
Soteh, Mohammad Bagher Hashemi [3 ]
Sharif, Mehdi [2 ]
Rahimi, Mohammad Taghi [4 ]
Valadan, Reza [3 ]
Tehrani, Mohsen [3 ]
Khalilian, Alireza [5 ]
Montazeri, Mahbobeh [2 ]
Fasihi-Ramandi, Mandi [6 ]
Daryani, Ahmad [2 ]
机构
[1] Tabriz Univ Med Sci, Immunol Res Ctr, Tabriz, Iran
[2] Mazandaran Univ Med Sci, Toxoplasmosis Res Ctr, Sari, Iran
[3] Mazandaran Univ Med Sci, Mol & Cell Biol Res Ctr, Sari, Iran
[4] Shahroud Univ Med Sci, Sch Med, Shahroud, Iran
[5] Mazandaran Univ Med Sci, Biostat Dept, Sari, Iran
[6] Baqiyatallah Univ Med Sci, Mol Biol Res Ctr, Tehran, Iran
关键词
Toxoplasma gondii; DNA vaccine; Calcium phosphate nanoparticles; Nano-adjuvant; GRA14; gene; Dense granule; Immune response; EXCRETORY-SECRETORY ANTIGENS; PROTECTIVE IMMUNITY; MICE; IMMUNIZATION; INFECTION; MICROPARTICLES; METAANALYSIS; INDUCTION; DELIVERY; PROTEIN;
D O I
10.1016/j.imlet.2017.03.006
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Several approaches have been used to improve the immunogenicity of DNA vaccines. In the current study, we constructed the plasmid encoding T. gondii dense granule 14 (GRA14) and investigated the immunological properties of calcium phosphate nanoparticles (CaPNs) as nano-adjuvant to enhance the protective efficacy of pcGRA14. BALB/c mice intramuscularly injected three times at two-week intervals and the immune responses were evaluated using lymphocyte proliferation assay, cytokine and antibody measurements, survival times, and parasite load of mice challenged with the virulent T. gondii RH strain. The results showed that the immune responses were induced in mice receiving pcGRA14 DNA vaccine. Interestingly, pcGRA14 coated with nanoparticles led to statistically significant enhancements of cellular and humoral immune responses against Toxoplasma infection (P < 0.05). After challenge with RH strain of T. gondii, immunized mice with pcGRA14 showed prolong survival time compared to control groups (P < 0.05). In addition, pcGRA14 coated with nano-adjuvant exhibited the lowest parasitic load in the infected mice tissues. For the first time, our data indicate that the pcGRA14 coated with CaPN was more effective for stimulation of immune responses and should be considered as an adjuvant in the design of vaccines against toxoplasmosis. (C) 2017 European Federation of Immunological Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:40 / 47
页数:8
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