Protective Effect Against Toxoplasmosis in BALB/c Mice Vaccinated With Recombinant Toxoplasma gondii MIF, CDPK3, and 14-3-3 Protein Cocktail Vaccine.
Protective Effect Against Toxoplasmosis in BALB/c Mice Vaccinated With Recombinant Toxoplasma gondii MIF, CDPK3, and 14-3-3 Protein Cocktail Vaccine.
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接种重组弓形虫 MIF、CDPK3 和 14-3-3 蛋白混合物疫苗的 BALB/c 小鼠对弓形虫病的保护作用
DOI:
10.3389/fimmu.2021.755792
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发表时间:
2021
影响因子:
7.3
通讯作者:
Du J
中科院分区:
文献类型:
--
作者:
Liu F;Wu M;Wang J;Wen H;An R;Cai H;Yu L;Shen J;Chen L;Du J
Toxoplasma gondii can infect almost all endotherm organisms including humans and cause life-threatening toxoplasmosis in immunocompromised individuals, which leads to serious public health problems. Developing an excellent vaccine against this disease is impending. In present study, we formulated a cocktail protein vaccine including the TgMIF, TgCDPK3, and Tg14-3-3 proteins, which play critical roles in T. gondii infection. The recombinant protein vaccines were constructed and assessed by vaccination in BALB/c mice. We organized the mice in various protein combination groups of vaccines, and all mice were immunized with corresponding proteins at 0, 2, and 4 weeks. The specific protective effects of the vaccines on mice against T. gondii were analyzed by the mensuration of cytokines, serum antibodies, splenocyte proliferation assay, survival time, and parasite cyst burden of mice after the challenge. The study indicated that mice immunized with all three multicomponent proteins vaccine triggered a strong immune response with highest levels of IFN-γ production and IgG antibody compared with the other two protein combinations and controls. Moreover, there was an increase in IL-4 production and antigen-specific lymphocyte proliferation. The parasite cysts were significantly reduced (resulting in an 82.7% reduction), and survival time was longer in immunized mice with three multicomponent proteins compared with the other groups of mice. The enhanced humoral and cell-mediated immunity indicated that the protein cocktail vaccine containing three antigens provided effective protection for mice. These results indicated that recombinant TgMIF, TgCDPK3, and Tg14-3-3 multicomponent proteins were potential candidates for vaccine against toxoplasmosis.
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影响因子:
5.7
作者:
Czarnewski P;Araújo ECB;Oliveira MC;Mineo TWP;Silva NM
通讯作者:
Silva NM
影响因子:
2.4
作者:
BUXTON, D;INNES, EA
通讯作者:
INNES, EA
DOI:
10.1016/j.bbrc.2009.01.030
发表时间:
2009-03-13
影响因子:
3.1
作者:
Richardson, Julia M.;Morrison, Lesley S.;Bland, Nicholas D.;Bruce, Sandra;Coombs, Graham H.;Mottram, Jeremy C.;Walkinshaw, Malcolm D.
通讯作者:
Walkinshaw, Malcolm D.
影响因子:
2.1
作者:
Dziadek, Bozena;Gatkowska, Justyna;Dlugonska, Henryka
通讯作者:
Dlugonska, Henryka
影响因子:
3.2
作者:
Chuang SC;Ko JC;Chen CP;Du JT;Yang CD
通讯作者:
Yang CD