含可溶性抗原脂质体(SA)对BALB/c小鼠弓形虫感染存活率的评价

IF 1.4 Q4 NANOSCIENCE & NANOTECHNOLOGY Nanomedicine Journal Pub Date : 2021-07-01 DOI:10.22038/NMJ.2021.56226.1573
M. Kavand, A. Mehravaran, Elham Pahlavani, H. Mirahmadi, J. Akhtari, M. Rahmati-Balaghaleh, S. Etemadi, L. Mohammadi
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引用次数: 0

摘要

目的弓形虫是一种专性细胞内原生动物寄生虫,广泛分布于世界各地。它会导致人类和家畜的先天性疾病和流产。因此,寄生虫学的主要关注点之一是开发有效的疫苗来控制弓形虫病。材料与方法本研究设计了一种含有可溶性抗原(SA)的纳米脂质体疫苗,用于评估BALB/c小鼠对弓形虫感染的免疫力和保护作用。从速殖子中获得可溶性抗原(SA),将其包裹在脂质体中,并通过扫描电子显微镜进行研究。用不同的制剂对BALB/c小鼠进行三次皮下免疫,间隔2周。通过用弓形虫RH株的速殖子攻击后BALB/c小鼠的存活百分比调查来评估对感染的保护水平;此外,通过评估细胞因子(IFN-γ、IL-4)的产生和IgG同种型的滴定来确定产生的免疫反应的类型。结果脂质体DSPC+SA和脂质体DSPC+咪喹莫特+SA免疫组弓形虫IgG抗体较PBS组显著增加(p<0.05),其中脂质体DSPC/咪喹莫特-SA免疫组IgG2a和IFN-γ分泌量最高,分别高于对照组(p<0.01)和对照组(p<0.0001)。用速殖子攻击后,脂质体DSPC+咪喹莫特+SA免疫小鼠的死亡率较低,与其他组相比有显著差异(p<0.01)。结论脂质体DSPC+咪喹莫特+SA对弓形虫具有较高的存活率和细胞免疫反应。
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Evaluation of survival rate using liposome containing soluble antigens (SA) against Toxoplasma gondii infection in BALB/c mice
Objective(s)Toxoplasma gondii, an obligate intracellular protozoan parasite, is widespread across the world. It causes congenital disease and abortion in humans and domestic animals. One of the major concerns in parasitology, thus, is an effective vaccine development to control Toxoplasmosis.Materials and MethodsIn the present research, a nano-liposomal vaccine containing soluble antigens (SA) was designed to evaluate the immunity and protective efficacy against T. gondii infection in BALB/c mice. Soluble antigens (SA) were achieved from tachyzoites, encapsulated in the liposome, and investigated via scanning electron microscope. Three times with 2-week intervals, BALB/c mice were immunized subcutaneously with different formulations. The level of protection against infection was assessed through the percent survival survey of BALB/c mice after challenge with tachyzoites of T. gondii RH strain; also, the type of generated immune response was determined by evaluating the generation of cytokine (IFN-γ, IL-4) and titration of IgG isotypes.ResultsThe immunization with liposome DSPC+ SA and liposome DSPC+ Imiquimod + SA induced a substantial increase in anti-Toxoplasma IgG antibody as compared to the PBS group (p <0.05). The IgG2a and IFN-γ secretion highest levels were seen with liposome DSPC+ Imiquimod + SA more than the control group (p <0.01) and (p <0.0001), respectively. After challenge with tachyzoites, less mortality was detected in the immunized mice by liposome DSPC + Imiquimod + SA that was meaningfully different (p <0.01) in comparison to other groups.ConclusionVaccination with liposome DSPC + Imiquimod + SA showed more survival rate and cellular immune reaction against T. gondii.
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来源期刊
Nanomedicine Journal
Nanomedicine Journal NANOSCIENCE & NANOTECHNOLOGY-
CiteScore
3.40
自引率
0.00%
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0
审稿时长
12 weeks
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