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SAG4 DNA和肽疫苗接种为BALB/c小鼠提供了部分抗感染保护。

SAG4 DNA and Peptide Vaccination Provides Partial Protection against Infection in BALB/c Mice.

作者信息

Zhou Jian, Wang Lin

机构信息

Department of Orthopedics, The Second Xiangya Hospital, Central South UniversityChangsha, China.

Department of Electroneurophysiology, Jinan Children's HospitalJinan, China.

出版信息

Front Microbiol. 2017 Sep 7;8:1733. doi: 10.3389/fmicb.2017.01733. eCollection 2017.

Abstract

can lead to congenital infections in human. Surface antigen protein 4 (SAG4) of is a potential stimulator for humoral and cellular immune responses. In the present study, a DNA vaccine encoding SAG4 from was constructed and used to immunize BALB/c mice with peptide to evaluate the protective efficacy of the vaccine. The productions of IgG antibodies and cytokines (gamma interferon) from the vaccine (pSAG4/peptide) group were significantly higher than pSAG4 or peptide groups. After a lethal challenge by 1 × 10 tachyzoites from the I strain (RH), the survival time of mice immunized by pSAG4/peptide was longer than that of pSAG4 or peptide immunized mice or control mice. Moreover, after challenging by 20 cysts of the II strain (PRU) of , the number of brain cysts from pSAG4/peptide vaccinated mice was only 31% of the number in PBS injected mice. The findings suggested the SAG4 DNA vaccine with peptide led significant immune responses and improved the protection against challenges.

摘要

可导致人类先天性感染。其表面抗原蛋白4(SAG4)是体液免疫和细胞免疫反应的潜在刺激物。在本研究中,构建了一种编码来自的SAG4的DNA疫苗,并用肽免疫BALB/c小鼠,以评估该疫苗的保护效果。疫苗(pSAG4/肽)组的IgG抗体和细胞因子(γ干扰素)产生量显著高于pSAG4组或肽组。在用I株(RH)的1×10速殖子进行致死性攻击后,pSAG4/肽免疫的小鼠存活时间长于pSAG4或肽免疫的小鼠或对照小鼠。此外,在用II株(PRU)的20个包囊进行攻击后,pSAG4/肽疫苗接种小鼠的脑包囊数量仅为注射PBS小鼠数量的31%。这些发现表明,带有肽的SAG4 DNA疫苗引发了显著的免疫反应,并增强了对攻击的保护作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f26/5594090/bc96cbf87413/fmicb-08-01733-g001.jpg

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