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乙胺嗪在实验性丝虫病中的免疫佐剂作用。

Immunoadjuvant effect of diethylcarbamazine in experimental filariasis.

作者信息

Parasurama Jawaharlal Jeya Prita, Rajaiah Prabhu Prince, Gandhirajan Anugraha, Krishnan Nithya, Perumal Kaliraj

机构信息

Centre for Biotechnology, Anna University, Chennai, Tamil Nadu 600 025, India.

出版信息

Int Immunopharmacol. 2015 Feb;24(2):458-462. doi: 10.1016/j.intimp.2014.12.034. Epub 2015 Jan 7.

Abstract

Lymphatic filariasis caused by tissue dwelling nematodes is endemic in 73 countries and drugs have been administered to control or stop the infection. Resurgence of the infection after mass drug administration necessitates the study of several parasite antigens or adjuvants for vaccine developments. In this study, diethylcarbamazine (DEC) was evaluated for its efficacy as adjuvant against the filarial parasite; Brugia malayi microfilariae (mf) by combining with the Escherichia coli expressed recombinant BmShp-1 protein. Shp-1 is one of the sheath proteins expressed by adult female and microfilarial stage of the filarial parasite. Hence, immunoprophylactic efficacy of Shp-1 using DEC and alum adjuvants was compared in BALB/c mice model by an in situ micropore chamber method. Shp-1 antibody titre was high when the mice were immunized with Shp-1 along with DEC and they exhibited balanced Th1/Th2 profile. DEC also induced significantly high T-cell proliferation (P<0.001) when stimulated with Shp-1 compared to alum. Significantly high percentage protection against B. malayi microfilariae was observed in Shp-1+DEC immunized mice groups (P<0.05) and hence it is concluded that the need of repeated drug administration can be controlled when there is a possibility of developing protective immunity in the host against mf by vaccination.

摘要

由组织内寄生线虫引起的淋巴丝虫病在73个国家呈地方性流行,人们已使用药物来控制或阻止感染。大规模药物给药后感染的复发使得有必要研究多种寄生虫抗原或佐剂以开发疫苗。在本研究中,通过将乙胺嗪(DEC)与大肠杆菌表达的重组BmShp-1蛋白结合,评估了其作为抗丝虫寄生虫佐剂的功效。Shp-1是丝虫寄生虫成年雌性和微丝蚴阶段表达的鞘蛋白之一。因此,通过原位微孔室法在BALB/c小鼠模型中比较了使用DEC和明矾佐剂的Shp-1的免疫预防功效。当小鼠用Shp-1和DEC一起免疫时,Shp-1抗体滴度很高,并且它们表现出平衡的Th1/Th2谱。与明矾相比,当用Shp-1刺激时,DEC还诱导了显著高的T细胞增殖(P<0.001)。在Shp-1+DEC免疫的小鼠组中观察到对马来布鲁线虫微丝蚴的显著高百分比保护(P<0.05),因此得出结论,当宿主有可能通过疫苗接种产生针对微丝蚴的保护性免疫时,可以控制重复给药的需求。

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