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LmjMAPK10 offers protection against Leishmania donovani infection.
Parasite Immunology ( IF 2.2 ) Pub Date : 2020-02-01 , DOI: 10.1111/pim.12687 Sunil Kumar 1 , Shubhranshu Zutshi 1 , Ashok Patidar 1 , Neelam Bodhale 1, 2 , Somenath Roy 3 , Arup Sarkar 4 , Bhaskar Saha 1, 4
Parasite Immunology ( IF 2.2 ) Pub Date : 2020-02-01 , DOI: 10.1111/pim.12687 Sunil Kumar 1 , Shubhranshu Zutshi 1 , Ashok Patidar 1 , Neelam Bodhale 1, 2 , Somenath Roy 3 , Arup Sarkar 4 , Bhaskar Saha 1, 4
Affiliation
AIMS
This study aimed at evaluating the DNA vaccination efficacy of Leishmania major-derived MAPK10 against Leishmania donovani infection.
METHODS AND RESULTS
MAPK10 is one of the 15 mitogen-activated protein kinases (MAPKs) of Leishmania major. Herein, we expressed the gene through a mammalian vector and tested whether priming with this gene would offer protection against L donovani infection. We report that LmjMAPK10 DNA vaccination using a mammalian expression vector significantly reduces the parasite burden. The protection is accompanied by host-protective T-cell functions, TH 1-type cytokines and elevated leishmanial antigen-specific IgG2a isotype response. T-cell response to the L donovani/challenge infection is associated with increase in IL-12 and IFN-γ, but reduced IL-10 and IL-4 production.
CONCLUSIONS
LmjMAPK10 is cross-protective against L donovani infection.
中文翻译:
LmjMAPK10提供了针对多形利什曼原虫感染的保护作用。
目的本研究旨在评估利什曼原虫主要来源的MAPK10的DNA疫苗接种疫苗对利什曼原虫donovani感染的功效。方法和结果MAPK10是利什曼原虫(Leishmania major)的15种丝裂原活化蛋白激酶(MAPK)之一。在本文中,我们通过哺乳动物载体表达了该基因,并测试了用该基因引发是否可以提供抗L donovani感染的保护。我们报告说,使用哺乳动物表达载体的LmjMAPK10 DNA疫苗接种显着降低了寄生虫负担。该保护伴随有宿主保护性T细胞功能,TH 1型细胞因子和利什曼原虫抗原特异性IgG2a同种型应答升高。T细胞对L多诺维尼/挑战感染的反应与IL-12和IFN-γ的增加有关,但IL-10和IL-4的产生减少。
更新日期:2019-11-01
中文翻译:
LmjMAPK10提供了针对多形利什曼原虫感染的保护作用。
目的本研究旨在评估利什曼原虫主要来源的MAPK10的DNA疫苗接种疫苗对利什曼原虫donovani感染的功效。方法和结果MAPK10是利什曼原虫(Leishmania major)的15种丝裂原活化蛋白激酶(MAPK)之一。在本文中,我们通过哺乳动物载体表达了该基因,并测试了用该基因引发是否可以提供抗L donovani感染的保护。我们报告说,使用哺乳动物表达载体的LmjMAPK10 DNA疫苗接种显着降低了寄生虫负担。该保护伴随有宿主保护性T细胞功能,TH 1型细胞因子和利什曼原虫抗原特异性IgG2a同种型应答升高。T细胞对L多诺维尼/挑战感染的反应与IL-12和IFN-γ的增加有关,但IL-10和IL-4的产生减少。