Characteristics and function of cathepsin L3 from Schistosoma japonicum.
Adjuvants, Immunologic
Animals
Antibody-Dependent Cell Cytotoxicity
/ immunology
Blotting, Western
Cathepsins
/ immunology
Cloning, Molecular
Female
Macrophages
/ immunology
Mice
Mice, Inbred BALB C
Protozoan Vaccines
/ immunology
Schistosoma japonicum
/ immunology
Schistosomiasis japonica
/ immunology
Vaccination
Antibody-dependent cell-mediated cytotoxicity
Cathepsin L3
Immune
Lung-stage schistosomula
Schistosoma japonicum
Journal
Parasitology research
ISSN: 1432-1955
Titre abrégé: Parasitol Res
Pays: Germany
ID NLM: 8703571
Informations de publication
Date de publication:
May 2020
May 2020
Historique:
received:
25
11
2019
accepted:
04
03
2020
pubmed:
19
3
2020
medline:
1
7
2020
entrez:
19
3
2020
Statut:
ppublish
Résumé
Schistosomiasis is still prevalent and seriously endangering the health of people and livestock in many countries. There have been great efforts to develop vaccines against schistosomiasis for prolonged protection in epidemic areas. Molecules from lung-stage schistosomula have been regarded as potential vaccine candidates against schistosomiasis. Our previous work has shown that cathepsin L3 from Schistosoma japonicum (SjCL3) is expressed in lung-stage schistosomula, but its role is not well known. In the present study, we characterized SjCL3 and detected its effect as a possible vaccine in vivo and in vitro. From the results of quantitative PCR (qPCR) and western blot, SjCL3 was present throughout the lifecycle of the worm, and its relative expressed level was higher in the liver eggs and adult worms than other stages. Additionally, immunofluorescence assay showed that SjCL3 was mainly concentrated in the eggshell, alimentary canal, and musculature of worms. Compared with the adjuvant group, the immunization of SjCL3 in mice resulted in a 28.9% decrease in worm burden and a 29.2% reduction in egg number in the host liver. In antibody-dependent cell-mediated cytotoxicity (ADCC) insecticidal experiments in vitro, the existence of SjCL3 could in part suppress adherence between macrophages and worm. The above results indicated that the immunization of SjCL3 could induce limited immune protection against S. japonicum infection in mice, and this protease played a role in breaking the process of ADCC, which was beneficial to the survival of worms.
Identifiants
pubmed: 32185481
doi: 10.1007/s00436-020-06647-x
pii: 10.1007/s00436-020-06647-x
doi:
Substances chimiques
Adjuvants, Immunologic
0
Protozoan Vaccines
0
Cathepsins
EC 3.4.-
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
1619-1628Subventions
Organisme : National Natural Science Foundation of China
ID : 81273010
Organisme : Scientific Research Subject of the Health and Family Planning Commission of Hubei Province
ID : XF2012-18
Commentaires et corrections
Type : CommentIn
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