Kunitz-type protease inhibitor as a vaccine candidate against schistosomiasis mansoni

Objective: The aim of this study was to develop a vaccine against schistosomiasis, which is a major challenge due to the complex lifecycle of the causative schistosome parasite. Methods: SmKI-1 is a 16-kDa Kunitz-type protease inhibitor present in the excretory–secretory products and tegument of adu...

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Main Authors: Shiwanthi L. Ranasinghe, Mary Duke, Marina Harvie, Donald P. McManus
Format: Article
Language:English
Published: Elsevier 2018-01-01
Series:International Journal of Infectious Diseases
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S1201971217302813
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spelling doaj-9ecf20d34d4f444b8fef9d01f2d36cec2020-11-24T23:13:40ZengElsevierInternational Journal of Infectious Diseases1201-97121878-35112018-01-0166C263210.1016/j.ijid.2017.10.024Kunitz-type protease inhibitor as a vaccine candidate against schistosomiasis mansoniShiwanthi L. RanasingheMary DukeMarina HarvieDonald P. McManusObjective: The aim of this study was to develop a vaccine against schistosomiasis, which is a major challenge due to the complex lifecycle of the causative schistosome parasite. Methods: SmKI-1 is a 16-kDa Kunitz-type protease inhibitor present in the excretory–secretory products and tegument of adult worms and eggs of Schistosoma mansoni. Two independent vaccine trials were performed in mice to determine the efficacy of rSmKI-1 in developing protective immunity. Results: The results obtained showed reductions of 23–33% in adult worms, 28–31% in intestinal eggs, 33–39% in faecal eggs, and 20–43% in liver eggs. Furthermore, rSmKI-1 significantly increased the production of interferon gamma, interleukin (IL)-10, and IL-6 in vaccinated mice, maintaining a Th1/Th2-type balanced protective response. Conclusions: rSmKI-1 generated partial protection against schistosomiasis mansoni in the murine model of infection and could be developed as part of a combination vaccine with other vaccine candidates to provide an even more solid level of protection.http://www.sciencedirect.com/science/article/pii/S1201971217302813Kunitz proteinSchistosomiasis mansoniSmKI-1ES products
collection DOAJ
language English
format Article
sources DOAJ
author Shiwanthi L. Ranasinghe
Mary Duke
Marina Harvie
Donald P. McManus
spellingShingle Shiwanthi L. Ranasinghe
Mary Duke
Marina Harvie
Donald P. McManus
Kunitz-type protease inhibitor as a vaccine candidate against schistosomiasis mansoni
International Journal of Infectious Diseases
Kunitz protein
Schistosomiasis mansoni
SmKI-1
ES products
author_facet Shiwanthi L. Ranasinghe
Mary Duke
Marina Harvie
Donald P. McManus
author_sort Shiwanthi L. Ranasinghe
title Kunitz-type protease inhibitor as a vaccine candidate against schistosomiasis mansoni
title_short Kunitz-type protease inhibitor as a vaccine candidate against schistosomiasis mansoni
title_full Kunitz-type protease inhibitor as a vaccine candidate against schistosomiasis mansoni
title_fullStr Kunitz-type protease inhibitor as a vaccine candidate against schistosomiasis mansoni
title_full_unstemmed Kunitz-type protease inhibitor as a vaccine candidate against schistosomiasis mansoni
title_sort kunitz-type protease inhibitor as a vaccine candidate against schistosomiasis mansoni
publisher Elsevier
series International Journal of Infectious Diseases
issn 1201-9712
1878-3511
publishDate 2018-01-01
description Objective: The aim of this study was to develop a vaccine against schistosomiasis, which is a major challenge due to the complex lifecycle of the causative schistosome parasite. Methods: SmKI-1 is a 16-kDa Kunitz-type protease inhibitor present in the excretory–secretory products and tegument of adult worms and eggs of Schistosoma mansoni. Two independent vaccine trials were performed in mice to determine the efficacy of rSmKI-1 in developing protective immunity. Results: The results obtained showed reductions of 23–33% in adult worms, 28–31% in intestinal eggs, 33–39% in faecal eggs, and 20–43% in liver eggs. Furthermore, rSmKI-1 significantly increased the production of interferon gamma, interleukin (IL)-10, and IL-6 in vaccinated mice, maintaining a Th1/Th2-type balanced protective response. Conclusions: rSmKI-1 generated partial protection against schistosomiasis mansoni in the murine model of infection and could be developed as part of a combination vaccine with other vaccine candidates to provide an even more solid level of protection.
topic Kunitz protein
Schistosomiasis mansoni
SmKI-1
ES products
url http://www.sciencedirect.com/science/article/pii/S1201971217302813
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