Characterization of protective immunity induced against Schistosoma mansoni via DNA priming with the large subunit of calpain (Sm-p80) in the presence of genetic adjuvants

Despite advances in control via snail eradication and large-scale chemotherapy using praziquental, schistosomiasis continues to spread to new geographic areas particularly in sub-Saharan Africa. Presently, there is no vaccine for controlling this disease. We have concentrated on a functionally impor...

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Main Authors: Siddiqui A.A., Pinkston J.R., Quinlin M.L., Kavikondala V., Rewers-Felkins K.A., Phillips T., Pompa J.
Format: Article
Language:English
Published: EDP Sciences 2005-03-01
Series:Parasite
Subjects:
Online Access:http://dx.doi.org/10.1051/parasite/2005121003
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author Siddiqui A.A.
Pinkston J.R.
Quinlin M.L.
Kavikondala V.
Rewers-Felkins K.A.
Phillips T.
Pompa J.
author_facet Siddiqui A.A.
Pinkston J.R.
Quinlin M.L.
Kavikondala V.
Rewers-Felkins K.A.
Phillips T.
Pompa J.
author_sort Siddiqui A.A.
collection DOAJ
description Despite advances in control via snail eradication and large-scale chemotherapy using praziquental, schistosomiasis continues to spread to new geographic areas particularly in sub-Saharan Africa. Presently, there is no vaccine for controlling this disease. We have concentrated on a functionally important schistosome antigen Sm-p80 as a possible vaccine candidate for schistosomiasis. Here we report the proliferation of spleen cells in response to the recombinant Sm-p80 protein and cytokine (IFN-γ and IL-4) production by the splenocytes. These spleen cells were obtained from groups of mice that were vaccinated with a DNA vaccine formulation containing Sm-p80 and one of the Th-1 (IL-2 or IL-12) or Th-2 (GM-CSF, IL-4) enhancer cytokines. The splenocytes from the groups of mice vaccinated with Sm-p80 DNA in the presence of Th-2 enhancer cytokines showed moderate but detectable proliferation. The splenocytes obtained from mice vaccinated with Sm-p80 DNA with Th-1 enhancer cytokines IL-2 and IL-12 provided the highest proliferation. The IFN-γ production by splenocytes was found to follow the similar pattern [(Sm-p80) < (Sm-p80 + IL-4) < (Sm-p80 + GM-CSF) < (Sm-p80 + IL-12) < (Sm-p80 + IL-2)], as has been observed for the proliferation and protection data. However, the elevated IL-4 production was inversely correlated to Sm-p80-induced splenocyte proliferation or the protection. These results show again that protective immune response induced by Sm-p80 is of Th-1 type.
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spelling doaj.art-8fcf12ce79e84a6a9467ee823bb56ac92023-12-02T00:19:28ZengEDP SciencesParasite1252-607X1776-10422005-03-011213810.1051/parasite/2005121003parasite2005121p3Characterization of protective immunity induced against Schistosoma mansoni via DNA priming with the large subunit of calpain (Sm-p80) in the presence of genetic adjuvantsSiddiqui A.A.Pinkston J.R.Quinlin M.L.Kavikondala V.Rewers-Felkins K.A.Phillips T.Pompa J.Despite advances in control via snail eradication and large-scale chemotherapy using praziquental, schistosomiasis continues to spread to new geographic areas particularly in sub-Saharan Africa. Presently, there is no vaccine for controlling this disease. We have concentrated on a functionally important schistosome antigen Sm-p80 as a possible vaccine candidate for schistosomiasis. Here we report the proliferation of spleen cells in response to the recombinant Sm-p80 protein and cytokine (IFN-γ and IL-4) production by the splenocytes. These spleen cells were obtained from groups of mice that were vaccinated with a DNA vaccine formulation containing Sm-p80 and one of the Th-1 (IL-2 or IL-12) or Th-2 (GM-CSF, IL-4) enhancer cytokines. The splenocytes from the groups of mice vaccinated with Sm-p80 DNA in the presence of Th-2 enhancer cytokines showed moderate but detectable proliferation. The splenocytes obtained from mice vaccinated with Sm-p80 DNA with Th-1 enhancer cytokines IL-2 and IL-12 provided the highest proliferation. The IFN-γ production by splenocytes was found to follow the similar pattern [(Sm-p80) < (Sm-p80 + IL-4) < (Sm-p80 + GM-CSF) < (Sm-p80 + IL-12) < (Sm-p80 + IL-2)], as has been observed for the proliferation and protection data. However, the elevated IL-4 production was inversely correlated to Sm-p80-induced splenocyte proliferation or the protection. These results show again that protective immune response induced by Sm-p80 is of Th-1 type.http://dx.doi.org/10.1051/parasite/2005121003schistosomiasisvaccineSm-p80 protein
spellingShingle Siddiqui A.A.
Pinkston J.R.
Quinlin M.L.
Kavikondala V.
Rewers-Felkins K.A.
Phillips T.
Pompa J.
Characterization of protective immunity induced against Schistosoma mansoni via DNA priming with the large subunit of calpain (Sm-p80) in the presence of genetic adjuvants
Parasite
schistosomiasis
vaccine
Sm-p80 protein
title Characterization of protective immunity induced against Schistosoma mansoni via DNA priming with the large subunit of calpain (Sm-p80) in the presence of genetic adjuvants
title_full Characterization of protective immunity induced against Schistosoma mansoni via DNA priming with the large subunit of calpain (Sm-p80) in the presence of genetic adjuvants
title_fullStr Characterization of protective immunity induced against Schistosoma mansoni via DNA priming with the large subunit of calpain (Sm-p80) in the presence of genetic adjuvants
title_full_unstemmed Characterization of protective immunity induced against Schistosoma mansoni via DNA priming with the large subunit of calpain (Sm-p80) in the presence of genetic adjuvants
title_short Characterization of protective immunity induced against Schistosoma mansoni via DNA priming with the large subunit of calpain (Sm-p80) in the presence of genetic adjuvants
title_sort characterization of protective immunity induced against schistosoma mansoni via dna priming with the large subunit of calpain sm p80 in the presence of genetic adjuvants
topic schistosomiasis
vaccine
Sm-p80 protein
url http://dx.doi.org/10.1051/parasite/2005121003
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