Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/12727
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dc.contributor.authorSangpairoj K.
dc.contributor.authorApisawetakan S.
dc.contributor.authorChangklungmoa N.
dc.contributor.authorKueakhai P.
dc.contributor.authorChaichanasak P.
dc.contributor.authorSobhon P.
dc.contributor.authorChaithirayanon K.
dc.date.accessioned2021-04-05T03:05:19Z-
dc.date.available2021-04-05T03:05:19Z-
dc.date.issued2018
dc.identifier.issn144894
dc.identifier.other2-s2.0-85054808400
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/12727-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85054808400&doi=10.1016%2fj.exppara.2018.09.005&partnerID=40&md5=3f571a66f3383896e347fcbd3b15ff2c
dc.description.abstractHelminth 2-cys peroxiredoxin (Prx) is a major antioxidant enzyme that protects parasites against hydrogen peroxide-generating oxidative stress from the hosts’ immune responses. This enzyme has been found in all stages of the tropical liver fluke, Fasciola gigantica. To investigate the potential of the recombinant F. gigantica Prx-2 (rFgPrx-2) as a vaccine candidate, vaccine trials in mice were carried out. In this study, the ICR mice were immunized with rFgPrx-2 combined with Freund's adjuvant and infected with F. gigantica metacercariae. The vaccine efficacy was estimated by quantitate fluke recovery, antibody levels and liver function. The protection by rFgPrx-2 against F. gigantica infection was achieved at 43–46% compared with adjuvant-infected and non-immunized-infected control groups, respectively. The vaccine elicited both Th1 and Th2 humoral immune responses with predominance of Th2 as indicated by the higher level of IgG1 in sera of immunized mice. However, the levels of liver damage markers, serum glutamate oxalic transaminase (SGOT) and serum glutamic pyruvate transaminase (SGPT) in rFgPrx-2 immunized group did not show significant difference in comparison with the controls. This study suggested that rFgPrx-2 may have a potential as a vaccine against tropical fasciolosis. © 2018
dc.subjectalanine aminotransferase
dc.subjectantibody
dc.subjectaspartate aminotransferase
dc.subjectFreund adjuvant
dc.subjectimmunoglobulin G1
dc.subjectperoxiredoxin 2
dc.subjectalanine aminotransferase
dc.subjectaspartate aminotransferase
dc.subjectFreund adjuvant
dc.subjecthelminth antibody
dc.subjectimmunoglobulin G
dc.subjectperoxiredoxin
dc.subjectrecombinant protein
dc.subjectvaccine
dc.subjectalanine aminotransferase blood level
dc.subjectanimal cell
dc.subjectanimal experiment
dc.subjectanimal model
dc.subjectanimal tissue
dc.subjectantibody blood level
dc.subjectArticle
dc.subjectaspartate aminotransferase blood level
dc.subjectcontrolled study
dc.subjectdrug efficacy
dc.subjectFasciola gigantica
dc.subjectfascioliasis
dc.subjectfemale
dc.subjecthumoral immunity
dc.subjectinfection prevention
dc.subjectliver function
dc.subjectliver injury
dc.subjectmetacercaria
dc.subjectmouse
dc.subjectnonhuman
dc.subjectpriority journal
dc.subjectTh1 cell
dc.subjectTh2 cell
dc.subjectanimal
dc.subjectblood
dc.subjectenzyme linked immunosorbent assay
dc.subjectenzymology
dc.subjectFasciola
dc.subjectfascioliasis
dc.subjectimmunology
dc.subjectInstitute for Cancer Research mouse
dc.subjectliver
dc.subjectLymnaea
dc.subjectparasitology
dc.subjectpathology
dc.subjectphysiology
dc.subjectrandomization
dc.subjectAlanine Transaminase
dc.subjectAnimals
dc.subjectAntibodies, Helminth
dc.subjectAspartate Aminotransferases
dc.subjectEnzyme-Linked Immunosorbent Assay
dc.subjectFasciola
dc.subjectFascioliasis
dc.subjectFemale
dc.subjectFreund's Adjuvant
dc.subjectImmunoglobulin G
dc.subjectLiver
dc.subjectLymnaea
dc.subjectMice
dc.subjectMice, Inbred ICR
dc.subjectPeroxiredoxins
dc.subjectRandom Allocation
dc.subjectRecombinant Proteins
dc.subjectVaccines
dc.titlePotential of recombinant 2-Cys peroxiredoxin protein as a vaccine for Fasciola gigantica infection
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationExperimental Parasitology. Vol 194, (2018), p.16-23
dc.identifier.doi10.1016/j.exppara.2018.09.005
Appears in Collections:Scopus 1983-2021

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