Publication:
Potential of recombinant 2-Cys peroxiredoxin protein as a vaccine for Fasciola gigantica infection

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.date.issuedBE2561
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.format.mimetypeapplication/pdf
dc.identifier.citationExperimental Parasitology. Vol 194, (2018), p.16-23
dc.identifier.doi10.1016/j.exppara.2018.09.005
dc.identifier.issn144894
dc.identifier.other2-s2.0-85054808400
dc.identifier.urihttps://hdl.handle.net/20.500.14740/5809
dc.rights.holderมหาวิทยาลัยศรีนครินทรวิโรฒ
dc.subject.otherAlanine aminotransferase
dc.subject.otherAntibody
dc.subject.otherAspartate aminotransferase
dc.subject.otherFreund adjuvant
dc.subject.otherImmunoglobulin G1
dc.subject.otherPeroxiredoxin 2
dc.subject.otherAlanine aminotransferase
dc.subject.otherAspartate aminotransferase
dc.subject.otherFreund adjuvant
dc.subject.otherHelminth antibody
dc.subject.otherImmunoglobulin G
dc.subject.otherPeroxiredoxin
dc.subject.otherRecombinant protein
dc.subject.otherVaccine
dc.subject.otherAlanine aminotransferase blood level
dc.subject.otherAnimal cell
dc.subject.otherAnimal experiment
dc.subject.otherAnimal model
dc.subject.otherAnimal tissue
dc.subject.otherAntibody blood level
dc.subject.otherArticle
dc.subject.otherAspartate aminotransferase blood level
dc.subject.otherControlled study
dc.subject.otherDrug efficacy
dc.subject.otherFasciola gigantica
dc.subject.otherFascioliasis
dc.subject.otherFemale
dc.subject.otherHumoral immunity
dc.subject.otherInfection prevention
dc.subject.otherLiver function
dc.subject.otherLiver injury
dc.subject.otherMetacercaria
dc.subject.otherMouse
dc.subject.otherNonhuman
dc.subject.otherPriority journal
dc.subject.otherTh1 cell
dc.subject.otherTh2 cell
dc.subject.otherAnimal
dc.subject.otherBlood
dc.subject.otherEnzyme linked immunosorbent assay
dc.subject.otherEnzymology
dc.subject.otherFasciola
dc.subject.otherFascioliasis
dc.subject.otherImmunology
dc.subject.otherInstitute for Cancer Research mouse
dc.subject.otherLiver
dc.subject.otherLymnaea
dc.subject.otherParasitology
dc.subject.otherPathology
dc.subject.otherPhysiology
dc.subject.otherRandomization
dc.subject.otherAlanine Transaminase
dc.subject.otherAnimals
dc.subject.otherAntibodies, Helminth
dc.subject.otherAspartate Aminotransferases
dc.subject.otherEnzyme-Linked Immunosorbent Assay
dc.subject.otherFasciola
dc.subject.otherFascioliasis
dc.subject.otherFemale
dc.subject.otherFreund's Adjuvant
dc.subject.otherImmunoglobulin G
dc.subject.otherLiver
dc.subject.otherLymnaea
dc.subject.otherMice
dc.subject.otherMice, Inbred ICR
dc.subject.otherPeroxiredoxins
dc.subject.otherRandom Allocation
dc.subject.otherRecombinant Proteins
dc.subject.otherVaccines
dc.titlePotential of recombinant 2-Cys peroxiredoxin protein as a vaccine for Fasciola gigantica infection
dc.typeArticle
dspace.entity.typePublication
swu.datasource.scopushttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85054808400&doi=10.1016%2fj.exppara.2018.09.005&partnerID=40&md5=3f571a66f3383896e347fcbd3b15ff2c

Files