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

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dc.contributor.author Sangpairoj K.
dc.contributor.author Apisawetakan S.
dc.contributor.author Changklungmoa N.
dc.contributor.author Kueakhai P.
dc.contributor.author Chaichanasak P.
dc.contributor.author Sobhon P.
dc.contributor.author Chaithirayanon K.
dc.date.accessioned 2021-04-05T03:05:19Z
dc.date.available 2021-04-05T03:05:19Z
dc.date.issued 2018
dc.identifier.issn 144894
dc.identifier.other 2-s2.0-85054808400
dc.identifier.uri https://ir.swu.ac.th/jspui/handle/123456789/12727
dc.identifier.uri https://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.abstract Helminth 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.subject alanine aminotransferase
dc.subject antibody
dc.subject aspartate aminotransferase
dc.subject Freund adjuvant
dc.subject immunoglobulin G1
dc.subject peroxiredoxin 2
dc.subject alanine aminotransferase
dc.subject aspartate aminotransferase
dc.subject Freund adjuvant
dc.subject helminth antibody
dc.subject immunoglobulin G
dc.subject peroxiredoxin
dc.subject recombinant protein
dc.subject vaccine
dc.subject alanine aminotransferase blood level
dc.subject animal cell
dc.subject animal experiment
dc.subject animal model
dc.subject animal tissue
dc.subject antibody blood level
dc.subject Article
dc.subject aspartate aminotransferase blood level
dc.subject controlled study
dc.subject drug efficacy
dc.subject Fasciola gigantica
dc.subject fascioliasis
dc.subject female
dc.subject humoral immunity
dc.subject infection prevention
dc.subject liver function
dc.subject liver injury
dc.subject metacercaria
dc.subject mouse
dc.subject nonhuman
dc.subject priority journal
dc.subject Th1 cell
dc.subject Th2 cell
dc.subject animal
dc.subject blood
dc.subject enzyme linked immunosorbent assay
dc.subject enzymology
dc.subject Fasciola
dc.subject fascioliasis
dc.subject immunology
dc.subject Institute for Cancer Research mouse
dc.subject liver
dc.subject Lymnaea
dc.subject parasitology
dc.subject pathology
dc.subject physiology
dc.subject randomization
dc.subject Alanine Transaminase
dc.subject Animals
dc.subject Antibodies, Helminth
dc.subject Aspartate Aminotransferases
dc.subject Enzyme-Linked Immunosorbent Assay
dc.subject Fasciola
dc.subject Fascioliasis
dc.subject Female
dc.subject Freund's Adjuvant
dc.subject Immunoglobulin G
dc.subject Liver
dc.subject Lymnaea
dc.subject Mice
dc.subject Mice, Inbred ICR
dc.subject Peroxiredoxins
dc.subject Random Allocation
dc.subject Recombinant Proteins
dc.subject Vaccines
dc.title Potential of recombinant 2-Cys peroxiredoxin protein as a vaccine for Fasciola gigantica infection
dc.type Article
dc.rights.holder Scopus
dc.identifier.bibliograpycitation Experimental Parasitology. Vol 194, (2018), p.16-23
dc.identifier.doi 10.1016/j.exppara.2018.09.005


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