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Title: | Potential of recombinant 2-Cys peroxiredoxin protein as a vaccine for Fasciola gigantica infection |
Authors: | Sangpairoj K. Apisawetakan S. Changklungmoa N. Kueakhai P. Chaichanasak P. Sobhon P. Chaithirayanon K. |
Keywords: | alanine aminotransferase antibody aspartate aminotransferase Freund adjuvant immunoglobulin G1 peroxiredoxin 2 alanine aminotransferase aspartate aminotransferase Freund adjuvant helminth antibody immunoglobulin G peroxiredoxin recombinant protein vaccine alanine aminotransferase blood level animal cell animal experiment animal model animal tissue antibody blood level Article aspartate aminotransferase blood level controlled study drug efficacy Fasciola gigantica fascioliasis female humoral immunity infection prevention liver function liver injury metacercaria mouse nonhuman priority journal Th1 cell Th2 cell animal blood enzyme linked immunosorbent assay enzymology Fasciola fascioliasis immunology Institute for Cancer Research mouse liver Lymnaea parasitology pathology physiology randomization Alanine Transaminase Animals Antibodies, Helminth Aspartate Aminotransferases Enzyme-Linked Immunosorbent Assay Fasciola Fascioliasis Female Freund's Adjuvant Immunoglobulin G Liver Lymnaea Mice Mice, Inbred ICR Peroxiredoxins Random Allocation Recombinant Proteins Vaccines |
Issue Date: | 2018 |
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 |
URI: | https://ir.swu.ac.th/jspui/handle/123456789/12727 https://www.scopus.com/inward/record.uri?eid=2-s2.0-85054808400&doi=10.1016%2fj.exppara.2018.09.005&partnerID=40&md5=3f571a66f3383896e347fcbd3b15ff2c |
ISSN: | 144894 |
Appears in Collections: | Scopus 1983-2021 |
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