Background And Aim: Immunoglobulin (Ig) G1 and IgG2a are the surrogate markers respectively for humoral and cellular immune responses of hosts against antigens including cystic fluid proteins of . A study was conducted to investigate the IgG1 and IgG2a responses of Balb/c mice against some individual cystic fluid proteins of in an effort to determine the roles of each protein in inducing the humoral and cellular immune responses in host.
Materials And Methods: Individual p71, p31, and p14 proteins of were purified by separation of the proteins using sodium dodecyl sulfate-polyacrylamide gel electrophoresis and elution of individual proteins from the gel. Six female Balb/c mice were immunized 4 times at 10-day intervals with the crude cystic fluid proteins, and sera were collected for the measurement of IgG1 and IgG2a levels against the individual proteins. Sera samples collected before the first immunization were used as negative antibody control, sera samples collected after the fourth immunization were used as positive antibody control, and crude cystic fluid protein was used as positive antigen control.
Results: All immunized mice were immune to p71, p31, p14, and crude cystic fluid proteins of . The crude cystic fluid proteins of induced a higher IgG2a than IgG1 level following the first and the second immunizations but switched into a higher IgG1 than IgG2a level following the fourth immunization. Protein 71 kDa (p71) induced a higher IgG2a than IgG1 level following the fourth immunization. In contrast, p14 induced a higher IgG1 than IgG2a level following the fourth immunization. Low and balance IgG1 and IgG2a levels against p31 were observed following the first to the fourth immunizations.
Conclusion: Using IgG1 and IgG2a levels as the surrogate markers, it appears that cystic fluid antigens of induce both humoral and cellular immune responses in Balb/c mice. The p71 appears to be a better inducer of cellular immune response, whereas p14 is a better inducer of humoral immune response of mice.
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| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6303487 | PMC |
| http://dx.doi.org/10.14202/vetworld.2018.1641-1647 | DOI Listing |
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