Efficacy of thiolated eudragit microspheres as an oral vaccine delivery system to induce mucosal immunity against enterotoxigenic Escherichia coli in mice
To investigate the efficay of thiolated eudragit microspheres (TEMS) as an oral vaccine delivery system, F4 and F18 in E.coli were loaded in TEMS and orally immunized to mice. Induced immune responses such as IgG an IgA levels were investigated with sera, saliva, feces, splenocyte, peyer’s patch, la...
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Published in | European journal of pharmaceutics and biopharmaceutics Vol. 81; no. 1; pp. 43 - 48 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Amsterdam
Elsevier B.V
01.05.2012
Elsevier |
Subjects | |
Online Access | Get full text |
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Summary: | To investigate the efficay of thiolated eudragit microspheres (TEMS) as an oral vaccine delivery system, F4 and F18 in E.coli were loaded in TEMS and orally immunized to mice. Induced immune responses such as IgG an IgA levels were investigated with sera, saliva, feces, splenocyte, peyer’s patch, lamina propria cells in mice.
A vaccine delivery system based on thiolated eudragit microsphere (TEMS) was studied in vivo for its ability to elicit mucosal immunity against enterotoxigenic Escherichia coli (ETEC). Groups of mice were orally immunized with F4 or F18 fimbriae of ETEC and F4 or F18 loaded in TEMS. Mice that were orally administered with F4 or F18 loaded TEMS showed higher antigen-specific IgG antibody responses in serum and antigen-specific IgA in saliva and feces than mice that were immunized with antigens only. In addition, oral vaccination of F4 or F18 loaded TEMS resulted in higher numbers of IgG and IgA antigen-specific antibody secreting cells in the spleen, lamina propria, and Peyer’s patches of immunized mice than other groups. Moreover, TEMS administration loaded with F4 or F18 induced mixed Th1 and Th2 type responses based on similarly increased levels of IgG1 and IgG2a. These results suggest that F4 or F18 loaded TEMS may be a promising candidate for an oral vaccine delivery system to elicit systemic and mucosal immunity against ETEC. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0939-6411 1873-3441 |
DOI: | 10.1016/j.ejpb.2012.01.010 |