Role of murine Peyer's patch lymphocytes against primary and challenge infections with Cryptosporidium parvum.
10.3347/kjp.2007.45.3.175
- Author:
Sang Mee GUK
1
;
Jong Yil CHAI
Author Information
1. Department of Parasitology and Tropical Medicine, Seoul National University College of Medicine, and Institute of Endemic Diseases, Seoul National University Medical Research Center, Seoul, Korea. cjy@snu.ac.kr
- Publication Type:Original Article
- Keywords:
Cryptosporidium parvum;
Peyer's patch lymphocytes;
mucosal immunity;
cytokines
- MeSH:
Animals;
Antibodies, Protozoan/analysis/metabolism;
Cattle;
Cryptosporidiosis/*immunology/parasitology;
Cryptosporidium parvum/*immunology;
Feces/parasitology;
Female;
Humans;
Immunoglobulin A/analysis/biosynthesis;
Immunoglobulin G/analysis/biosynthesis;
Interferon-gamma/analysis/biosynthesis;
Interleukin-2/analysis/biosynthesis;
Lymphocytes/*immunology;
Male;
Mice;
Mice, Inbred C57BL;
Peyer's Patches/cytology/*immunology;
Specific Pathogen-Free Organisms
- From:The Korean Journal of Parasitology
2007;45(3):175-180
- CountryRepublic of Korea
- Language:English
-
Abstract:
In order to determine the role of Peyer's patch lymphocytes (PPL) in self-clearing of Cryptosporidium parvum infection in murine models, changes in PPL subsets, their cytokine expression, and in vitro IgG1 and IgA secretions by PPL were observed in primary- and challenge-infected C57BL/6 mice. In primary-infected mice, the percentages of CD4+ T cells, CD8+ T cells, sIgA+ B cells, IL-2+ T cells, and IFN-gamma+ T cells among the PPL, increased significantly (P < 0.05) on day 10 post-infection (PI). Secretion of IgG1 and IgA in vitro by PPL also increased on day 10 PI. However, all these responses, with the exception of IgG1 and IgA secretions, decreased in challenge-infected mice on day 7 post-challenge (= day 13 PI); their IgG1 and IgA levels were higher (P > 0.05) than those in primaryinfected mice. The results suggest that murine PPL play an important role in self-clearing of primary C. parvum infections through proliferation of CD4+, CD8+, IL-2+, and IFN-gamma+ T cells, and IgG1 and IgA-secreting B cells. In challenge infections, the role of T cells is reduced whereas that of B cells secreting IgA appeared to be continuously important.
