Ileal Peyer's patches are not necessary for systemic B cell development and maintenance and do not contribute significantly to the overall B cell pool in swine

• Published in: The Journal of immunology (1950) 2011-11, Vol.187 (10), p.5150-5161
• Main Authors: Sinkora, Marek, Stepanova, Katerina, Butler, John E, Francis, David, Santiago-Mateo, Kristina, Potockova, Hana, Karova, Kristyna, Sinkorova, Jana
• Format: Article
• Language: English
• Subjects: Animals; Animals, Newborn; B-Lymphocyte Subsets - cytology; B-Lymphocyte Subsets - immunology; B-Lymphocyte Subsets - metabolism; Cell Differentiation - immunology; Cell Lineage - immunology; Female; Germ-Free Life; Ileum - cytology; Ileum - immunology; Ileum - surgery; Lymphocyte Count; Lymphopoiesis - immunology; Peyer's Patches - cytology; Peyer's Patches - immunology; Peyer's Patches - surgery; Swine
• ISSN: 0022-1767; 1550-6606
• DOI: 10.4049/jimmunol.1101879

Based on studies of sheep, ileal Peyer's patches (IPP) have been regarded as a type of primary lymphoid tissue similar to the bursa of Fabricius in chicken. Because bursectomy results in B cell deficiency, we wondered whether resection of the IPP of piglets would have a similar effect. Comparison of IPP-resected, surgical shams and untreated germ-free piglets, all of which were later colonized with a defined commensal flora, demonstrated that resection of the IPP did not alter the level and phenotype of B and T cells in lymphoid tissues and the blood 10 wk after surgery. Additionally, colonization of IPP caused a shift from the fetal type of lymphocyte distribution to the adult type that is characterized by prevalence of B cells, with many of them representing IgA(+) switched B cells or displaying a more mature CD2(-)CD21(+) and CD2(-)CD21(-) phenotype. Moreover, colonization leads to appearance of effector CD4(+)CD8(+) αβ T helper and CD2(+)CD8(-) γδ T cells. Comparison of germ-free with colonized pigs and experiments utilizing surgical transposition of jejunal Peyer's patch into terminal ileum or construction of isolated ileal loops indicated that lymphocyte development in IPP is dependent on colonization. Although our studies confirmed higher mitotic and apoptotic rates in IPP, they failed to identify any cell populations that resemble developing B lineage cells in the bone marrow. These results indicate that porcine IPP are not required for systemic B cell generation or maintenance, but they are secondary lymphoid tissue that appears important in immune responses to colonizing bacteria.