Department of Food Science and Technology, College of Bioresource Sciences, Nihon University, 1866, Kameino, Fujisawa-shi, Kanagawa, 252-8510, Japan.
Cytotechnology. 2005 Jan;47(1-3):69-77. doi: 10.1007/s10616-005-3776-1.
We demonstrate immunomodulatory effects, especially those involving murine intestinal IgA secretion, in Peyer's patch cells following oral administration of Bifidobacterium immunomodulator (BIM) derived from sonicated B. pseudocatenulatum 7041. BALB/c mice were administered BIM orally for 7 consecutive days. The PP cells demonstrated upregulated secretion of total IgA including BIM-specific IgA following BIM administration. In observing the response of PP cells co-cultured with BIM, we found enhanced secretion of interferon-gamma (IFN-gamma) and interleukin (IL)-6 in the CD4(+) T cells. In contrast, IL-12 secretion by Thy1.2(-) PP cells was enhanced, but secretion of IFN-gamma, IL-5, and IL-6 was not significantly affected. Furthermore, the population of CD4(+) CD45RB(high) T cells in PP increased following oral administration of BIM. These data suggest that CD4(+) T cells were affected by BIM administration. Overall, the results show that oral administration of BIM induced CD4(+) PP cells to change their expression of cell surface antigen and cytokine production.
我们证明了双歧杆菌免疫调节剂(BIM)经超声处理的双歧杆菌假链状菌 7041 口服后,在派尔氏结细胞中具有免疫调节作用,特别是涉及到鼠肠道 IgA 分泌的作用。BALB/c 小鼠连续 7 天口服 BIM。在观察与 BIM 共培养的 PP 细胞的反应时,我们发现 CD4(+)T 细胞中干扰素-γ(IFN-γ)和白细胞介素(IL)-6 的分泌增强。相反,Thy1.2(-)PP 细胞中 IL-12 的分泌增强,但 IFN-γ、IL-5 和 IL-6 的分泌没有明显影响。此外,口服 BIM 后派尔氏结中 CD4(+)CD45RB(high)T 细胞的数量增加。这些数据表明,BIM 给药影响 CD4(+)T 细胞。总的来说,结果表明口服 BIM 诱导 PP 细胞中的 CD4(+)改变其细胞表面抗原的表达和细胞因子的产生。