Chang Sun-Young, Cha Hye-Ran, Igarashi Osamu, Rennert Paul D, Kissenpfennig Adrien, Malissen Bernard, Nanno Masanobu, Kiyono Hiroshi, Kweon Mi-Na
Mucosal Immunology Section, International Vaccine Institute, Seoul, Republic of Korea.
J Immunol. 2008 Apr 1;180(7):4361-5. doi: 10.4049/jimmunol.180.7.4361.
Topical transcutaneous immunization (TCI) presents many clinical advantages, but its underlying mechanism remains unknown. TCI induced Ag-specific IgA Ab-secreting cells expressing CCR9 and CCR10 in the small intestine in a retinoic acid-dependent manner. These intestinal IgA Abs were maintained in Peyer's patch-null mice but abolished in the Peyer's patch- and lymph node-null mice. The mesenteric lymph node (MLN) was shown to be the site of IgA isotype class switching after TCI. Unexpectedly, langerin(+)CD8alpha(-) dendritic cells emerged in the MLN after TCI; they did not migrate from the skin but rather differentiated rapidly from bone marrow precursors. Depletion of langerin(+) cells impaired intestinal IgA Ab responses after TCI. Taken together, these findings suggest that MLN is indispensable for the induction of intestinal IgA Abs following skin immunization and that cross-talk between the skin and gut immune systems might be mediated by langerin(+) dendritic cells in the MLN.
局部经皮免疫(TCI)具有许多临床优势,但其潜在机制尚不清楚。TCI 以视黄酸依赖的方式在小肠中诱导表达 CCR9 和 CCR10 的抗原特异性 IgA 抗体分泌细胞。这些肠道 IgA 抗体在派氏结缺失的小鼠中得以维持,但在派氏结和淋巴结均缺失的小鼠中消失。肠系膜淋巴结(MLN)被证明是 TCI 后 IgA 同种型类别转换的部位。出乎意料的是,TCI 后 MLN 中出现了 langerin(+)CD8alpha(-)树突状细胞;它们并非从皮肤迁移而来,而是迅速从骨髓前体分化而来。去除 langerin(+)细胞会损害 TCI 后的肠道 IgA 抗体反应。综上所述,这些发现表明 MLN 对于皮肤免疫后肠道 IgA 抗体的诱导不可或缺,并且皮肤和肠道免疫系统之间的相互作用可能由 MLN 中的 langerin(+)树突状细胞介导。