Cutting edge: Uniqueness of lymphoid chemokine requirement for the initiation and maturation of nasopharynx-associated lymphoid tissue organogenesis

被引:34
作者
Fukuyama, Satoshi
Nagatake, Takahiro
Kim, Dong-Young
Takamura, Kaoru
Park, Eun Jeong
Kaisho, Tsuneyasu
Tanaka, Norimitsu
Kurono, Yuichi
Kiyono, Hiroshi
机构
[1] Univ Tokyo, Dept Microbiol & Immunol, Div Mucosal Immunol, Inst Med Sci,Minato Ku, Tokyo 1088639, Japan
[2] RIKEN, Res Ctr Allergy & Immunol, Yokohama, Kanagawa, Japan
[3] Kagoshima Univ, Grad Sch Med & Dent Sci, Dept Otolaryngol Head & Neck Surg, Kagoshima 890, Japan
关键词
D O I
10.4049/jimmunol.177.7.4276
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
CD3(-) CD4(+) CD45(+) inducer cells are required for the initiation of mucosa-associated organogenesis of both nasopharynx-associated lymphoid tissues (NALT) and Peyer's patches (PP) in the aerodigestive tract. CXCL13(-/-) mice and mice carrying the paucity of lymph node T cell (plt) mutation and lacking expression of CCL19 and CCL21 accumulate CD3(-) CD4(+) CD45(+) cells at the site of NALT but not of PP genesis. Although NALT was observed to develop in adult CXCL13(-/-) and plt/plt mice, the formation of germinal centers in CXCL13(-/-) mice was affected, and their population of B cells was much lower than in the NALT of CXCL13(+/-) mice. Similarly, fewer T cells were observed in the NALT of plt/plt mice than in control mice. These findings indicate that the initiation of NALT organogenesis is independent of CXCL13, CCL19, and CCL21. However, the expression of these lymphoid chemokines is essential for the maturation of NALT microarchitecture.
引用
收藏
页码:4276 / 4280
页数:5
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