Kreisel Daniel, Richardson Steven B, Li Wenjun, Lin Xue, Kornfeld Christopher G, Sugimoto Seiichiro, Hsieh Chyi-Song, Gelman Andrew E, Krupnick Alexander S
Department of Surgery, Washington University School of Medicine, St. Louis, MO 63110, USA.
J Immunol. 2010 Oct 1;185(7):3809-13. doi: 10.4049/jimmunol.1000971. Epub 2010 Sep 1.
The interaction of CD4(+) T cells with MHC class II (MHCII)-expressing hematopoietic APCs plays a critical role in both the generation of protective immune responses and maintenance of tolerance in the lung. The functional significance of MHCII expression by nonhematopoietic stromal cells, however, has not been defined in vivo. Using a novel mouse model of orthotopic left lung transplantation, we demonstrate that selective elimination of MHCII expression on nonhematopoietic cells leads to an inflammatory response as a result of reduced peripheral generation of regulatory CD4(+) T cells. Absence of MHCII expression on nonhematopoietic cells also inhibits local growth of metastatic pulmonary tumor. These findings indicate that nonhematopoietic cells play a previously unrecognized role in downregulating inflammatory responses in nonlymphoid tissues.
CD4(+) T细胞与表达主要组织相容性复合体II类分子(MHCII)的造血抗原呈递细胞(APC)之间的相互作用,在肺部保护性免疫反应的产生和耐受性的维持中均起着关键作用。然而,非造血基质细胞表达MHCII的功能意义在体内尚未明确。利用一种新型的原位左肺移植小鼠模型,我们证明非造血细胞上MHCII表达的选择性消除,会因调节性CD4(+) T细胞外周生成减少而导致炎症反应。非造血细胞上缺乏MHCII表达也会抑制转移性肺肿瘤的局部生长。这些发现表明,非造血细胞在下调非淋巴组织中的炎症反应方面发挥了以前未被认识到的作用。