Futagawa Toshiro, Akiba Hisaya, Kodama Tomohiro, Takeda Kazuyoshi, Hosoda Yasuyuki, Yagita Hideo, Okumura Ko
Department of Immunology, Juntendo University School of Medicine, 2-1-1 Hongo, Bunkyo-ku, Tokyo 113-8421, Japan.
Int Immunol. 2002 Mar;14(3):275-86. doi: 10.1093/intimm/14.3.275.
4-1BB (CDw137) and its ligand (4-1BBL) have been implicated in cellular immune responses. To further characterize the expression and function of 4-1BBL, we newly generated an anti-mouse 4-1BBL mAb (TKS-1), which can inhibit the interaction of 4-1BBL with 4-1BB. Flow cytometric analyses using TKS-1 and an anti-mouse 4-1BB mAb indicated that 4-1BB was inducible on both CD4(+) and CD8(+) splenic T cells by stimulation with immobilized anti-CD3 mAb, but 4-1BBL was not expressed on resting or activated T cells. 4-1BBL expression was inducible on splenic B cells by stimulation with anti-IgM antibody plus anti-CD40 mAb, on peritoneal macrophages by stimulation with lipopolysaccharide (LPS) and on splenic dendritic cells (DC) by stimulation with anti-CD40 mAb or LPS. Interestingly, splenic DC expressed 4-1BB constitutively, which was down-regulated by anti-CD40 stimulation. Co-culture of splenic DC with 4-1BBL-transfected cells or 4-1BBL-expressing tumor cell lines led to cytokine (IL-6 and IL-12) production and co-stimulatory molecule up-regulation by splenic DC, indicating that 4-1BBL can directly activate DC. Moreover, IL-12 production by anti-CD40-stimulated DC was partially inhibited by TKS-1. These results suggest that 4-1BB expressed on DC may be involved in DC activation through DC--tumor interaction and DC--DC interaction.
4-1BB(CDw137)及其配体(4-1BBL)与细胞免疫反应有关。为了进一步表征4-1BBL的表达和功能,我们新制备了一种抗小鼠4-1BBL单克隆抗体(TKS-1),它可以抑制4-1BBL与4-1BB的相互作用。使用TKS-1和抗小鼠4-1BB单克隆抗体进行的流式细胞术分析表明,通过固定化抗CD3单克隆抗体刺激,CD4(+)和CD8(+)脾T细胞上均可诱导4-1BB表达,但静息或活化的T细胞上不表达4-1BBL。用抗IgM抗体加抗CD40单克隆抗体刺激可诱导脾B细胞表达4-1BBL,用脂多糖(LPS)刺激可诱导腹腔巨噬细胞表达4-1BBL,用抗CD40单克隆抗体或LPS刺激可诱导脾树突状细胞(DC)表达4-1BBL。有趣的是,脾DC组成性表达4-1BB,抗CD40刺激可使其下调。脾DC与4-1BBL转染细胞或表达4-1BBL的肿瘤细胞系共培养可导致脾DC产生细胞因子(IL-6和IL-12)并上调共刺激分子,表明4-1BBL可直接激活DC。此外,TKS-1可部分抑制抗CD40刺激的DC产生IL-12。这些结果表明,DC上表达的4-1BB可能通过DC-肿瘤相互作用和DC-DC相互作用参与DC激活。