CCL19型
促炎细胞因子
趋化因子
树突状细胞
C-C趋化因子受体7型
细胞生物学
CCL21型
生物
T细胞
免疫学
滤泡树突状细胞
免疫系统
抗原提呈细胞
炎症
趋化因子受体
作者
Benjamin J. Marsland,Patrick Bättig,Monika Bauer,Christiane Ruedl,Ute Lässing,Roger R. Beerli,Klaus Dietmeier,Lidia Ivanova,Thomas D. Pfister,Lorenz Vogt,Hideki Nakano,Chiara Nembrini,Philippe Saudan,Manfred Köpf,Martin F. Bachmann
出处
期刊:Immunity
[Cell Press]
日期:2005-04-01
卷期号:22 (4): 493-505
被引量:243
标识
DOI:10.1016/j.immuni.2005.02.010
摘要
Dendritic cells (DCs) are key instigators of adaptive immune responses. Using an alphaviral expression cloning technology, we have identified the chemokine CCL19 as a potent inducer of T cell proliferation in a DC-T cell coculture system. Subsequent studies showed that CCL19 enhanced T cell proliferation by inducing maturation of DCs, resulting in upregulation of costimulatory molecules and the production of proinflammatory cytokines. Moreover, CCL19 programmed DCs for the induction of T helper type (Th) 1 rather than Th2 responses. Importantly, only activated DCs that migrated from the periphery to draining lymph nodes, but not resting steady-state DCs residing within lymph nodes, expressed high levels of CCR7 in vivo and responded to CCL19 with the production of proinflammatory cytokines. Migrating DCs isolated from mice genetically deficient in CCL19 and CCL21 (plt/plt) presented an only partially mature phenotype, highlighting the importance of these chemokines for full DC maturation in vivo. Our findings indicate that CCL19 and CCL21 are potent natural adjuvants for terminal activation of DCs and suggest that chemokines not only orchestrate DC migration but also regulate their immunogenic potential for the induction of T cell responses.
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