Guarda Greta, Hons Miroslav, Soriano Silvia F, Huang Alex Y, Polley Rosalind, Martín-Fontecha Alfonso, Stein Jens V, Germain Ronald N, Lanzavecchia Antonio, Sallusto Federica
Institute for Research in Biomedicine, CH-6500 Bellinzona, Switzerland.
Nat Immunol. 2007 Jul;8(7):743-52. doi: 10.1038/ni1469. Epub 2007 May 27.
T lymphocytes lacking the lymph node-homing receptors L-selectin and CCR7 do not migrate to lymph nodes in the steady state. Instead, we found here that lymph nodes draining sites of mature dendritic cells or adjuvant inoculation recruited L-selectin-negative CCR7- effector and memory CD8+ T cells. This recruitment required CXCR3 expression on T cells and occurred through high endothelial venules in concert with lumenal expression of the CXCR3 ligand CXCL9. In reactive lymph nodes, recruited T cells established stable interactions with and killed antigen-bearing dendritic cells, limiting the ability of these dendritic cells to activate naive CD4+ and CD8+ T cells. The inducible recruitment of blood-borne effector and memory T cells to lymph nodes may represent a mechanism for terminating primary and limiting secondary immune responses.
缺乏淋巴结归巢受体L-选择素和CCR7的T淋巴细胞在稳态下不会迁移至淋巴结。相反,我们在此发现,引流成熟树突状细胞部位或接种佐剂部位的淋巴结会募集L-选择素阴性CCR7效应性和记忆性CD8⁺T细胞。这种募集需要T细胞上表达CXCR3,并且通过高内皮微静脉发生,同时CXCR3配体CXCL9在管腔内表达。在反应性淋巴结中,募集的T细胞与携带抗原的树突状细胞建立稳定的相互作用并将其杀伤,从而限制这些树突状细胞激活初始CD4⁺和CD8⁺T细胞的能力。血源性效应性和记忆性T细胞向淋巴结的可诱导募集可能代表了一种终止初次免疫反应并限制二次免疫反应的机制。