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Alteration of Lymphocyte Trafficking by Sphingosine- 1-Phosphate Receptor Agonists

机译:鞘氨醇-1-磷酸受体激动剂对淋巴细胞运输的影响

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摘要

Blood lymphocyte numbers, essential for the development of efficient immune responses, are maintained by recirculation through secondary lymphoid organs. We show that lymphocyte trafficking is altered by the lysophospholipid sphingosine- 1- phosphate (S1P) and by a phosphoryl metabolite of the immunosuppressive agent FTY720. Both species were high-affinity agonists of at least four of the five S1P receptors. These agonists produce lymphopenia in blood and thoracic duct Lymph by sequestration of lymphocytes in lymph nodes, but not spleen. S1P Receptor agonists induced emptying of lymphoid sinuses by retention of lympho- Cytes on the abluminal side of sinus-lining endothelium and inhibition of egress into Lymph. Inhibition of lymphocyte recirculation by activation of S1P receptors may Result in therapeutically useful immunosuppresison.
机译:通过有效的继发性淋巴器官再循环,可以维持有效的免疫应答发展所必需的血淋巴细胞数量。我们显示淋巴细胞运输被溶血磷脂鞘氨醇-1-磷酸(S1P)和免疫抑制剂FTY720的磷酰基代谢物改变。两种物种都是五个S1P受体中至少四个的高亲和力激动剂。这些激动剂通过螯合淋巴结而不是脾脏中的淋巴细胞而在血液和胸导管淋巴中产生淋巴细胞减少症。 S1P受体激动剂通过将淋巴细胞保留在鼻窦衬里的内皮小腔侧并抑制进入淋巴而诱导淋巴窦排空。通过激活S1P受体来抑制淋巴细胞再循环可能会导致治疗上有用的免疫抑制。

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