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Emerging roles of lymphatic endothelium in regulating adaptive immunity
Catherine M. Card, … , Shann S. Yu, Melody A. Swartz
Catherine M. Card, … , Shann S. Yu, Melody A. Swartz
Published March 3, 2014
Citation Information: J Clin Invest. 2014;124(3):943-952. https://doi.org/10.1172/JCI73316.
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Emerging roles of lymphatic endothelium in regulating adaptive immunity

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Abstract

Emerging research on the roles of stromal cells in modulating adaptive immune responses has included a new focus on lymphatic endothelial cells (LECs). LECs are presumably the first cells that come into direct contact with peripheral antigens, cytokines, danger signals, and immune cells travelling from peripheral tissues to lymph nodes. LECs can modulate dendritic cell function, present antigens to T cells on MHC class I and MHC class II molecules, and express immunomodulatory cytokines and receptors, which suggests that their roles in adaptive immunity are far more extensive than previously realized. This Review summarizes the emergent evidence that LECs are important in maintaining peripheral tolerance, limiting and resolving effector T cell responses, and modulating leukocyte function.

Authors

Catherine M. Card, Shann S. Yu, Melody A. Swartz

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Figure 2

LECs actively recruit leukocytes.

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LECs actively recruit leukocytes.
Tissue-resident DCs (red) take up anti...
Tissue-resident DCs (red) take up antigens in peripheral tissues, home to nearby draining lymphatic vessels via CCL21-driven chemotaxis, and engage ICAM-1, VCAM, and Sema3A for transmigration. Under inflammatory conditions, LECs can increase their expression of adhesion molecules and chemokines that further promote the lymphatic recruitment of DCs and other cell subsets, including macrophages via CCL2. LEC expression of decoy receptors such as D6 helps limit local chemokine concentrations and shape gradients.

Copyright © 2025 American Society for Clinical Investigation
ISSN: 0021-9738 (print), 1558-8238 (online)

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