Lymphatic vessels and tertiary lymphoid organs
Identifieur interne : 002892 ( Main/Exploration ); précédent : 002891; suivant : 002893Lymphatic vessels and tertiary lymphoid organs
Auteurs : Nancy H. RuddleSource :
- The Journal of Clinical Investigation [ 0021-9738 ] ; 2014.
Descripteurs français
- KwdFr :
- Animaux, Humains, Inflammation (anatomopathologie), Lymphoedème (immunologie), Maladies auto-immunes (immunologie), Noeuds lymphatiques (immunologie), Tumeurs (anatomopathologie), Vaisseaux lymphatiques (anatomopathologie), Vaisseaux lymphatiques (immunologie), Vaisseaux lymphatiques (physiopathologie).
- MESH :
- anatomopathologie : Inflammation, Tumeurs, Vaisseaux lymphatiques.
- immunologie : Lymphoedème, Maladies auto-immunes, Noeuds lymphatiques, Vaisseaux lymphatiques.
- physiopathologie : Vaisseaux lymphatiques.
- Animaux, Humains.
English descriptors
- KwdEn :
- MESH :
- immunology : Autoimmune Diseases, Lymph Nodes, Lymphatic Vessels, Lymphedema.
- pathology : Inflammation, Lymphatic Vessels, Neoplasms.
- physiopathology : Lymphatic Vessels.
- Animals, Humans.
Abstract
Tertiary lymphoid organs (TLOs) are accumulations of lymphoid cells in chronic inflammation that resemble LNs in their cellular content and organization, high endothelial venules, and lymphatic vessels (LVs). Although acute inflammation can result in defective LVs, TLO LVs appear to function normally in that they drain fluid and transport cells that respond to chemokines and sphingosine-1-phosphate (S1P) gradients. Molecular regulation of TLO LVs differs from lymphangiogenesis in ontogeny with a dependence on cytokines and hematopoietic cells. Ongoing work to elucidate the function and molecular regulation of LVs in TLOs is providing insight into therapies for conditions as diverse as lymphedema, autoimmunity, and cancer.
Url:
DOI: 10.1172/JCI71611
PubMed: 24590281
PubMed Central: 3934190
Affiliations:
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Le document en format XML
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<term>Lymph Nodes (immunology)</term>
<term>Lymphatic Vessels (immunology)</term>
<term>Lymphatic Vessels (pathology)</term>
<term>Lymphatic Vessels (physiopathology)</term>
<term>Lymphedema (immunology)</term>
<term>Neoplasms (pathology)</term>
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<term>Humains</term>
<term>Inflammation (anatomopathologie)</term>
<term>Lymphoedème (immunologie)</term>
<term>Maladies auto-immunes (immunologie)</term>
<term>Noeuds lymphatiques (immunologie)</term>
<term>Tumeurs (anatomopathologie)</term>
<term>Vaisseaux lymphatiques (anatomopathologie)</term>
<term>Vaisseaux lymphatiques (immunologie)</term>
<term>Vaisseaux lymphatiques (physiopathologie)</term>
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<keywords scheme="MESH" qualifier="anatomopathologie" xml:lang="fr"><term>Inflammation</term>
<term>Tumeurs</term>
<term>Vaisseaux lymphatiques</term>
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<term>Noeuds lymphatiques</term>
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<term>Lymph Nodes</term>
<term>Lymphatic Vessels</term>
<term>Lymphedema</term>
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<front><div type="abstract" xml:lang="en"><p>Tertiary lymphoid organs (TLOs) are accumulations of lymphoid cells in chronic inflammation that resemble LNs in their cellular content and organization, high endothelial venules, and lymphatic vessels (LVs). Although acute inflammation can result in defective LVs, TLO LVs appear to function normally in that they drain fluid and transport cells that respond to chemokines and sphingosine-1-phosphate (S1P) gradients. Molecular regulation of TLO LVs differs from lymphangiogenesis in ontogeny with a dependence on cytokines and hematopoietic cells. Ongoing work to elucidate the function and molecular regulation of LVs in TLOs is providing insight into therapies for conditions as diverse as lymphedema, autoimmunity, and cancer.</p>
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