The anti-microbial peptide LL-37 modulates immune responses in the palatine tonsils where it is exclusively expressed by neutrophils and a subset of dendritic cells.

To access publisher full text version of this article. Please click on the hyperlink in Additional Links field. Antimicrobial peptides are essential elements of epithelial defense against invading micro-organisms. The palatine tonsils are positioned at the entry of the airway and the gut and as such...

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Bibliographic Details
Published in:Clinical Immunology
Main Authors: Sigurdardottir, Sigrun L, Thorleifsdottir, Ragna H, Guzman, Andrew M, Gudmundsson, Gudmundur H, Valdimarsson, Helgi, Johnston, Andrew
Other Authors: Department of Immunology, Landspitali-University Hospital, Reykjavik, Iceland.
Format: Article in Journal/Newspaper
Language:English
Published: Elsevier Science 2012
Subjects:
Antimicrobial Cationic Peptides
Chemokine CXCL5
Chemokine CXCL9
Dendritic Cells
Down-Regulation
Epithelium
GTP-Binding Proteins
Humans
Interferon-gamma
Leukocytes
Mononuclear
Neutrophils
Palatine Tonsil
Receptors
CCR4
CCR6
Up-Regulation
Iceland
Online Access:http://hdl.handle.net/2336/238368
https://doi.org/10.1016/j.clim.2011.09.013
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Summary:To access publisher full text version of this article. Please click on the hyperlink in Additional Links field. Antimicrobial peptides are essential elements of epithelial defense against invading micro-organisms. The palatine tonsils are positioned at the entry of the airway and the gut and as such are ideally situated to act as immune sentinels in the pharynx protecting against microbial invasion. Tonsils express a number of antimicrobial peptides including hCAP18/LL-37. Here we clearly define the expression of hCAP18/LL-37 in the tonsils showing unequivocally that hCAP18/LL-37 is mainly expressed by infiltrating neutrophils and follicular CD11c+CD13+HLA-DR+ dendritic cells, rarely by macrophages, and never by the epithelium itself. To explore possible functions for follicle-derived LL-37, we stimulated tonsil mononuclear cells with LL-37 in vitro and observed the secretion of the proinflammatory cytokines CCL5 and CXCL9, expression of IFN-γ and MX-1 and down-regulation of chemokine receptors CCR4 and CCR6 which are involved in tissue-selective T cell trafficking. Taken together, these data illustrate new potential immunoregulatory functions for hCAP18/LL-37 in the tonsils. Icelandic Research Fund 080448021-23, Landspitali University Hospital, University of Iceland, Babcock Endowment Fund

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