Human Beta Defensin 3 induces maturation of human langerhans cell like dendritic cells: An antimicrobial peptide that functions as an endogenous adjuvant

Autor: Adriana T. Larregina, Eric Fluharty, Yvonne K. Mburu, Alicia R. Mathers, Robert L. Ferris, Louis D. Falo, Laura K. Ferris
Jazyk: angličtina
Rok vydání: 2012
Předmět:
Langerhans cell
beta-Defensins
MAP Kinase Signaling System
T-Lymphocytes
Antimicrobial peptides
Human skin
chemical and pharmacologic phenomena
Dermatology
Biology
GTP-Binding Protein alpha Subunits
Gi-Go

Biochemistry
Article
Immunophenotyping
03 medical and health sciences
Interferon-gamma
0302 clinical medicine
Immune system
Adjuvants
Immunologic

Cell Movement
medicine
Humans
Molecular Biology
030304 developmental biology
Cell Proliferation
0303 health sciences
Innate immune system
integumentary system
Chemokine CCL21
CCL19
NF-kappa B
Cell Polarity
Cell Biology
Acquired immune system
3. Good health
Cell biology
Beta defensin
medicine.anatomical_structure
Langerhans Cells
Immunology
Skin-derived dendritic cells
Myeloid Differentiation Factor 88
Human beta-defensin 3
Chemokine CCL19
Immunization
030215 immunology
Antimicrobial Cationic Peptides
Zdroj: The Journal of investigative dermatology
ISSN: 1523-1747
0022-202X
Popis: Human beta-defensins (hBDs) are antimicrobial peptides that have an important role in innate immune responses at epithelial barriers such as the skin. However, the role that hBDs have in initiating cellular immune responses that contribute to antigen-specific adaptive immunity is not well understood. Here we show that one member of the hBD family, hBD3, can induce maturation and T-helper type 1 skewing function in human Langerhans cell–like dendritic cells (LC-DCs). Specifically, hBD3 potently induces phenotypic maturation of LC-DCs, including increased expression of CCR7, which mediates functional chemotactic responses to CCL19 and CCL21. hBD3-stimulated LC-DCs induce strong proliferation of and IFN-γ secretion by naive human T cells. hBD3 also induces phenotypic maturation of primary human skin–migratory DCs derived from human skin explants. These results suggest an important role for hBD3 in inducing DC activation, migration, and polarization. Thus, hBD3 contributes to the integration of innate and adaptive immune responses in the skin, and may be a useful adjuvant for skin immunization and an important factor in the pathophysiology of inflammatory skin diseases.
Databáze: OpenAIRE