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Human Flt-3-ligand-mobilized dendritic cells require additional activation to drive effective immune responses


Diener, KR and Moldenhauer, L and Lyons, AB and Brown, MP and Hayball, JD, Human Flt-3-ligand-mobilized dendritic cells require additional activation to drive effective immune responses, Experimental Hematology, 36, (1) pp. 51-60. ISSN 0301-472X (2008) [Refereed Article]

DOI: doi:10.1016/j.exphem.2007.08.024


OBJECTIVE: Dendritic cells (DCs) play a pivotal role in the induction of immunity in response to pathogenic challenge or vaccination. As such, the fms-like tyrosine kinase 3-ligand (Flt-3L) has been used to increase DC populations in vivo, with contrasting outcomes, which include an increase in immunity, tolerance induction, or expansion of regulatory cells. This study examines the adjuvant role that human Flt-3L (hFL) administration has in generating immune responses upon immunization with a poorly immunogenic and soluble protein antigen. MATERIALS AND METHODS: Mice were immunized with the nominal antigen, ovalbumin, alone or with antigen emulsified in complete Freund's adjuvant (CFA), with or without prior hFL-mediated expansion of DC subsets. The maturation of DC subsets and activation status of antigen-specific T cells were analyzed by flow cytometry, with effector function assessed in cytolytic T-lymphocyte assays. RESULTS: hFL treatment expanded both conventional DC and plasmacytoid DC in vivo, resulting in increased antigen presentation by both direct and cross-presentation pathways. However, it was only in the context of CFA that antigen immunization could mature DCs and subsequently fully activate antigen-specific T cells with enhanced cytolytic activity. CONCLUSIONS: Our studies reveal that hFL essentially acts as a coadjuvant, as hFL augments the size of an immune response but requires further adjuvant activation to alter the quality of the response

Item Details

Item Type:Refereed Article
Research Division:Biomedical and Clinical Sciences
Research Group:Immunology
Research Field:Applied immunology (incl. antibody engineering, xenotransplantation and t-cell therapies)
Objective Division:Health
Objective Group:Clinical health
Objective Field:Clinical health not elsewhere classified
UTAS Author:Lyons, AB (Associate Professor Bruce Lyons)
ID Code:73627
Year Published:2008
Web of Science® Times Cited:16
Deposited By:Medicine
Deposited On:2011-10-19
Last Modified:2011-10-19

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