## Abstract Understanding of biomaterial adjuvant effect and its mechanisms is essential for the effective design and selection of appropriate materials for specific applications. We have previously shown that poly(lactic‐__co__‐glycolic acid) (PLGA), one of the most commonly studied polymers in ti
Poly(lactic-co-glycolic acid) enhances maturation of human monocyte-derived dendritic cells
✍ Scribed by Yoshida, Mutsumi ;Babensee, Julia E.
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 307 KB
- Volume
- 71A
- Category
- Article
- ISSN
- 0021-9304
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✦ Synopsis
Abstract
Immature dendritic cells (iDCs) were derived from human peripheral blood monocytes, and treated with 75:25 poly(lactic‐co‐glycolic acid) (PLGA) microparticles (MPs) or film to assess the resultant dendritic cell (DC) maturation as compared to positive control of lipopolysaccharide (LPS) treatment for DC maturation or negative control of untreated iDCs. The effect of PLGA contact on DC maturation was examined as one possible explanation for the PLGA adjuvant effect we have observed in the enhancement of an immune response to codelivered model antigen, as adjuvants act through the maturation of DCs. Culturing iDCs with PLGA MPs or PLGA film resulted in morphology similar to that of LPS‐matured DCs and the association, or possible internalization, of PLGA MPs. Furthermore, biomaterial‐treated iDCs demonstrated an increase in MHC class II and costimulatory molecule expression compared to iDCs but to a lower level than that of LPS‐matured DCs. Direct iDC contact with PLGA MPs was necessary for maturation. Immature DCs exposed to PLGA MPs were stimulatory of allogeneic T‐cell proliferation, whereas cells exposed to PLGA film were not. Further, PLGA MPs supported a moderate delayed type hypersensitivity reaction in mice indicative of in vivo DC maturation. Taken together, these results suggest that PLGA is a DC maturation stimulus and that the form of the biomaterial may influence the extent of DC maturation. © 2004 Wiley Periodicals, Inc. J Biomed Mater Res 71A: 45–54, 2004
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