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ARS Home » Northeast Area » Beltsville, Maryland (BARC) » Beltsville Agricultural Research Center » Animal Biosciences & Biotechnology Laboratory » Research » Publications at this Location » Publication #279893

Title: Characterization of chicken dendritic cell markers

item Lillehoj, Hyun
item Lee, Sung

Submitted to: Journal of Immunology
Publication Type: Peer Reviewed Journal
Publication Acceptance Date: 5/1/2012
Publication Date: 5/4/2012
Citation: Lillehoj, H.S., Lee, S.H. 2012. Characterization of chicken dendritic cell markers. Journal of Immunology. 181(1):188.

Interpretive Summary:

Technical Abstract: Animal and Natural Resources Institute, ARS-USDA, Beltsville, MD, USA. New mouse monoclonal antibodies which detect CD80 and CD83 were developed to characterize chicken dendritic cells (DCs). The characteristics of these molecules have been studied in human, swine, ovine, feline, and canine but not in chickens. MAbs to chCD80 showed staining of chicken macrophage cell line (HD11), bursa, and spleen. onoclonal antibodies (MAbs) against chCD80 reduced chCD80’s ability inducing T cell proliferation and IFN-' production in blast chicken spleen cells, and no secretion in the HD11. Two mAbs, CD83-159 and CD83-227, reacted with a HD11 and recognized a single 53 kDa protein on Western blots of lysates from LPS-stimulated spleen mononuclear cells. Immunostaining of chicken secondary lymphoid organs identified CD80+ and CD83+cells with morphologic and subtissue localization properties comparable to mammalian DCs. In vitro stimulation of spleen monocytes with concanavalin A (Con A) decreased the percentage of CD83+ cells compared with cells treated with medium alone. Interestingly, spleen cells treated with Con A in the presence of chCD83-227 mAb exhibited decreased percentage of MHCII+ cells compared with cells treated with plus an isotype-matched negative control mAb. These mAbs will be useful for future investigations of DC maturation and mechanisms of action in chickens. (This project is funded by USDA-AFRI proposal #2010-65121-20649 and was carried out as part of the US Veterinary Immune Reagent Network,