Human Tissues Contain CD141hi Cross-Presenting Dendritic Cells with Functional Homology to Mouse CD103+ Nonlymphoid Dendritic Cells

Muzlifah Haniffa(Agency for Science, Technology and Research), Amanda Shin(Agency for Science, Technology and Research), Venetia Bigley(Newcastle University), Naomi McGovern(Newcastle University), Pearline Teo(Agency for Science, Technology and Research), Peter See(Agency for Science, Technology and Research), Pavandip Singh Wasan(Agency for Science, Technology and Research), Xiao-Nong Wang(Newcastle University), Frano Malinarich(Agency for Science, Technology and Research), Benoît Malleret(Agency for Science, Technology and Research), Anis Larbi(Agency for Science, Technology and Research), Pearlie W.W. Tan(Singapore General Hospital), Helen Zhao(Agency for Science, Technology and Research), Michael Poidinger(Agency for Science, Technology and Research), Sarah Pagan(Newcastle University), Sharon Cookson(Newcastle University), Rachel Dickinson(Newcastle University), Ian Dimmick(Newcastle University), Ruth F. Jarrett(MRC University of Glasgow Centre for Virus Research), Laurent Rénia(Agency for Science, Technology and Research), John Kit Chung Tam(National University of Singapore), Colin Song(Singapore General Hospital), John E. Connolly(Agency for Science, Technology and Research), Jerry Kok Yen Chan(National University of Singapore), Adam J. Gehring(Agency for Science, Technology and Research), Antonio Bertoletti(Agency for Science, Technology and Research), Matthew Collin(Newcastle University), Florent Ginhoux(Agency for Science, Technology and Research)
Immunity
July 1, 2012
Cited by 693Open Access
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Abstract

Dendritic cell (DC)-mediated cross-presentation of exogenous antigens acquired in the periphery is critical for the initiation of CD8(+) T cell responses. Several DC subsets are described in human tissues but migratory cross-presenting DCs have not been isolated, despite their potential importance in immunity to pathogens, vaccines, and tumors and tolerance to self. Here, we identified a CD141(hi) DC present in human interstitial dermis, liver, and lung that was distinct from the majority of CD1c(+) and CD14(+) tissue DCs and superior at cross-presenting soluble antigens. Cutaneous CD141(hi) DCs were closely related to blood CD141(+) DCs, and migratory counterparts were found among skin-draining lymph node DCs. Comparative transcriptomic analysis with mouse showed tissue DC subsets to be conserved between species and permitted close alignment of human and mouse DC subsets. These studies inform the rational design of targeted immunotherapies and facilitate translation of mouse functional DC biology to the human setting.


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