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10.1038/ncomms12623

http://scihub22266oqcxt.onion/10.1038/ncomms12623
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C4999515!4999515!27554168
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suck abstract from ncbi


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pmid27554168      Nat+Commun 2016 ; 7 (ä): ä
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  • Graft-infiltrating host dendritic cells play a key role in organ transplant rejection #MMPMID27554168
  • Zhuang Q; Liu Q; Divito SJ; Zeng Q; Yatim KM; Hughes AD; Rojas-Canales DM; Nakao A; Shufesky WJ; Williams AL; Humar R; Hoffman RA; Shlomchik WD; Oberbarnscheidt MH; Lakkis FG; Morelli AE
  • Nat Commun 2016[]; 7 (ä): ä PMID27554168show ga
  • Successful engraftment of organ transplants has traditionally relied on preventing the activation of recipient (host) T cells. Once T-cell activation has occurred, however, stalling the rejection process becomes increasingly difficult, leading to graft failure. Here we demonstrate that graft-infiltrating, recipient (host) dendritic cells (DCs) play a key role in driving the rejection of transplanted organs by activated (effector) T cells. We show that donor DCs that accompany heart or kidney grafts are rapidly replaced by recipient DCs. The DCs originate from non-classical monocytes and form stable, cognate interactions with effector T cells in the graft. Eliminating recipient DCs reduces the proliferation and survival of graft-infiltrating T cells and abrogates ongoing rejection or rejection mediated by transferred effector T cells. Therefore, host DCs that infiltrate transplanted organs sustain the alloimmune response after T-cell activation has already occurred. Targeting these cells provides a means for preventing or treating rejection.
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