作者
Hehua Dai,Peixiang Lan,Daqiang Zhao,Khodor I. Abou-Daya,Wentao Liu,Wenhao Chen,Andrew J. Friday,Amanda Williams,Tao Sun,Jianjiao Chen,Wei Chen,Steven Mortin-Toth,Jayne S. Danska,Chris Wiebe,Peter Nickerson,Tengfang Li,Lisa Mathews,Hēth Turnquist,Matthew L. Nicotra,Sébastien Gingras,Eiji Takayama,Hiromi Kubagawa,Mark J. Shlomchik,Martin H. Oberbarnscheidt,Li X,Fadi G. Lakkis
摘要
Innate immune cells remember Immunological memory is a phenomenon by which immune cells can quickly recognize an antigen that the host has previously encountered. Certain cells of the innate immune system exhibit memory-like responses know as trained immunity. Rapid, antigen-specific secondary (anamnestic) responses were long thought to be the domain of B and T cells. However, Dai et al. report that monocytes and macrophages can acquire memory specific for particular major histocompatibility complex I antigens using paired A-type immunoglobulin-like receptors (PIR-As) (see the Perspective by Dominguez-Andrés and Netea). This pathway contributes to recognition and rejection of allograft-transplanted tissue from a donor of the same species. Genetic depletion or blockade of PIR-As in mice diminished the rejection of kidney and heart allografts. This work, which expands immunological memory to include myeloid cells, points to targets that may improve organ transplantation outcomes in the future. Science , this issue p. 1122 ; see also p. 1052