Identification of the target self-antigens in reperfusion injury

被引:176
作者
Zhang, M
Alicot, EM
Chiu, I
Li, JN
Verna, N
Vorup-Jensen, T
Kessler, B
Shimaoka, M
Chan, R
Friend, D
Mahmood, U
Weissleder, R
Moore, FD
Carroll, MC [1 ]
机构
[1] CBR Inst Biomed Res Inc, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dept Pathol, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Dept Surg, Boston, MA 02115 USA
[4] Harvard Univ, Sch Med, Dept Pediat, Boston, MA 02115 USA
[5] Harvard Univ, Sch Med, Brigham & Womens Hosp, Boston, MA 02115 USA
[6] Massachusetts Gen Hosp, Ctr Mol Imaging Res, Boston, MA 02129 USA
[7] Harvard Univ, Sch Med, Boston, MA 02129 USA
[8] Declmmune Therapeut, Boston, MA 02115 USA
关键词
D O I
10.1084/jem.20050390
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Reperfusion injury ( RI), a potential life-threatening disorder, represents an acute inflammatory response after periods of ischemia resulting from myocardial infarction, stroke, surgery, or trauma. The recent identification of a monoclonal natural IgM that initiates RI led to the identification of nonmuscle myosin heavy chain type II A and C as the self-targets in two different tissues. These results identify a novel pathway in which the innate response to a highly conserved self-antigen expressed as a result of hypoxic stress results in tissue destruction.
引用
收藏
页码:141 / 152
页数:12
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