Anti-GPVI-associated ITP:: an acquired platelet disorder caused by autoantibody-mediated clearance of the GPVI/FcRγ-chain complex from the human platelet surface

被引:114
作者
Boylan, B
Chen, H
Rathore, V
Paddock, C
Salacz, M
Friedman, KD
Curtis, BR
Stapleton, M
Newman, DK
Kahn, ML
Newman, PJ
机构
[1] Blood Ctr SE Wisconsin Inc, Blood Res Inst, Milwaukee, WI 53201 USA
[2] Univ Penn, Dept Med, Div Cardiol, Philadelphia, PA 19104 USA
[3] Med Coll Wisconsin, Dept Med, Milwaukee, WI 53226 USA
[4] Med Coll Wisconsin, Dept Microbiol, Milwaukee, WI 53226 USA
[5] Med Coll Wisconsin, Dept Pharmacol, Milwaukee, WI 53226 USA
[6] Med Coll Wisconsin, Dept Cellular Biol, Milwaukee, WI 53226 USA
[7] Med Coll Wisconsin, Cardiovasc Res Ctr, Milwaukee, WI 53226 USA
关键词
D O I
10.1182/blood-2004-03-0896
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Platelet glycoprotein (GP) VI is a 62-kDa membrane glycoprotein that exists on both human and murine platelets in a noncovalent complex with the Fc receptor (FcR) gamma chain. The GPVI/FcRgamma-chain complex serves as the major activating receptor for Collagen, as evidenced by observations that platelets genetically deficient in GPVI or the FCRgamma Chain are highly refractory to collagen-induced platelet activation. Recently, several different rat anti-murine GPVI monoclonal antibodies, termed JAQs 1, 2, and 3, were produced that had the unique property of "immunodepleting" GPVI from the murine platelet surface and rendering it unresponsive to Collagen or GPVI-specific agonists like convuixin or collagen-related peptide (CRP). Herein, we describe a patient with a mild bleeding disorder and a moderately reduced platelet count whose platelets fail to become activated in response to Collagen or CRP and inefficiently adhere to and form thrombi on immobilized Collagen under conditions of arterial shear. Although the amount of GPVI platelet mRNA and the nucleotide sequence of the GPVI gene were found to be normal, both GPVI and the FcRgamma chain were nearly absent from the platelet surface and were markedly reduced in whole-platelet detergent lysates. Patient plasma contained an autoantibody that bound specifically to GPVI-positive, normal platelets, and cleared soluble GPVI from the plasma, suggesting that the patient suffers from a rare form of idiopathic thrombocytopenic purpura caused by a GPVI-specific autoantibody that mediates clearance of the GPVI/FCRgamma-chain complex from the platelet surface. Since antibody-induced GPVI shedding now has been demonstrated in both, humans and mice, these studies may provide a rationale for developing therapeutic reagents that induce temporary depletion of GPVI for the treatment of clinical thrombosis. (C) 2004 by The American Society of Hematology.
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收藏
页码:1350 / 1355
页数:6
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