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Role of complement in patients with autoimmune hemolytic anemia and platelet transfusion refractoriness
被引:0
|作者:
Fontaine, Magali J.
[1
]
机构:
[1] Univ Maryland, Sch Med, Dept Pathol, 22 S Greene St N2W50a, Baltimore, MD 21201 USA
关键词:
Complement;
Hemolysis;
Autoimmune;
Platelet transfusion refractoriness;
HLA ANTIBODIES;
IMMUNE;
ALLOIMMUNIZATION;
AUTOANTIBODIES;
MANAGEMENT;
MECHANISMS;
FAILURE;
BLOOD;
D O I:
10.1016/j.tracli.2019.06.232
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
The complement is a key player of the innate immune response. It provides defense mechanisms that are not specific, but very efficient at neutralizing any invader, accounting for 4% of the proteins in the peripheral blood. Nevertheless, there is a dark side to the complement system, as it may activate its machinery against healthy cells such as peripheral blood red blood cells and platelets resulting in undesired hemolysis and thrombocytopenia, respectively. Understanding and identifying the role of complement in these settings allow physicians to adjust their diagnostic and therapeutic modalities accordingly. The role of complement in the pathophysiology and management of autoimmune hemolytic anemia and of alloimmune-mediated thrombocytopenia is under investigation and discussed. (C) 2019 Societe francaise de transfusion sanguine (SFTS). Published by Elsevier Masson SAS. All rights reserved.
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页码:152 / 154
页数:3
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