| Literature DB >> 27038460 |
Anton Neschadim1, Donald R Branch1,2,3.
Abstract
Immune thrombocytopenia (ITP) is a debilitating, life-threatening autoimmune disorder affecting more than 4 in every 100,000 adults annually, stemming from the production of antiplatelet antibody resulting in accelerated platelet destruction and thrombocytopenia. Numerous animal models of ITP have been developed that contributed to the basic understanding of the underlying mechanisms of ITP onset, progression, and maintenance. Rodent models that develop ITP spontaneously, or by passive transfer of an antiplatelet sera or antibody, play an instrumental role in the investigation of ITP mechanisms responsible for the breakdown of tolerance in human ITP, in studies of the immunopathology underlying the progression of platelet destruction, and in elucidation of the mechanisms of therapeutic amelioration of ITP by existing and new therapeutic modalities. This unit captures the protocols for the implementation and readout of passive antibody transfer mouse models of ITP, established by the infusion of a commercially-available monoclonal rat anti-mouse CD41 platelet antibody.Entities:
Keywords: ITP; IVIg; autoimmune disease: mouse model; immune thrombocytopenia; intravenous immunoglobulin; platelets
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Year: 2016 PMID: 27038460 DOI: 10.1002/0471142735.im1530s113
Source DB: PubMed Journal: Curr Protoc Immunol ISSN: 1934-3671