MD Zhen-Yi Wang (Professor of Haematology and Pathophysiology, Honorary Director) , MD Zhi-Xiang Shen (Professor, Chief)
{"title":"5 Megakaryocytes and platelets in immune thrombocytopenic purpura","authors":"MD Zhen-Yi Wang (Professor of Haematology and Pathophysiology, Honorary Director) , MD Zhi-Xiang Shen (Professor, Chief)","doi":"10.1016/S0950-3536(97)80052-2","DOIUrl":null,"url":null,"abstract":"<div><p>In idiopathic thrombocytopenic purpura, 90% of the patients have an elevated platelet-associated immunoglobulin. The most important related antigens are glycoprotein IIb-IIIa (GPIIb-IIIa) (16.7–83.3%), GPIb-IX (13.3–83%), GPIb (3.3–47.1%) and GPIIIa (21.6–33.3%), and less commonly GPIa-IIa, GPIV and GPV. Other related antigens can be platelet granule membrane protein, phospholipid, intraplatelet and cytoplasmic antigens, and rarely human platelet antigen (HPA) la and HLA-DR antigens. The marrow megakaryocytes are usually normal or increased in number with maturation impairment. There are discrepancies regarding megakaryocytopoiesis in vitro. A low dose of heparin could elevate the platelet number in certain cases. The expression of c-<em>sis</em> was reported to be inhibited in ITP, when the plasma β-thromboglobin-platelet factor 4 level was elevated.</p><p>In secondary immune thrombocytopenia, platelet antibodies can be (1) alloantibodies against the (HPA) system and (2) autoantibodies most commonly against platelet GPIIb-IIIa or GPIb-IX. Other antigens can be 30–52 kDa proteins of the platelet membrane. Platelet survival is usually shortened, and marrow megakaryocytes are normal in number. Megakaryocyte colony-forming units could be reduced.</p></div>","PeriodicalId":77029,"journal":{"name":"Bailliere's clinical haematology","volume":"10 1","pages":"Pages 89-107"},"PeriodicalIF":0.0000,"publicationDate":"1997-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0950-3536(97)80052-2","citationCount":"23","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bailliere's clinical haematology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0950353697800522","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 23
Abstract
In idiopathic thrombocytopenic purpura, 90% of the patients have an elevated platelet-associated immunoglobulin. The most important related antigens are glycoprotein IIb-IIIa (GPIIb-IIIa) (16.7–83.3%), GPIb-IX (13.3–83%), GPIb (3.3–47.1%) and GPIIIa (21.6–33.3%), and less commonly GPIa-IIa, GPIV and GPV. Other related antigens can be platelet granule membrane protein, phospholipid, intraplatelet and cytoplasmic antigens, and rarely human platelet antigen (HPA) la and HLA-DR antigens. The marrow megakaryocytes are usually normal or increased in number with maturation impairment. There are discrepancies regarding megakaryocytopoiesis in vitro. A low dose of heparin could elevate the platelet number in certain cases. The expression of c-sis was reported to be inhibited in ITP, when the plasma β-thromboglobin-platelet factor 4 level was elevated.
In secondary immune thrombocytopenia, platelet antibodies can be (1) alloantibodies against the (HPA) system and (2) autoantibodies most commonly against platelet GPIIb-IIIa or GPIb-IX. Other antigens can be 30–52 kDa proteins of the platelet membrane. Platelet survival is usually shortened, and marrow megakaryocytes are normal in number. Megakaryocyte colony-forming units could be reduced.