PLATELET-BOUND IGM IN AUTOIMMUNE THROMBOCYTOPENIA
- 1 January 1983
- journal article
- research article
- Vol. 61 (1) , 119-124
Abstract
Elevated levels of platelet-bound IgG (PA-IgG) are a feature of autoimmune thrombocytopenia (ATP), but this does not occur in all cases. The role of platelet-bound IgM (PA-IgM) in these patients was investigated by using a quantitative enzyme-linked immunosorbent assay (ELISA). Determinations (45) of PA-IgM and PA-IgG were done on 24 patients with ATP. Elevated levels of PA-IgM were found in 93.3% of the determinations, while PA-IgG was elevated in only 71.7%. In 64.4% of determinations, both were elevated. Elevated PA-IgM or PA-IgG alone occurred in 28.9 and 6.7% of determinations, respectively. The frequent involvement of PA-IgM in ATP was shown; a complex interrelationship exists between the 2 Ig classes in ATP. Some of the possibilities that might explain this interrelationship are discussed.This publication has 15 references indexed in Scilit:
- Autoimmune Thrombocytopenia in PregnancyBritish Journal of Haematology, 1980
- A New Method for the Simultaneous Quantitation of Platelet‐bound Immunoglobuin (IgG) and Complement (C3) Employing an Enzyme‐linked Immunosorbent Assay (ELISA) ProcedureBritish Journal of Haematology, 1980
- COMPARISON OF 2 DIRECT ASSAYS FOR PLATELET-ASSOCIATED IGG (PAIGG) IN ASSESSMENT OF IMMUNE AND NON-IMMUNE THROMBOCYTOPENIA1980
- PLATELET ANTIBODIES IN IDIOPATHIC THROMBOCYTOPENIC PURPURA1980
- Immune ThrombocytopeniaNew England Journal of Medicine, 1979
- SOLID-PHASE RADIOIMMUNOASSAY FOR BOUND ANTI-PLATELET ANTIBODY - STUDIES ON 45 PATIENTS WITH AUTO-IMMUNE PLATELET DISORDERS1979
- PLATELET-BOUND COMPLEMENT (C3) IN IMMUNE THROMBOCYTOPENIA1977
- Inhibition of Complementary Lysis by Rheumatoid SeraNature, 1967
- SIMILARITIES BETWEEN KNOWN ANTIPLATELET ANTIBODIES AND THE FACTOR RESPONSIBLE FOR THROMBOCYTOPENIA IN IDIOPATHIC PURPURA. PHYSIOLOGIC, SEROLOGIC AND ISOTOPIC STUDIESAnnals of the New York Academy of Sciences, 1965
- Platelet Sequestration in Man. I. Methods*Journal of Clinical Investigation, 1964