Autoantibodies against Erythropoietin in a Patient with Pure Red-Cell Aplasia
Open Access
- 7 March 1996
- journal article
- research article
- Published by Massachusetts Medical Society in New England Journal of Medicine
- Vol. 334 (10) , 630-633
- https://doi.org/10.1056/nejm199603073341004
Abstract
Autoimmunity is often implicated in pure red-cell aplasia. Approximately 10 to 15 percent of patients with pure red-cell aplasia have thymomas,1 and remission of the anemia occurs in 25 to 30 percent of these patients after the thymoma is removed.2 In other patients there are immunologic abnormalities, such as hypogammaglobulinemia,3 monoclonal immunoglobulins,4 antithyroid antibodies,5 antinuclear antibodies,6,7 and autoimmune hemolytic anemia.3,8 Immunosuppressive therapy is successful in many patients,2,9-12 and a good response to plasmapheresis has been reported in two patients.13,14Keywords
This publication has 28 references indexed in Scilit:
- Pure red cell aplasia: further evidence of T cell clonal disorderBritish Journal of Haematology, 1994
- Solubilization and hydrodynamic characteristics of the erythropoietin receptorEuropean Journal of Biochemistry, 1990
- Glycosylation of the murine erythropoietin receptorFEBS Letters, 1990
- Autoreactive erythroid progenitor‐T suppressor cells in the pure red cell aplasia associated with thymoma and panhypogammaglobulinemiaAmerican Journal of Hematology, 1986
- Remission of acquired pure red cell aplasia following plasma exchanges:Scandinavian Journal of Haematology, 1985
- Pure red-cell aplasia: association with systemic lupus erythematosus and primary autoimmune hypothyroidism.BMJ, 1982
- Control of Antibody-Mediated Pure Red-Cell Aplasia by PlasmapheresisNew England Journal of Medicine, 1981
- Pure Red Cell Aplasia: Studies on an IgG Serum Inhibitor Neutralizing ErythropoietinBritish Journal of Haematology, 1975
- Studies on Red Cell Aplasia. V. PRESENCE OF ERYTHROBLAST CYTOTOXICITY IN γG-GLOBULIN FRACTION OF PLASMAJournal of Clinical Investigation, 1973
- REFRACTORY ANqMIA WITH THYMOMAThe Lancet, 1966