Intravenous anti-D treatment of immune thrombocytopenic purpura: analysis of efficacy, toxicity, and mechanism of effect

Blood. 1991 May 1;77(9):1884-93.

Abstract

The efficacy, toxicity, and mechanism of effect of intravenous Anti-D (Winrho) were studied in 43 Rh+ patients with immune thrombocytopenia purpura (ITP) who had not undergone splenectomy and in three already splenectomized patients. The mean platelet increase for the 43 nonsplenectomized patients was 95,000/microL (median 43,000/microL). Children had greater acute platelet responses than did adults. Human immunodeficiency virus status and duration of thrombocytopenia did not affect response. Maintenance treatment was given to patients as needed: the average interval between infusions was 24 days. The three splenectomized patients had no platelet response whatsoever. Toxicity was minimal; infusions were completed in less than 5 minutes. The generally accepted mechanism of effect of Anti-D has been Fc receptor blockade by substitution of antibody-coated red blood cells for antibody-coated platelets. Evidence is presented suggesting that the effect of IV Anti-D is not limited to Fc receptor blockade, including: (1) no correlation of parameters of hemolysis with platelet increase; (2) a 48- to 72-hour delay before platelet increase; (3) a tendency of the change in monocyte Fc receptor I expression to correlate with platelet increase; and (4) increased in vitro production of antibodies to sheep red blood cells following IV Anti-D infusion.

Publication types

  • Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Child
  • Erythrocyte Count
  • HIV Seropositivity / complications
  • Hemoglobins / metabolism
  • Humans
  • Immunization, Passive* / adverse effects
  • Immunoglobulins / administration & dosage*
  • Immunoglobulins / adverse effects
  • Infusions, Intravenous
  • Platelet Count
  • Purpura, Thrombocytopenic / blood
  • Purpura, Thrombocytopenic / complications
  • Purpura, Thrombocytopenic / immunology*
  • Purpura, Thrombocytopenic / therapy
  • Receptors, Fc / metabolism
  • Reticulocytes / pathology
  • Rho(D) Immune Globulin
  • Splenectomy

Substances

  • Hemoglobins
  • Immunoglobulins
  • Receptors, Fc
  • Rho(D) Immune Globulin