Evaluation of Platelet Antibodies in Idiopathic Thrombocytopenic Purpura

Abstract

<h3>Introduction</h3> The suggestion that antibodies to platelets are responsible for the thrombocytopenia of "idiopathic" thrombocytopenic purpura (ITP) is based on three observations: (<i>a</i>) infants born of mothers with ITP sometimes exhibit thrombocytopenia¹; (<i>b</i>) normal volunteers who receive infusions of plasma from patients with ITP sometimes develop thrombocytopenia²; (<i>c</i>) transfused platelets do not circulate as long in patients with ITP as in normal recipients.³These phenomena indicate that a constituent of the blood of some patients with ITP is able to depress platelet levels of normal persons. These observations, however, are not proof of an antigen-antibody reaction, and it is not known whether this platelet-depressing activity is, in fact, capable of affecting the patient's own platelets. Platelet antibodies have been demonstrated in patients with thrombocytopenia induced by drugs, such as allyl-isopropyl-acetyl-carbamide (Sedormid),⁴quinidine,⁵quinine,⁶and novobiocin⁷; and in patients who have received transfusions.^8-10