Graafland H, Seignalet J, Donadio D, Navarro M, Izarn P
Rev Fr Transfus Immunohematol. 1981 Sep;24(4):389-404. doi: 10.1016/s0338-4535(81)80069-4.
We measured the quantity of IgG bound to platelets (IgGP) by the antiglobulin consumption test (Dixon technic). In controls, the IgG level did not exceed 10 X 10(-15) g for one platelet. The amount of IgGP was often incraeased (more than 10 X 10(-l5) g) in some autoimmune diseases as lupus erythematosus, chronic lymphocytic leukemia and chronic active hepatitis. Among 26 patients presenting an idiopathic thrombocytopenic purpura (ITP) with a low number of platelets, 21 (77%) had a high titer of IgGP. In 6 ITP in remission, the IgGP titer was normal. After a review of the different technics detecting the IgG bound to platelets, we explain why we choose the antiglobulin consumption. This test is excellent for the research of anti-platelets auto-antibodies in ITP. Yet, the reaction remains negative in a minority of ITP. Several explanations are possible: low quantity of IgGP, presence of other anto-antibodies as IgM or IgA, cellular auto-immunity anti-platelets without antibodies, non immunologic ITP.
我们通过抗球蛋白消耗试验(狄克逊技术)测量结合于血小板的IgG量(IgGP)。在对照组中,单个血小板的IgG水平不超过10×10⁻¹⁵克。在一些自身免疫性疾病如红斑狼疮、慢性淋巴细胞白血病和慢性活动性肝炎中,IgGP量常增加(超过10×10⁻¹⁵克)。在26例血小板数量低的特发性血小板减少性紫癜(ITP)患者中,21例(77%)IgGP滴度高。在6例缓解期的ITP患者中,IgGP滴度正常。在回顾了检测结合于血小板的IgG的不同技术后,我们解释了选择抗球蛋白消耗试验的原因。该试验对于ITP中抗血小板自身抗体的检测非常出色。然而,在少数ITP患者中反应仍为阴性。可能有几种解释:IgGP量低、存在其他自身抗体如IgM或IgA、无抗体的细胞性抗血小板自身免疫、非免疫性ITP。