Inhibition of platelet-aggregating activity in thrombotic thrombocytopenic purpura plasma by normal adult immunoglobulin G.
Open Access
- 1 February 1984
- journal article
- Published by American Society for Clinical Investigation in Journal of Clinical Investigation
- Vol. 73 (2) , 548-555
- https://doi.org/10.1172/JCI111242
Abstract
Plasma from patients with thrombotic thrombocytopenic purpura (TTP) caused the aggregation of autologous and homologous platelets, and effect which was inhibited by normal plasma. IgG purified from seven normal adults at a concentration of 0.7 mg/ml completely inhibited the platelet aggregation induced by plasma obtained from two TTP patients with active disease. The inhibition of platelet aggregation by human adult IgG was concentration dependent, and the inhibitory activity of human IgG was neutralized by rabbit antihuman IgG. Fab fragments inhibited the TTP plasma-induced platelet aggregation as well as intact IgG, whereas Fc fragments had no effect. Platelet aggregation caused by ADP, collagen, epinephrine, or thrombin was not affected by purified human IgG. The prior incubation of IgG with TTP plasma caused a significantly greater reduction of platelet aggregation by TTP plasma than that of IgG and platelet suspension, suggesting that the IgG inhibits TTP plasma-induced platelet aggregation through direct interaction with platelet aggregating factor in TTP plasma. IgG obtained initially from five infants and young children under the age of 4 yr did not possess any inhibitory activity. When one of the children reached 3 yr of age, his IgG inhibited the aggregation induced by one TTP plasma, but not that caused by another plasma. The IgG procured from the same boy at 4 yr of age inhibited the aggregation induced by both TTP plasmas. The IgG purified from the TTP plasma during active disease failed to inhibit the aggregation caused by the same plasma. After recovery, however, the IgG effectively inhibited aggregation. These observations suggest that platelet-aggregating factors present in the TTP plasma are heterogeneous in nature and that the IgG present in the normal adult plasma, which inhibits the TTP plasma-induced platelet aggregation, may be partially responsible for the success of plasma infusion therapy in TTP.Keywords
This publication has 33 references indexed in Scilit:
- COMBINED PLASMAPHERESIS AND HEMODIALYSIS TREATMENT FOR SEVERE HEMOLYTIC‐UREMIC SYNDROME FOLLOWING CAMPYLOBACTER COLITISActa Paediatrica, 1982
- ACCELERATED PROSTACYCLIN DEGRADATION IN THROMBOTIC THROMBOCYTOPENIC PURPURAThe Lancet, 1981
- Immunologic and Other Factors in Thrombotic Thrombocytopenic Purpura (TTP)Seminars in Thrombosis and Hemostasis, 1980
- PROSTACYCLIN DEFICIENCY IN THROMBOTIC THROMBOCYTOPENIC PURPURAThe Lancet, 1979
- How Carbon Monoxide Reduces Plasma VolumeNew England Journal of Medicine, 1978
- TTP: New Clues to the Etiology of an Enigmatic DiseaseNew England Journal of Medicine, 1977
- Thrombotic thrombocytopenic purpuraThe Journal of Pediatrics, 1974
- Thrombotic thrombocytopenic purpura after influenza vaccination.BMJ, 1973
- Elektronenmikroskopische Untersuchungen über die Adsorption und Phagocytose von Influenza-Viren durch ThrombocytenKlinische Wochenschrift, 1966
- Thrombotic thrombocytopenic purpuraThe Journal of Pediatrics, 1962