Affiliation:
1. Clinical Hematology and Bone Marrow Transplantation Unit, Department of Internal Medicine, Faculty of Medicine, Ain Shams University, Cairo, Egypt
2. Department of Cinical Pathology, Faculty of Medicine, Assiut University, Assiut, Egypt
Abstract
Background
Glycoprotein (GP) V is a well-characterized immune target in Varicella-associated and drug-induced thrombocytopenia. Recent studies have focused on the involvement of anti-GP V in the mechanism of platelet clearance as a recent paradigm in the pathophysiology of immune thrombocytopenia (ITP), rather than other anti-GPs like GP IIb/IIIa, GP Ib/IX and less frequently GP Ia/IIa.
Objectives
This study was conducted to determine the prevalence of anti-GP V in adult ITP Egyptian patients and to detect its impact on the outcome in these patients.
Patients and methods
This was a cross-sectional study in which, using enzyme-linked immunosorbent assay, the level of serum anti-GP antibodies V was measured in the peripheral blood of 90 patients with primary ITP compared with 20 age-matched and sex-matched normal healthy controls and its relationship with clinical, laboratory parameters, and response to treatment.
Results
Our study revealed that anti-GP antibodies V level in the cases group was statistically significantly higher as compared with the control group (P=0.005). There was weak statistically significant positive correlation between platelet count and anti-GP V level antibodies in the cases group after treatment with a P value of 0.0548. However, the level of anti-GP V did not show significant correlation with the bleeding score (P=0.123), degree of thrombocytopenia (P=0.967), sex (P=0.067), bone marrow findings (P=0.448), spleen size (P=0.992), or with the response to steroid therapy (P=0.171).
Conclusion
This study points out that GP V is a frequent immune target in ITP and that the detection of GP-specific autoantibodies being of value in the pathogenesis of ITP. We recommend that further studies including GP V are required before ITP treatment can be tailored according to platelet autoantibody specificity.