Abstract | OBJECTIVES: To study the effect of monoclonal antibody (McAb) against helicobacter pylori (Hp) ureB, 1F11 on platelet aggregation and activation, and its mechanism. METHODS: The relativity between human platelet glycoproteins (GPs) and Hp ureB was identified by Western blot and FCM. Platelet aggregation was measured by turbidimetry, and P-selectin and TXB2 assay by ELISA. RESULTS: 1F11 could bind to platelet GPIIIa, and ADP-induced platelet aggregation was inhibited by 1F11 in a dose-dependent manner. However, 1F11 had no effect on plasma P-selectin and TXB2 induced by ADP. The FCM results show that the positive rates of platelet binding to FITC-SZ21 was decreased from 99.5% to 77.4% after addition of 1F11. CONCLUSION: McAb against Hp ureB 1F11 inhibits platelet aggregation through binding to platelet GPIIIa but does not block platelet activation. There might be crossed- epitopes on Hp ureB and platelet GPIIIa, and Hp infection might be involved in ITP immunopathology.
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Authors | Yan-yan Bai, Zhao-yue Wang, Xia Bai, Jing-cheng Miao, Wei Zhang, Lan Dai, Wen-hong Shen, Chang-geng Ruan |
Journal | Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi
(Zhonghua Xue Ye Xue Za Zhi)
Vol. 27
Issue 3
Pg. 166-9
(Mar 2006)
ISSN: 0253-2727 [Print] China |
PMID | 16792917
(Publication Type: Journal Article)
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Chemical References |
- Antibodies, Bacterial
- Antibodies, Monoclonal
- Bacterial Proteins
- Integrin beta3
- P-Selectin
- Urokinase-Type Plasminogen Activator
- Urease
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Topics |
- Antibodies, Bacterial
(pharmacology)
- Antibodies, Monoclonal
(pharmacology)
- Bacterial Proteins
(immunology, metabolism)
- Helicobacter pylori
(immunology)
- Humans
- Integrin beta3
(immunology)
- P-Selectin
(immunology)
- Platelet Activation
(drug effects)
- Platelet Aggregation
(drug effects)
- Urease
(immunology)
- Urokinase-Type Plasminogen Activator
(immunology)
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