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Antiphospholipid syndrome: Reversal of antiphosphatidylserine/prothrombin-induced activated protein C resistance
被引:5
|作者:
Pontara, Elena
[1
]
Cattini, Maria Grazia
[1
]
Bison, Elisa
[1
]
Cheng, Chunyan
[1
]
Denas, Gentian
[1
]
Pengo, Vittorio
[1
,2
,3
]
机构:
[1] Univ Padua, Thrombosis Res Lab, Padua, Italy
[2] Arianna Fdn Anticoagulat, Bologna, Italy
[3] Univ Padua, Thrombosis Res Lab, Campus Biomed,Via Orus 2-B, I-35129 Padua, Italy
关键词:
Antibodies;
Antiphospholipid syndrome;
Lupus coagulation inhibitor;
beta 2-glycoprotein I;
Protein C;
Prothrombin;
ANTICARDIOLIPIN ANTIBODIES;
CLINICAL-COURSE;
THROMBOSIS;
RISK;
ARTERIAL;
UPDATE;
HEMOSTASIS;
INHIBITION;
GUIDELINES;
COFACTOR;
D O I:
10.1016/j.thromres.2022.08.004
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Background: Anti-phosphatidylserine/prothrombin (aPS/PT) antibodies are the major contributor to activated Protein C resistance (APC-R) in tetra-positive thrombotic high-risk patients with Antiphospholipid Syndrome (APS). Objectives: To evaluate the role of phospholipids (PL) on aPS/PT mediated APC-R. Patients/methods: Total IgG were purified from plasma of 6 tetra-positive patients and IgG aPS/PT were affinitypurified from 3 of these patients. Purified material was spiked into Normal Pooled Plasma (NPP) and tested for APC-R in thrombin generation assay and in Factor Va inactivation assay using increasing amounts of phospholipids. Results and conclusions: Total IgG showed APC-R at low PL concentration (1.5 mu g/mL) that disappeared at increasing PL concentrations (5.8, 11.6 and 46.6 mu g/mL). In the same way, affinity purified aPS/PT showed a robust (59 %, 52 %, 36 %) APC-R in patients #4, #5 and #6, respectively at low PL concentration (1.5 mu g/mL) that was completely reversed at higher concentration (11.6 mu g/mL). The inactivation of FVa by activated Protein C (aPC) was impaired in the presence of aPS/PT at low aPL concentration and reversed by increasing amounts of PL. These data point out the relevance of PL in reversing APC-R in this 'in vitro' system. The mechanism for reversal might be explained by loss of PL availability for aPC. These results may give some insight into the pathogenesis of thrombosis or suggestions for alternative treatments.
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页码:17 / 23
页数:7
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