Poor responder to plasma exchange therapy in acquired thrombotic thrombocytopenic purpura is associated with ADAMTS13 inhibitor boosting: visualization of an ADAMTS13 inhibitor complex and its proteolytic clearance from plasma

被引:20
作者
Isonishi, Ayami [1 ]
Bennett, Charles L. [2 ,3 ]
Plaimauer, Barbara [4 ]
Scheiflinger, Friedrich [4 ]
Matsumoto, Masanori [1 ]
Fujimura, Yoshihiro [1 ]
机构
[1] Nara Med Univ, Dept Blood Transfus Med, Kashihara, Nara 6348522, Japan
[2] South Carolina Coll Pharm, Southern Network Adverse React SONAR, South Carolina Ctr Econ Excellence Medicat Safety, Columbia, SC USA
[3] William Jennings Bryan Dorn Vet Adm Med Ctr, Columbia, SC USA
[4] Baxter Biosci, Dept Discovery Res & Tech Assessment, Vienna, Austria
关键词
VON-WILLEBRAND-FACTOR; FACTOR-CLEAVING PROTEASE; ANTI-ADAMTS13; ANTIBODIES; ENZYME-IMMUNOASSAY; FACTOR MULTIMERS; RITUXIMAB; MICROANGIOPATHIES; EFFICACY; SAFETY;
D O I
10.1111/trf.13182
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUNDPlasma exchange (PE) is the first-line treatment for primary acquired thrombotic thrombocytopenic purpura (aTTP) with severe deficiency of ADAMTS13 activity (ADAMTS13:AC). Some patients are poor responders to PE, raising concern over multiple pathogenetic pathways. STUDY DESIGN AND METHODSBased on 52 aTTP patients in our national cohort study, we monitored plasma levels of ADAMTS13, clinical and laboratory findings, and outcomes. In a representative poor responder to PE, we examined an ADAMTS13 inhibitor (ADAMTS13:INH) complex in plasma milieu, by means of a large-pore isoelectric focusing (IEF) analysis. RESULTSOf 52 aTTP patients, 20 were good responders and 32 were poor responders. In the latter group, plasma ADAMTS13:AC levels never increased to more than 10% of normal during 14 days after PE initiation. Mean (SD) plasma ADAMTS13:INH titers (Bethesda unit/mL) were 5.7 (+/- 4.5) before PE, but decreased to 1.4 (+/- 0.8) on the fourth PE day and then remarkably increased to 14.8 (+/- 10.0) on the 10th PE day, termed inhibitor boosting, and then slowly decreased to undetectable level over 1 month. On admission, none of the routinely available clinical and laboratory markers differentiated these two groups. However, elevated pre-PE levels of ADAMTS13:INH were correlated with a poor response. We visualized an ADAMTS13:INH (immunoglobulin G) complex in a patient plasma by an IEF analysis and found proteolytic fragment of ADAMTS13 antigen by a two-dimensional IEF and sodium dodecyl sulfate-polyacrylamide gel electrophoresis analysis. CONCLUSIONFindings from this cohort of aTTP patients demonstrated that inhibitor boosting often occurs in aTTP patients in Japan. Poor responders could be predicted by elevated pre-PE ADAMTS13:INH levels on admission, but not by routinely collected clinical or laboratory data.
引用
收藏
页码:2321 / 2330
页数:10
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