TY - CHAP
T1 - Automated and rapid ADAMTS13 testing using chemiluminescence
T2 - Utility for identification or exclusion of TTP and beyond
AU - Favaloro, Emmanuel J
AU - Chapman, Kent
AU - Mohammed, Soma
AU - Vong, Ronny
AU - Pasalic, Leonardo
N1 - Publisher Copyright:
© 2023, The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature.
PY - 2023
Y1 - 2023
N2 - Thrombotic thrombocytopenic purpura (TTP) is a prothrombotic condition caused by a significant deficiency of the enzyme, ADAMTS13 (a disintegrin and metalloproteinase with a thrombospondin type 1 motif, member 13). In the absence of adequate levels of ADAMTS13 (i.e., in TTP), plasma VWF accumulates, in particular as "ultra-large" VWF multimers, and this leads to pathological platelet aggregation and thrombosis. In addition to TTP, ADAMTS13 may be mildly to moderately reduced in a range of other conditions, including secondary thrombotic microangiopathies (TMA) such as those caused by infections (e.g., hemolytic uremic syndrome (HUS)), liver disease, disseminated intravascular coagulation (DIC), and sepsis, during acute/chronic inflammatory conditions, and sometimes also in COVID-19 (coronavirus disease 2019)). ADAMTS13 can be detected by a variety of techniques, including ELISA (enzyme-linked immunosorbent assay), FRET (fluorescence resonance energy transfer) and by chemiluminescence immunoassay (CLIA). The current report describes a protocol for assessment of ADAMTS13 by CLIA. This protocol reflects a rapid test able to be performed within 35 min on the AcuStar instrument (Werfen/Instrumentation Laboratory), although certain regional approvals may also permit this testing to be performed on a BioFlash instrument from the same manufacturer.
AB - Thrombotic thrombocytopenic purpura (TTP) is a prothrombotic condition caused by a significant deficiency of the enzyme, ADAMTS13 (a disintegrin and metalloproteinase with a thrombospondin type 1 motif, member 13). In the absence of adequate levels of ADAMTS13 (i.e., in TTP), plasma VWF accumulates, in particular as "ultra-large" VWF multimers, and this leads to pathological platelet aggregation and thrombosis. In addition to TTP, ADAMTS13 may be mildly to moderately reduced in a range of other conditions, including secondary thrombotic microangiopathies (TMA) such as those caused by infections (e.g., hemolytic uremic syndrome (HUS)), liver disease, disseminated intravascular coagulation (DIC), and sepsis, during acute/chronic inflammatory conditions, and sometimes also in COVID-19 (coronavirus disease 2019)). ADAMTS13 can be detected by a variety of techniques, including ELISA (enzyme-linked immunosorbent assay), FRET (fluorescence resonance energy transfer) and by chemiluminescence immunoassay (CLIA). The current report describes a protocol for assessment of ADAMTS13 by CLIA. This protocol reflects a rapid test able to be performed within 35 min on the AcuStar instrument (Werfen/Instrumentation Laboratory), although certain regional approvals may also permit this testing to be performed on a BioFlash instrument from the same manufacturer.
KW - a disintegrin and metalloproteinase with a thrombospondin type 1 motif, member 13
KW - ADAMTS13
KW - Chemiluminescence immunoassay
KW - CLIA
KW - COVID-19
KW - Thrombotic thrombocytopenic purpura
KW - TTP
UR - http://www.scopus.com/inward/record.url?scp=85159764629&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85159764629&partnerID=8YFLogxK
U2 - 10.1007/978-1-0716-3175-1_32
DO - 10.1007/978-1-0716-3175-1_32
M3 - Chapter (peer-reviewed)
C2 - 37204732
SN - 9781071631744
T3 - Methods in Molecular Biology
SP - 487
EP - 504
BT - Hemostasis and Thrombosis
A2 - , Emmanuel J. Favaloro
A2 - , Robert C. Gosselin
PB - Humana Press
CY - New York
ER -