PF4-Dependent Immunoassays in Patients with Vaccine-Induced Immune Thrombotic Thrombocytopenia: Results of an Interlaboratory Comparison

• Published in: Thrombosis and haemostasis Vol. 121; no. 12; p. 1622
• Main Authors: Sachs, Ulrich J, Cooper, Nina, Czwalinna, Andreas, Müller, Jens, Pötzsch, Bernd, Tiede, Andreas, Althaus, Karina
• Format: Journal Article
• Language: English
• Published: Germany 01-12-2021
• Subjects: Antibodies - blood; Biomarkers - blood; ChAdOx1 nCoV-19 - administration & dosage; ChAdOx1 nCoV-19 - adverse effects; Enzyme-Linked Immunosorbent Assay; Humans; Luminescent Measurements; Platelet Factor 4 - immunology; Predictive Value of Tests; Purpura, Thrombocytopenic, Idiopathic - blood; Purpura, Thrombocytopenic, Idiopathic - chemically induced; Purpura, Thrombocytopenic, Idiopathic - diagnosis; Purpura, Thrombocytopenic, Idiopathic - immunology; Reproducibility of Results; Vaccination - adverse effects
• DOI: 10.1055/a-1535-9002
• EISSN: 2567-689X

Coronavirus disease 2019 vaccine ChAdOx1 nCov-19 may rarely lead to vaccine-induced thrombotic thrombocytopenia (VITT). Antibody-mediated, platelet factor 4 (PF4)-dependent platelet activation appears to resemble a key mechanism in VITT, partially comparable to heparin-induced thrombocytopenia. The use of PF4/heparin immunoassays has been proposed as part of a diagnostic approach, but their sensitivity has not been established.
 Sera from 12 well-defined VITT patients were first studied by two different laboratories in functional assays. Sera where then used for an interlaboratory comparison, in which five different PF4/heparin immunoassays were used by four laboratories.
 Results for functional testing were highly concordant. VITT antibodies were also reliably detected by PF4/heparin enzyme-linked immunosorbent assays (ELISAs) (92-100%). In contrast, only 25% of VITT antibodies were reactive in a particle gel immunoassay (PaGIA), and 8% in a lateral flow assay (LFA). An automated chemiluminescence immunoassay (CLIA) was negative for all sera tested (0%).
 It seems feasible to establish functional antibody testing for the confirmation of VITT. For the initial screening of suspected VITT cases, PaGIA, LFA, and CLIA are useless when applied as single tests. Only ELISA-based PF4/heparin immunoassays are sensitive enough to be incorporated in the diagnostic workup. However, a combination of a positive ELISA and a negative CLIA may be useful to identify VITT antibodies in the absence of confirmatory functional assays.