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Editorial
. 2021 Dec 2;138(22):2159-2160.
doi: 10.1182/blood.2021014195.

VITT(al) insights into vaccine-related clots

Affiliations
Editorial

VITT(al) insights into vaccine-related clots

Jeffrey R Strich et al. Blood. .
No abstract available

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Conflict of interest statement

Conflict-of-interest disclosure: Y.K. serves as a board member for the Society for Vascular Medicine, participates in the National Heart, Lung and Blood Institute (NHLBI) CONNECTS program and ACTIV-4 Host Tissue trial, and is an author on an unrelated patent application by the University of Michigan for the use of biogases in vascular disease. J.R.S. was the principal investigator of a clinical trial sponsored by the NHLBI to evaluate fostamatinib in acute COVID and participates in the ACTIV-4 Host Tissue trial.

Figures

None
Two-step process for VITT pathogenesis. (A) Shortly after vaccine administration, components of the adenovirus vaccine and PF4 generate immune complexes, whereas EDTA sequesters calcium, leading to vascular leak and an inflammatory response serving as a danger signal to provoke antibody generation. (B) One to 3 weeks after vaccine administration, polyanion/PF4/anti-PF4 antibody immune complexes trigger neutrophil extracellular trap formation and platelet aggregation in an FcγRIIA-dependent manner, resulting in thrombosis. Illustration by Alan Hoofring, National Institutes of Health.

Comment on

  • Insights in ChAdOx1 nCoV-19 vaccine-induced immune thrombotic thrombocytopenia.
    Greinacher A, Selleng K, Palankar R, Wesche J, Handtke S, Wolff M, Aurich K, Lalk M, Methling K, Völker U, Hentschker C, Michalik S, Steil L, Reder A, Schönborn L, Beer M, Franzke K, Büttner A, Fehse B, Stavrou EX, Rangaswamy C, Mailer RK, Englert H, Frye M, Thiele T, Kochanek S, Krutzke L, Siegerist F, Endlich N, Warkentin TE, Renné T. Greinacher A, et al. Blood. 2021 Dec 2;138(22):2256-2268. doi: 10.1182/blood.2021013231. Blood. 2021. PMID: 34587242 Free PMC article.

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