Journal
CURRENT OPINION IN HEMATOLOGY
Volume 21, Issue 5, Pages 380-387Publisher
LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/MOH.0000000000000066
Keywords
Fc gamma RII alpha; heparin; heparin-induced thrombocytopenia; immune-mediated thrombocytopenia and thrombosis; platelet factor 4
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Funding
- NIH [P01HL110860]
- Wolfgang Bergmeier [R01HL106009]
- Michael Holinstat [R01HL114405]
- Paul Bray and Leonard Edelstein (Cardeza Foundation for Hematological Research)
- Portola Pharmaceuticals
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Purpose of review To review the recent developments in understanding the pathophysiology of heparin-induced thrombocytopenia (HIT) and in applying this knowledge to the treatment of patients with suspected and proven HIT. Recent findings HIT pathophysiology is dynamic and complex. HIT pathophysiology is initiated by four essential components - heparin (Hep), platelet factor 4 (PF4), IgG antibodies against the Hep-PF4 complex, and platelet Fc gamma RII alpha. HIT is propagated by activated platelets, monocytes, endothelial cells, and coagulation proteins. Insights into the unique HIT antibody response continue to emerge, but without consensus as to the relative roles of B cells, T cells, and antigen-presenting cells. Platelet activation via Fc gamma RII alpha, the sine qua non of HIT, has become much better appreciated. Therapy remains challenging for several reasons. Suspected HIT is more frequent than proven HIT, because of the widespread use of Hep and the inadequacies of current diagnostic tests and scoring systems. In proven HIT, approved treatments reduce but do not eliminate thrombosis, and have substantial bleeding risk. Rational novel therapeutic strategies, directed at the initiating steps in HIT pathophysiology and with potential combinations staged over time, are in various phases of development. Summary Progress continues in understanding the breadth of molecular and cellular players in HIT. Translation to improved diagnosis and treatment is needed.
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