<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Greinacher A</submitter><funding>German Research Foundation</funding><funding>Deutsche Forschungsgemeinschaft</funding><pagination>2092-2101</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8095372</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>384(22)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Several cases of unusual thrombotic events and thrombocytopenia have developed after vaccination with the recombinant adenoviral vector encoding the spike protein antigen of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) (ChAdOx1 nCov-19, AstraZeneca). More data were needed on the pathogenesis of this unusual clotting disorder.&lt;h4>Methods&lt;/h4>We assessed the clinical and laboratory features of 11 patients in Germany and Austria in whom thrombosis or thrombocytopenia had developed after vaccination with ChAdOx1 nCov-19. We used a standard enzyme-linked immunosorbent assay to detect platelet factor 4 (PF4)-heparin antibodies and a modified (PF4-enhanced) platelet-activation test to detect platelet-activating antibodies under various reaction conditions. Included in this testing were samples from patients who had blood samples referred for investigation of vaccine-associated thrombotic events, with 28 testing positive on a screening PF4-heparin immunoassay.&lt;h4>Results&lt;/h4>Of the 11 original patients, 9 were women, with a median age of 36 years (range, 22 to 49). Beginning 5 to 16 days after vaccination, the patients presented with one or more thrombotic events, with the exception of 1 patient, who presented with fatal intracranial hemorrhage. Of the patients with one or more thrombotic events, 9 had cerebral venous thrombosis, 3 had splanchnic-vein thrombosis, 3 had pulmonary embolism, and 4 had other thromboses; of these patients, 6 died. Five patients had disseminated intravascular coagulation. None of the patients had received heparin before symptom onset. All 28 patients who tested positive for antibodies against PF4-heparin tested positive on the platelet-activation assay in the presence of PF4 independent of heparin. Platelet activation was inhibited by high levels of heparin, Fc receptor-blocking monoclonal antibody, and immune globulin (10 mg per milliliter). Additional studies with PF4 or PF4-heparin affinity purified antibodies in 2 patients confirmed PF4-dependent platelet activation.&lt;h4>Conclusions&lt;/h4>Vaccination with ChAdOx1 nCov-19 can result in the rare development of immune thrombotic thrombocytopenia mediated by platelet-activating antibodies against PF4, which clinically mimics autoimmune heparin-induced thrombocytopenia. (Funded by the German Research Foundation.).</pubmed_abstract><journal>The New England journal of medicine</journal><pubmed_title>Thrombotic Thrombocytopenia after ChAdOx1 nCov-19 Vaccination.</pubmed_title><pmcid>PMC8095372</pmcid><funding_grant_id>Projektnummer 374031971 - TRR 240</funding_grant_id><funding_grant_id>Projektnummer 374031971 – TRR 240</funding_grant_id><pubmed_authors>Warkentin TE</pubmed_authors><pubmed_authors>Thiele T</pubmed_authors><pubmed_authors>Kyrle PA</pubmed_authors><pubmed_authors>Eichinger S</pubmed_authors><pubmed_authors>Greinacher A</pubmed_authors><pubmed_authors>Weisser K</pubmed_authors></additional><is_claimable>false</is_claimable><name>Thrombotic Thrombocytopenia after ChAdOx1 nCov-19 Vaccination.</name><description>&lt;h4>Background&lt;/h4>Several cases of unusual thrombotic events and thrombocytopenia have developed after vaccination with the recombinant adenoviral vector encoding the spike protein antigen of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) (ChAdOx1 nCov-19, AstraZeneca). More data were needed on the pathogenesis of this unusual clotting disorder.&lt;h4>Methods&lt;/h4>We assessed the clinical and laboratory features of 11 patients in Germany and Austria in whom thrombosis or thrombocytopenia had developed after vaccination with ChAdOx1 nCov-19. We used a standard enzyme-linked immunosorbent assay to detect platelet factor 4 (PF4)-heparin antibodies and a modified (PF4-enhanced) platelet-activation test to detect platelet-activating antibodies under various reaction conditions. Included in this testing were samples from patients who had blood samples referred for investigation of vaccine-associated thrombotic events, with 28 testing positive on a screening PF4-heparin immunoassay.&lt;h4>Results&lt;/h4>Of the 11 original patients, 9 were women, with a median age of 36 years (range, 22 to 49). Beginning 5 to 16 days after vaccination, the patients presented with one or more thrombotic events, with the exception of 1 patient, who presented with fatal intracranial hemorrhage. Of the patients with one or more thrombotic events, 9 had cerebral venous thrombosis, 3 had splanchnic-vein thrombosis, 3 had pulmonary embolism, and 4 had other thromboses; of these patients, 6 died. Five patients had disseminated intravascular coagulation. None of the patients had received heparin before symptom onset. All 28 patients who tested positive for antibodies against PF4-heparin tested positive on the platelet-activation assay in the presence of PF4 independent of heparin. Platelet activation was inhibited by high levels of heparin, Fc receptor-blocking monoclonal antibody, and immune globulin (10 mg per milliliter). Additional studies with PF4 or PF4-heparin affinity purified antibodies in 2 patients confirmed PF4-dependent platelet activation.&lt;h4>Conclusions&lt;/h4>Vaccination with ChAdOx1 nCov-19 can result in the rare development of immune thrombotic thrombocytopenia mediated by platelet-activating antibodies against PF4, which clinically mimics autoimmune heparin-induced thrombocytopenia. (Funded by the German Research Foundation.).</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Jun</publication><modification>2025-04-26T09:05:55.395Z</modification><creation>2025-04-06T12:52:58.908Z</creation></dates><accession>S-EPMC8095372</accession><cross_references><pubmed>33835769</pubmed><doi>10.1056/NEJMoa2104840</doi></cross_references></HashMap>