Publication:
COVID-19 Vaccines and Autoimmune Hematologic Disorders.

dc.contributor.authorMingot-Castellano, María Eva
dc.contributor.authorButta, Nora
dc.contributor.authorCanaro, Mariana
dc.contributor.authorGómez Del Castillo Solano, María Del Carmen
dc.contributor.authorSánchez-González, Blanca
dc.contributor.authorJiménez-Bárcenas, Reyes
dc.contributor.authorPascual-Izquierdo, Cristina
dc.contributor.authorCaballero-Navarro, Gonzalo
dc.contributor.authorEntrena Ureña, Laura
dc.contributor.authorJosé González-López, Tomás
dc.contributor.authorOn Behalf Of The Gepti,
dc.date.accessioned2023-05-03T14:24:22Z
dc.date.available2023-05-03T14:24:22Z
dc.date.issued2022-06-16
dc.description.abstractWorldwide vaccination against SARS-CoV-2 has allowed the detection of hematologic autoimmune complications. Adverse events (AEs) of this nature had been previously observed in association with other vaccines. The underlying mechanisms are not totally understood, although mimicry between viral and self-antigens plays a relevant role. It is important to remark that, although the incidence of these AEs is extremely low, their evolution may lead to life-threatening scenarios if treatment is not readily initiated. Hematologic autoimmune AEs have been associated with both mRNA and adenoviral vector-based SARS-CoV-2 vaccines. The main reported entities are secondary immune thrombocytopenia, immune thrombotic thrombocytopenic purpura, autoimmune hemolytic anemia, Evans syndrome, and a newly described disorder, so-called vaccine-induced immune thrombotic thrombocytopenia (VITT). The hallmark of VITT is the presence of anti-platelet factor 4 autoantibodies able to trigger platelet activation. Patients with VITT present with thrombocytopenia and may develop thrombosis in unusual locations such as cerebral beds. The management of hematologic autoimmune AEs does not differ significantly from that of these disorders in a non-vaccine context, thus addressing autoantibody production and bleeding/thromboembolic risk. This means that clinicians must be aware of their distinctive signs in order to diagnose them and initiate treatment as soon as possible.
dc.identifier.doi10.3390/vaccines10060961
dc.identifier.issn2076-393X
dc.identifier.pmcPMC9231220
dc.identifier.pmid35746569
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9231220/pdf
dc.identifier.unpaywallURLhttps://www.mdpi.com/2076-393X/10/6/961/pdf?version=1655888544
dc.identifier.urihttp://hdl.handle.net/10668/21609
dc.issue.number6
dc.journal.titleVaccines
dc.journal.titleabbreviationVaccines (Basel)
dc.language.isoen
dc.organizationHospital Universitario Virgen de las Nieves
dc.organizationÁrea de Gestión Sanitaria Serrania de Malaga
dc.organizationHospital Universitario Virgen del Rocío
dc.organizationInstituto de Biomedicina de Sevilla-IBIS
dc.organizationAGS - Serranía de Málaga
dc.pubmedtypeJournal Article
dc.pubmedtypeReview
dc.rightsAttribution 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectAIHA and Evans syndrome
dc.subjectCOVID-19
dc.subjectITP
dc.subjectTTP
dc.subjectVITT
dc.subjectantiphospholipid syndrome
dc.subjectcatastrophic antiphospholipid syndrome
dc.subjectvaccines
dc.titleCOVID-19 Vaccines and Autoimmune Hematologic Disorders.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number10
dspace.entity.typePublication

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