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Third primary SARS-CoV-2 mRNA vaccines enhance antibody responses in most patients with haematological malignancies

SARS-CoV-2 infection, and resulting disease, COVID-19, has a high mortality amongst patients with haematological malignancies. Global vaccine rollouts have reduced hospitalisations and deaths, but vaccine efficacy in patients with haematological malignancies is known to be reduced. The UK-strategy o...

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Detalles Bibliográficos
Autores principales: Cook, Lucy B., O’Dell, Gillian, Vourvou, Eleni, Palanicawandar, Renuka, Marks, Sasha, Milojkovic, Dragana, Apperley, Jane F., Loaiza, Sandra, Claudiani, Simone, Bua, Marco, Hockings, Catherine, Macdonald, Donald, Chaidos, Aris, Pavlu, Jiri, Cooper, Nichola, Fidler, Sarah, Randell, Paul, Innes, Andrew J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9662771/
https://www.ncbi.nlm.nih.gov/pubmed/36376307
http://dx.doi.org/10.1038/s41467-022-34657-z
Descripción
Sumario:SARS-CoV-2 infection, and resulting disease, COVID-19, has a high mortality amongst patients with haematological malignancies. Global vaccine rollouts have reduced hospitalisations and deaths, but vaccine efficacy in patients with haematological malignancies is known to be reduced. The UK-strategy offered a third, mRNA-based, vaccine as an extension to the primary course in these patients. The MARCH database is a retrospective observational study of serological responses in patients with blood disorders. Here we present data on 381 patients with haematological malignancies. By comparison with healthy controls, we report suboptimal responses following two primary vaccines, with significantly enhanced responses following the third primary dose. These responses however are heterogeneous and determined by haematological malignancy sub-type and therapy. We identify a group of patients with continued suboptimal vaccine responses who may benefit from additional doses, prophylactic extended half-life neutralising monoclonal therapies (nMAB) or prompt nMAB treatment in the event of SARS-CoV-2 infection.