Abstract
This cohort study examines the ability of patients receiving chimeric antigen receptor T-cell treatments to mount T-cell immunity in response to messenger RNA vaccines for severe acute respiratory syndrome coronavirus 2 despite substantial B-cell depletion.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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B-Lymphocytes
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COVID-19* / immunology
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Humans
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Immunotherapy, Adoptive*
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Receptors, Chimeric Antigen
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SARS-CoV-2
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Spike Glycoprotein, Coronavirus / immunology*
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T-Lymphocytes / immunology*
Substances
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Receptors, Chimeric Antigen
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Spike Glycoprotein, Coronavirus
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spike protein, SARS-CoV-2