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Immune responses against SARS-CoV-2 variants after two and three doses of vaccine in B-cell malignancies: UK PROSECO study.

Sean H LimBeth StuartDebora Joseph-PietrasMarina JohnsonNicola CampbellAdam KellyDanielle JeffreyAnna H TurajKate RolfvondenbaumenCeline GallowayThomas WynnAdam R ColemanBenjamin WardKaren LongHelen ColemanCarina MundyAndrew T BatesDiana AyresRobert LownJanlyn FalconerOliver BrakeJames BatchelorVictoria WillimottAnna Bowzyk Al-NaeebLisa RobinsonAnn O'CallaghanGraham P CollinsTobias MenneSaul N FaustChristopher P FoxMatthew AhearnePeter W M JohnsonAndrew J DaviesDavid Goldblatt
Published in: Nature cancer (2022)
Patients with hematological malignancies are at increased risk of severe COVID-19 outcomes due to compromised immune responses, but the insights of these studies have been compromised due to intrinsic limitations in study design. Here we present the PROSECO prospective observational study ( NCT04858568 ) on 457 patients with lymphoma that received two or three COVID-19 vaccine doses. We show undetectable humoral responses following two vaccine doses in 52% of patients undergoing active anticancer treatment. Moreover, 60% of patients on anti-CD20 therapy had undetectable antibodies following full vaccination within 12 months of receiving their anticancer therapy. However, 70% of individuals with indolent B-cell lymphoma displayed improved antibody responses following booster vaccination. Notably, 63% of all patients displayed antigen-specific T-cell responses, which increased after a third dose irrespective of their cancer treatment status. Our results emphasize the urgency of careful monitoring of COVID-19-specific immune responses to guide vaccination schemes in these vulnerable populations.
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