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 GoldblattPublished 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.
Keyphrases
- sars cov
- immune response
- coronavirus disease
- patients undergoing
- end stage renal disease
- ejection fraction
- newly diagnosed
- diffuse large b cell lymphoma
- dendritic cells
- prognostic factors
- toll like receptor
- respiratory syndrome coronavirus
- gene expression
- metabolic syndrome
- early onset
- adipose tissue
- mesenchymal stem cells
- dna methylation
- copy number
- patient reported
- hodgkin lymphoma
- case control
- weight loss
- bone marrow
- cell therapy
- genetic diversity
- replacement therapy