4.5 Article

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

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NATURE CANCER
卷 3, 期 5, 页码 552-+

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NATURE PORTFOLIO
DOI: 10.1038/s43018-022-00364-3

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  1. Blood Cancer UK Vaccine Research Collaborative
  2. British Society for Haematology [21009]
  3. Cancer Research UK Advanced Clinician Scientist Fellowship [A27179]
  4. Cancer Research UK/National Institute for Health Research (NIHR) Southampton Experimental Cancer Medicine Center [A25141]
  5. NIHR Southampton Clinical Research Facility (Southampton Research Biorepository)
  6. NIHR Southampton Biomedical Research Center
  7. NIHR Oxford Biomedical Research Center
  8. CRUK Experimental Cancer Medicines Center
  9. Myeloma UK
  10. Anthony Nolan

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Patients with hematological malignancies, especially those undergoing active anticancer treatment or on anti-CD20 therapy, show compromised immune responses to COVID-19 vaccination. However, booster vaccination can significantly improve antibody responses in indolent B-cell lymphoma patients, and antigen-specific T-cell responses are observed in the majority of patients after a third dose, regardless of their cancer treatment status.
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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