4.6 Article

BCG-induced trained immunity enhances acellular pertussis vaccination responses in an explorative randomized clinical trial

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NPJ VACCINES
卷 7, 期 1, 页码 -

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NATURE PORTFOLIO
DOI: 10.1038/s41541-022-00438-4

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资金

  1. National Institute of Public Health and the Environment (RIVM), The Netherlands (SPR project) [S112200]
  2. ERC Advanced Grant [833247]
  3. Spinoza grant of the Netherlands Organization for Scientific Research

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This study demonstrates that prior Bacille Calmette-Guerin (BCG) vaccination enhances immune responses to pertussis vaccines. Simultaneous BCG and acellular pertussis (aP) vaccinations do not show the same effect. Biomarkers of trained immunity are identified as the most reliable correlates of the enhanced immune responses.
Acellular pertussis (aP) booster vaccines are central to pertussis immunization programs, although their effectiveness varies. The Bacille Calmette-Guerin (BCG) vaccine is a prototype inducer of trained immunity, which enhances immune responses to subsequent infections or vaccinations. While previous clinical studies have demonstrated that trained immunity can protect against heterologous infections, its effect on aP vaccines in humans is unknown. We conducted a clinical study in order to determine the immunological effects of trained immunity on pertussis vaccination. Healthy female volunteers were randomly assigned to either receive BCG followed by a booster dose of tetanus-diphteria-pertussis inactivated polio vaccine (Tdap-IPV) 3 months later (BCG-trained), BCG + Tdap-IPV concurrently, or Tdap-IPV followed by BCG 3 months later. Primary outcomes were pertussis-specific humoral, T- and B-cell responses and were quantified at baseline of Tdap-IPV vaccination and 2 weeks thereafter. As a secondary outcome in the BCG-trained cohort, ex vivo leukocyte responses were measured in response to unrelated stimuli before and after BCG vaccination. BCG vaccination 3 months prior to, but not concurrent with, Tdap-IPV improves pertussis-specific Th1-cell and humoral responses, and also increases total memory B cell responses. These responses were correlated with enhanced IL-6 and IL-1 beta production at the baseline of Tdap-IPV vaccination in the BCG-trained cohort. Our study demonstrates that prior BCG vaccination potentiates immune responses to pertussis vaccines and that biomarkers of trained immunity are the most reliable correlates of those responses.

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