4.7 Article

BCG vaccination improves DTaP immune responses in mice and is associated with lower pertussis incidence in ecological epidemiological studies

Journal

EBIOMEDICINE
Volume 65, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.ebiom.2021.103254

Keywords

Live-tuberculosis vaccines; Heterologous immunity; Non-specific effects; DTP; BCG; MTBVAC

Funding

  1. Instituto de Salud Carlos III (Proyecto de Investigacion en Salud, Accion Estrategica en Salud, Cofinanciado FEDER) [GePEM ISCIII/PI16/01478, ISCIII/PI16/01569]
  2. Instituto de Salud Carlos III (Conselleria de Sanidade, Xunta de Galicia) [PS09749, 10PXIB918184PR, RHI07/2]
  3. Instituto de Salud Carlos III (Intensificacion de la actividad investigadora 2007-2012) [PI16/01569]
  4. Fondo de Investigacion Sanitaria (FIS) del plan nacional de I + D + I [PI070069, PI1000540, PI1901090]
  5. Grupo Gallego de Genetica Vacunas Infecciones y Pediatria [REDES 2016GI-1344 G3VIP, ED341D R2016/021, 2016-PG071]
  6. Spanish Ministry of Economia y Competitividad [BFU2015-72190-EXP, BES-2012-052937]
  7. Spanish Ministry of Ciencia, Innovacion y Universidades [RTI2018-097625-B-I00]
  8. European Commission H2020 program European Union European & Developing Countries Clinical Trials Partnership (EDCTP) [RIA2016V-1637]
  9. Gobierno de Aragon-Fondo Europeo de Desarrollo Regional (FEDER) 2014~2020: Construyendo Europa Desde Aragon
  10. Fundacao Butantan
  11. fondos FEDER

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The study showed that BCG and MTBVAC administered before DTaP can induce Th1 immune responses against diphtheria, tetanus, and pertussis in mice, while DTaP alone fails to trigger the same response. Analysis of human epidemiological data revealed that countries using both DTaP and BCG had significantly lower pertussis incidence compared to countries using only DTaP.
Background: The Bacillus Calmette-Guerin (BCG), the only vaccine against tuberculosis (TB) currently in use, has shown beneficial effects against unrelated infections and to enhance immune responses to vaccines. However, there is little evidence regarding the influence of BCG vaccination on pertussis. Methods: Here, we studied the ability of BCG to improve the immune responses to diphtheria, tetanus, and acellular (DTaP) or whole-cell pertussis (DTwP) vaccination in a mouse model. We included MTBVAC, an experimental live-attenuated vaccine derived from Mycobacterium tuberculosis, in our studies to explore if it presents similar heterologous immunity as BCG. Furthermore, we explored the potential effect of routine BCG vaccination on pertussis incidence worldwide. Findings: We found that both BCG and MTBVAC when administered before DTaP, triggered Th1 immune responses against diphtheria, tetanus, and pertussis in mice. Immunization with DTaP alone failed to trigger a Th1 response, as measured by the production of IFN-gamma. Humoral responses against DTaP antigens were also enhanced by previous immunization with BCG or MTBVAC. Furthermore, exploration of human epidemiological data showed that pertussis incidence was 10-fold lower in countries that use DTaP and BCG compared to countries that use only DTaP. Interpretation: BCG vaccination may have a beneficial impact on the protection against pertussis conferred by DTaP. Further randomized controlled trials are needed to properly define the impact of BCG on pertussis incidence in a controlled setting. This could be a major finding that would support changes in immunization policies. (C) 2021 The Authors. Published by Elsevier B.V.

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