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Distinct early cellular kinetics in participants protected against colonization upon Bordetella pertussis challenge.
Diks, Annieck M; de Graaf, Hans; Teodosio, Cristina; Groenland, Rick J; de Mooij, Bas; Ibrahim, Muktar; Hill, Alison R; Read, Robert C; van Dongen, Jacques Jm; Berkowska, Magdalena A.
Afiliação
  • Diks AM; Department of Immunology, Leiden University Medical Center, Leiden, Netherlands.
  • de Graaf H; Faculty of Medicine and.
  • Teodosio C; NIHR Southampton Biomedical Research Centre, University of Southampton, University Hospital Southampton NHS Foundation Trust, Southampton, United Kingdom.
  • Groenland RJ; Department of Immunology, Leiden University Medical Center, Leiden, Netherlands.
  • de Mooij B; Centro de Investigación del Cáncer-Instituto de Biología Molecular y Celular del Cáncer (CIC-IBMCC, USAL-CSIC-FICUS) and Department of Medicine, University of Salamanca, Salamanca, Spain.
  • Ibrahim M; Department of Immunology, Leiden University Medical Center, Leiden, Netherlands.
  • Hill AR; Department of Immunology, Leiden University Medical Center, Leiden, Netherlands.
  • Read RC; NIHR Southampton Biomedical Research Centre, University of Southampton, University Hospital Southampton NHS Foundation Trust, Southampton, United Kingdom.
  • van Dongen JJ; NIHR Southampton Biomedical Research Centre, University of Southampton, University Hospital Southampton NHS Foundation Trust, Southampton, United Kingdom.
  • Berkowska MA; NIHR Southampton Biomedical Research Centre, University of Southampton, University Hospital Southampton NHS Foundation Trust, Southampton, United Kingdom.
J Clin Invest ; 133(5)2023 03 01.
Article em En | MEDLINE | ID: mdl-36649086
BACKGROUNDTo date, only limited data are available on the mechanisms of protection against colonization with Bordetella pertussis in humans.METHODSIn this study, the cellular responses to B. pertussis challenge were monitored longitudinally using high-dimensional EuroFlow-based flow cytometry, allowing quantitative detection of more than 250 different immune cell subsets in the blood of 15 healthy donors.RESULTSParticipants who were protected against colonization showed different early cellular responses compared with colonized participants. Especially prominent for colonization-protected participants were the early expansion of CD36- nonclassical monocytes on day 1 (D1), natural killer cells (D3), follicular T helper cells (D1-D3), and plasma cells (D3). Plasma cell expansion on D3 correlated negatively with the CFU load on D7 and D9 after challenge. Increased plasma cell maturation on D11-D14 was found in participants with seroconversion.CONCLUSIONThese early cellular immune responses following experimental infection can now be further characterized and potentially linked to an efficient mucosal immune response, preventing colonization. Ultimately, their presence may be used to evaluate whether new B. pertussis vaccine candidates are protective against B. pertussis colonization, e.g., by bacterial challenge after vaccination.TRIAL REGISTRATIONClinicalTrials.gov NCT03751514.FUNDINGInnovative Medicines Initiative 2 Joint Undertaking and the EuroFlow Consortium.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Bordetella pertussis / Coqueluche Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Bordetella pertussis / Coqueluche Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article