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Controlled Human Infection of Healthy Adults with Lyophilized Neisseria lactamica Induces Asymptomatic, Immunogenic Nasopharyngeal Carriage in the United Kingdom and Mali

  • D. F. Gbesemete*
  • , F. Haidara
  • , J. R. Laver
  • , M. Ibrahim
  • , J. MacLennan
  • , A. P. Dale
  • , A. R. Gorringe
  • , Y. Traore
  • , F. Diallo
  • , H. Badji
  • , A. Traore
  • , U. Onwuchekwa
  • , E. Jones
  • , C. Webb
  • , J. Guy
  • , A. A. Theodosiou
  • , S. N. Faust
  • , S. O. Sow
  • , R. S. Heyderman
  • , M. D. Tapia
  • R. C. Read
*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

Background Carriage of Neisseria lactamica (Nlac), a harmless nasopharyngeal commensal, correlates inversely with carriage of Neisseria meningitidis (Nmen), a common cause of meningitis and sepsis outbreaks in sub-Saharan Africa. Nasally administered lyophilized Nlac (LyoNlac) might interrupt carriage and transmission of Nmen in sub-Saharan settings without requirement of a cold chain, but whether LyoNlac can establish colonization is undetermined. Methods Healthy adult volunteers aged 18-45 years were inoculated intranasally with 104-107 colony forming units (CFU) of reconstituted, lyophilized Nlac strain Y92-1009 (LyoNlac) in 2 dose-ranging controlled human infection studies conducted in the United Kingdom and Mali. Safety was measured as a primary objective. Secondary objectives included the dose achieving ≥70% colonization rates for each setting, colonization kinetics, and serological responses. Both trials were registered with ClinicalTrials.gov (United Kingdom: NCT04135053, Mali: NCT04665791) and are complete. Results Intranasal inoculation with LyoNlac was well tolerated with no significant safety concerns. In the United Kingdom, 105 CFU yielded 100% colonization (n = 10/10) while in Mali, 107 CFU achieved 65% colonization (n = 13/20). An increase in Nlac- and Nmen-specific IgG from pre-challenge to day 28 post-challenge was observed in colonized participants - median fold-change [interquartile range] United Kingdom: Nlac 2.24 [1.37-4.24], Nmen 1.39 [1.20-3.70] and Mali: Nlac 1.31 [1.04-1.94], Nmen 1.32 [0.99-1.73]. No significant seroconversion occurred in non-colonized participants. Conclusions Intranasal inoculation with LyoNlac was safe and induced immunogenic nasopharyngeal colonization in healthy adults in the United Kingdom and Mali. Future clinical trials to determine whether LyoNlac reduces meningococcal carriage and transmission in the meningitis belt are warranted.

Original languageEnglish
Article numberofaf809
JournalOpen Forum Infectious Diseases
Volume13
Issue number1
DOIs
Publication statusPublished - 7 Jan 2026

Bibliographical note

Publisher Copyright:
© 2026 The Author(s). Published by Oxford University Press on behalf of Infectious Diseases Society of America.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • African meningitis belt
  • Neisseria lactamica
  • Neisseria meningitidis
  • controlled human infection
  • lyophilization

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