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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

Controlled human infection of healthy adults with lyophilized Neisseria lactamica induces asymptomatic, immunogenic nasopharyngeal carriage in the United Kingdom and Mali
Controlled human infection of healthy adults with lyophilized Neisseria lactamica induces asymptomatic, immunogenic nasopharyngeal carriage in the United Kingdom and Mali

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 10 4-10 7 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, 10 5 CFU yielded 100% colonization (n = 10/10) while in Mali, 10 7 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.

African meningitis belt, Neisseria lactamica, Neisseria meningitidis, controlled human infection, lyophilization
2328-8957
Gbesemete, D.F.
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Haidara, F.
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Laver, J.R.
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Ibrahim, M.
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Maclennan, J.
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Dale, A.P.
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Gorringe, A.R.
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Traore, Y.
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Diallo, F.
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Badji, H.
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Traore, A.
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Onwuchekwa, U.
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Jones, E.
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Webb, C.
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Guy, J.
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Theodosiou, A.A.
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Faust, S.N.
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Sow, S.O.
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Heyderman, R.S.
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Tapia, M.D.
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Read, R.C.
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Gbesemete, D.F.
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Haidara, F.
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Laver, J.R.
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Ibrahim, M.
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Maclennan, J.
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Dale, A.P.
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Gorringe, A.R.
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Traore, Y.
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Diallo, F.
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Badji, H.
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Traore, A.
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Onwuchekwa, U.
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Jones, E.
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Webb, C.
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Guy, J.
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Theodosiou, A.A.
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Faust, S.N.
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Sow, S.O.
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Heyderman, R.S.
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Tapia, M.D.
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Read, R.C.
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Gbesemete, D.F., Haidara, F., Laver, J.R., Ibrahim, M., Maclennan, J., Dale, A.P., Gorringe, A.R., Traore, Y., Diallo, F., Badji, H., Traore, A., Onwuchekwa, U., Jones, E., Webb, C., Guy, J., Theodosiou, A.A., Faust, S.N., Sow, S.O., Heyderman, R.S., Tapia, M.D. and Read, R.C. (2026) Controlled human infection of healthy adults with lyophilized Neisseria lactamica induces asymptomatic, immunogenic nasopharyngeal carriage in the United Kingdom and Mali. Open Forum Infectious Diseases, 13 (1), [ofaf809]. (doi:10.1093/ofid/ofaf809).

Record type: Article

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 10 4-10 7 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, 10 5 CFU yielded 100% colonization (n = 10/10) while in Mali, 10 7 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.

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Accepted/In Press date: 26 December 2025
e-pub ahead of print date: 7 January 2026
Keywords: African meningitis belt, Neisseria lactamica, Neisseria meningitidis, controlled human infection, lyophilization

Identifiers

Local EPrints ID: 509720
URI: http://eprints.soton.ac.uk/id/eprint/509720
ISSN: 2328-8957
PURE UUID: 0b962653-8db0-41b2-8152-66c182cc5579
ORCID for J.R. Laver: ORCID iD orcid.org/0000-0003-3314-5989
ORCID for M. Ibrahim: ORCID iD orcid.org/0009-0000-1169-8545
ORCID for A.A. Theodosiou: ORCID iD orcid.org/0000-0002-0096-4825
ORCID for S.N. Faust: ORCID iD orcid.org/0000-0003-3410-7642
ORCID for R.C. Read: ORCID iD orcid.org/0000-0002-4297-6728

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Date deposited: 03 Mar 2026 17:55
Last modified: 07 Mar 2026 04:17

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Contributors

Author: D.F. Gbesemete
Author: F. Haidara
Author: J.R. Laver ORCID iD
Author: M. Ibrahim ORCID iD
Author: J. Maclennan
Author: A.P. Dale
Author: A.R. Gorringe
Author: Y. Traore
Author: F. Diallo
Author: H. Badji
Author: A. Traore
Author: U. Onwuchekwa
Author: E. Jones
Author: C. Webb
Author: J. Guy
Author: A.A. Theodosiou ORCID iD
Author: S.N. Faust ORCID iD
Author: S.O. Sow
Author: R.S. Heyderman
Author: M.D. Tapia
Author: R.C. Read ORCID iD

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