Wellcome Open Research (Aug 2024)

Experimental Human Pneumococcal Carriage using Streptococcus pneumoniae serotype 3 in Malawi: a dose ranging and reproducibility human infection study [version 1; peer review: 2 approved, 1 approved with reservations]

  • Clara Ngoliwa,
  • Kondwani Jambo,
  • Neema Toto,
  • Vitumbiko S. Nkhoma,
  • Lorensio Chimgoneko,
  • Marc Henrion,
  • Lumbani Makhaza,
  • John Ndaferankhande,
  • Stephen B. Gordon,
  • Gift Chiwala,
  • Gareth Lipunga,
  • Anthony Emeritus Chirwa,
  • Bridgette Galafa,
  • Faith Thole,
  • Evarista Kudowa,
  • Morrison Peace Kamanga,
  • Godwin Tembo,
  • Dingase Dula,
  • Daniela M. Ferreira,
  • Tarsizio Chikaonda,
  • Ndaziona Peter Kwanjo Banda,
  • Edna Nsomba

Journal volume & issue
Vol. 9

Abstract

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Background Streptococcus pneumoniae is a major cause of morbidity and mortality from respiratory tract infections, pneumonia, meningitis, and sepsis. Nasopharyngeal carriage of pneumococcus is a prerequisite for pneumococcal disease and transmission. Since the global introduction of pneumococcal conjugated vaccines, rates of pneumococcal disease have declined for many vaccine type serotypes but serotype 3 (SPN3) continues to cause significant disease. The Experimental Human Pneumococcal Challenge (EHPC) model is a unique method of determining pneumococcal colonisation, understanding the impact of colonisation on acquired immunity and for testing pneumococcal vaccines. This study will develop a serotype 3 EHPC model to address some pertinent questions on the burden of pneumococcal disease in Malawi. Methods Healthy adults aged 18-50 years will be recruited, with a maximum target of 83 participants to complete all study visits. The study will consist of a dose ranging and safety study, followed by a reproducibility study. Sequential cohorts of 10 healthy participants will be challenged with escalating doses of SPN3 in the dose ranging study. Samples will be collected before inoculation and on days 2, 7, 13, 16, 21 and 28 following inoculations, for determination of carriage. A total of 33 participants will be enrolled in the reproducibility part and will use a dose that established ≥60% of carriage, and with a high safety profile. Samples will be collected for determination of both local and systemic immunological responses to pneumococcal challenge. Upon completion of study visits, participants will complete a questionnaire establish acceptability. Interpretations We expect to establish an optimal SPN3 dose required to establish nasopharyngeal colonisation in healthy adults in an EHPC model. The model can then be used to evaluate pneumococcal vaccines in both healthy and at-risk populations.

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