Morton, Ben 
ORCID: 0000-0002-6164-2854, Jambo, Kondwani ORCID: 0000-0002-3195-2210, Chikaonda, Tarsizio, Rylance, Jamie ORCID: 0000-0002-2323-3611, Henrion, Marc YR ORCID: 0000-0003-1242-839X, Banda, Ndaziona Peter, Nsomba, Edna, Gondwe, Joel, Ferreira, Daniela ORCID: 0000-0002-0594-0902, Gordon, Stephen ORCID: 0000-0001-6576-1116 et al (show 1 more authors)
(2021)
The influence of pneumococcal conjugate vaccine-13 on nasal colonisation in a controlled human infection model of pneumococcal carriage in Malawi: a double-blinded randomised controlled trial protocol.
Wellcome Open Res, 6.
240-.
Abstract
Streptococcus pneumoniae is the leading cause of morbidity and mortality due to community acquired pneumonia, bacterial meningitis and bacteraemia worldwide. Pneumococcal conjugate vaccines protect against invasive disease, but are expensive to manufacture, limited in serotype coverage, associated with serotype replacement, and demonstrate reduced effectiveness against mucosal colonisation. For Malawi, nasopharyngeal carriage of vaccine-type pneumococci is common in vaccinated children despite national roll-out of 13-valent pneumococcal conjugate vaccine (PCV13) since 2011. Our team has safely transferred an established experimental human pneumococcal carriage method from Liverpool School of Tropical Medicine to the Malawi-Liverpool Wellcome Trust Clinical Research Programme, Malawi. This study will determine potential immunological mechanisms for the differential effects of PCV13 on nasal carriage between healthy Malawian and UK populations. We will conduct a double-blinded randomised controlled trial to vaccinate (1:1) participants with either PCV13 or control (normal saline). After a period of one month, participants will be inoculated with S. pneumoniae serotype 6B to experimentally induce nasal carriage using the EHPC method. Subsequently, participants will be invited for a second inoculation after one year to determine longer-term vaccine-induced immunological effects. Primary endpoint: detection of inoculated pneumococci by classical culture from nasal wash recovered from the participants after pneumococcal challenge. Secondary endpoints: local and systemic innate, humoral and cellular responses to PCV-13 with and without pneumococcal nasal carriage The primary objective of this controlled human infection model study is to determine if PCV-13 vaccination is protective against pneumococcal carriage in healthy adult Malawian volunteers. This study will help us to understand the observed differences in PCV-13 efficacy between populations and inform the design of future vaccines relevant to the Malawian population. Trial Registration: Pan African Clinical Trial Registry (REF: PACTR202008503507113 )
| Item Type: | Article |
|---|---|
| Uncontrolled Keywords: | MARVELS Consortium |
| Divisions: | Faculty of Health and Life Sciences Faculty of Health and Life Sciences > Institute of Infection, Veterinary and Ecological Sciences |
| Depositing User: | Symplectic Admin |
| Date Deposited: | 17 Oct 2022 09:25 |
| Last Modified: | 18 Jan 2023 20:36 |
| DOI: | 10.12688/wellcomeopenres.17172.1 |
| Open Access URL: | https://wellcomeopenresearch.org/articles/6-240/v1 |
| Related URLs: | |
| URI: | https://livrepository.liverpool.ac.uk/id/eprint/3165512 |
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