Haidara, Fadima C; Umesi, Ama; Sow, Samba O; Ochoge, Magnus; Diallo, Fatoumata; Imam, Abdulazeez; Traore, Youssouf; Affleck, Lucy; Doumbia, Moussa F; Daffeh, Bubacarr; +23 more... Kodio, Mamoudou; Wariri, Oghenebrume; Traoré, Awa; Jallow, Edrissa; Kampmann, Beate; Kapse, Dhananjay; Kulkarni, Prasad S; Mallya, Asha; Goel, Sunil; Sharma, Pankaj; Sarma, Annamraju D; Avalaskar, Nikhil; LaForce, F Marc; Alderson, Mark R; Naficy, Abdi; Lamola, Steve; Tang, Yuxiao; Martellet, Lionel; Hosken, Nancy; Simeonidis, Evangelos; Welsch, Jo Anne; Tapia, Milagritos D; Clarke, Ed; (2023) Meningococcal ACWYX Conjugate Vaccine in 2-to-29-Year-Olds in Mali and Gambia. The New England journal of medicine, 388 (21). pp. 1942-1955. ISSN 0028-4793 DOI: https://doi.org/10.1056/NEJMoa2214924
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Abstract
BACKGROUND: An effective, affordable, multivalent meningococcal conjugate vaccine is needed to prevent epidemic meningitis in the African meningitis belt. Data on the safety and immunogenicity of NmCV-5, a pentavalent vaccine targeting the A, C, W, Y, and X serogroups, have been limited. METHODS: We conducted a phase 3, noninferiority trial involving healthy 2-to-29-year-olds in Mali and Gambia. Participants were randomly assigned in a 2:1 ratio to receive a single intramuscular dose of NmCV-5 or the quadrivalent vaccine MenACWY-D. Immunogenicity was assessed at day 28. The noninferiority of NmCV-5 to MenACWY-D was assessed on the basis of the difference in the percentage of participants with a seroresponse (defined as prespecified changes in titer; margin, lower limit of the 96% confidence interval [CI] above -10 percentage points) or geometric mean titer (GMT) ratios (margin, lower limit of the 98.98% CI >0.5). Serogroup X responses in the NmCV-5 group were compared with the lowest response among the MenACWY-D serogroups. Safety was also assessed. RESULTS: A total of 1800 participants received NmCV-5 or MenACWY-D. In the NmCV-5 group, the percentage of participants with a seroresponse ranged from 70.5% (95% CI, 67.8 to 73.2) for serogroup A to 98.5% (95% CI, 97.6 to 99.2) for serogroup W; the percentage with a serogroup X response was 97.2% (95% CI, 96.0 to 98.1). The overall difference between the two vaccines in seroresponse for the four shared serogroups ranged from 1.2 percentage points (96% CI, -0.3 to 3.1) for serogroup W to 20.5 percentage points (96% CI, 15.4 to 25.6) for serogroup A. The overall GMT ratios for the four shared serogroups ranged from 1.7 (98.98% CI, 1.5 to 1.9) for serogroup A to 2.8 (98.98% CI, 2.3 to 3.5) for serogroup C. The serogroup X component of the NmCV-5 vaccine generated seroresponses and GMTs that met the prespecified noninferiority criteria. The incidence of systemic adverse events was similar in the two groups (11.1% in the NmCV-5 group and 9.2% in the MenACWY-D group). CONCLUSIONS: For all four serotypes in common with the MenACWY-D vaccine, the NmCV-5 vaccine elicited immune responses that were noninferior to those elicited by the MenACWY-D vaccine. NmCV-5 also elicited immune responses to serogroup X. No safety concerns were evident. (Funded by the U.K. Foreign, Commonwealth, and Development Office and others; ClinicalTrials.gov number, NCT03964012.).
Item Type | Article |
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Faculty and Department |
MRC Gambia > GM-Vaccinology Theme Faculty of Infectious and Tropical Diseases > Dept of Clinical Research |
PubMed ID | 37224196 |
Elements ID | 203318 |
Official URL | http://dx.doi.org/10.1056/nejmoa2214924 |
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