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Statistical Modelling of Waning Immunity After Shanchol™ Vaccination: A Prospective Cohort Study

  • Samuel Bosomprah
  • , Fraser Liswaniso
  • , Bernard Phiri
  • , Mwelwa Chibuye
  • , Charlie C. Luchen
  • , Harriet Ng’ombe
  • , Kennedy Chibesa
  • , Dennis Ngosa
  • , Mutinta Muchimba
  • , Amanda K. Debes
  • , Roma Chilengi
  • , David A. Sack
  • , Caroline C. Chisenga
  • Centre for Infectious Disease Research in Zambia
  • University of Zambia
  • University of Amsterdam
  • Stellenbosch University
  • University of the Free State, School of Medicine
  • Johns Hopkins Bloomberg School of Public Health
  • Zambia National Public Health Institute
  • Wellcome Sanger Institute

Research output: Contribution to journalArticlepeer-review

Abstract

Introduction: Cholera remains a major public health threat in endemic settings, and oral cholera vaccine (Shanchol™) campaigns are increasingly used amid constrained global supply. However, practical decisions on revaccination require clearer, setting-specific estimates of how rapidly vaccine-induced vibriocidal antibodies peak and wane. Methods: We conducted a prospective cohort kinetics analysis in Lukanga Swamps (Central Province, Zambia), enrolling adults (18–65 years) stratified by prior Shanchol™ exposure (0, 1, or 2 previous doses). All participants received two Shanchol™ doses 14 days apart, with serum collected at baseline and days 14, 28, 60, and 90 (end of follow-up). Ogawa and Inaba vibriocidal titres were measured using a complement-based assay and analysed on the log10 scale. Serotype-specific mixed-effects models with natural cubic splines for time (knots: 14, 28, 60 days) assessed trajectories by prior-dose strata, adjusting for age, sex, and HIV status. Peak timing and post-peak half-life were derived from model-based predictions with participant-level bootstrap CIs (1000 replications). Results: The analysis included 225 participants: 68 (30.2%) with zero prior doses, 89 (39.6%) with one, and 68 (30.2%) with two; median age was 33 years (IQR 25–49), 56.4% were female, and 19.2% were HIV-positive. Modelled titres for both serotypes rose steeply after vaccination, peaking around day 36–37 across prior-dose strata. Ogawa titres reached half of peak by about day 73–78, corresponding to post-peak half-lives of 37–41 days; Inaba declined more slowly with half-lives of 42–46 days. Confidence intervals overlapped across prior-dose strata, indicating minimal differences by vaccination history. Conclusions: In this cholera-endemic adult population, Shanchol™ induced vibriocidal responses that peaked at ~5 weeks and waned over the following 5–7 weeks, with broadly similar kinetics regardless of prior vaccination and slightly slower decay for Inaba than Ogawa. These parameters can inform booster timing in hotspot settings.

Original languageEnglish
Article number147
JournalVaccines
Volume14
Issue number2
DOIs
Publication statusPublished - Feb 2026

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

  • Shanchol™
  • antibodies
  • cholera
  • vibriocidal
  • waning

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