The Impact of Improved Water, Sanitation, and Hygiene on Oral Rotavirus Vaccine Immunogenicity in Zimbabwean Infants: Substudy of a Cluster-randomized Trial

Author:

Church James A12ORCID,Rukobo Sandra1,Govha Margaret1,Lee Benjamin34,Carmolli Marya P35,Chasekwa Bernard1,Ntozini Robert1,Mutasa Kuda1,McNeal Monica M6,Majo Florence D1,Tavengwa Naume V1,Moulton Lawrence H7,Humphrey Jean H17,Kirkpatrick Beth D35,Prendergast Andrew J126

Affiliation:

1. Zvitambo Institute for Maternal and Child Health Research, Harare, Zimbabwe

2. Centre for Genomics and Child Health, Blizard Institute, Queen Mary University of London, United Kingdom

3. Vaccine Testing Center, Larner College of Medicine, University of Vermont, Burlington

4. Department of Pediatrics, Larner College of Medicine, University of Vermont, Burlington

5. Department of Microbiology and Molecular Genetics, Larner College of Medicine, University of Vermont, Burlington

6. Department of Pediatrics, University of Cincinnati College of Medicine, Division of Infectious Diseases, Cincinnati Children’s Hospital Medical Center, Ohio

7. Department of International Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland

Abstract

Abstract Background Oral vaccines have lower efficacy in developing compared to developed countries. Poor water, sanitation, and hygiene (WASH) may contribute to reduced oral vaccine immunogenicity. Methods We conducted a cluster-randomized 2 × 2 factorial trial in rural Zimbabwe. Pregnant women and their infants were eligible if they lived in clusters randomized to (1) standard of care (52 clusters); (2) improved infant feeding (53 clusters); (3) WASH: ventilated improved pit latrine, 2 hand-washing stations, liquid soap, chlorine, infant play space, and hygiene counseling (53 clusters); or (4) feeding plus WASH (53 clusters). This substudy compared oral rotavirus vaccine (RVV) seroconversion (primary outcome), and seropositivity and geometric mean titer (GMT) (secondary outcomes), in WASH vs non-WASH infants by intention-to-treat analysis. Results We included 801 infants with documented RVV receipt and postvaccine titer measurements (329 from 84 WASH clusters; 472 from 102 non-WASH clusters); 328 infants with prevaccination titers were included in the primary outcome. Thirty-three of 109 (30.3%) infants in the WASH group seroconverted following rotavirus vaccination, compared to 43 of 219 (19.6%) in the non-WASH group (absolute difference, 10.6% [95% confidence interval {CI}, .54%–20.7%]; P = .031). In the WASH vs non-WASH groups, 90 of 329 (27.4%) vs 107 of 472 (22.7%) were seropositive postvaccination (absolute difference, 4.7% [95% CI, –1.4% to 10.8%]; P = .130), and antirotavirus GMT was 18.4 (95% CI, 15.6–21.7) U/mL vs 14.9 (95% CI, 13.2–16.8) U/mL (P = .072). Conclusions Improvements in household WASH led to modest but significant increases in seroconversion to RVV in rural Zimbabwean infants. Clinical Trials Registration NCT01824940.

Funder

Wellcome Trust

Bill & Melinda Gates Foundation

Swiss Agency for Development and Cooperation and the US National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

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