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Age-dependent acquisition of IgG antibodies to Shigella serotypes-a retrospective analysis of seroprevalence in Kenyan children with implications for infant vaccination.
Kapulu, Melissa C; Muthumbi, Esther; Otieno, Edward; Rossi, Omar; Ferruzzi, Pietro; Necchi, Francesca; Acquaviva, Alessandra; Martin, Laura B; Orindi, Benedict; Mwai, Kennedy; Kibet, Hillary; Mwanzu, Alfred; Bigogo, Godfrey M; Verani, Jennifer R; Mbae, Cecilia; Nyundo, Christopher; Agoti, Charles N; Nakakana, Usman Nasir; Conti, Valentino; Bejon, Philip; Kariuki, Samuel; Scott, J Anthony G; Micoli, Francesca; Podda, Audino.
Afiliação
  • Kapulu MC; KEMRI-Wellcome Trust Programme, Kilifi, Kenya.
  • Muthumbi E; Centre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom.
  • Otieno E; KEMRI-Wellcome Trust Programme, Kilifi, Kenya.
  • Rossi O; Department of Infectious Disease Epidemiology, London School of Hygiene and Tropical Medicine, London, United Kingdom.
  • Ferruzzi P; KEMRI-Wellcome Trust Programme, Kilifi, Kenya.
  • Necchi F; GSK Vaccines Institute for Global Health, Siena, Italy.
  • Acquaviva A; GSK Vaccines Institute for Global Health, Siena, Italy.
  • Martin LB; GSK Vaccines Institute for Global Health, Siena, Italy.
  • Orindi B; GSK Vaccines Institute for Global Health, Siena, Italy.
  • Mwai K; GSK Vaccines Institute for Global Health, Siena, Italy.
  • Kibet H; KEMRI-Wellcome Trust Programme, Kilifi, Kenya.
  • Mwanzu A; KEMRI-Wellcome Trust Programme, Kilifi, Kenya.
  • Bigogo GM; Epidemiology and Biostatistics Division, School of Public Health, University of the Witwatersrand, Johannesburg, South Africa.
  • Verani JR; KEMRI-Wellcome Trust Programme, Kilifi, Kenya.
  • Mbae C; KEMRI-Wellcome Trust Programme, Kilifi, Kenya.
  • Nyundo C; Centre for Global Health Research, Kenya Medical Research Institute, Kisumu, Kenya.
  • Agoti CN; Division of Global Health Protection, US Centers for Disease Control and Prevention, Nairobi, Kenya.
  • Nakakana UN; Centre for Microbiology Research, Kenya Medical Research Institute, Nairobi, Kenya.
  • Conti V; KEMRI-Wellcome Trust Programme, Kilifi, Kenya.
  • Bejon P; KEMRI-Wellcome Trust Programme, Kilifi, Kenya.
  • Kariuki S; GSK Vaccines Institute for Global Health, Siena, Italy.
  • Scott JAG; GSK Vaccines Institute for Global Health, Siena, Italy.
  • Micoli F; KEMRI-Wellcome Trust Programme, Kilifi, Kenya.
  • Podda A; Centre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of Oxford, Oxford, United Kingdom.
Front Immunol ; 15: 1340425, 2024.
Article em En | MEDLINE | ID: mdl-38361949
ABSTRACT

Background:

Shigellosis mainly affects children under 5 years of age living in low- and middle-income countries, who are the target population for vaccination. There are, however, limited data available to define the appropriate timing for vaccine administration in this age group. Information on antibody responses following natural infection, proxy for exposure, could help guide vaccination strategies.

Methods:

We undertook a retrospective analysis of antibodies to five of the most prevalent Shigella serotypes among children aged <5 years in Kenya. Serum samples from a cross-sectional serosurvey in three Kenyan sites (Nairobi, Siaya, and Kilifi) were analyzed by standardized ELISA to measure IgG against Shigella sonnei and Shigella flexneri 1b, 2a, 3a, and 6. We identified factors associated with seropositivity to each Shigella serotype, including seropositivity to other Shigella serotypes.

Results:

A total of 474 samples, one for each participant, were analyzed Nairobi (n = 169), Siaya (n = 185), and Kilifi (n = 120). The median age of the participants was 13.4 months (IQR 7.0-35.6), and the malefemale ratio was 11. Geometric mean concentrations (GMCs) for each serotype increased with age, mostly in the second year of life. The overall seroprevalence of IgG antibodies increased with age except for S. flexneri 6 which was high across all age subgroups. In the second year of life, there was a statistically significant increase of antibody GMCs against all five serotypes (p = 0.01-0.0001) and a significant increase of seroprevalence for S. flexneri 2a (p = 0.006), S. flexneri 3a (p = 0.006), and S. sonnei (p = 0.05) compared with the second part of the first year of life. Among all possible pairwise comparisons of antibody seropositivity, there was a significant association between S. flexneri 1b and 2a (OR = 6.75, 95% CI 3-14, p < 0.001) and between S. flexneri 1b and 3a (OR = 23.85, 95% CI 11-54, p < 0.001).

Conclusion:

Children living in low- and middle-income settings such as Kenya are exposed to Shigella infection starting from the first year of life and acquire serotype-specific antibodies against multiple serotypes. The data from this study suggest that Shigella vaccination should be targeted to infants, ideally at 6 or at least 9 months of age, to ensure children are protected in the second year of life when exposure significantly increases.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Shigella / Disenteria Bacilar Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Child / Child, preschool / Female / Humans / Infant / Male País/Região como assunto: Africa Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Shigella / Disenteria Bacilar Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Child / Child, preschool / Female / Humans / Infant / Male País/Região como assunto: Africa Idioma: En Ano de publicação: 2024 Tipo de documento: Article