Distribution of pneumococcal serotypes causing invasive and non-invasive diseases in children in Mexico after introduction of PCV13 (2012−2023). Results from the GIVEBPVac group
Araceli Soto-Noguerón , María Noemí Carnalla-Barajas , Gilberto Sánchez-González , Fortino Solórzano-Santos , Mercedes Macías-Parra , Virginia Díaz-Jiménez , Damaris Manzano-Arredonda , Antonino Lara-Barbosa , Lilia Pichardo-Villalón , Sarbelio Moreno-Espinoza , Martha Josefina Avilés-Robles , Rayo Morfín-Otero , Antonio Luévanos-Velázquez , Rosario Vázquez-Larios , Eduardo Rivera-Martínez , Mariana Gil-Veloz , Elvira Garza-González , Víctor Antonio Monroy-Colín , José Manuel Feliciano-Guzmán , Juan Carlos Tinoco-Favila , Gabriela Echaniz-Aviles
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Abstract
Background
The introduction of pneumococcal conjugate vaccines (PCVs) since 2000 has altered the epidemiology of invasive (IPD) and non-invasive pneumococcal diseases (NIPD). This study aims to analyze trends in pneumococcal serotype distribution among children in Mexico, focusing on the period following the introduction of PCV13, and assess the potential impact of future vaccines.
Material and methods
Pneumococcal isolates were collected from hospitalized children in participating hospitals from January 2012 to December 2023. Serotype distribution was analyzed in children under <5 years and those aged ≥5 to 17.9 years. The average annual change (AAC) in serotype proportions was calculated, and trends were analyzed using the Cochran-Armitage test.
Results
Serotype 19A was the most frequent PCV13 serotype, followed by serotypes 3 and 19F, in both age groups. Serotype 33F, included in PCV15 and PCV20, was absent in children aged ≥5‐17.9 years. Among PCV20 serotypes, serotype 15B was the most common, and serotype 17F, covered by PCV24, showed a significant increase in the older age group (p = 0.037). No significant trends in the increase or decrease of individual serotypes were found, except for serotypes 17F and serotype 34, which increased in both age groups. A decrease in serotypes covered by PCV13 (excluding serotypes 3, 19A, and 19F) was observed in both age groups (p = 0.04, 0.002). A significant increase in non-PCV13 serotypes occurred in children aged ≥5‐17.9 years (p = 0.023).
Conclusions
After a decade of the introduction of PCV13 in Mexico, 10 of the 13 vaccine serotypes have not been detected in the past six years. However, serotypes 3, 19A, and 19F persist at high frequencies as causes of IPD and NIPD in children. Ongoing robust surveillance is critical for identifying emerging pneumococcal serotypes, selecting appropriate vaccines for each country, and developing next-generation vaccine formulations.
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