» Articles » PMID: 34960136

Pneumococcal Immunization Strategies for High-Risk Pediatric Populations Worldwide: One Size Does Not Fit All

Overview
Date 2021 Dec 28
PMID 34960136
Citations 2
Authors
Affiliations
Soon will be listed here.
Abstract

Despite the significant reduction in pneumococcal disease due to pneumococcal vaccines, protection of vulnerable high-risk individuals, especially pediatric populations, remains a great challenge. In an effort to maximize the protection of high-risk children against pneumococcal disease, a combined schedule that includes both conjugate and polysaccharide vaccines is recommended by several countries in the developed world. On the other hand, middle- and low-income countries do not have in place established policies for pneumococcal immunization of children at risk. Pneumococcal conjugate vaccines, despite their benefits, have several limitations, mainly associated with serotype replacement and the wide range of serotype coverage worldwide. In addition, PPV23-impaired immunogenicity and the hyporesponsiveness effect among populations at risk have been well-documented. Therefore, the added value of continuing to include PPV23 in vaccination schedules for high-risk individuals in the years to come remains to be determined by monitoring whether the replacing/remaining serotypes causing IPD are covered by PPV23 to determine whether its benefits outweigh its limitations. In this review, we aim to describe serotype distribution and vaccine efficacy data on pneumococcal disease in the pre- and post-PCV implementation era among high-risk children in both developed and developing countries, assessing the optimization of current recommendations for their vaccination against pneumococcal disease.

Citing Articles

Changes in pneumococcal serotypes distribution and penicillin resistance in healthy children five years after generalization of PCV10.

Warda K, Amari S, Boureddane M, Elkamouni Y, Arsalane L, Zouhair S Heliyon. 2024; 10(4):e25741.

PMID: 38380016 PMC: 10877248. DOI: 10.1016/j.heliyon.2024.e25741.


Epidemiology of Serotypes in Jordan Amongst Children Younger than the Age of 5: A National Cross-Sectional Study.

Abu-Helalah M, Al-Mnayyis A, Alzoubi H, Al-Abdallah R, Jdaitawi H, Nafi O Vaccines (Basel). 2023; 11(9).

PMID: 37766074 PMC: 10536609. DOI: 10.3390/vaccines11091396.

References
1.
van Hoek A, Andrews N, Waight P, Stowe J, Gates P, George R . The effect of underlying clinical conditions on the risk of developing invasive pneumococcal disease in England. J Infect. 2012; 65(1):17-24. DOI: 10.1016/j.jinf.2012.02.017. View

2.
McCavit T, Xuan L, Zhang S, Flores G, Quinn C . Hospitalization for invasive pneumococcal disease in a national sample of children with sickle cell disease before and after PCV7 licensure. Pediatr Blood Cancer. 2011; 58(6):945-9. PMC: 4248562. DOI: 10.1002/pbc.23259. View

3.
Gilks C, Ojoo S, Ojoo J, Brindle R, Paul J, Batchelor B . Invasive pneumococcal disease in a cohort of predominantly HIV-1 infected female sex-workers in Nairobi, Kenya. Lancet. 1996; 347(9003):718-23. DOI: 10.1016/s0140-6736(96)90076-8. View

4.
Madhi S, Nunes M . The potential impact of pneumococcal conjugate vaccine in Africa: Considerations and early lessons learned from the South African experience. Hum Vaccin Immunother. 2015; 12(2):314-25. PMC: 5049711. DOI: 10.1080/21645515.2015.1084450. View

5.
Shatz D . Vaccination considerations in the asplenic patient. Expert Rev Vaccines. 2005; 4(1):27-34. DOI: 10.1586/14760584.4.1.27. View