Application of a Pneumococcal Serotype-specific Urinary Antigen Detection Test for Identification of Pediatric Pneumonia in Burkina Faso

被引:6
作者
Bountogo, Mamadou [1 ,2 ,3 ]
Sanogo, Bintou [4 ]
Pride, Michael W. [5 ]
Jiang, Qin [5 ]
Nikiema, Zakari [4 ]
Njanpop-Lafourcade, Berthe-Marie [1 ]
Ouedraogo, Abdou Salam [4 ]
van der Linden, Mark P. G. [6 ]
Moisi, Jennifer [1 ]
Tall, Haoua [1 ]
Essoh, Alima [1 ]
Betsem, Edouard [1 ]
Gessner, Bradford D. [1 ,5 ]
Meda, Nicolas [3 ,7 ]
机构
[1] Agence Med Prevent, Abidjan, Cote Ivoire
[2] Ctr Rech Sante Nouna, Nouna, Burkina Faso
[3] Univ Pr Joseph Ki Zerbo, Ouagadougou, Burkina Faso
[4] Univ Souro Sanou, Ctr Hosp, Bobo Dioulasso, Burkina Faso
[5] Pfizer Inc, Collegeville, PA USA
[6] German Natl Reference Ctr Streptococci, Aachen, Germany
[7] Ctr Muraz, Bobo Dioulasso, Burkina Faso
关键词
Burkina Faso; pneumonia; serotype; Streptococcus pneumoniae; urinary antigen detection assay; STREPTOCOCCUS-PNEUMONIAE; CONJUGATE VACCINE; CHILDREN; DIAGNOSIS; COMMUNITY; IMPACT; CARRIAGE; DENSITY; DISEASE;
D O I
10.1097/INF.0000000000003065
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: Serotype-specific diagnosis of pneumococcal community-acquired pneumonia in children under age 5 years would mark a major advancement for understanding pneumococcal epidemiology and supporting vaccine decision-making. Methods: A Luminex technology-based multiplex urinary antigen detection (UAD) diagnostic assay was developed and subsequently validated in adults, but its applicability to children is unknown. This study aimed to set appropriate cutoffs for use of the UAD in a healthy pediatric population and apply these cutoffs in children with pneumonia in sub-Saharan Africa. The cutoffs were determined by assessing 379 urines obtained from healthy children under age 5 years from the Bobo-Dioulasso area for serotypes included in 13-valent pneumococcal conjugate vaccine (UAD-1) and the 11 other serotypes unique to 23-valent pneumococcal polysaccharide vaccine (UAD-2). Results: Based on the assigned cutoff values, among 108 children who met the World Health Organization consolidation endpoint criteria, UAD-1 and UAD-2 were positive in 23.3% and 8.3%, respectively; among 364 children with clinically suspected pneumonia who did not meet the World Health Organization criteria, UAD-1 and UAD-2 were positive for 6.6% and 3.6%, respectively. Pneumococcal carriage prevalence was similar among pneumonia cases (30%) versus controls (35%) as was semiquantitative carriage density. Conclusions: UAD-1 and UAD-2 were able to distinguish community controls from children with pneumonia, particularly pneumonia with consolidation. Future studies are needed to confirm these results and more fully assess the contribution of pneumococcal carriage and concurrent viral infection.
引用
收藏
页码:418 / 425
页数:8
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