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Use of Mpox Multiplex Serology in the Identification of Cases and Outbreak Investigations in the Democratic Republic of the Congo (DRC)

Human Mpox cases are increasingly reported in Africa, with the highest burden in the Democratic Republic of Congo (DRC). While case reporting on a clinical basis can overestimate infection rates, laboratory confirmation by PCR can underestimate them, especially on suboptimal samples like blood, comm...

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Detalles Bibliográficos
Autores principales: Kinganda-Lusamaki, Eddy, Baketana, Lionel Kinzonzi, Ndomba-Mukanya, Etienne, Bouillin, Julie, Thaurignac, Guillaume, Aziza, Adrienne Amuri, Luakanda-Ndelemo, Gradi, Nuñez, Nicolas Fernandez, Kalonji-Mukendi, Thierry, Pukuta, Elisabeth Simbu, Nkuba-Ndaye, Antoine, Lofiko, Emmanuel Lokilo, Kibungu, Emile Malembi, Lushima, Robert Shongo, Ayouba, Ahidjo, Mbala-Kingebeni, Placide, Muyembe-Tamfum, Jean-Jacques, Delaporte, Eric, Peeters, Martine, Ahuka-Mundeke, Steve
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10385798/
https://www.ncbi.nlm.nih.gov/pubmed/37513764
http://dx.doi.org/10.3390/pathogens12070916
Descripción
Sumario:Human Mpox cases are increasingly reported in Africa, with the highest burden in the Democratic Republic of Congo (DRC). While case reporting on a clinical basis can overestimate infection rates, laboratory confirmation by PCR can underestimate them, especially on suboptimal samples like blood, commonly used in DRC. Here we used a Luminex-based assay to evaluate whether antibody testing can be complementary to confirm cases and to identify human transmission chains during outbreak investigations. We used left-over blood samples from 463 patients, collected during 174 outbreaks between 2013 and 2022, with corresponding Mpox and VZV PCR results. In total, 157 (33.9%) samples were orthopox-PCR positive and classified as Mpox+; 124 (26.8%) had antibodies to at least one of the three Mpox peptides. The proportion of antibody positive samples was significantly higher in Mpox positive samples (36.9%) versus negative (21.6%) (p < 0.001). By combining PCR and serology, 66 additional patients were identified, leading to an Mpox infection rate of 48.2% (223/463) versus 33.9% when only PCR positivity is considered. Mpox infections were as such identified in 14 additional health zones and 23 additional outbreaks (111/174 (63.8%) versus 88/174 (50.6%)). Our findings highlight the urgent need of rapid on-site diagnostics to circumvent Mpox spread.