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Vaccine-derived poliovirus serotype 2 outbreaks and response in the Democratic Republic of the Congo, 2017-2021.
Alleman, Mary M; Jorba, Jaume; Riziki, Yogolelo; Henderson, Elizabeth; Mwehu, Anicet; Seakamela, Lerato; Howard, Wayne; Kadiobo Mbule, Albert; Nsamba, Renee Ntumbannji; Djawe, Kpandja; Yapi, Moïse Désiré; Mengouo, Marcellin Nimpa; Gumede, Nicksy; Ndoutabe, Modjirom; Kfutwah, Anfumbom K W; Senouci, Kamel; Burns, Cara C.
Afiliación
  • Alleman MM; Global Immunization Division, Centers for Disease Control and Prevention, Atlanta, USA. Electronic address: mea4@cdc.gov.
  • Jorba J; Division of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, USA.
  • Riziki Y; Institut National de Recherche Biomédicale, Ministry of Public Health, Hygiene and Prevention, Democratic Republic of the Congo.
  • Henderson E; Division of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, USA.
  • Mwehu A; Emergency Operations Center for Polio, Ministry of Public Health, Hygiene and Prevention, Democratic Republic of the Congo.
  • Seakamela L; National Institute for Communicable Diseases, National Health Laboratory Services, South Africa.
  • Howard W; National Institute for Communicable Diseases, National Health Laboratory Services, South Africa.
  • Kadiobo Mbule A; Polio, Office of the Regional Director, World Health Organization, Democratic Republic of the Congo Country Office, Democratic Republic of the Congo.
  • Nsamba RN; Polio, Office of the Regional Director, World Health Organization, Democratic Republic of the Congo Country Office, Democratic Republic of the Congo.
  • Djawe K; Polio, Office of the Regional Director, World Health Organization, Democratic Republic of the Congo Country Office, Democratic Republic of the Congo.
  • Yapi MD; Polio, Office of the Regional Director, World Health Organization, Democratic Republic of the Congo Country Office, Democratic Republic of the Congo.
  • Mengouo MN; Polio, Office of the Regional Director, World Health Organization, Democratic Republic of the Congo Country Office, Democratic Republic of the Congo.
  • Gumede N; Polio, Office of the Regional Director, World Health Organization, Regional Office for Africa, Republic of the Congo.
  • Ndoutabe M; Polio, Office of the Regional Director, World Health Organization, Regional Office for Africa, Republic of the Congo.
  • Kfutwah AKW; Polio, Office of the Regional Director, World Health Organization, Regional Office for Africa, Republic of the Congo.
  • Senouci K; Bill and Melinda Gates Foundation, Washington, USA.
  • Burns CC; Division of Viral Diseases, Centers for Disease Control and Prevention, Atlanta, USA.
Vaccine ; 41 Suppl 1: A35-A47, 2023 04 06.
Article en En | MEDLINE | ID: mdl-36907733
ABSTRACT
Vaccine-derived polioviruses (VDPVs) can emerge from Sabin strain poliovirus serotypes 1, 2, and 3 contained in oral poliovirus vaccine (OPV) after prolonged person-to-person transmission where population vaccination immunity against polioviruses is suboptimal. VDPVs can cause paralysis indistinguishable from wild polioviruses and outbreaks when community circulation ensues. VDPV serotype 2 outbreaks (cVDPV2) have been documented in The Democratic Republic of the Congo (DRC) since 2005. The nine cVDPV2 outbreaks detected during 2005-2012 were geographically-limited and resulted in 73 paralysis cases. No outbreaks were detected during 2013-2016. During January 1, 2017-December 31, 2021, 19 cVDPV2 outbreaks were detected in DRC. Seventeen of the 19 (including two first detected in Angola) resulted in 235 paralysis cases notified in 84 health zones in 18 of DRC's 26 provinces; no notified paralysis cases were associated with the remaining two outbreaks. The DRC-KAS-3 cVDPV2 outbreak that circulated during 2019-2021, and resulted in 101 paralysis cases in 10 provinces, was the largest recorded in DRC during the reporting period in terms of numbers of paralysis cases and geographic expanse. The 15 outbreaks occurring during 2017-early 2021 were successfully controlled with numerous supplemental immunization activities (SIAs) using monovalent OPV Sabin-strain serotype 2 (mOPV2); however, suboptimal mOPV2 vaccination coverage appears to have seeded the cVDPV2 emergences detected during semester 2, 2018 through 2021. Use of the novel OPV serotype 2 (nOPV2), designed to have greater genetic stability than mOPV2, should help DRC's efforts in controlling the more recent cVDPV2 outbreaks with a much lower risk of further seeding VDPV2 emergence. Improving nOPV2 SIA coverage should decrease the number of SIAs needed to interrupt transmission. DRC needs the support of polio eradication and Essential Immunization (EI) partners to accelerate the country's ongoing initiatives for EI strengthening, introduction of a second dose of inactivated poliovirus vaccine (IPV) to increase protection against paralysis, and improving nOPV2 SIA coverage.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Poliomielitis / Poliovirus Límite: Humans País/Región como asunto: Africa Idioma: En Revista: Vaccine Año: 2023 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Poliomielitis / Poliovirus Límite: Humans País/Región como asunto: Africa Idioma: En Revista: Vaccine Año: 2023 Tipo del documento: Article