<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Mbala-Kingebeni P</submitter><funding>Fogarty International Center NIH/CRDF</funding><funding>Bill &amp; Melinda Gates Foundation</funding><funding>World Health Organization</funding><funding>FIC NIH HHS</funding><funding>NIAID NIH HHS</funding><funding>National Cancer Institute</funding><funding>NCI NIH HHS</funding><funding>National Institutes of Health</funding><funding>Bill and Melinda Gates Foundation</funding><funding>NIH HHS</funding><funding>NIGMS NIH HHS</funding><funding>National Science Foundation</funding><pagination>1240-1247</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7888312</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>384(13)</volume><pubmed_abstract>During the 2018-2020 Ebola virus disease (EVD) outbreak in North Kivu province in the Democratic Republic of Congo, EVD was diagnosed in a patient who had received the recombinant vesicular stomatitis virus-based vaccine expressing a ZEBOV glycoprotein (rVSV-ZEBOV) (Merck). His treatment included an Ebola virus (EBOV)-specific monoclonal antibody (mAb114), and he recovered within 14 days. However, 6 months later, he presented again with severe EVD-like illness and EBOV viremia, and he died. We initiated epidemiologic and genomic investigations that showed that the patient had had a relapse of acute EVD that led to a transmission chain resulting in 91 cases across six health zones over 4 months. (Funded by the Bill and Melinda Gates Foundation and others.).</pubmed_abstract><journal>The New England journal of medicine</journal><pubmed_title>Ebola Virus Transmission Initiated by Relapse of Systemic Ebola Virus Disease.</pubmed_title><pmcid>PMC7888312</pmcid><funding_grant_id>3U19AI135995</funding_grant_id><funding_grant_id>U01AI151812</funding_grant_id><funding_grant_id>UL1TR002550</funding_grant_id><funding_grant_id>U19 AI135995</funding_grant_id><funding_grant_id>INV-003565</funding_grant_id><funding_grant_id>DGE-1256082</funding_grant_id><funding_grant_id>001</funding_grant_id><funding_grant_id>U01 AI151812</funding_grant_id><funding_grant_id>U19AI135995</funding_grant_id><funding_grant_id>INV-004176</funding_grant_id><funding_grant_id>GM119774-01</funding_grant_id><funding_grant_id>Contract# 75N91019D00024 Task Order No. 75N91019F0</funding_grant_id><funding_grant_id>FOGX-19-90402-1</funding_grant_id><funding_grant_id>R35 GM119774</funding_grant_id><pubmed_authors>Sana-Paka E</pubmed_authors><pubmed_authors>Mutafali-Ruffin M</pubmed_authors><pubmed_authors>Suchard MA</pubmed_authors><pubmed_authors>Mbala-Kingebeni P</pubmed_authors><pubmed_authors>Mambu F</pubmed_authors><pubmed_authors>Bula Bula J</pubmed_authors><pubmed_authors>Hensley L</pubmed_authors><pubmed_authors>Nkuba-Ndaye A</pubmed_authors><pubmed_authors>Wiley MR</pubmed_authors><pubmed_authors>Faye O</pubmed_authors><pubmed_authors>Faye M</pubmed_authors><pubmed_authors>Ploquin A</pubmed_authors><pubmed_authors>Mulangu S</pubmed_authors><pubmed_authors>Mukadi D</pubmed_authors><pubmed_authors>Gangavarapu K</pubmed_authors><pubmed_authors>Bedford T</pubmed_authors><pubmed_authors>Aziza A</pubmed_authors><pubmed_authors>Diallo B</pubmed_authors><pubmed_authors>Sall A</pubmed_authors><pubmed_authors>Sullivan NJ</pubmed_authors><pubmed_authors>Belizaire MRD</pubmed_authors><pubmed_authors>Pratt C</pubmed_authors><pubmed_authors>Kinganda-Lusamaki E</pubmed_authors><pubmed_authors>Pauthner MG</pubmed_authors><pubmed_authors>Crozier I</pubmed_authors><pubmed_authors>Rambaut A</pubmed_authors><pubmed_authors>Epaso V</pubmed_authors><pubmed_authors>Muyembe Tamfum JJ</pubmed_authors><pubmed_authors>Yam A</pubmed_authors><pubmed_authors>Diagne MM</pubmed_authors><pubmed_authors>Akonga M</pubmed_authors><pubmed_authors>Keita M</pubmed_authors><pubmed_authors>Rimoin AW</pubmed_authors><pubmed_authors>Fall IS</pubmed_authors><pubmed_authors>N'kasar YTT</pubmed_authors><pubmed_authors>Bile F</pubmed_authors><pubmed_authors>Edidi F</pubmed_authors><pubmed_authors>White B</pubmed_authors><pubmed_authors>Ahuka-Mundeke S</pubmed_authors><pubmed_authors>Black A</pubmed_authors><pubmed_authors>Hadfield J</pubmed_authors><pubmed_authors>Salfati E</pubmed_authors><pubmed_authors>Kazadi D</pubmed_authors><pubmed_authors>Nsunda B</pubmed_authors><pubmed_authors>Tshiani O</pubmed_authors><pubmed_authors>Andersen KG</pubmed_authors><pubmed_authors>Bisento N</pubmed_authors><pubmed_authors>Matondo M</pubmed_authors><pubmed_authors>Misasi J</pubmed_authors><pubmed_authors>Torkamani A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Ebola Virus Transmission Initiated by Relapse of Systemic Ebola Virus Disease.</name><description>During the 2018-2020 Ebola virus disease (EVD) outbreak in North Kivu province in the Democratic Republic of Congo, EVD was diagnosed in a patient who had received the recombinant vesicular stomatitis virus-based vaccine expressing a ZEBOV glycoprotein (rVSV-ZEBOV) (Merck). His treatment included an Ebola virus (EBOV)-specific monoclonal antibody (mAb114), and he recovered within 14 days. However, 6 months later, he presented again with severe EVD-like illness and EBOV viremia, and he died. We initiated epidemiologic and genomic investigations that showed that the patient had had a relapse of acute EVD that led to a transmission chain resulting in 91 cases across six health zones over 4 months. (Funded by the Bill and Melinda Gates Foundation and others.).</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Apr</publication><modification>2024-11-12T15:01:21.995Z</modification><creation>2022-02-09T11:05:50.828Z</creation></dates><accession>S-EPMC7888312</accession><cross_references><pubmed>33789012</pubmed><doi>10.1056/NEJMoa2024670</doi></cross_references></HashMap>