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      Vaccination of contacts of Ebola virus disease survivors to prevent further transmission

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          Abstract

          On April 10, 2020, just 2 days before the anticipated declaration of the end of the North Kivu and Ituri Ebola virus disease (EVD) outbreak in DR Congo, and 53 days after the last confirmed case of EVD had been reported, a new case was confirmed. Sequencing of patient samples from the case in April and six others that followed indicated that these cases were likely to have come from a reintroduction of the virus from a persistently infected survivor. 1 This group of cases marked the second flare-up linked to an EVD survivor during this outbreak. In November, 2019, a relapse case in North Kivu resulted in widespread transmission across multiple health zones, helping to extend the outbreak by at least 3 months. Ebola virus is known to persist in immune-privileged sites in survivors. 2,3 Viral RNA has been detected in semen up to 2 years after recovery, 2 and clinical relapse has been documented. 3 In North Kivu and Ituri, there are 1171 known EVD survivors, and although the vast majority will no longer transmit the virus, transmission events linked to survivors continue to pose a risk. 1 Unlike previous Ebola outbreaks, the current EVD response strategy has benefited from new investigational tools, including a safe and effective vaccine that protects against Ebola virus. 4 The rVSVΔG-ZEBOV-GP vaccine has been used since the beginning of the North Kivu and Ituri outbreak under a compassionate use protocol using ring vaccination. 4,5 The success of ring vaccination is dependent on strong case investigation, contact identification, and follow-up to ensure all contacts are identified. The ring is defined using the list of contact names ascertained and routinely updated by contact tracers during the investigation, and those on the contact list and their contacts (ie, contacts of contacts) are offered the vaccine. Rings are closed when all identified individuals have been offered vaccination or 21 days have passed. Eligible individuals who do not receive the vaccine due to refusal or because they were not listed might not have another opportunity to be vaccinated unless they are part of a newly defined ring. In theory, the majority of contacts and contacts of contacts should have been vaccinated, or at least offered vaccination, while the ring was open. However, during the North Kivu and Ituri outbreak, and now the Equateur outbreak, many new cases have not been previously identified as contacts, suggesting incomplete contact identification. Additionally, the ring vaccination strategy, as currently implemented, does not account for the fact that a survivor’s contacts are dynamic and can change over time. There is a need to incorporate additional risk reduction strategies, such as regular re-elicitation and vaccination of new and previously unvaccinated contacts of survivors. Offering ongoing vaccination to contacts of survivors early and throughout the outbreak could potentially have prevented both the November, 2019, and April, 2020, flare-ups. In eastern DR Congo, there is an established survivor programme, which includes dedicated clinics that provide health services, including testing of semen to detect the persistence of Ebola virus, counselling on sexual transmission, and specialised psychological support. Monthly follow-up visits are encouraged for survivors up to 18 months after infection. Survivor clinics present an opportunity to expand vaccination to contacts of survivors. Trained counsellors can work with survivors during monthly clinic visits to reassess close contacts and contacts of contacts. The vaccine should be offered to all newly identified or previously unvaccinated contacts to prevent potential sexual transmission and transmission from a relapse case. In the event of insufficient vaccine supply, a more targeted approach could be considered, such as prioritising vaccination of the contacts of male survivors only, or even just the contacts of Ebola-PCR-positive male survivors. Regardless of the approach, the number of doses needed would be minimal. Given the stigma around EVD, appropriate and socially sensitive communication strategies need to be developed in consultation with survivor associations to educate survivors and facilitate community engagement. Educating community members and highlighting the protective value of vaccinating contacts and contacts of contacts should reduce the perceived risk of survivors and overall EVD stigma. The elicitation of sexual partners could be challenging because of intimate partner violence, the sexual exploitation of underage girls, and the need to protect partner anonymity. It is important that mitigation policies and procedures designed for HIV partner services be incorporated into survivor clinics. These concerns could be further addressed by eliciting a broader range of contacts without distinguishing between sexual and close contacts and revealing the nature of their contact with the survivor. In the past 7 years, we have witnessed the two largest and most complex EVD outbreaks in history. Given the continued risk of flare-ups from the North Kivu and Ituri outbreak and, now, the Equateur outbreak, and the likelihood of future EVD outbreaks in DR Congo and elsewhere, response methods need to be updated and improved, and any new tools available need to be strategically used to efficiently stop the prolonged spread of EVD. Transmission events associated with survivors have hampered outbreak containment and highlight the urgent need to incorporate vaccination into survivor programmes as standard practice. It is time to develop, implement, and standardise a protocol for vaccination of contacts of survivors during Ebola outbreaks to prevent survivor-related infections in the future.

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          Most cited references4

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          Efficacy and effectiveness of an rVSV-vectored vaccine in preventing Ebola virus disease: final results from the Guinea ring vaccination, open-label, cluster-randomised trial (Ebola Ça Suffit!)

          Summary Background rVSV-ZEBOV is a recombinant, replication competent vesicular stomatitis virus-based candidate vaccine expressing a surface glycoprotein of Zaire Ebolavirus. We tested the effect of rVSV-ZEBOV in preventing Ebola virus disease in contacts and contacts of contacts of recently confirmed cases in Guinea, west Africa. Methods We did an open-label, cluster-randomised ring vaccination trial (Ebola ça Suffit!) in the communities of Conakry and eight surrounding prefectures in the Basse-Guinée region of Guinea, and in Tomkolili and Bombali in Sierra Leone. We assessed the efficacy of a single intramuscular dose of rVSV-ZEBOV (2×107 plaque-forming units administered in the deltoid muscle) in the prevention of laboratory confirmed Ebola virus disease. After confirmation of a case of Ebola virus disease, we definitively enumerated on a list a ring (cluster) of all their contacts and contacts of contacts including named contacts and contacts of contacts who were absent at the time of the trial team visit. The list was archived, then we randomly assigned clusters (1:1) to either immediate vaccination or delayed vaccination (21 days later) of all eligible individuals (eg, those aged ≥18 years and not pregnant, breastfeeding, or severely ill). An independent statistician generated the assignment sequence using block randomisation with randomly varying blocks, stratified by location (urban vs rural) and size of rings (≤20 individuals vs >20 individuals). Ebola response teams and laboratory workers were unaware of assignments. After a recommendation by an independent data and safety monitoring board, randomisation was stopped and immediate vaccination was also offered to children aged 6–17 years and all identified rings. The prespecified primary outcome was a laboratory confirmed case of Ebola virus disease with onset 10 days or more from randomisation. The primary analysis compared the incidence of Ebola virus disease in eligible and vaccinated individuals assigned to immediate vaccination versus eligible contacts and contacts of contacts assigned to delayed vaccination. This trial is registered with the Pan African Clinical Trials Registry, number PACTR201503001057193. Findings In the randomised part of the trial we identified 4539 contacts and contacts of contacts in 51 clusters randomly assigned to immediate vaccination (of whom 3232 were eligible, 2151 consented, and 2119 were immediately vaccinated) and 4557 contacts and contacts of contacts in 47 clusters randomly assigned to delayed vaccination (of whom 3096 were eligible, 2539 consented, and 2041 were vaccinated 21 days after randomisation). No cases of Ebola virus disease occurred 10 days or more after randomisation among randomly assigned contacts and contacts of contacts vaccinated in immediate clusters versus 16 cases (7 clusters affected) among all eligible individuals in delayed clusters. Vaccine efficacy was 100% (95% CI 68·9–100·0, p=0·0045), and the calculated intraclass correlation coefficient was 0·035. Additionally, we defined 19 non-randomised clusters in which we enumerated 2745 contacts and contacts of contacts, 2006 of whom were eligible and 1677 were immediately vaccinated, including 194 children. The evidence from all 117 clusters showed that no cases of Ebola virus disease occurred 10 days or more after randomisation among all immediately vaccinated contacts and contacts of contacts versus 23 cases (11 clusters affected) among all eligible contacts and contacts of contacts in delayed plus all eligible contacts and contacts of contacts never vaccinated in immediate clusters. The estimated vaccine efficacy here was 100% (95% CI 79·3–100·0, p=0·0033). 52% of contacts and contacts of contacts assigned to immediate vaccination and in non-randomised clusters received the vaccine immediately; vaccination protected both vaccinated and unvaccinated people in those clusters. 5837 individuals in total received the vaccine (5643 adults and 194 children), and all vaccinees were followed up for 84 days. 3149 (53·9%) of 5837 individuals reported at least one adverse event in the 14 days after vaccination; these were typically mild (87·5% of all 7211 adverse events). Headache (1832 [25·4%]), fatigue (1361 [18·9%]), and muscle pain (942 [13·1%]) were the most commonly reported adverse events in this period across all age groups. 80 serious adverse events were identified, of which two were judged to be related to vaccination (one febrile reaction and one anaphylaxis) and one possibly related (influenza-like illness); all three recovered without sequelae. Interpretation The results add weight to the interim assessment that rVSV-ZEBOV offers substantial protection against Ebola virus disease, with no cases among vaccinated individuals from day 10 after vaccination in both randomised and non-randomised clusters. Funding WHO, UK Wellcome Trust, the UK Government through the Department of International Development, Médecins Sans Frontières, Norwegian Ministry of Foreign Affairs (through the Research Council of Norway's GLOBVAC programme), and the Canadian Government (through the Public Health Agency of Canada, Canadian Institutes of Health Research, International Development Research Centre and Department of Foreign Affairs, Trade and Development).
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            Late Ebola virus relapse causing meningoencephalitis: a case report

            Summary Background There are thousands of survivors of the 2014 Ebola outbreak in west Africa. Ebola virus can persist in survivors for months in immune-privileged sites; however, viral relapse causing life-threatening and potentially transmissible disease has not been described. We report a case of late relapse in a patient who had been treated for severe Ebola virus disease with high viral load (peak cycle threshold value 13·2). Methods A 39-year-old female nurse from Scotland, who had assisted the humanitarian effort in Sierra Leone, had received intensive supportive treatment and experimental antiviral therapies, and had been discharged with undetectable Ebola virus RNA in peripheral blood. The patient was readmitted to hospital 9 months after discharge with symptoms of acute meningitis, and was found to have Ebola virus in cerebrospinal fluid (CSF). She was treated with supportive therapy and experimental antiviral drug GS-5734 (Gilead Sciences, San Francisco, Foster City, CA, USA). We monitored Ebola virus RNA in CSF and plasma, and sequenced the viral genome using an unbiased metagenomic approach. Findings On admission, reverse transcriptase PCR identified Ebola virus RNA at a higher level in CSF (cycle threshold value 23·7) than plasma (31·3); infectious virus was only recovered from CSF. The patient developed progressive meningoencephalitis with cranial neuropathies and radiculopathy. Clinical recovery was associated with addition of high-dose corticosteroids during GS-5734 treatment. CSF Ebola virus RNA slowly declined and was undetectable following 14 days of treatment with GS-5734. Sequencing of plasma and CSF viral genome revealed only two non-coding changes compared with the original infecting virus. Interpretation Our report shows that previously unanticipated, late, severe relapses of Ebola virus can occur, in this case in the CNS. This finding fundamentally redefines what is known about the natural history of Ebola virus infection. Vigilance should be maintained in the thousands of Ebola survivors for cases of relapsed infection. The potential for these cases to initiate new transmission chains is a serious public health concern. Funding Royal Free London NHS Foundation Trust.
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              Prevention of sexual transmission of Ebola in Liberia through a national semen testing and counselling programme for survivors: an analysis of Ebola virus RNA results and behavioural data.

              Ebola virus has been detected in semen of Ebola virus disease survivors after recovery. Liberia's Men's Health Screening Program (MHSP) offers Ebola virus disease survivors semen testing for Ebola virus. We present preliminary results and behavioural outcomes from the first national semen testing programme for Ebola virus.
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                Author and article information

                Contributors
                Journal
                101613665
                42402
                Lancet Glob Health
                Lancet Glob Health
                The Lancet. Global health
                2214-109X
                14 November 2023
                December 2020
                21 November 2023
                : 8
                : 12
                : e1455-e1456
                Affiliations
                Global Immunization Division, Centers for Disease Control and Prevention, Atlanta, GA 30329, USA
                Global Immunization Division, Centers for Disease Control and Prevention, Atlanta, GA 30329, USA
                Expanded Programme on Immunization, Kinshasa, Democratic Republic of the Congo
                Global Immunization Division, Centers for Disease Control and Prevention, Atlanta, GA 30329, USA
                Global Immunization Division, Centers for Disease Control and Prevention, Atlanta, GA 30329, USA
                Division of High-Consequence Pathogens and Pathology, National Center for Emerging and Zoonotic Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA
                Expanded Programme on Immunization, Kinshasa, Democratic Republic of the Congo
                Expanded Programme on Immunization, Goma, Democratic Republic of the Congo
                Center for Global Health, Centers for Disease Control and Prevention, Atlanta, GA 30329, USA
                Division of High-Consequence Pathogens and Pathology, National Center for Emerging and Zoonotic Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA
                Division of High-Consequence Pathogens and Pathology, National Center for Emerging and Zoonotic Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA
                Division of Foodborne, Waterborne and Environmental Diseases, National Center for Emerging and Zoonotic Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA
                Expanded Programme on Immunization, Kinshasa, Democratic Republic of the Congo
                Global Immunization Division, Centers for Disease Control and Prevention, Atlanta, GA 30329, USA
                Author notes
                Article
                HHSPA1942427
                10.1016/S2214-109X(20)30454-X
                10662388
                33220205
                eb80f055-023c-4d0b-b1f2-84c45888d23a

                This is an Open Access article under the CC BY 4.0 license.

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