Journal Article > ProtocolSubscription Only
Marburg Virus: Methods and Protocols. 26 November 2024; Volume 2877; 3-24.; DOI:10.1007/978-1-0716-4256-6_1
Sprecher A, Van Herp M
Marburg Virus: Methods and Protocols. 26 November 2024; Volume 2877; 3-24.; DOI:10.1007/978-1-0716-4256-6_1
In many ways, Marburg virus disease resembles the more well-known Ebola virus disease: The clinical syndrome is similar, management of outbreaks is similar, and the fear engendered in the population experiencing the outbreak is similar. However, diagnostics, therapeutics, and vaccines to manage patients and outbreaks are not similarly available. These have been developed but not yet approved, as outbreaks have not provided the opportunity to establish an evidence base for regulators to evaluate their use in humans. The history of outbreaks of Marburg virus disease suggests that this opportunity will not come, and so alternative pathways to regulatory approval are needed.
Conference Material > Poster
Soubrier H, Talla C, Gaye A, Mbala P, Van Herp M, et al.
Epicentre Scientific Day 2024. 23 May 2024
Conference Material > Poster
Elsinga J, Sunyoto T, Di Stefano L, Giorgetti PF, Kyi HA, et al.
MSF Scientific Day International 2024. 16 May 2024; DOI:10.57740/63l6oZ
Journal Article > CommentaryFull Text
Science. 15 March 2024; Volume 383 (Issue 6688); 1181-1182.; DOI:10.1126/science.ado6257
Sprecher A, Van Herp M
Science. 15 March 2024; Volume 383 (Issue 6688); 1181-1182.; DOI:10.1126/science.ado6257
Journal Article > CommentarySubscription Only
Lancet Infect Dis. 18 August 2023; Volume S1473-3099 (Issue 23); 00506-6.; DOI:10.1016/S1473-3099(23)00506-6
Kofman AD, Haberling DL, Mbuyi G, Martel LD, Whitesell AN, et al.
Lancet Infect Dis. 18 August 2023; Volume S1473-3099 (Issue 23); 00506-6.; DOI:10.1016/S1473-3099(23)00506-6
Journal Article > CommentaryFull Text
NPJ Vaccines. 2 November 2022; Volume 7; 137.; DOI:10.1038/s41541-022-00552-3
Lindsey NP, Horton J, Barrett ADT, Demanou M, Monath TP, et al.
NPJ Vaccines. 2 November 2022; Volume 7; 137.; DOI:10.1038/s41541-022-00552-3
Journal Article > ResearchFull Text
Vaccine. 9 June 2022; Volume S0264-410X (Issue 22); 00552-7.; DOI:10.1016/j.vaccine.2022.04.093
Lightowler M, Manangazira P, Nackers F, Van Herp M, Phiri I, et al.
Vaccine. 9 June 2022; Volume S0264-410X (Issue 22); 00552-7.; DOI:10.1016/j.vaccine.2022.04.093
BACKGROUND
Zimbabwe suffers from regular outbreaks of typhoid fever (TF), worse since 2017. Most cases were in Harare and a vaccination campaign with Typhoid Conjugate Vaccine (TCV) was conducted in March 2019. The vaccine effectiveness (VE) was assessed against culture-confirmed S. Typhi in children six months to 15 years and in individuals six months to 45 years in Harare.
METHODS
A matched case-control study was conducted in three urban suburbs of Harare targeted by the TCV vaccination campaign. Suspected TF cases were enrolled prospectively in four health facilities and were matched to facility (1:1) and community (1:5) controls.
FINDINGS
Of 504 suspected cases from July 2019 to March 2020, 148 laboratory-confirmed TF cases and 153 controls confirmed-negative were identified. One hundred and five (47 aged six months to 15 years) cases were age, sex, and residence matched with 105 facility-based controls while 96 cases were matched 1:5 by age, sex, and immediate-neighbour with 229 community controls.
The adjusted VE against confirmed TF was 75% (95%CI: 1–94, p = 0.049) compared to facility controls, and 84% (95%CI: 57–94, p < 0.001) compared to community controls in individuals six months to 15 years. The adjusted VE against confirmed TF was 46% (95%CI: 26–77, p = 0.153) compared to facility controls, and 67% (95%CI: 35–83, p = 0.002) compared to community controls six months to 45 years old.
INTERPRETATION
This study confirms that one vaccine dose of TCV is effective to control TF in children between six months and 15 years old in an African setting.
Zimbabwe suffers from regular outbreaks of typhoid fever (TF), worse since 2017. Most cases were in Harare and a vaccination campaign with Typhoid Conjugate Vaccine (TCV) was conducted in March 2019. The vaccine effectiveness (VE) was assessed against culture-confirmed S. Typhi in children six months to 15 years and in individuals six months to 45 years in Harare.
METHODS
A matched case-control study was conducted in three urban suburbs of Harare targeted by the TCV vaccination campaign. Suspected TF cases were enrolled prospectively in four health facilities and were matched to facility (1:1) and community (1:5) controls.
FINDINGS
Of 504 suspected cases from July 2019 to March 2020, 148 laboratory-confirmed TF cases and 153 controls confirmed-negative were identified. One hundred and five (47 aged six months to 15 years) cases were age, sex, and residence matched with 105 facility-based controls while 96 cases were matched 1:5 by age, sex, and immediate-neighbour with 229 community controls.
The adjusted VE against confirmed TF was 75% (95%CI: 1–94, p = 0.049) compared to facility controls, and 84% (95%CI: 57–94, p < 0.001) compared to community controls in individuals six months to 15 years. The adjusted VE against confirmed TF was 46% (95%CI: 26–77, p = 0.153) compared to facility controls, and 67% (95%CI: 35–83, p = 0.002) compared to community controls six months to 45 years old.
INTERPRETATION
This study confirms that one vaccine dose of TCV is effective to control TF in children between six months and 15 years old in an African setting.
Journal Article > ResearchFull Text
PLOS One. 8 December 2014; Volume 9 (Issue 12); DOI:10.1371/journal.pone.0114702
Polonsky JA, Martinez-Pino I, Nackers F, Chonzi P, Manangazira P, et al.
PLOS One. 8 December 2014; Volume 9 (Issue 12); DOI:10.1371/journal.pone.0114702
Typhoid fever remains a significant public health problem in developing countries. In October 2011, a typhoid fever epidemic was declared in Harare, Zimbabwe - the fourth enteric infection epidemic since 2008. To orient control activities, we described the epidemiology and spatiotemporal clustering of the epidemic in Dzivaresekwa and Kuwadzana, the two most affected suburbs of Harare.
Journal Article > ResearchFull Text
Disasters. 1 June 2003; Volume 27 (Issue 2); 141-153.; DOI:10.1111/1467-7717.00225
Van Herp M, Parqué V, Rackley E, Ford NP
Disasters. 1 June 2003; Volume 27 (Issue 2); 141-153.; DOI:10.1111/1467-7717.00225
The people of the Democratic Republic of Congo for decades have been living in a situation of chronic crisis. Violence, population displacement and the destruction of infrastructure and health services have devastated the health of the population. In 2001, Médicins Sans Frontières conducted a survey in five areas of western and central DRC to assess mortality, access to health-care, vaccination coverage and exposure to violence. High mortality rates were found in front-line zones, mainly due to malnutrition and infectious diseases. In Basankusu approximately 10 per cent of the total population and 25 per cent of the under-five population had perished in the year before the survey. Humanitarian needs remain acute across the country, particularly near the front line. Infectious-disease control and treatment are a priority, as is increasing access to health-care. Humanitarian assistance must be increased considerably, especially in rural areas and zones that have been affected directly by conflict.
Journal Article > ResearchFull Text
Euro Surveill. 9 October 2014; Volume 19 (Issue 40); 20924.
Fitzpatrick G, Vogt F, Gbabai O, Black B, Santantonio M, et al.
Euro Surveill. 9 October 2014; Volume 19 (Issue 40); 20924.
Case management centres (CMCs) are part of the outbreak control plan for Ebola virus disease (EVD). A CMC in Sierra Leone had 33% (138/419) of primary admissions discharged as EVD negative (not a case). Fifteen of these were readmitted within 21 days, nine of which were EVD positive. All readmissions had contact with an Ebola case in the community in the previous 21 days indicating that the infection was likely acquired outside the CMC.