Sudan virus disease in humans

In 2025, Uganda had Africa's ninth outbreak of disease caused by Sudan virus (SUDV), a filovirus similar to Ebola virus (EBOV) that causes severe febrile disease in humans. In this Review, we summarise the evidence on the epidemiology, natural history, and immunology of Sudan virus disease (SVD) from outbreaks since 1976. Following an incubation period averaging about 1 week, SVD typically presents with an influenza-like illness followed by a severe diarrhoeal disease, often accompanied by cardiorespiratory symptoms and dehydration. Clinical findings can include kidney and liver injury, acute inflammation, and coagulopathy. Severe cases can progress rapidly to shock, multiorgan failure, and death. The pooled case-fatality rate until 2022 was 49% (95% CI 39-58), although a lower case-fatality rate of 29% was recorded during the 2025 outbreak. The virus is detectable in blood from symptom onset, peaking during acute illness. Transmission occurs mainly through close contact with acutely symptomatic individuals and their body fluids, driving household and nosocomial spread. Early T-cell responses and SUDV-specific antibodies might be important for survival, and suppressed immunity and uncontrolled inflammation might predict fatal outcomes. Survivors present durable humoral and cellular immunity for up to 15 years after infection. Although outbreaks to date offer valuable insights into SVD, substantial evidence gaps and limitations exist. Future outbreak preparedness should include prospective planning for high-quality research that can be rapidly implemented to address key evidence gaps. Strengthening these data, together with advancing the development and evaluation of vaccines and therapeutics, will be essential for timely and effective outbreak response.