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Understanding the immune response to West Nile and Usutu Viruses

Virological characterization and analysis of the immune response in subjects with West Nile virus and Usutu virus infection

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ISRCTN
Registry ID
ISRCTN99840298
Enrollment
80
Registered
2026-07-13
Start date
2025-07-15
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Innate and adaptive immune response in subjects with West Nile virus and Usutu virus infections Infections and Infestations

Interventions

This is an in vitro study on biological fluids to investigate the adaptive humoral and cell-mediated immune responses in blood donors with West Nile virus (WNV) and Usutu virus (USUV) infections. The

Sponsors

University of Padua
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Male or female individuals aged between 18 and 60 years 2. WNV/USUV infection detected through WNV NAT testing as part of blood donor screening 3. Individuals without other acute infections or active chronic diseases, apart from WNV or USUV infection 4. Willingness to provide written informed consent after being adequately informed about the risks and benefits of the study 5. Availability to participate in at least two scheduled study visits

Exclusion criteria

Exclusion criteria: 1. Any individual who, in the investigator's opinion, does not comply with the study objectives and protocol 2. Anticipated absence from the study center during the study period, for example, due to a planned vacation

Design outcomes

Primary

MeasureTime frame
1. Quantification of neutralizing antibody titers by PRNT and MNT at 1, 7, 40 days, and 6 and 12 months post-infection 2. Detection of WNV- and USUV-specific antigen antibodies by EIA at 1, 7, 40 days, and 6 and 12 months post-infection 3. Assessment of cross-reactivity against other orthoflaviviruses by EIA and neutralization assays at 1, 40 days, and 12 months post-infection 4. Analysis of CD4+ and CD8+ T lymphocyte responses measured using flow cytometry at 1 day and 12 months post-infection

Secondary

MeasureTime frame
There are no secondary outcome measures

Countries

Italy

Contacts

Public ContactLuisa Barzon
luisa.barzon@unipd.it+390498218946

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Aug 10, 2026