Flavivirus Cross-priming Potential of IMOJEV

Japanese Encephalitis Clinical Trial

— FlaviPrime  

Official title:

Flavivirus Cross-priming Potential of Live Attenuated Japanese Encephalitis (JE) Vaccine IMOJEV in Flavivirus naïve and Flavivirus Experienced Participants

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03920111
• Other study ID #: UoL001462 - 4833
• Status: Completed
• Phase: N/A
• Start date: April 16, 2021
• Est. completion date: May 11, 2022

Study information

• Verified date: October 2022
• Source: University of Liverpool
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

There is a pressing need for a better experimental system to understand flavivirus antibody responses, beyond dengue, to make sure the investigators are using current vaccines to greatest effect and to inform the development of next-generation vaccines. This study will use live chimeric JE vaccine IMOJEV® as a tool for flavivirus epitope discovery. This will allow experimental JEV infection using replication competent, live, attenuated virus as a model, in a setting where the flavivirus infection history of humans can be tightly controlled.

Description:

This study will test the hypothesis that in previously flavivirus-exposed individuals, the antibody response is more broadly cross neutralising, and that this will lead to the identification of conserved virion surface epitopes that could be the target of second generation vaccines. Exploratory Primary Objectives/Specific aims: 1. To establish a human model system of JEV infection in healthy adult volunteers using live attenuated JE vaccine IMOJEV®. 2. To sort and sequence individual responding B cells (plasmablasts) after vaccination with IMOJEV®, and to generate human monoclonal antibodies to JEV. 3. To generate JEV specific human monoclonal antibodies from the sequences derived in (2). 4. To describe the development, specificity, cross-reactivity and function of the T cell response to IMOJEV®. 5. To establish a sample bank for future work on cross-reactive and other responses to flaviviruses, flavivirus vaccines and other emergent viruses. Exploratory Secondary Objectives: 1. To examine the specificity and cross-reactivity of the antibody response after JE vaccination, using serum and human monoclonal antibodies. 2. To determine whether there are epitopes which can serve as the target of broadly cross-neutralising antibody responses. Experimentally the fine specificity and cross-reactivity of the antibody response will be studied by cloning antibodies from plasmablasts (B cells responding to the vaccine) that have been single cell sorted by flow cytometry then sequenced at one week post vaccine. These human monoclonal antibodies will then be mapped on to the surface of the virus particle using established approaches, and tested to look for cross-reactive antibodies. T cell responses to the vaccine will be studied using custom pools of synthetic peptides by ELISpot and flow cytometry.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 18
• Est. completion date: May 11, 2022
• Est. primary completion date: December 23, 2021
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 70 Years

Eligibility

Inclusion Criteria:

1. A male or female adult between 18 and 70 years of age at consent.

2. Written and informed consent obtained from participant and agreement of participant to comply with the requirements of the study

3. Able to attend regularly to donate study blood samples for the duration of the study (8 weeks), no planned re-location or travel to a flavivirus endemic area during the study period.

4. Satisfactory medical screen, as demonstrated by study screening document normal physical examination and normal screening blood tests

5. Group 1: Any flavivirus exposure status; Group 2: No previous flavivirus vaccination (JE, tick borne encephalitis or yellow fever (YF)), no residence in a flavivirus endemic area nor planned travel to a flavivirus endemic area during the period of the study; Group 3: JE vaccine and/or yellow fever vaccine or other proven flavivirus infection within the last 10 years or other proven flavivirus infection (lifetime).

6. An efficacious method of contraception must be used during the study for women of childbearing potential.

Exclusion Criteria:

1. Use of any investigational or non-registered drug within 5 half-lives of the drug, or 30 days preceding administration of study JE vaccine, whichever is longer; or planned use during the study period.

2. Receipt of any investigational biologic agents with mechanisms of action that might affect the immune system, at the discretion of the CI and local PI.

3. Administration of immunosuppressants or other immune-modifying drugs within a period of six months before vaccination or at any time during the study period; participants who have received these agents may also be excluded at the discretion of the CI and local PI.

4. Any confirmed or suspected immunosuppressive or immunodeficient condition.

5. A family history of congenital or hereditary immunodeficiency.

6. Any antiviral drug therapy within a period of 5 drug half-lives or 30 days before vaccination, whichever is longer, or at any time during the study period.

7. History of significant allergic reactions likely to be exacerbated by any component of the study vaccine, especially allergic disease or reactions to any previous dose of any vaccine.

8. History of having received JE vaccine, yellow fever vaccine, tick-borne encephalitis vaccine or experimental flavivirus vaccine (group 2 only).

9. Detectable anti Flavivirus neutralizing antibodies in screening tests (group 2 only).

10. Acute disease (for example acute infection) at the time of enrolment or vaccination, if symptoms are rated as anything more significant than a mild adverse event. Entry into the study and/or vaccination may be deferred until the illness has resolved for at least one week.

11. Acute or chronic, clinically significant in the opinion of the investigator, disease in any organ system, as determined by history, physical examination or laboratory testing.

12. Presence of any inflammatory condition that might require immunomodulatory therapy.

13. Recent blood donation (inclusion can be delayed under these circumstances; the participant should be enrolled 16 weeks after their last blood donation. Each participant should give no more than 470 ml per 16 weeks, so regular blood donation should be suspended during the study and can re-commence 1 month after the last study sample).

14. Current or previous abattoir worker or sheep farmer in Scotland (risk of Louping ill virus exposure; group 2 only).

15. Administration of immunoglobulins and/or any blood products within the three months preceding administration of vaccine, or planned administration during the study period.

16. Seropositive for HIV.

17. Pregnancy or Lactation.

18. History of excessive alcohol consumption (>28 units per week), drug abuse or significant psychiatric illness.

19. Any other condition or consideration that, in the opinion of the Investigator, would pose a health risk to the participant if they were enrolled in the study, or would otherwise interfere with the evaluation of the study aims (e.g. difficult venesection).

Related Conditions & MeSH terms

• Encephalitis
• Encephalitis, Japanese
• Japanese Encephalitis

Intervention

Biological:
• IMOJEV
live attenuated Japanese encephalitis (JE) vaccine IMOJEV®

Locations

Country	Name	City	State
United Kingdom	Liverpool University Hospitals NHS Foundation Trust	Liverpool

Sponsors (1)

Lead Sponsor	Collaborator
University of Liverpool

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Primary: Plasmablast percentage of total B cells at 7 days post vaccine	Plasmablast percentage of total B cells at 7 days post vaccine Number of plasmablasts sorted by flow cytometry at 7 days post vaccine	1 week
Primary	Primary: Neutralising antibody titre, measured by 50% of viral plaque reduction at one and two months post vaccine	Neutralising antibody titre, measured by 50% of viral plaque reduction at one and two months post vaccine	two months
Secondary	Secondary: Number of adverse events occurring in all participants in one month post vaccine	Number of adverse events occurring in all participants in one month post vaccine	one month