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Characterization of T Cell Responses Following Yellow Fever Virus Vaccination in Healthy Adults

Characterization of T Cell Responses Following Yellow Fever Virus Vaccination in Healthy Adults

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00616356
Enrollment
8
Registered
2008-02-15
Start date
2007-12-31
Completion date
2008-06-30
Last updated
2011-11-08

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

Conditions

Yellow Fever

Keywords

Yellow Fever

Brief summary

The investigators at Rockefeller University are doing this research to study how the immune system responds to viruses and other infectious agents by using the yellow fever 17D vaccine as a model. The YFV-17D vaccine is one of the safest and most effective vaccines known and has been used to vaccinate humans against yellow fever virus (YFV) infection since the 1930s. By studying how the human immune system responds to the YFV vaccine we hope to learn more about the normal functioning of the immune system so that it might be possible to design new, more effective types of vaccines to prevent important infectious diseases. The reason for doing this research is: Currently there is very little information about which factors determine the effectiveness of the initial (primary) immune response to a foreign substance (antigen), such as a virus, that person may be exposed to. There is also very little known about what determines how effectively and for how long a person's immune system can react to the same antigen to prevent another infection. Studies in animals have given us important information about how the immune systems of other animals behave upon initial or repeated exposure to antigens,but these topics have not been studied in detail in humans. The following hypotheses will be tested: * The magnitude of the initial expansion of T lymphocytes (the clonal burst) specific for the infecting virus determines the level at which memory T cell responses are generated against the specific viral antigen and the duration of the memory T cell response generated in the body. * The majority of CD8 T cells generated after immunization are yellow fever specific and not bystander activation of non-specific cells.

Interventions

None listed

Sponsors

Emory University
CollaboratorOTHER
Rockefeller University
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

1. Able to give informed consent. 2. Age 18-45 years. 3. Agrees not to take any vaccines within 30 days before or 30 days after YFV vaccination.

Exclusion criteria

1. Previously vaccinated with yellow fever vaccine. 2. A history of a medical condition resulting in impaired immunity. 3. Use of immunosuppressive medications. 4. Thymus gland dysfunction. 5. Recipient of a blood product or immune globulin product within 42 days of the screening visit or 30 days after the YFV vaccination.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026