Characterization of T Cell Responses Following Yellow Fever Virus Vaccination in Healthy Adults
|The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.|
|ClinicalTrials.gov Identifier: NCT00616356|
Recruitment Status : Completed
First Posted : February 15, 2008
Last Update Posted : November 8, 2011
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.
|Condition or disease|
|Study Type :||Observational|
|Estimated Enrollment :||8 participants|
|Official Title:||Characterization of T Cell Responses Following Yellow Fever Virus Vaccination in Healthy Adults|
|Study Start Date :||December 2007|
|Actual Primary Completion Date :||June 2008|
|Actual Study Completion Date :||June 2008|
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00616356
|United States, New York|
|New York, New York, United States, 10021|
|Principal Investigator:||Charles M Rice, PhD||Rockefeller University|