The purpose of this study is to elucidate the molecular mechanism by which novel adjuvants enhance the immunogenicity of Respiratory Syncytial Virus (RSV) vaccines by regulating antigen-specific B cell affinity maturation and T cell memory formation.
Age range
20 Years
Sex
ALL
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The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Neutralizing Antibodies against both the RSV-A and RSV-B subtypes.
Timeframe: At pre-vaccination (Day 1), and at 1, 12, and 24 months post-vaccination.
Specific IgG Antibodies to RSV pre-F of both RSV-A and RSV-B subtypes.
Timeframe: At pre-vaccination (Day 1), and at 1 month, 12 months, and 24 months post-vaccination.
The Frequency of RSV pre-F Specific Cluster of Differentiation 4+ (CD4+) T Cells or Cluster of Differentiation 8+ (CD8+) T cells Expressing.
Timeframe: At pre-vaccination (Day 1), and at 1 month, 12 months, and 24 months post-vaccination.