Penn Presbyterian Medical Center
Philadelphia, Pennsylvania, 19104, United States
Location status: Recruiting
Location contact
Tachianna Griffiths
CONTACT
NCT Number: NCT06807840
Cellular and humoral immune responses in individuals with active influenza infection will be assessed. Each year, up to 50 participants will be enrolled. The investigators hypothesize that influenza infection will elicit mostly memory immune responses rather than de novo immune responses to infection.
Interested in participating?
Request Info18 year and older
All sexes
Observational
Philadelphia, Pennsylvania, 19104, United States
Location status: Recruiting
Tachianna Griffiths
CONTACT
Using samples collected from individuals after influenza virus vaccination, the investigators have shown that immune cells primed by previous influenza exposures are recruited to produce antibodies against newer viral strains. The investigators previous work indicate that the majority of the immune cells that respond to influenza vaccination are from the memory compartment, suggesting that 'immune imprinting' greatly affects the specificity of antibodies elicited by influenza vaccines. It remains less clear how prior influenza virus exposures impact immunity elicited by influenza virus infections. Compared to vaccinated individuals, it is more difficult to enroll influenza virus infected patients and track their immune responses over time. Viral antigens can persist for longer amounts of time following influenza virus infections relative to influenza vaccinations. It is therefore possible that influenza virus infections more efficiently prime de novo immune responses compared to influenza virus vaccinations. In this study, the investigators will longitudinally collect serum, PBMC, and respiratory samples from influenza virus-infected individuals from the University of Pennsylvania Health System characterize the cellular and humoral immune responses elicited by influenza virus infections.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Participants with active influenza virus infection will be enrolled in this study.
Time frame: 2 years
The investigators will compare neutralizing antibodies in sera, plasma, and nasal swab samples against the influenza strain that each participant is infected with as well as historical and recently circulating influenza virus strains. Antibody titers between different strains will be compared to understand if memory or de novo immune responses are generated following influenza infection based on inferred influenza exposure history.
Time frame: 2 years
The investigators will compare binding antibodies in sera, plasma, and nasal swab samples against the influenza strain that each participant is infected with as well as historical and recently circulating influenza virus strains. Antibody titers between different strains will be compared to understand if memory or de novo immune responses are generated following influenza infection based on inferred influenza exposure history.
Time frame: 2 years
Influenza specific B cells will be identified in PBMC samples and their specificity and functionality to different influenza virus strains will be assessed to understand how influenza infection influences the generation of memory and de novo immune responses.
Time frame: 2 years
T cells specific to influenza will be identified in PBMC samples and their specificity and functionality to different influenza virus strains will be assessed to understand how influenza infection influences the generation of memory and de novo immune responses.
Contact information is provided by the study sponsor or research team.
Elizabeth Drapeau, PhD
CONTACT
Scott Hensley, PhD
CONTACT
University of Pennsylvania
Other
Evaluating Immune Imprinting in the Context of Influenza Virus Infections
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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