Genetic and Environmental Factors in the Response to Influenza Vaccination

Completed · Phase 1

Conditions studied: Influenza, Healthy

In brief

The purpose of the study is to investigate and compare the immune responses to influenza vaccination in monozygotic (identical) and dizygotic (fraternal) twins to determine the roles of genetics and environment in the response to flu vaccination.

Key facts

Study ID

NCT03088904

Run by

Stanford University

People needed

109

Starts

2014-10-03

Expected to finish

2018-12-12

Last updated by the study team

2020-02-13

Who can join

Age: 12 and older, up to 49. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Otherwise healthy, 12-49 years old, identical (MZ) or fraternal (DZ) twins.
• Willing to complete the informed consent process (including assent for minors 12-17 years of age, inclusive).
• Availability for follow-up for the planned duration of the study at least 28 days after immunization.
• Acceptable medical history by review of inclusion/exclusion criteria and vital signs.

You may not qualify if…

• Prior off-study vaccination with the current year's seasonal influenza vaccine.
• Allergy to egg or egg products, or to vaccine components, (including gentamicin, gelatin, arginine or MSG in LAIV)
• Life-threatening reactions to previous influenza vaccinations.
• Asthma (If yes, not eligible for Group C).
• Active systemic or serious concurrent illness, including febrile illness on the day of vaccination.
• History of immunodeficiency (including HIV infection).
• Known or suspected impairment of immunologic function, including, but not limited to, clinically significant liver disease, diabetes mellitus treated with insulin, moderate to severe renal disease, or any other chronic disorder which, in the opinion of the investigator, might jeopardize volunteer safety or compliance with the protocol.
• Blood pressure >150 systolic or >95 diastolic at first study visit and the day of vaccination.
• Hospitalization in the past year for congestive heart failure or emphysema.
• Chronic Hepatitis B or C.
• Recent or current use of immunosuppressive medication, including systemic glucocorticoids (corticosteroid nasal sprays and topical steroids are permissible in all groups; inhaled steroid use is not permissible).
• In close contact with anyone who has a severely weakened immune system and requires a protective environment (If yes, may be ineligible for Group C; exposure to such persons should be avoided for 7 days after receipt of LAIV).
• Malignancy, other than squamous cell or basal cell skin cancer (includes solid tumors such as breast cancer or prostate cancer with recurrence in the past year, and any hematologic cancer such as leukemia).
• Autoimmune disease (including rheumatoid arthritis treated with immunosuppressive medication such as Plaquenil, methotrexate, prednisone, Enbrel) which, in the opinion of the investigator, might jeopardize volunteer safety or compliance with the protocol.
• History of blood dyscrasias, renal disease, or hemoglobinopathies requiring regular medical follow up or hospitalization during the preceding year.
• Use of any anti-coagulation medication such as Coumadin or Lovenox, or anti-platelet agents such as aspirin (except up to 325 mg. per day), Plavix, or Aggrenox must be reviewed by investigator to determine if this would affect the volunteer's safety.
• For children or adolescents through 17 years of age, receiving aspirin therapy or aspirin-containing products (If yes, not eligible for Group C).
• Receipt of blood or blood products within the past 6 months or planned used during the study.
• Medical or psychiatric condition or occupational responsibilities that preclude participant compliance with the protocol.
• Receipt of inactivated vaccine 14 days prior to study enrollment, or planned vaccinations prior to completion of last study visit (\~ 28 days after study vaccination).
• Receipt of live, attenuated vaccine within 60 days prior to enrollment of planned vaccination prior to completion of last study visit (\~ 28 days after study vaccination).
• Need for allergy immunization (that cannot be postponed) during the study period.
• Has taken an influenza antiviral medication within 48 hours prior to study vaccination (If yes, not eligible for Group C).
• History of Guillain-Barré syndrome
• Pregnant woman

Where it is running

• Stanford University — Stanford, California, United States

Full record on ClinicalTrials.gov

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