D1. Primary Objective: 1\. Determine the immunogenicity of FDA approved COVID-19 vaccination in patients with hematologic malignancies D2. Secondary Objectives: 1. Assess the safety of FDA approved COVID-19 vaccination in patients with hematologic malignancies 2. Analyze the kinetics of immunogenic response over time after receipt of the COVID-19 vaccination 3. Compare the immunogenicity of different COVID-19 vaccinations that will be approved by the FDA 4. Analyze advanced flow immunophenotyping of innate and adaptive immune blood cells in all participants and correlate with response to vaccination
Study Type
OBSERVATIONAL
Enrollment
358
Mayo Clinic
Rochester, Minnesota, United States
Humoral Immunogenicity
Number of participants who have detectable antibodies to SARS-Co-V2 vaccination
Time frame: Assessed 14 days following the second dose of the vaccine
Cellular Immunogenicity
Number of participants who have a SARS-CoV-2 specific memory B cell ELISPOT response
Time frame: Assessed 14 days following the second dose of the vaccine
Cellular Immunogenicity
Number of participants who have a SARS-CoV-2 specific IFNγ ELISPOT T cell response
Time frame: Assessed 14 days following the second dose of the vaccine
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