Humoral and Cellular Immune Response to COVID-19 Vaccines in Immunocompromised and Healthy Individuals

Medical University of Graz373 enrolled

Overview

Currently, the efficacy of COVID-19 vaccination in immunodeficient patients is unknown. Here the investigators aim to evaluate the efficacy of COVID-19 vaccines in immunodeficient patients compared to healthy controls. The investigators will assess the humoral and cellular response to COVID-19 vaccination in these subjects in detail. Furthermore, factors associated with good response to vaccination will be identified. The results of this study will help to guide future recommendations on COVID-19 vaccination in this population.

The total duration of the study is 38 months, starting in March 2021 with a recruiting period until 31. December 2021 and termination of all scheduled visits until 31 May 2024. Individuals having consented and fulfilling the inclusion and exclusion criteria are included in the trial. A baseline visit will take place up to 60 days before the planned date of vaccination according to the Austrian vaccination plan. Scheduled vaccination with any COVID-19 vaccine approved in Austria will allow recruitment. If appropriate pre-vaccine samples from study participants exist in the biobank of the Medical University of Graz, patients may also be included in the study after vaccination starting with visit 3. In this case the biomaterial available at the biobank will be used for the analyses planned on visit 1. The investigators will not influence the date of vaccination or the type of the vaccine used. After first vaccination a telephone visit (visit 2) will assess adverse events and schedule visit 3 at the appropriate time after the second vaccination. At visit 3 the patient's vaccination certificate will be checked to verify correct vaccination and document the type of vaccine received. Further visits (5-6) will be performed for up to two years after the second vaccination. This follow-up period will allow an assessment of the duration of the immune response. The data recorded directly on the Case Report Form (CRF) are considered to be source data. COVID-19 vaccination, COVID-19 infection, Vaccination history, Pregnancy test, Adverse Events, BMI (Body Mass Index), and Laboratory Specimen Collection are recorded directly on the CRF and therefore are considered to be source data. Data will be merged in an electronic database (RDA Research, Documentation \& Analysis; Medical University of Graz, version 07.03.2019). Case Report Forms (CRFs) will be inspected in respect of their accuracy and completeness and compared to original data by the monitor.

Study Type

OBSERVATIONAL

Enrollment

Eligibility

Sex: ALLMin age: 16 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: 1. Noninfectious immunocompetent participants (i.e., healthy participants) as determined by medical history and clinical judgement. or 2. Patients with primary immunodeficiencies or 3. Patients with B-cell depleting therapy due to autoimmune disease or 4. Patients with benign and malignant hematological diseases receiving specific Treatments with known immunosuppressive effects including cytotoxic agents, systemic corticosteroids, monoclonal antibodies and targeted therapies. or 5. Patients with active hematological diseases and secondary immunoglobulin deficiency (e.g. chronic lymphatic leukemia, MM) currently not receiving specific treatment. or 6. Patients \>3 months but \<12 months after autologous HSCT (hematopoietic stem cell transplantation). or 7. Patients \>3 months but \<12 months after allogeneic HSCT. or 8. Recipients of HSCT \>12 months after allogeneic HSCT but under immunosuppressive therapy. or 9. Patients with chronic GvHD (graft-versus-host disease) and persistent immunodeficiency. Exclusion Criteria: Healthy participants 1. Presence of diseases or therapies that are likely to interfere with the immune response to vaccination. 2. Presence of a disease requiring change in therapy during 4 weeks before enrollment. 3. Any contraindications to the vaccine planned to receive as listed in the product characteristics. 4. Lack of willingness to undergo serial blood draws and attend follow-up appointments. 5. Women who are pregnant or breastfeeding. 6. Previous vaccination with any coronavirus vaccine. 7. Persons who are not willing to sign the informed consents (biobank informed consent and study specific informed consent). Immunodeficient participants 1. Patients with hematological diseases within three months from B-cell-depleting immunotherapy (rituximab, ofatumumab, obinutuzumab, blinatumomab, CAR-T cells (Chimeric Antigen Receptor). 2. Patients with hematological malignancies in remission and \>12 months after end of specific therapy. 3. Patients within three months from HSCT. 4. Any contraindications to the vaccine planned to receive as listed in the product characteristics. 5. Lack of willingness to undergo serial blood draws and attend follow-up appointments. 6. Women who are pregnant or breastfeeding. 7. Previous vaccination with any coronavirus vaccine (exception: if serum prior to vaccination is available from the biobank). 8. Patients who are not willing to sign the informed consents (biobank informed consent and study specific informed consent).

Outcomes

Primary Outcomes

The levels of anti-SARS-CoV-2 spike protein humoral immune response.

The levels of anti-SARS-CoV-2 (severe acute respiratory syndrome-Covid Virus) spike protein humoral immune response measured by SARS-CoV-2 antigen-binding Ig assay comparing immunocompromised patients to healthy controls.

Time frame: At day 21-28 after the second vaccination

Secondary Outcomes

Seroconversion

Change of Seroconversion measured by SARS-CoV-2 antigen-binding Ig assay 6, 12 and 24 months after vaccination.

Time frame: 6, 12 and 24 months after vaccination.

Concentrations of recombinant S protein-binding IgG (immunoglobulin G)

Change of Concentrations of recombinant S protein-binding IgG after second vaccination in comparison to response after first vaccination.