RECOVAC Repeated Vaccination Study

• OBJECTIVES

Primary objective:

To assess the immunogenicity (expressed as percentage of responders) of various COVID-19 third or fourth vaccination strategies in kidney transplant patients that failed to mount a sufficient antibody response after two or three primary doses of a mRNA vaccine (either mRNA-1273 (Moderna) or BNT162b2 (Pfizer) or any combination of both).

Secondary Objectives:

• To measure the concentration of SARS-CoV-2 spike S1-specific IgG antibodies in serum at 28 days after the 3rd or 4th vaccine administration
• To measure the presence and titer of neutralizing anti-SARS-CoV-2 antibodies after third or fourth vaccination
• To evaluate SARS-CoV-2 specific T cell responses
• To measure anti-S1 antibody (IgG and IgA) responses and neutralizing capacity of these antibodies in nasal mucosal fluid
• To evaluate vaccine safety in terms of incidence of solicited local and systemic adverse events (AEs) graded according to severity.

Exploratory Objectives:

• To assess the association between baseline clinical and immunological parameters and the immune response to third or fourth vaccinations
• To correlate RNA-seq data at one week after vaccination to the subsequent antibody and T cell response

• STUDY DESIGN

This is a prospective, multicentre, open-label, randomized study to evaluate the immunogenicity and safety of various third or fourth vaccination strategies in kidney transplant patients without a sufficient antibody response after two or three primary doses of a mRNA vaccine (either mRNA-1273 (Moderna) or BNT162b2 (Pfizer) or any combination of both).

The four participating study sites are: Amsterdam UMC, ErasmusMC, Radboudumc and UMCG.

Based on their immunosuppressive treatment, patients will participate in one of the following strata:

• stratum A: patients treated with triple immunosuppressive therapy consisting of a calcineurin inhibitor, MMF/MPA, and steroids,
• stratum B: patients treated with any combination of immunosuppressive drugs.

In stratum A, patients will be randomized to one of two third or fourth vaccination strategies:

• A1: one extra dose of mRNA-1273 (100 μg, i.m)
• A2: one extra dose of mRNA-1273 (100 μg, i.m), with temporary discontinuation of MMF/MPA during one week before and one week after the 3rd dose

In stratum B, patients will be randomized to one of three third vaccination strategies:

• B1: 3rd dose of mRNA-1273 (100 μg, i.m)
• B2: 3rd dose of mRNA-1273 (100 μg, i.m) in both upper arms
• B3: Ad26.COV2.S vaccine (Janssen, 5x1010 viral particles i.m.)

To assess the immune response after vaccination, blood samples will be collected at baseline (i.e. prior to third dose administration) and at 28 days after the third or fourth dose administration. A complete blood count, kidney function, and liver enzymes will be determined at the same time points.

In a subset of patients we will collect a blood sample at 1 week after the third vaccin administration for specific immunological assays.

For safety reasons, a blood sample will be collected in stratum A at one and two weeks after discontinuing MMF/MPA.

The maximum volume of blood collected for this study is 66 mL per timepoint, and no more than 200 mL for the one year study period, which is well within the safe limits of blood collection for clinical studies.

Nasal mucosal lining fluid (MLF) will be collected for assessment of secreted mucosal antibodies at the same time points used to collect blood. MLF will be collected by use of soft synthetic absorptive matrix (SAM) strips, which are gently inserted into one nostril of the participant and placed along the surface of the inferior turbinate. The index finger is then lightly pressed against the side of the nostril to keep the SAM strip in place and to allow MLF absorption for 60 seconds, after which the SAM strip is placed back in the protective plastic tube. The procedure may tickle slightly but is completely painless.

To evaluate vaccination related AEs, patients will be asked to collect solicited local and systemic AEs for 7 days after each vaccination using a questionnaire, as vaccination related AEs are mainly expected in the first week after vaccination.

Inclusion criteria

• Age 18 years or older
• Received 2 doses of mRNA-1273 (stratum B) according to the recommended vaccination schedule, with the last administration within the last nine months. For stratum A, also patients who received 2 doses of BNT162b2 and/or a third dose with a mRNA vaccine (mRNA-1273 or BNT162b2) within the last three months are eligible.
• At least 6 months after kidney transplantation
• Negative seroresponse 14 to 56 days after vaccination, measured by a validated anti-spike IgG assay of which the definition is dependent on the assay that is used.
• Eligible for COVID-19 vaccination as described by the instructions of the manufacturers of the vaccine (Moderna and Janssen)
• Capable of understanding the purpose and risks of the study, fully informed and given written informed consent (signed informed consent form has been obtained)
• Willing to adhere to the protocol and be available during the study period

Additional inclusion criteria to be eligible for stratum A:

• Maintenance immunosuppressive therapy consisting of a calcineurin inhibitor (tacrolimus or cyclosporine), MMF/MPA, and prednisone
• In case of tacrolimus treatment: last tacrolimus pre-dose level while on current dosage above 4 μg/l
• In case of cyclosporine treatment: last cyclosporine pre-dose level while on current dosage above 75 μg/l
• Prednisone dose at least 5 mg/day
• First or second transplantation
• Calculated level of panel reactive antibodies prior to last transplantation below 85%
• No signs of acute rejection during the preceding year

Exclusion criteria

• Multi-organ transplant recipient
• History of severe adverse reaction associated with a vaccine and/or severe allergic reaction (e.g. anaphylaxis) to any component of the study intervention(s).
• Previous or active COVID-19 disease
• Active malignancy, except non-melanoma skin cancer
• Inherited immune deficiency
• Infection with Human Immunodeficiency Virus (HIV)
• Administration of T cell, B cell, or plasma cell depleting antibodies during the last 6 months
• Any vaccination within a week before enrolment
• Bleeding diathesis or condition associated with prolonged bleeding that would, in the opinion of the investigator, contraindicate intramuscular injection.

Additional exclusion criteria for stratum B:

• History of recurrent venous thrombosis or venous thrombosis <2 years before baseline
• Immune-mediated diseases associated with thrombocytopenia such as ITP and aHUS