An interventional study of Blood draw in HIV Seropositivity, Immunodeficiency and Vaccination Reaction, sponsored by University Hospital, Ghent. Withdrawn at 1 site in Belgium. Open to participants aged 16 Years to 100 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-09-19.
Sponsored by University Hospital, Ghent · Not applicable, Interventional, and Screening
The aim of this study is to identify both the humoral immunological response through the detection of induced antibodies and the cellular immunological response through the detection of interferon gamma production by functional CD4+ and CD8+ cells in different groups of immunocompromised patients. For antibody detection, LIAISON® SARS-CoV-2 TrimericS assay (DiaSorin) will be used and for the evaluation of cellular immunity - QuantiFERON SARS-CoV-2 assay (QIAGEN).
The national vaccination campaign against COVID-19 is ongoing and high risk patients are invited. Within the group of high risk patients, there are several groups of people who are for some reason immune-compromised and whose immune system is not functioning adequately. As vaccines against COVID-19 have become available in Europe as a matter of urgency, there are currently insufficient or no data available on the generation of post-vaccinal response in different groups of these immunocompromised patients. The theoretical assumption that the generation of post-vaccinal response in these patients is different from that in immunocompetent individuals is valid, as it has been shown for other vaccines, e.g. against influenza and pneumococcal disease, that the use of immunosuppressive treatments such as asrituximab, methotrexate and rituximab suppress the production of neutralising antibodies. It is known that vaccines against COVID-19 are also capable of inducing a clear functional cellular response in addition to neutralising antibody production, the modalities of which are also insufficiently or not known in these patients.
As mentioned is the goal of VACCIm to identify both the humoral immunological response through the detection of induced antibodies and the cellular immunological response through the detection of interferon gamma production by functional CD4+ and CD8+ cells in different groups of immunocompromised patients.
Within this prospective observational study, serum samples (for subsequent measurement with LIAISON® SARS-CoV-2 TrimericS assay) and lithium-heparin whole blood samples (for subsequent measurement with QuantiFERON SARS-CoV-2 assay) will be collected from control immune-competent individuals and immune-compromised patients within the following groups:
In order to assess both humoral and cellular responses as fully as possible, both measurements are performed at the following time points:
T0: before (=prior) or at time of first dose of vaccine T1: 21-28 days after first dose of vaccine T2: at least 10 days after second dose of vaccine T3: after 3 months after second dose of vaccine T4: after 6 months from second dose of vaccine T5: after 12 months from second dose of vaccine
215 studies on the registry are indexed under HIV Seropositivity; 10 are open to participants now.
Browse HIV Seropositivity studies →University Hospital, Ghent is the lead sponsor of 685 studies on the registry; 158 are open to participants now.
Of its 5 completed or terminated interventional studies of FDA-regulated products, 4 (80%) have results posted.
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Following patient groups receiving the Pfizer vaccine
Exclusion Criteria:
Diagnostic Test: Blood draw
Diagnostic Test: Blood draw
Diagnostic Test: Blood draw
Diagnostic Test: Blood draw
Diagnostic Test: Blood draw
Diagnostic Test: Blood draw
Blood draw
Humoral immune response
Detection of Antibodies
Time frame: prior or at the time of first dose of vaccine until 12 months after second dose of vaccine
Cellular immune response
DetectionINF-gamma by functional CD4+ and CD8+ cells
Time frame: prior or at the time of first dose of vaccine until 12 months after second dose of vaccine
Plan to share: Undecided
No publications or documents are linked to this record.
This study is withdrawn, as verified in Sep 2024. You cannot join it, but the record below documents what was studied.
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