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Reduced Humoral and Cellular Immune Response to Primary COVID-19 mRNA Vaccination in Kidney Transplanted Children
Jasmin K Lalia1, Raphael Schild2, Marc Lütgehetmann3,4
1University Children's Research, UCR@Kinder-UKE, University Medical Center Hamburg-Eppendorf, Martinistr. 52, 20246 Hamburg, Germany.
Insights
COVID-19 mRNA vaccines elicited a weaker antibody response in kidney transplant children compared to healthy children. T cell responses varied, with reduced antiviral capacity observed in transplant recipients.
Area of Science:
- Immunology
- Vaccinology
- Pediatrics
Background:
- Limited data exists on COVID-19 mRNA vaccine responses in immunocompromised children.
- Secondary immunodeficiency in children, such as post-kidney transplant, may impact vaccine efficacy.
Purpose of the Study:
- To investigate humoral and T cell responses to BNT162b2 vaccination in immunocompromised children.
- To compare responses between children post-kidney transplant, with glomerulonephritis, and healthy controls.
Main Methods:
- Prospective observational study of children aged 5-11 years.
- Assessed antibody levels and T cell responses (cytokine secretion, activation markers) after primary vaccination.
- Stimulated peripheral blood mononuclear cells (PBMCs) with SARS-CoV-2 spike protein peptides (Wuhan Hu-1 and Omicron BA.5).
Main Results:
- Seroconversion rates were 56% in kidney transplant (KTx) patients vs. 100% in glomerulonephritis (GN) and controls.
- Antibody titers were significantly lower in KTx patients compared to GN patients and controls.
- Humoral response improved in KTx patients after a third dose.
- No significant differences in antigen-specific CD4+ and CD8+ T cell frequencies were observed.
- T cell antiviral cytokine secretion capacity was reduced in KTx patients.
Conclusions:
- COVID-19 mRNA vaccination induces a variable humoral response in immunocompromised children, with lower efficacy in KTx patients.
- While T cell frequency was similar, functional antiviral capacity was diminished in KTx patients.
- Further immunization may be necessary for immunocompromised children to achieve adequate protection.
Abstract:
The situation of limited data concerning the response to COVID-19 mRNA vaccinations in immunocom-promised children hinders evidence-based recommendations. This prospective observational study investigated humoral and T cell responses after primary BNT162b2 vaccination in secondary immunocompromised and healthy children aged 5-11 years. Participants were categorized as: children after kidney transplantation (KTx, n = 9), proteinuric glomerulonephritis (GN, n = 4) and healthy children (controls, n = 8). Expression of activation-induced markers and cytokine secretion were determined to quantify the T cell response from PBMCs stimulated with peptide pools covering the spike glycoprotein of SARS-CoV-2 Wuhan Hu-1 and Omicron BA.5. Antibodies against SARS-CoV-2 spike receptor-binding domain were quantified in serum. Seroconversion was detected in 56% of KTx patients and in 100% of the GN patients and controls. Titer levels were significantly higher in GN patients and controls than in KTx patients. In Ktx patients, the humoral response increased after a third immunization. No differences in the frequency of antigen-specific CD4+ and CD8+ T cells between all groups were observed. T cells showed a predominant anti-viral capacity in their secreted cytokines; however, this capacity was reduced in KTx patients. This study provides missing evidence concerning the humoral and T cell response in immunocompromised children after COVID-19 vaccination.
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