Humoral and Innate Immunological Profile of Paediatric Recipients of Pfizer-BioNTech BNT162b2 mRNA Vaccine.

Humoral and Innate Immunological Profile of Paediatric Recipients of Pfizer-BioNTech BNT162b2 mRNA Vaccine.

Publication date: Jul 09, 2024

The Pfizer-BioNTech vaccine was one of the essential tools in curtailing the COVID-19 pandemic. Unlike conventional vaccines, this newly approved mRNA vaccine is taken up by cells, which leads to the synthesis of the specific viral Spike antigen. The vaccine was initially introduced for adults, and the immunological profile of adult recipients is well-characterized. The vaccine was approved for paediatric use much later after its efficacy and safety had been confirmed in children. However, the complete picture of how the paediatric immune system in children reacts to the vaccine is not well documented. Therefore, in order to better understand the immune response in children, we analysed the humoral response, immune cell count, and interferon signalling in paediatric vaccine recipients ranging between 5 and 17 years of age. Our findings suggest that the paediatric recipients elicit a robust humoral response that is sustained for at least three months. We also found that the vaccine triggered a transient lymphocytopenia similar to that observed during viral infection. Interestingly, we also found that the vaccine may sensitise the interferon signalling pathway, priming the cells to mount a potent response when exposed to interferons during a subsequent infection. The study offers new insights into the workings of the paediatric immune system and innate immunity, thereby opening the doors for further research in this field.

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Concepts Keywords
Adults COVID-19
Bnt162b2 innate immunity
Lymphocytopenia interferons
Newly neutralizing antibodies
Vaccine paediatric immunity
Pfizer vaccine

Semantics

Type Source Name
disease VO vaccine
disease MESH COVID-19 pandemic
pathway REACTOME Immune System
drug DRUGBANK Tropicamide
disease IDO immune response
disease IDO cell
disease MESH lymphocytopenia
disease MESH viral infection
disease MESH infection
drug DRUGBANK Coenzyme M
drug DRUGBANK Efavirenz
disease MESH Infectious Diseases
disease VO vaccination
disease VO vaccinated
disease IDO host
disease VO effective
disease VO population
disease IDO history
pathway KEGG Viral replication
disease VO vaccine efficacy
disease VO dose
disease VO inactivated vaccine
disease VO time
disease VO vaccination protocol
disease VO manufacturer
disease IDO blood
disease VO vein
drug DRUGBANK Edetic Acid
disease VO USA
disease IDO assay
drug DRUGBANK Flunarizine
drug DRUGBANK Dimethyl sulfoxide
drug DRUGBANK Isopropyl Alcohol
disease VO viability
drug DRUGBANK Water
disease VO viable
disease VO vaccine dose
drug DRUGBANK Ademetionine
drug DRUGBANK Trestolone
drug DRUGBANK Spinosad
disease MESH Breakthrough infections
disease MESH leukopenia
drug DRUGBANK L-Phenylalanine
disease VO efficiency
drug DRUGBANK Cycloserine
drug DRUGBANK BK-MDA
disease VO volume
disease IDO production
disease MESH long term infection
disease MESH reinfection
drug DRUGBANK Papain
drug DRUGBANK Gold
disease IDO facility
disease VO effectiveness
drug DRUGBANK Carboxyamidotriazole
disease VO immunization
disease VO vaccine effectiveness
disease MESH Emergency
drug DRUGBANK Guanosine
disease MESH Inflammation
disease MESH Abnormalities
drug DRUGBANK Clozapine
disease VO age
disease VO macrophage

Original Article

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