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

Author:

Jeremiah Sundararaj Stanleyraj1,Das Priya1,Venkatesan Manu2,Albinzayed Reem3,Ahmed Aysha3,Stevenson Nigel John1,Corbally Martin4,Alqahtani Manaf5ORCID,Al-Wedaie Fatima6,Farid Eman67ORCID,Hejres Suha2

Affiliation:

1. School of Postgraduate Studies and Research, Royal College of Surgeons in Ireland—Medical University of Bahrain, Building 2441, Road 2835, Busaiteen 228, Bahrain

2. Hematology and Hematopathology Laboratory, King Hamad University Hospital, Busaiteen 228, Bahrain

3. Medical Internship, King Hamad University Hospital, Busaiteen 228, Bahrain

4. Department of Surgery, Royal College of Surgeons in Ireland—Medical University of Bahrain, Busaiteen 228, Bahrain

5. Department of Microbiology, Royal College of Surgeons in Ireland—Medical University of Bahrain, Busaiteen 228, Bahrain

6. Department of Pathology, Salmaniya Medical Complex, Government Hospital, Manama 329, Bahrain

7. Department of Microbiology, Immunology and Infectious Diseases, College of Medicine, Arabian Gulf University, Manama 329, Bahrain

Abstract

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.

Funder

RCSI internal grant

Adhoc grant

Publisher

MDPI AG

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