4.7 Article

Immunogenicity of an mRNA-Based COVID-19 Vaccine among Adolescents with Obesity or Liver Transplants

Journal

VACCINES
Volume 10, Issue 11, Pages -

Publisher

MDPI
DOI: 10.3390/vaccines10111867

Keywords

COVID-19; SARS-CoV-2; liver transplantation; obesity; BNT162b2 vaccine; SARS-CoV-2 variants

Funding

  1. Thai Association for the Study of the Liver (THASL)
  2. Royal College Pediatricians of Thailand [2564.2.1]
  3. Ratchadapisek Sompoch Endowment Fund of Chulalongkorn University [RA65/017]

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This study evaluated the humoral immune response in liver transplant recipients and obese adolescents after receiving the BNT162b2 vaccine. The results suggest the need for a booster vaccination for groups with a lower immunogenic response.
There are limited data regarding the immunogenicity of mRNA-based SARS-CoV-2 vaccine BNT162b2 among immunosuppressed or obese adolescents. We evaluated the humoral immune response in adolescents with obesity and adolescent liver transplant recipients (LTRs) after receiving two BNT162b2 doses. Sixty-eight participants (44 males; mean age 14.9 +/- 1.7 years), comprising 12 LTRs, 24 obese, and 32 healthy adolescents, were enrolled. Immunogenicity was evaluated by anti-SARS-CoV-2 spike protein immunoassay and surrogate viral neutralization tests (sVNT) against the Delta and Omicron (BA.1) variants. At 27.1 +/- 3.2 days after the second dose, the antibody levels were 1476.6 +/- 1185.4, 2999.4 +/- 1725.9, and 4960.5 +/- 2644.1 IU/mL in the LTRs, obese adolescents, and controls, respectively (p < 0.001). Among obese individuals, liver stiffness <5.5 kPa was associated with higher antibody levels. The %inhibition of sVNT was significantly lower for the Omicron than that for the Delta variant. Injection site pain was the most common local adverse event. Nine participants (three obese and six controls) developed COVID-19 at 49 +/- 11 days after the second vaccination; four were treated with favipiravir. All infections were mild, and the patients recovered without any consequences. Our study supports the need for the booster regimen in groups with an inferior immunogenic response, including LTRs and obese individuals.

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