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Age-Related Differences in Neutralizing Antibody Responses against SARS-CoV-2 Delta and Omicron Variants in 151 SARS-CoV-2-Naïve Metropolitan Residents Boosted with BNT162b2

Authors
Lee, BeomkiBae, Go EunJeong, In HwaKim, Jong-HunKwon, Min-JungKim, JayoungKim, ByounggukLee, June-WooNam, Jeong-HyunHuh, Hee JinKang, Eun-Suk
Issue Date
Mar-2024
Publisher
Oxford University Press
Keywords
Antibodies, Neutralizing; Antibodies, Viral; Bnt162 Vaccine; Covid-19 Vaccines; Bnt 162 Vaccine; Neutralizing Antibody; Sars-cov-2 Vaccine; Virus Antibody; Adult; Age; Aged; Blood; Coronavirus Disease 2019; Female; Human; Immunology; Male; Middle Aged; Neutralization Test; Prevention And Control; Procedures; Severe Acute Respiratory Syndrome Coronavirus 2; Virology; Young Adult; Adult; Age Factors; Aged; Antibodies, Neutralizing; Antibodies, Viral; Bnt162 Vaccine; Covid-19; Covid-19 Vaccines; Female; Humans; Male; Middle Aged; Neutralization Tests; Sars-cov-2; Sars-cov-2 Variants; Young Adult
Citation
The Journal of Applied Laboratory Medicine, v.9, no.4, pp 1 - 11
Pages
11
Indexed
SCOPUS
ESCI
Journal Title
The Journal of Applied Laboratory Medicine
Volume
9
Number
4
Start Page
1
End Page
11
URI
https://scholarworks.dongguk.edu/handle/sw.dongguk/22673
DOI
10.1093/jalm/jfae014
ISSN
2576-9456
2475-7241
Abstract
Background: Although age negatively correlates with vaccine-induced immune responses, whether the vaccine-induced neutralizing effect against variants of concern (VOCs) substantially differs across age remains relatively poorly explored. In addition, the utility of commercial binding assays developed with the wild-type SARS-CoV-2 for predicting the neutralizing effect against VOCs should be revalidated. Methods: We analyzed 151 triple-vaccinated SARS-CoV-2-naive individuals boosted with BNT162b2 (Pfizer-BioNTech). The study population was divided into young adults (age < 30), middle-aged adults (30 <= age < 60), and older adults (age >= 60). The plaque reduction neutralization test (PRNT) titers against Delta (B.1.617.2) and Omicron (B.1.1.529) variants were compared across age. Antibody titers measured with commercial binding assays were compared with PRNT titers. Results: Age-related decline in neutralizing titers was observed for both Delta and Omicron variants. Neutralizing titers for Omicron were lower than those against Delta in all ages. The multiple linear regression model demonstrated that duration from third dose to sample collection and vaccine types were also significant factors affecting vaccine-induced immunity along with age. The correlation between commercial binding assays and PRNT was acceptable for all age groups with the Delta variant, but relatively poor for middle-aged and older adults with the Omicron variant due to low titers. Conclusions: This study provides insights into the age-related dynamics of vaccine-induced immunity against SARS-CoV-2 VOCs, corroborating the need for age-specific vaccination strategies in the endemic era where new variants continue to evolve. Moreover, commercial binding assays should be used cautiously when estimating neutralizing titers against VOCs, particularly Omicron.
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