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Multiplex Magnetic Biosensor Microarrays Facilitate Personalized Vaccination Schedules for SARS-CoV-2 Variants

Title
Multiplex Magnetic Biosensor Microarrays Facilitate Personalized Vaccination Schedules for SARS-CoV-2 Variants
Authors
Um H.-K.; Kim S.; Hwang J.; Lee Y.; Wang S.X.; Lee J.-R.
Ewha Authors
이정록
SCOPUS Author ID
이정록scopus
Issue Date
2026
Journal Title
Biochip Journal
ISSN
1976-0280JCR Link
Citation
Biochip Journal vol. 20, no. 1, pp. 124 - 132
Keywords
Giant magnetoresistance; Magnetic biosensors; Magnetic nanoparticles; Neutralizing antibodies; Vaccination; Viral variants
Indexed
SCIE; SCOPUS; KCI WOS scopus
Document Type
Article
Abstract
Rapid, sensitive, multiplexed antibody detection technologies are essential for assessing vaccine efficacy and recipient immunity against viruses. As severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants continue to emerge and novel viruses may pose potential threats in the near future, personalized vaccines can be precisely tailored to an individual’s measured immunity to help mitigate the symptoms of infection and viral spread. Here, we present giant magnetoresistive (GMR) biosensor microarrays for the quantitative multiplexed detection of antibodies against SARS-CoV-2 variants. The multiplexed GMR biosensor microarrays demonstrated high sensitivity, comparable to that of the single-plex enzyme-linked immunosorbent assay, enabling multiplexed measurements using blood obtained from finger pricks. Additionally, the GMR biosensor microarrays demonstrated compatibility with clinical samples and could detect variant-specific antibodies in serum, allowing for the assessment of current immunity status. Notably, an increased concentration of antibodies against the Omicron variant was clearly observed two weeks after receiving an Omicron-based booster vaccination. These results indicate that GMR biosensor microarrays offer a practical point-of-care tool for monitoring humoral immunity and guiding personalized vaccination schedules, thereby supporting immunity management against SARS-CoV-2 and future viral threats. © The Korean BioChip Society 2025.
DOI
10.1007/s13206-025-00244-9
Appears in Collections:
공과대학 > 휴먼기계바이오공학과 > Journal papers
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