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Updated: Mar 8, 2026

Use of an Influenza Antigen Microarray to Measure the Breadth of Serum Antibodies Across Virus Subtypes
Published on: July 26, 2019
Pathogen-specific deep sequence-coupled biopanning: A method for surveying human antibody responses.
Kathryn M Frietze1, Juan M Pascale2, Brechla Moreno2
1Department of Molecular Genetics and Microbiology, University of New Mexico School of Medicine, MSC08 4660, 1 University of New Mexico, Albuquerque, NM, United States of America.
We developed a new method to identify antibody targets during infection. This approach helps find Dengue virus (DENV) epitopes for better vaccines and diagnostics.
Area of Science:
- Immunology
- Virology
- Biotechnology
Background:
- Identifying antibody targets is crucial for vaccine design, diagnostics, and understanding disease.
- Current methods may not fully capture the breadth of antibody responses in polyclonal human serum.
Purpose of the Study:
- To adapt a deep sequence-coupled biopanning approach for identifying pathogen-specific epitopes recognized by antibodies during acute infection.
- To demonstrate the utility of this method by applying it to Dengue virus (DENV) infection.
Main Methods:
- Developed and applied a deep sequence-coupled biopanning technique using bacteriophage MS2 virus-like particles displaying DENV antigen fragments.
- Analyzed affinity-selected peptide epitopes from sera of patients with acute secondary DENV infection via deep sequence analysis.
Main Results:
- Identified several commonly enriched epitopes within the DENV Envelope glycoprotein and Non-Structural Protein 1.
- Observed significant individual variation in antibody responses, highlighting personalized epitope recognition.
Conclusions:
- Established a novel, powerful approach for characterizing pathogen-specific antibody responses in human sera.
- The method has significant potential for identifying new diagnostic markers and vaccine targets for infectious diseases.
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