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Multi-Level Model to Predict Antibody Response to Influenza Vaccine Using Gene Expression Interaction Network Feature
Saeid Parvandeh1, Greg A Poland2, Richard B Kennedy3
1Tandy School of Computer Science, University of Tulsa, Tulsa, OK 74104, USA. parvandehsaied@gmail.com.
Identifying individuals at risk for influenza infection post-vaccination is crucial. Machine learning models using pre-vaccination gene expression and antibody titers can predict vaccine response, improving influenza prevention strategies.
Area of Science:
- Immunology and Computational Biology
- Genomics and Machine Learning Applications
Background:
- Vaccination is key for influenza prevention, but some individuals show reduced antibody response, increasing infection risk.
- Identifying individuals with poor vaccine response is vital for personalized health strategies.
Purpose of the Study:
- To develop a predictive model for influenza vaccine response using baseline gene expression and antibody titers.
- To identify individuals at higher risk of infection despite vaccination.
Main Methods:
- A multi-level machine learning strategy combining pre-vaccination antibody titers and gene expression network interactions.
- Clustering individuals by baseline antibody titers (HAI) to refine gene-based modeling.
- Utilizing a gene-association interaction network (GAIN) for feature selection and identifying interacting gene pairs.
Main Results:
- The multi-level model effectively predicts post-vaccination antibody response, particularly in individuals with high baseline titers.
- GAIN feature selection enhanced model generalizability and identified key genes in B Cell Receptor signaling and antigen processing.
- Stratifying by baseline HAI enabled more targeted gene-based predictive modeling.
Conclusions:
- A multi-level machine learning approach can accurately predict influenza vaccine response by integrating baseline antibody levels and gene expression data.
- The developed model and interactive tool offer a promising strategy for identifying at-risk individuals and could be adapted for other vaccine studies.
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