Quantitative profiling reveals minor changes of T cell receptor repertoire in response to subunit inactivated influenza vaccine
Language English Country Netherlands Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
29454515
DOI
10.1016/j.vaccine.2018.02.027
PII: S0264-410X(18)30201-9
Knihovny.cz E-resources
- Keywords
- High-throughput sequencing, Inactivated influenza vaccine, T cell receptor, TCR repertoires,
- MeSH
- Influenza, Human prevention & control MeSH
- Genetic Variation MeSH
- Vaccines, Inactivated administration & dosage immunology MeSH
- Clonal Evolution genetics MeSH
- Middle Aged MeSH
- Humans MeSH
- Receptors, Antigen, T-Cell genetics metabolism MeSH
- Vaccines, Subunit administration & dosage immunology MeSH
- T-Lymphocytes immunology metabolism MeSH
- Influenza Vaccines administration & dosage immunology MeSH
- High-Throughput Nucleotide Sequencing MeSH
- Check Tag
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Vaccines, Inactivated MeSH
- Receptors, Antigen, T-Cell MeSH
- Vaccines, Subunit MeSH
- Influenza Vaccines MeSH
Vaccination against influenza is widely used to protect against seasonal flu epidemic although its effectiveness is debated. Here we performed deep quantitative T cell receptor repertoire profiling in peripheral blood of a healthy volunteer in response to trivalent subunit influenza vaccine. We did not observe significant rebuilding of peripheral blood T cell receptors composition in response to vaccination. However, we found several clonotypes in memory T cell fraction that were undetectable before the vaccination and had a maximum concentration at day 45 after vaccine administration. These cells were found in lower concentration in the course of repertoire monitoring for two years period. Our observation suggests a potential for recruitment of only a limited number of new T cells after each seasonal influenza vaccination.
References provided by Crossref.org
Benchmarking of T cell receptor repertoire profiling methods reveals large systematic biases