Abstract
T cells play an important role in adaptive immunity. An enormous clonal diversity of T cells with a different specificity, encoded by the T cell receptor (TCR), protect the body against infection. Most TCRβ chains are generated from a V, D, and J segment during recombination in the thymus. Although complete absence of the D segment is not easily detectable from sequencing data, we find convincing evidence for a substantial proportion of TCRβ rearrangements lacking a D segment. Additionally, sequences without a D segment are more likely to be abundant within individuals and/or shared between individuals. Our analysis indicates that such sequences are preferentially generated during fetal development and persist within the elderly. Summarizing, TCRβ rearrangements without a D segment are not uncommon, and tend to allow for TCRβ chains with a high abundance in the naive repertoire.
| Original language | English |
|---|---|
| Article number | e2104367118 |
| Pages (from-to) | 1-7 |
| Journal | Proceedings of the National Academy of Sciences of the United States of America |
| Volume | 118 |
| Issue number | 39 |
| DOIs | |
| Publication status | Published - 28 Sept 2021 |
Bibliographical note
Funding Information:ACKNOWLEDGMENTS This work was supported by The Netherlands Organization for Scientific Research Graduate Program 22.005.023 (to P.C.d.G.). We gratefully acknowledge all authors involved in generating the TCR sequencing datasets we studied, for providing access to their data.
Publisher Copyright:
© 2021 National Academy of Sciences. All rights reserved.
Funding
ACKNOWLEDGMENTS This work was supported by The Netherlands Organization for Scientific Research Graduate Program 22.005.023 (to P.C.d.G.). We gratefully acknowledge all authors involved in generating the TCR sequencing datasets we studied, for providing access to their data.
Keywords
- Immune repertoire
- T cell receptor
- V(D)J recombination
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