Detecting T-cell clonal expansions and quantifying clone survival using deep profiling of immune repertoires
An individual’s T-cell repertoire constantly changes under the influence of external and internal factors. Cells that do not receive a stimulatory signal die, while those that encounter and recognize a pathogen or receive a co-stimulatory signal divide, resulting in clonal expansions. T-cell clones...
Main Authors: | Anastasia V. Pavlova, Ivan V. Zvyagin, Mikhail Shugay |
---|---|
Format: | Article |
Language: | English |
Published: |
Frontiers Media S.A.
2024-04-01
|
Series: | Frontiers in Immunology |
Subjects: | |
Online Access: | https://www.frontiersin.org/articles/10.3389/fimmu.2024.1321603/full |
Similar Items
-
Preparing unbiased T cell receptor and antibody cDNA libraries for the deep next generation sequencing profiling
by: Ilgar Z Mamedov, et al.
Published: (2013-12-01) -
A Framework for Annotation of Antigen Specificities in High-Throughput T-Cell Repertoire Sequencing Studies
by: Mikhail V. Pogorelyy, et al.
Published: (2019-09-01) -
Overview of methodologies for T-cell receptor repertoire analysis
by: Elisa Rosati, et al.
Published: (2017-07-01) -
Inactivated tick-borne encephalitis vaccine elicits several overlapping waves of T cell response
by: Anastasiia L. Sycheva, et al.
Published: (2022-08-01) -
T cell receptor beta germline variability is revealed by inference from repertoire data
by: Aviv Omer, et al.
Published: (2022-01-01)