Analysis of CDR3 Sequences from T-Cell Receptor β in Acute Respiratory Distress Syndrome

Acute Respiratory Distress Syndrome (ARDS) is an illness that typically develops in people who are significantly ill or have serious injuries. ARDS is characterized by fluid build-up that occurs in the alveoli. T-cells are implicated as playing a role in the modulation of the aberrant response leadi...

Full description

Bibliographic Details
Main Authors: Sara Hey, Dayjah Whyte, Minh-Chau Hoang, Nick Le, Joseph Natvig, Claire Wingfield, Charles Onyeama, Judie Howrylak, Inimary T. Toby
Format: Article
Language:English
Published: MDPI AG 2023-05-01
Series:Biomolecules
Subjects:
Online Access:https://www.mdpi.com/2218-273X/13/5/825
_version_ 1797600885131444224
author Sara Hey
Dayjah Whyte
Minh-Chau Hoang
Nick Le
Joseph Natvig
Claire Wingfield
Charles Onyeama
Judie Howrylak
Inimary T. Toby
author_facet Sara Hey
Dayjah Whyte
Minh-Chau Hoang
Nick Le
Joseph Natvig
Claire Wingfield
Charles Onyeama
Judie Howrylak
Inimary T. Toby
author_sort Sara Hey
collection DOAJ
description Acute Respiratory Distress Syndrome (ARDS) is an illness that typically develops in people who are significantly ill or have serious injuries. ARDS is characterized by fluid build-up that occurs in the alveoli. T-cells are implicated as playing a role in the modulation of the aberrant response leading to excessive tissue damage and, eventually, ARDS. Complementarity Determining Region 3 (CDR3) sequences derived from T-cells are key players in the adaptive immune response. This response is governed by an elaborate specificity for distinct molecules and the ability to recognize and vigorously respond to repeated exposures to the same molecules. Most of the diversity in T-cell receptors (TCRs) is contained in the CDR3 regions of the heterodimeric cell-surface receptors. For this study, we employed the novel technology of immune sequencing to assess lung edema fluid. Our goal was to explore the landscape of CDR3 clonal sequences found within these samples. We obtained more than 3615 CDR3 sequences across samples in the study. Our data demonstrate that: (1) CDR3 sequences from lung edema fluid exhibit distinct clonal populations, and (2) CDR3 sequences can be further characterized based on biochemical features. Analysis of these CDR3 sequences offers insight into the CDR3-driven T-cell repertoire of ARDS. These findings represent the first step towards applications of this technology with these types of biological samples in the context of ARDS.
first_indexed 2024-03-11T03:55:10Z
format Article
id doaj.art-da11b6cb405145cd8a0c7f9c8571e217
institution Directory Open Access Journal
issn 2218-273X
language English
last_indexed 2024-03-11T03:55:10Z
publishDate 2023-05-01
publisher MDPI AG
record_format Article
series Biomolecules
spelling doaj.art-da11b6cb405145cd8a0c7f9c8571e2172023-11-18T00:39:44ZengMDPI AGBiomolecules2218-273X2023-05-0113582510.3390/biom13050825Analysis of CDR3 Sequences from T-Cell Receptor β in Acute Respiratory Distress SyndromeSara Hey0Dayjah Whyte1Minh-Chau Hoang2Nick Le3Joseph Natvig4Claire Wingfield5Charles Onyeama6Judie Howrylak7Inimary T. Toby8Department of Biology, University of Dallas, Irving, TX 75062, USADepartment of Biology, University of Dallas, Irving, TX 75062, USADepartment of Biology, University of Dallas, Irving, TX 75062, USADepartment of Biology, University of Dallas, Irving, TX 75062, USADepartment of Biology, University of Dallas, Irving, TX 75062, USADepartment of Biology, University of Dallas, Irving, TX 75062, USAT.C Pediatrics, Bedford, TX 76021, USAPulmonary, Allergy and Critical Care Division, Penn State Milton S. Hershey Medical Center, Hershey, PA 17033, USADepartment of Biology, University of Dallas, Irving, TX 75062, USAAcute Respiratory Distress Syndrome (ARDS) is an illness that typically develops in people who are significantly ill or have serious injuries. ARDS is characterized by fluid build-up that occurs in the alveoli. T-cells are implicated as playing a role in the modulation of the aberrant response leading to excessive tissue damage and, eventually, ARDS. Complementarity Determining Region 3 (CDR3) sequences derived from T-cells are key players in the adaptive immune response. This response is governed by an elaborate specificity for distinct molecules and the ability to recognize and vigorously respond to repeated exposures to the same molecules. Most of the diversity in T-cell receptors (TCRs) is contained in the CDR3 regions of the heterodimeric cell-surface receptors. For this study, we employed the novel technology of immune sequencing to assess lung edema fluid. Our goal was to explore the landscape of CDR3 clonal sequences found within these samples. We obtained more than 3615 CDR3 sequences across samples in the study. Our data demonstrate that: (1) CDR3 sequences from lung edema fluid exhibit distinct clonal populations, and (2) CDR3 sequences can be further characterized based on biochemical features. Analysis of these CDR3 sequences offers insight into the CDR3-driven T-cell repertoire of ARDS. These findings represent the first step towards applications of this technology with these types of biological samples in the context of ARDS.https://www.mdpi.com/2218-273X/13/5/825Complementarity Determining Region 3immune sequencingAcute Respiratory Distress SyndromeT-cell receptorsequence analysisbiochemical properties and clonality
spellingShingle Sara Hey
Dayjah Whyte
Minh-Chau Hoang
Nick Le
Joseph Natvig
Claire Wingfield
Charles Onyeama
Judie Howrylak
Inimary T. Toby
Analysis of CDR3 Sequences from T-Cell Receptor β in Acute Respiratory Distress Syndrome
Biomolecules
Complementarity Determining Region 3
immune sequencing
Acute Respiratory Distress Syndrome
T-cell receptor
sequence analysis
biochemical properties and clonality
title Analysis of CDR3 Sequences from T-Cell Receptor β in Acute Respiratory Distress Syndrome
title_full Analysis of CDR3 Sequences from T-Cell Receptor β in Acute Respiratory Distress Syndrome
title_fullStr Analysis of CDR3 Sequences from T-Cell Receptor β in Acute Respiratory Distress Syndrome
title_full_unstemmed Analysis of CDR3 Sequences from T-Cell Receptor β in Acute Respiratory Distress Syndrome
title_short Analysis of CDR3 Sequences from T-Cell Receptor β in Acute Respiratory Distress Syndrome
title_sort analysis of cdr3 sequences from t cell receptor β in acute respiratory distress syndrome
topic Complementarity Determining Region 3
immune sequencing
Acute Respiratory Distress Syndrome
T-cell receptor
sequence analysis
biochemical properties and clonality
url https://www.mdpi.com/2218-273X/13/5/825
work_keys_str_mv AT sarahey analysisofcdr3sequencesfromtcellreceptorbinacuterespiratorydistresssyndrome
AT dayjahwhyte analysisofcdr3sequencesfromtcellreceptorbinacuterespiratorydistresssyndrome
AT minhchauhoang analysisofcdr3sequencesfromtcellreceptorbinacuterespiratorydistresssyndrome
AT nickle analysisofcdr3sequencesfromtcellreceptorbinacuterespiratorydistresssyndrome
AT josephnatvig analysisofcdr3sequencesfromtcellreceptorbinacuterespiratorydistresssyndrome
AT clairewingfield analysisofcdr3sequencesfromtcellreceptorbinacuterespiratorydistresssyndrome
AT charlesonyeama analysisofcdr3sequencesfromtcellreceptorbinacuterespiratorydistresssyndrome
AT judiehowrylak analysisofcdr3sequencesfromtcellreceptorbinacuterespiratorydistresssyndrome
AT inimaryttoby analysisofcdr3sequencesfromtcellreceptorbinacuterespiratorydistresssyndrome