The role of TRECs/KRECs as immune indicators that reflect immunophenotypes and predict the risk of infection in systemic autoimmune diseases

T cell receptor rearrangement excision circles (TRECs) and immunoglobulin κ-deleting recombination excision circles (KRECs) represent the lymphopoiesis capacity, widely used for newborn screening of inborn errors of immunity. To clarify the significance of TRECs and KRECs as immune indicators in pat...

Full description

Saved in:
Bibliographic Details
Main Authors: Takuji Itakura, Hirokazu Sasaki, Tadashi Hosoya, Natsuka Umezawa, Tetsuya Saito, Hideyuki Iwai, Hisanori Hasegawa, Hiroyuki Sato, Akihiro Hirakawa, Kohsuke Imai, Tomohiro Morio, Naoki Kimura, Shinsuke Yasuda
Format: Article
Language:English
Published: Taylor & Francis Group 2025-02-01
Series:Immunological Medicine
Subjects:
Online Access:https://www.tandfonline.com/doi/10.1080/25785826.2025.2460275
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1832544906060496896
author Takuji Itakura
Hirokazu Sasaki
Tadashi Hosoya
Natsuka Umezawa
Tetsuya Saito
Hideyuki Iwai
Hisanori Hasegawa
Hiroyuki Sato
Akihiro Hirakawa
Kohsuke Imai
Tomohiro Morio
Naoki Kimura
Shinsuke Yasuda
author_facet Takuji Itakura
Hirokazu Sasaki
Tadashi Hosoya
Natsuka Umezawa
Tetsuya Saito
Hideyuki Iwai
Hisanori Hasegawa
Hiroyuki Sato
Akihiro Hirakawa
Kohsuke Imai
Tomohiro Morio
Naoki Kimura
Shinsuke Yasuda
author_sort Takuji Itakura
collection DOAJ
description T cell receptor rearrangement excision circles (TRECs) and immunoglobulin κ-deleting recombination excision circles (KRECs) represent the lymphopoiesis capacity, widely used for newborn screening of inborn errors of immunity. To clarify the significance of TRECs and KRECs as immune indicators in patients with systemic autoimmune diseases, we prospectively evaluated TREC and KREC levels with qPCR, lymphocyte phenotypes with flow cytometry, along with lymphocyte counts and serum immunoglobulin levels in peripheral blood samples from newly diagnosed patients. Each variable was assessed before immunosuppressive treatments (baseline), 3-, 6-, and 12-months after the treatment. Severe infections were recorded until 6 months after treatment. Among 35 patients, TREC and KREC levels were associated positively with the proportion of recent thymic emigrants, naïve T and B cells at all the timepoints. TREC and KREC levels decreased after treatment. The ratios of TREC and KREC levels under treatment to baseline were significantly lower in patients with severe infection than those without. In conclusion, TREC and KREC levels reflect peripheral blood immunophenotypes, specifically recent-emigrated T and B cells, in patients under treatment-naïve and immunosuppressive conditions. The longitudinal changes in TREC and KREC levels were beneficial markers for predicting the risk of severe infection during immunosuppressive treatments.
format Article
id doaj-art-9958cecd002f4362800b6719c4203b69
institution Kabale University
issn 2578-5826
language English
publishDate 2025-02-01
publisher Taylor & Francis Group
record_format Article
series Immunological Medicine
spelling doaj-art-9958cecd002f4362800b6719c4203b692025-02-03T08:48:28ZengTaylor & Francis GroupImmunological Medicine2578-58262025-02-0111210.1080/25785826.2025.2460275The role of TRECs/KRECs as immune indicators that reflect immunophenotypes and predict the risk of infection in systemic autoimmune diseasesTakuji Itakura0Hirokazu Sasaki1Tadashi Hosoya2Natsuka Umezawa3Tetsuya Saito4Hideyuki Iwai5Hisanori Hasegawa6Hiroyuki Sato7Akihiro Hirakawa8Kohsuke Imai9Tomohiro Morio10Naoki Kimura11Shinsuke Yasuda12Department of Rheumatology, Graduate School of Medical and Dental Sciences, Institute of Science Tokyo, Tokyo, JapanDepartment of Rheumatology, Graduate School of Medical and Dental Sciences, Institute of Science Tokyo, Tokyo, JapanDepartment of Rheumatology, Graduate School of Medical and Dental Sciences, Institute of Science Tokyo, Tokyo, JapanDepartment of Rheumatology, Graduate School of Medical and Dental Sciences, Institute of Science Tokyo, Tokyo, JapanDepartment of Rheumatology, Graduate School of Medical and Dental Sciences, Institute of Science Tokyo, Tokyo, JapanDepartment of Rheumatology, Graduate School of Medical and Dental Sciences, Institute of Science Tokyo, Tokyo, JapanOffice of Global Affairs, Institute of Science Tokyo, Tokyo, JapanDepartment of Clinical Biostatistics, Graduate School of Medical and Dental Sciences, Institute of Science Tokyo, Tokyo, JapanDepartment of Clinical Biostatistics, Graduate School of Medical and Dental Sciences, Institute of Science Tokyo, Tokyo, JapanDepartment of Pediatrics, National Defense Medical College, Tokorozawa, JapanDepartment of Pediatrics and Developmental Biology, Graduate School of Medical and Dental Sciences, Institute of Science Tokyo, Tokyo, JapanDepartment of Rheumatology, Graduate School of Medical and Dental Sciences, Institute of Science Tokyo, Tokyo, JapanDepartment of Rheumatology, Graduate School of Medical and Dental Sciences, Institute of Science Tokyo, Tokyo, JapanT cell receptor rearrangement excision circles (TRECs) and immunoglobulin κ-deleting recombination excision circles (KRECs) represent the lymphopoiesis capacity, widely used for newborn screening of inborn errors of immunity. To clarify the significance of TRECs and KRECs as immune indicators in patients with systemic autoimmune diseases, we prospectively evaluated TREC and KREC levels with qPCR, lymphocyte phenotypes with flow cytometry, along with lymphocyte counts and serum immunoglobulin levels in peripheral blood samples from newly diagnosed patients. Each variable was assessed before immunosuppressive treatments (baseline), 3-, 6-, and 12-months after the treatment. Severe infections were recorded until 6 months after treatment. Among 35 patients, TREC and KREC levels were associated positively with the proportion of recent thymic emigrants, naïve T and B cells at all the timepoints. TREC and KREC levels decreased after treatment. The ratios of TREC and KREC levels under treatment to baseline were significantly lower in patients with severe infection than those without. In conclusion, TREC and KREC levels reflect peripheral blood immunophenotypes, specifically recent-emigrated T and B cells, in patients under treatment-naïve and immunosuppressive conditions. The longitudinal changes in TREC and KREC levels were beneficial markers for predicting the risk of severe infection during immunosuppressive treatments.https://www.tandfonline.com/doi/10.1080/25785826.2025.2460275T cellsB cellsimmunosuppressantsTRECsKRECs
spellingShingle Takuji Itakura
Hirokazu Sasaki
Tadashi Hosoya
Natsuka Umezawa
Tetsuya Saito
Hideyuki Iwai
Hisanori Hasegawa
Hiroyuki Sato
Akihiro Hirakawa
Kohsuke Imai
Tomohiro Morio
Naoki Kimura
Shinsuke Yasuda
The role of TRECs/KRECs as immune indicators that reflect immunophenotypes and predict the risk of infection in systemic autoimmune diseases
Immunological Medicine
T cells
B cells
immunosuppressants
TRECs
KRECs
title The role of TRECs/KRECs as immune indicators that reflect immunophenotypes and predict the risk of infection in systemic autoimmune diseases
title_full The role of TRECs/KRECs as immune indicators that reflect immunophenotypes and predict the risk of infection in systemic autoimmune diseases
title_fullStr The role of TRECs/KRECs as immune indicators that reflect immunophenotypes and predict the risk of infection in systemic autoimmune diseases
title_full_unstemmed The role of TRECs/KRECs as immune indicators that reflect immunophenotypes and predict the risk of infection in systemic autoimmune diseases
title_short The role of TRECs/KRECs as immune indicators that reflect immunophenotypes and predict the risk of infection in systemic autoimmune diseases
title_sort role of trecs krecs as immune indicators that reflect immunophenotypes and predict the risk of infection in systemic autoimmune diseases
topic T cells
B cells
immunosuppressants
TRECs
KRECs
url https://www.tandfonline.com/doi/10.1080/25785826.2025.2460275
work_keys_str_mv AT takujiitakura theroleoftrecskrecsasimmuneindicatorsthatreflectimmunophenotypesandpredicttheriskofinfectioninsystemicautoimmunediseases
AT hirokazusasaki theroleoftrecskrecsasimmuneindicatorsthatreflectimmunophenotypesandpredicttheriskofinfectioninsystemicautoimmunediseases
AT tadashihosoya theroleoftrecskrecsasimmuneindicatorsthatreflectimmunophenotypesandpredicttheriskofinfectioninsystemicautoimmunediseases
AT natsukaumezawa theroleoftrecskrecsasimmuneindicatorsthatreflectimmunophenotypesandpredicttheriskofinfectioninsystemicautoimmunediseases
AT tetsuyasaito theroleoftrecskrecsasimmuneindicatorsthatreflectimmunophenotypesandpredicttheriskofinfectioninsystemicautoimmunediseases
AT hideyukiiwai theroleoftrecskrecsasimmuneindicatorsthatreflectimmunophenotypesandpredicttheriskofinfectioninsystemicautoimmunediseases
AT hisanorihasegawa theroleoftrecskrecsasimmuneindicatorsthatreflectimmunophenotypesandpredicttheriskofinfectioninsystemicautoimmunediseases
AT hiroyukisato theroleoftrecskrecsasimmuneindicatorsthatreflectimmunophenotypesandpredicttheriskofinfectioninsystemicautoimmunediseases
AT akihirohirakawa theroleoftrecskrecsasimmuneindicatorsthatreflectimmunophenotypesandpredicttheriskofinfectioninsystemicautoimmunediseases
AT kohsukeimai theroleoftrecskrecsasimmuneindicatorsthatreflectimmunophenotypesandpredicttheriskofinfectioninsystemicautoimmunediseases
AT tomohiromorio theroleoftrecskrecsasimmuneindicatorsthatreflectimmunophenotypesandpredicttheriskofinfectioninsystemicautoimmunediseases
AT naokikimura theroleoftrecskrecsasimmuneindicatorsthatreflectimmunophenotypesandpredicttheriskofinfectioninsystemicautoimmunediseases
AT shinsukeyasuda theroleoftrecskrecsasimmuneindicatorsthatreflectimmunophenotypesandpredicttheriskofinfectioninsystemicautoimmunediseases
AT takujiitakura roleoftrecskrecsasimmuneindicatorsthatreflectimmunophenotypesandpredicttheriskofinfectioninsystemicautoimmunediseases
AT hirokazusasaki roleoftrecskrecsasimmuneindicatorsthatreflectimmunophenotypesandpredicttheriskofinfectioninsystemicautoimmunediseases
AT tadashihosoya roleoftrecskrecsasimmuneindicatorsthatreflectimmunophenotypesandpredicttheriskofinfectioninsystemicautoimmunediseases
AT natsukaumezawa roleoftrecskrecsasimmuneindicatorsthatreflectimmunophenotypesandpredicttheriskofinfectioninsystemicautoimmunediseases
AT tetsuyasaito roleoftrecskrecsasimmuneindicatorsthatreflectimmunophenotypesandpredicttheriskofinfectioninsystemicautoimmunediseases
AT hideyukiiwai roleoftrecskrecsasimmuneindicatorsthatreflectimmunophenotypesandpredicttheriskofinfectioninsystemicautoimmunediseases
AT hisanorihasegawa roleoftrecskrecsasimmuneindicatorsthatreflectimmunophenotypesandpredicttheriskofinfectioninsystemicautoimmunediseases
AT hiroyukisato roleoftrecskrecsasimmuneindicatorsthatreflectimmunophenotypesandpredicttheriskofinfectioninsystemicautoimmunediseases
AT akihirohirakawa roleoftrecskrecsasimmuneindicatorsthatreflectimmunophenotypesandpredicttheriskofinfectioninsystemicautoimmunediseases
AT kohsukeimai roleoftrecskrecsasimmuneindicatorsthatreflectimmunophenotypesandpredicttheriskofinfectioninsystemicautoimmunediseases
AT tomohiromorio roleoftrecskrecsasimmuneindicatorsthatreflectimmunophenotypesandpredicttheriskofinfectioninsystemicautoimmunediseases
AT naokikimura roleoftrecskrecsasimmuneindicatorsthatreflectimmunophenotypesandpredicttheriskofinfectioninsystemicautoimmunediseases
AT shinsukeyasuda roleoftrecskrecsasimmuneindicatorsthatreflectimmunophenotypesandpredicttheriskofinfectioninsystemicautoimmunediseases