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Increase of CD3(+)CD7(−) T cells in bone marrow predicts invasion in patients with T-cell non-Hodgkin’s lymphoma
BACKGROUND: The T-cell non-Hodgkin’s lymphoma (T-NHL) patients with bone marrow (BM) invasion have a poor prognosis. Although BM biopsy is still a confirmed diagnosis method, the low sensitivity restricts its use to detect the minimal BM invasion. It is of great clinical significance to establish a...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9273714/ https://www.ncbi.nlm.nih.gov/pubmed/35836512 http://dx.doi.org/10.21037/tcr-21-2666 |
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author | Huang, Ziyang Chen, Binbin Ling, Yixin Pan, Yangya Jiang, Songfu Zhang, Shenghui Yu, Kang Han, Yixiang |
author_facet | Huang, Ziyang Chen, Binbin Ling, Yixin Pan, Yangya Jiang, Songfu Zhang, Shenghui Yu, Kang Han, Yixiang |
author_sort | Huang, Ziyang |
collection | PubMed |
description | BACKGROUND: The T-cell non-Hodgkin’s lymphoma (T-NHL) patients with bone marrow (BM) invasion have a poor prognosis. Although BM biopsy is still a confirmed diagnosis method, the low sensitivity restricts its use to detect the minimal BM invasion. It is of great clinical significance to establish a rapid and highly sensitive method to evaluate BM invasion. METHODS: We conducted a retrospective study of 85 patients with new diagnosed T-NHL patients enrolled in our institute. The bone marrow mononuclear cells (BMMNCs) cells were isolated, stained with different combinations of antibody and subjected to flow cytometry analysis. RESULTS: We found that CD3(+)CD7(−) T cells increased significantly in the BM in T-NHL patients with BM invasion. The patients were divided into the low and high groups according to the cutoff value of 1.035% obtained by analyzing the receiver operating characteristic (ROC) curve of the percentage of CD3(+)CD7(−) T cells of nucleated cells at diagnosis. The ratio of invasion in high group was markedly higher than that in low group. Furthermore, CD3(+)CD7(−) T cells presented significantly higher level of programmed cell death-1 (PD-1), lymphocyte-activation-gene-3 (LAG3) and CD4/CD8 ratio. CONCLUSIONS: Our study revealed the percentage of CD3(+)CD7(−) T cells of nucleated cells in BM was a potential diagnostic predictor of BM invasion with T-NHL. |
format | Online Article Text |
id | pubmed-9273714 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-92737142022-07-13 Increase of CD3(+)CD7(−) T cells in bone marrow predicts invasion in patients with T-cell non-Hodgkin’s lymphoma Huang, Ziyang Chen, Binbin Ling, Yixin Pan, Yangya Jiang, Songfu Zhang, Shenghui Yu, Kang Han, Yixiang Transl Cancer Res Original Article BACKGROUND: The T-cell non-Hodgkin’s lymphoma (T-NHL) patients with bone marrow (BM) invasion have a poor prognosis. Although BM biopsy is still a confirmed diagnosis method, the low sensitivity restricts its use to detect the minimal BM invasion. It is of great clinical significance to establish a rapid and highly sensitive method to evaluate BM invasion. METHODS: We conducted a retrospective study of 85 patients with new diagnosed T-NHL patients enrolled in our institute. The bone marrow mononuclear cells (BMMNCs) cells were isolated, stained with different combinations of antibody and subjected to flow cytometry analysis. RESULTS: We found that CD3(+)CD7(−) T cells increased significantly in the BM in T-NHL patients with BM invasion. The patients were divided into the low and high groups according to the cutoff value of 1.035% obtained by analyzing the receiver operating characteristic (ROC) curve of the percentage of CD3(+)CD7(−) T cells of nucleated cells at diagnosis. The ratio of invasion in high group was markedly higher than that in low group. Furthermore, CD3(+)CD7(−) T cells presented significantly higher level of programmed cell death-1 (PD-1), lymphocyte-activation-gene-3 (LAG3) and CD4/CD8 ratio. CONCLUSIONS: Our study revealed the percentage of CD3(+)CD7(−) T cells of nucleated cells in BM was a potential diagnostic predictor of BM invasion with T-NHL. AME Publishing Company 2022-06 /pmc/articles/PMC9273714/ /pubmed/35836512 http://dx.doi.org/10.21037/tcr-21-2666 Text en 2022 Translational Cancer Research. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/. |
spellingShingle | Original Article Huang, Ziyang Chen, Binbin Ling, Yixin Pan, Yangya Jiang, Songfu Zhang, Shenghui Yu, Kang Han, Yixiang Increase of CD3(+)CD7(−) T cells in bone marrow predicts invasion in patients with T-cell non-Hodgkin’s lymphoma |
title | Increase of CD3(+)CD7(−) T cells in bone marrow predicts invasion in patients with T-cell non-Hodgkin’s lymphoma |
title_full | Increase of CD3(+)CD7(−) T cells in bone marrow predicts invasion in patients with T-cell non-Hodgkin’s lymphoma |
title_fullStr | Increase of CD3(+)CD7(−) T cells in bone marrow predicts invasion in patients with T-cell non-Hodgkin’s lymphoma |
title_full_unstemmed | Increase of CD3(+)CD7(−) T cells in bone marrow predicts invasion in patients with T-cell non-Hodgkin’s lymphoma |
title_short | Increase of CD3(+)CD7(−) T cells in bone marrow predicts invasion in patients with T-cell non-Hodgkin’s lymphoma |
title_sort | increase of cd3(+)cd7(−) t cells in bone marrow predicts invasion in patients with t-cell non-hodgkin’s lymphoma |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9273714/ https://www.ncbi.nlm.nih.gov/pubmed/35836512 http://dx.doi.org/10.21037/tcr-21-2666 |
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