{"title":"[Expression and Clinical Significance of Co-inhibitory Molecules TIGIT/CD155 and PD-1 in Chronic Lymphocytic Leukemia].","authors":"Rui Zhang, Shuang Chen, Ting-Ting Luo, Jian-Hua Qu","doi":"10.19746/j.cnki.issn.1009-2137.2025.01.008","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>To investigate the expression of co-inhibitory molecules TIGIT/CD155 and PD-1 on CD4<sup>+</sup>T cells and Treg cells in peripheral blood of patients with chronic lymphocytic leukemia (CLL) and analyze their clinical significance.</p><p><strong>Methods: </strong>The expression of PD-1 and TIGIT on CD4<sup>+</sup>T cells and Treg cells was detected by flow cytometry in 40 CLL patients and 20 healthy controls. Additionally, the expression of CD155 on peripheral blood B cells and DC cells of the enrolled subjects was detected.</p><p><strong>Results: </strong>The proportions of PD-1<sup>+</sup>TIGIT<sup>+</sup>CD4<sup>+</sup>T cells, PD-1<sup>+</sup>TIGIT<sup>+</sup>Treg cells and CD155<sup>+</sup>DC cells in peripheral blood of CLL patients were significantly higher than those of healthy controls ( <i>P</i> < 0.05). The proportions of PD-1<sup>+</sup>TIGIT<sup>+</sup>CD4<sup>+</sup>T cells and PD-1<sup>+</sup>TIGIT<sup>+</sup>Treg cells in CLL patients were significantly higher than those of PD-1<sup>+</sup>TIGIT<sup>-</sup>CD4<sup>+</sup>T cells and PD-1<sup>+</sup>TIGIT<sup>-</sup>Treg cells, respectively ( <i>P</i> < 0.05). Both PD-1<sup>+</sup>TIGIT<sup>+</sup>CD4<sup>+</sup>T cells and PD-1<sup>+</sup>TIGIT<sup>+</sup>Treg cells were positively correlated with the level of CD155<sup>+</sup>DC cells (<i>r</i> =0.742, <i>r</i> =0.766). With the progression of Binet stage, the proportions of PD-1<sup>+</sup>TIGIT<sup>+</sup>CD4<sup>+</sup>T cells, PD-1<sup>+</sup>TIGIT<sup>+</sup>Treg cells, and CD155<sup>+</sup>DC cells gradually increased ( <i>P</i> < 0.05), and the aforementioned three types cells were all increased in patients with CD38≥30%, <i>IGVH</i> unmutated, or poor prognosis due to chromosomal abnormalities ( <i>P</i> < 0.05).</p><p><strong>Conclusion: </strong>Co-inhibitory molecules PD-1 and TIGIT may be involved in immunodepletion in patients with advanced CLL, which has clinical prognostic value. Dual inhibitor molecular targeted therapy provides a new direction for the individualized treatment of CLL.</p>","PeriodicalId":35777,"journal":{"name":"中国实验血液学杂志","volume":"33 1","pages":"54-61"},"PeriodicalIF":0.0000,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"中国实验血液学杂志","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.19746/j.cnki.issn.1009-2137.2025.01.008","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0
Abstract
Objective: To investigate the expression of co-inhibitory molecules TIGIT/CD155 and PD-1 on CD4+T cells and Treg cells in peripheral blood of patients with chronic lymphocytic leukemia (CLL) and analyze their clinical significance.
Methods: The expression of PD-1 and TIGIT on CD4+T cells and Treg cells was detected by flow cytometry in 40 CLL patients and 20 healthy controls. Additionally, the expression of CD155 on peripheral blood B cells and DC cells of the enrolled subjects was detected.
Results: The proportions of PD-1+TIGIT+CD4+T cells, PD-1+TIGIT+Treg cells and CD155+DC cells in peripheral blood of CLL patients were significantly higher than those of healthy controls ( P < 0.05). The proportions of PD-1+TIGIT+CD4+T cells and PD-1+TIGIT+Treg cells in CLL patients were significantly higher than those of PD-1+TIGIT-CD4+T cells and PD-1+TIGIT-Treg cells, respectively ( P < 0.05). Both PD-1+TIGIT+CD4+T cells and PD-1+TIGIT+Treg cells were positively correlated with the level of CD155+DC cells (r =0.742, r =0.766). With the progression of Binet stage, the proportions of PD-1+TIGIT+CD4+T cells, PD-1+TIGIT+Treg cells, and CD155+DC cells gradually increased ( P < 0.05), and the aforementioned three types cells were all increased in patients with CD38≥30%, IGVH unmutated, or poor prognosis due to chromosomal abnormalities ( P < 0.05).
Conclusion: Co-inhibitory molecules PD-1 and TIGIT may be involved in immunodepletion in patients with advanced CLL, which has clinical prognostic value. Dual inhibitor molecular targeted therapy provides a new direction for the individualized treatment of CLL.