[Expression and Clinical Significance of Co-inhibitory Molecules TIGIT/CD155 and PD-1 in Chronic Lymphocytic Leukemia].

Q4 Medicine
Rui Zhang, Shuang Chen, Ting-Ting Luo, Jian-Hua Qu
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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.

[慢性淋巴细胞白血病共抑制分子TIGIT/CD155和PD-1的表达及临床意义]。
目的:探讨共抑制分子TIGIT/CD155和PD-1在慢性淋巴细胞白血病(CLL)患者外周血CD4+T细胞和Treg细胞中的表达,并分析其临床意义。方法:采用流式细胞术检测40例慢性淋巴细胞白血病患者CD4+T细胞和Treg细胞上PD-1和TIGIT的表达。此外,还检测了CD155在入选受试者外周血B细胞和DC细胞上的表达。结果:CLL患者外周血中PD-1+TIGIT+CD4+T细胞、PD-1+TIGIT+Treg细胞和CD155+DC细胞的比例均显著高于健康对照组(P < 0.05)。PD-1+TIGIT+CD4+T细胞和PD-1+TIGIT+Treg细胞在CLL患者中的比例分别显著高于PD-1+TIGIT-CD4+T细胞和PD-1+TIGIT-Treg细胞(P < 0.05)。PD-1+TIGIT+CD4+T细胞和PD-1+TIGIT+Treg细胞均与CD155+DC细胞水平呈正相关(r =0.742, r =0.766)。随着Binet期的进展,PD-1+TIGIT+CD4+T细胞、PD-1+TIGIT+Treg细胞、CD155+DC细胞的比例逐渐增加(P < 0.05),且在CD38≥30%、IGVH未突变、染色体异常导致预后不良的患者中,上述三种细胞均增加(P < 0.05)。结论:共抑制分子PD-1和TIGIT可能参与了晚期CLL患者的免疫耗损,具有临床预后价值。双抑制剂分子靶向治疗为CLL的个体化治疗提供了新的方向。
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来源期刊
中国实验血液学杂志
中国实验血液学杂志 Medicine-Medicine (all)
CiteScore
0.40
自引率
0.00%
发文量
7331
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