Department of Hematology and Oncology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Tlalpan, Mexico.
Department of Inmunology and Rheumatology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Tlalpan, Mexico.
Cancer Med. 2024 Sep;13(18):e70200. doi: 10.1002/cam4.70200.
Testicular cancer survivors (TCS) exposed to chemotherapy have an increased expression of CDKN2A/p16 and a lymphocyte phenotype associated with immunosenescence. We seek to define whether the immunosenescent phenotype is associated with chemotherapy.
Case-control study of TCS, disease-free ≥3 months and stratified by primary treatment modality into orchiectomy only, chemotherapy, or bone marrow transplant (BMT). Each group was compared with age-matched healthy controls (HC). We measured the relative proportions of lymphocyte subpopulations using flow cytometry, levels of C-reactive protein, and relative expression of CDKN2A/p16 quantified by qPCR.
We included 65 patients; 19 were treated with orchiectomy only, 35 received different doses of chemotherapy, and 11 underwent BMT. The chemotherapy and BMT groups had decreased naïve CD4 cells compared to HC. The chemotherapy group showed increased central and effector memory CD4 cells, as well as effector and terminally differentiated CD8 cells, compared to HC. Chemotherapy (chemotherapy 1.84 vs. HC 0.92; p < 0.01) and BMT (BMT 6.96 vs. HC 1.25; p < 0.005) groups had higher expression of CDKN2A/p16 compared to HC. The orchiectomy group showed no significant difference with HC (orchiectomy 1.73 vs. HC 1.01; p = 0.17). CRP levels were higher in all groups when compared with HC; in the orchiectomy group, they were only marginally increased (chemotherapy 0.22 vs. HC 0.06; p < 0.01; BMT 0.26 vs. HC 0.06; p < 0.01; orchiectomy 0.09 vs. HC 0.07; p < 0.01).
Among TCS, only patients exposed to cytotoxic agents developed an immunosenescent phenotype. This finding supports the attribution of this alteration to the cytotoxic treatment.
接受化疗的睾丸癌幸存者(TCS)CDKN2A/p16 表达增加,并表现出与免疫衰老相关的淋巴细胞表型。我们旨在确定免疫衰老表型是否与化疗有关。
对 TCS 进行病例对照研究,患者无病生存期≥3 个月,并根据主要治疗方式分为仅行睾丸切除术、化疗或骨髓移植(BMT)。每组均与年龄匹配的健康对照(HC)进行比较。我们使用流式细胞术测量淋巴细胞亚群的相对比例,测量 C 反应蛋白(CRP)水平,并通过 qPCR 定量测定 CDKN2A/p16 的相对表达。
我们纳入了 65 例患者,其中 19 例仅接受睾丸切除术治疗,35 例接受不同剂量的化疗,11 例接受骨髓移植。与 HC 相比,化疗组和 BMT 组的幼稚 CD4 细胞减少。与 HC 相比,化疗组的中央记忆和效应记忆 CD4 细胞以及效应和终末分化 CD8 细胞增加。与 HC 相比,化疗组(化疗 1.84 比 HC 0.92;p<0.01)和 BMT 组(BMT 6.96 比 HC 1.25;p<0.005)CDKN2A/p16 的表达更高。与 HC 相比,睾丸切除术组无显著差异(睾丸切除术 1.73 比 HC 1.01;p=0.17)。与 HC 相比,所有组的 CRP 水平均升高;在睾丸切除术组中,CRP 水平仅略有升高(化疗 0.22 比 HC 0.06;p<0.01;BMT 0.26 比 HC 0.06;p<0.01;睾丸切除术 0.09 比 HC 0.07;p<0.01)。
在 TCS 中,仅接受细胞毒性药物治疗的患者出现免疫衰老表型。这一发现支持将这种改变归因于细胞毒性治疗。