← 返回

癌症患者抵御新病原体的淋巴细胞亚群

英文原题:Lymphocyte Subsets in Defense Against New Pathogens in Patients with Cancer.

查看英文原题

Lymphocyte Subsets in Defense Against New Pathogens in Patients with Cancer.

PubMed 2022/05/16(内容时间) MEDICC Rev

分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。

研究概要

癌症及常规癌症治疗会显著影响外周血 B 淋巴细胞水平,尤其是过渡型辅助性 T 淋巴细胞,从而降低免疫系统对新抗原触发初次免疫应答的能力。

研究思路结论见上方概要

癌症患者免疫受癌症本身和肿瘤特异性治疗的影响。患者适应性免疫是否受损取决于其初始淋巴细胞水平和其他细胞群体。在 COVID-19 大流行期间,癌症患者进展为重症的风险更高,死亡率也高于非癌症个体,尤其是在接受癌症特异性治疗期间。个体对感染的保护、对疫苗的反应,甚至测定 SARS-CoV-2 体液免疫反应的检测,都取决于淋巴细胞群体,值得对其进行研究。

评估癌症患者中对新病原体免疫应答所涉及的淋巴细胞血液浓度。

我们开展了一项对218名癌症患者的分析性研究;其中女性124名,男性94名,年龄26-93岁,他们于2020年3月至6月在古巴哈瓦那的国家肿瘤学和放射生物学研究所接受治疗。患者被分为五组:(1)疾病得到控制且未接受癌症特异性治疗的患者;(2)接受减瘤手术的患者;(3)接受化疗的患者;(4)接受放射治疗的患者,以及(5)目前正在对抗感染的患者。我们通过流式细胞术评估了以下外周血淋巴细胞亚群:B淋巴细胞(总B细胞、初始B细胞、过渡型B细胞、记忆B细胞、浆母细胞和浆细胞);T淋巴细胞(总T细胞、辅助T细胞、细胞毒性T细胞及其各自的初始、活化、中枢记忆和效应记忆亚群);以及总NK 细胞、分泌型NK 细胞和细胞毒性NK 细胞及TNK 细胞。我们还估算了中性粒细胞/淋巴细胞比值。淋巴细胞浓度与疾病控制和标准癌症治疗相关。对于不符合正态分布的变量,范围由中位数和2.5-97.5百分位数设定。采用双尾Mann-Whitney U检验来测量性别的影响并比较淋巴细胞群体。我们计算了比值比以估计淋巴细胞减少症风险。

所有癌症患者的初始辅助性T淋巴细胞和细胞毒性T淋巴细胞群体、初始B淋巴细胞以及NK 细胞的数值均低于正常参考中位数。初始辅助性T细胞是受影响最严重的亚群。记忆B细胞、浆母细胞、浆细胞、活化辅助性T细胞和细胞毒性中央记忆T细胞则有所增加。正在接受治疗的患者其初始淋巴细胞水平低于未治疗患者,尤其是在放疗期间。接受治疗的患者发生B淋巴细胞减少症的风险更高。接受手术的患者B淋巴细胞减少症的比值比为8.0,接受化疗的患者为12.9,接受放疗的患者为13.9。

展开英文摘要原文

Estimate blood concentrations of lymphocytes involved in the immune response to new pathogens in cancer patients.

We carried out an analytical study of 218 cancer patients; 124 women and 94 men, 26-93 years of age, who were treated at the National Oncology and Radiobiology Institute in Havana, Cuba, March-June, 2020. Patients were divided into five groups: (1) those with controlled disease who were not undergoing cancer-specific treatment; (2) those undergoing debulking surgery; (3) patients undergoing chemotherapy; (4) patients undergoing radiation therapy and (5) patients currently battling infection. We evaluated the following peripheral blood lymphocyte subpopulations via flow cytometry: B lymphocytes (total, naive, transitional, memory, plasmablasts and plasma cells); T lymphocytes (total, helper, cytotoxic and their respective naive, activated, central memory and effector memory subsets); and total, secretory and cytotoxic natural killer cells and T natural killer cells. We also estimated neutrophil/lymphocyte ratios. Lymphocyte concentrations were associated with controlled disease and standard cancer therapy. For variables that did not fall within a normal distribution, ranges were set by medians and 2.5-97.5 percentiles. The two-tailed Mann-Whitney U test was used to measure the effect of sex and to compare lymphocyte populations. We calculated odds ratios to estimate lymphopenia risk.

All cancer patients had lower values of naive helper and cytotoxic T lymphocyte populations, naive B lymphocytes, and natural killer cells than normal reference medians. Naive helper T cells were the most affected subpopulation. Memory B cells, plasmablasts, plasma cells, activated T helper cells, and cytotoxic central memory T cells were increased. Patients undergoing treatment had lower levels of naive lymphocytes than untreated patients, particularly during radiation therapy. The risk of B lymphopenia was higher in patients in treatment. The odds ratio for B lymphopenia was 8.0 in patients who underwent surgery, 12.9 in those undergoing chemotherapy, and 13.9 in patients in radiotherapy.

Cancer and conventional cancer therapies significantly affect peripheral blood B lymphocyte levels, particularly transitional T helper lymphocytes, reducing the immune system's ability to trigger primary immune responses against new antigens.

论文信息

作者
Arango-Prado MDC、Villegas-Valverde CA、Torres-López G、Soto-Pardeiro P、Suárez-Reyes A、Faxas-García ME、Diéguez-Rodríguez V、Gracia-Medina E
单位
Immunology Laboratory, National Oncology and Radiobiology Institute (INOR), Havana, Cuba.Cuba
期刊
MEDICC review2022 May 16
原文标识
PubMed 35648060 · DOI 10.37757/mr2022.v24.n2.5