首页|期刊导航|协和医学杂志|围术期肿瘤患者脓毒性休克前后淋巴细胞亚群变化特征及其对预后的影响

围术期肿瘤患者脓毒性休克前后淋巴细胞亚群变化特征及其对预后的影响OA

Altered Lymphocyte Subsets in Perioperative Cancer Patients Before and After Septic Shock:Characteristics and Prognostic Implications

中文摘要英文摘要

目的 探究恶性肿瘤患者发生脓毒性休克前后外周血免疫细胞变化情况,并分析这些免疫细胞与患者预后的关系.方法 回顾性纳入山西省肿瘤医院2018 年10 月—2019 年12 月因脓毒性休克转入重症监护病房(intensive care unit,ICU)的围术期肿瘤患者.比较脓毒性休克前后(分别于脓毒症休克发生前及发生脓毒症休克 72h内完成检测)淋巴细胞及其亚群变化,并采用多因素Logistic回归模型分析肿瘤患者发生脓毒性休克后上述免疫指标与 28d死亡风险的关系.结果 共纳入因脓毒性休克转入ICU的肿瘤患者 47 例.男性 32 例,女性 15 例;平均年龄(63.9±11.2)岁;胃肠道肿瘤为最常见的肿瘤类型(76.60%,36/47);腹盆腔感染(65.96%,31/47)是最主要的感染来源;转入ICU 后28d内死亡12例,存活35例.相较于脓毒性休克发生前,脓毒性休克后淋巴细胞计数显著降低[530(300,830)个/μL比1530(1020,2020)个/μL,P<0.001].淋巴细胞亚群分析显示,除总B细胞计数外,余免疫细胞计数在脓毒性休克后均显著降低(P均<0.05).组间比较显示,死亡组与存活组自然杀伤 T细胞计数、自然杀伤细胞计数无显著差异(P均>0.05),余免疫细胞计数显著低于存活组(P均<0.05).多因素Logistic回归分析校正年龄、乳酸、急性生理学与慢性健康状况评估Ⅱ评分后显示,脓毒性休克后调节性T细胞计数与发生脓毒性休克的肿瘤患者 28d全因死亡率呈显著负相关(OR=0.938,95%CI:0.886~0.993,P=0.028).结论 围术期肿瘤患者发生脓毒性休克后,外周血淋巴细胞亚群普遍存在急性耗竭现象.在众多免疫指标中,调节性T细胞计数是患者短期死亡风险的独立预测因素.对此类患者进行基础免疫功能评估,有助于优化治疗策略,从而改善总体预后.

Objective To investigate the changes in peripheral blood immune cells before and after the onset of septic shock in patients with malignant tumors,and to analyze the relationship between these immune cells and patient prognosis.Methods A retrospective study was conducted,enrolling perioperative tumor patients who were transferred to the intensive care unit(ICU)due to septic shock at Shanxi Provincial Canc-er Hospital between October 2018 and December 2019.Changes in lymphocyte counts and subsets were com-pared before and after septic shock(measured prior to septic shock onset and within 72 hours after onset).A multivariate Logistic regression model was used to analyze the relationship between these immune indicators and the 28-day mortality risk in tumor patients following septic shock.Results A total of 47 tumor patients transferred to the ICU due to septic shock were included.There were 32 males and 15 females,with a mean age of(63.9±11.2)years.Gastrointestinal tumors were the most common tumor type(76.60%,36/47),and abdominal/pelvic infection(65.96%,31/47)was the primary source of infection.Within28 days after ICU transfer,12 patients died and 35 survived.Compared to pre-septic shock levels,lymphocyte counts sig-nificantly decreased after septic shock[530(300,830)cells/μL vs.1530(1020,2020)cells/μL,P<0.001].Lymphocyte subset analysis revealed that,compared to pre-septic shock levels,counts of all other immune cells significantly decreased after septic shock except for total B-cell count(all P<0.05).Be-tween-group comparisons demonstrated no significant differences in natural killer T-cell or natural killer cell counts between non-survivors and survivors(all P>0.05);however,the remaining immune cell counts were significantly lower in non-survivors compared with survivors(all P<0.05).Multivariate Logistic re-gression analysis[adjusted for age,lactate level,and acute physiology and chronic health evaluation Ⅱ(APACHE Ⅱ)score]showed that regulatory T cell counts after septic shock were significantly negatively correlated with 28-day all-cause mortality(OR = 0.938,95%CI:0.886-0.993,P = 0.028).Conclusions Perioperative tumor patients experience acute depletion of peripheral blood lymphocyte subsets following septic shock.Among various immune indicators,regulatory T cell count serves as an independent predictor of short-term mortality risk.Evaluating baseline immune function in such patients may help optimize treatment strategies and improve overall prognosis.

魏苗;杨丽丽;李晓燕;吕慧芳;段燕

山西省肿瘤医院中国医学科学院肿瘤医院山西医院山西医科大学附属肿瘤医院重症医学科,太原 030013山西省肿瘤医院中国医学科学院肿瘤医院山西医院山西医科大学附属肿瘤医院重症医学科,太原 030013山西省肿瘤医院中国医学科学院肿瘤医院山西医院山西医科大学附属肿瘤医院重症医学科,太原 030013山西省肿瘤医院中国医学科学院肿瘤医院山西医院山西医科大学附属肿瘤医院重症医学科,太原 030013山西省肿瘤医院中国医学科学院肿瘤医院山西医院山西医科大学附属肿瘤医院重症医学科,太原 030013

医药卫生

恶性肿瘤脓毒性休克淋巴细胞减少症淋巴细胞亚群调节性T细胞计数

malignancyseptic shocklymphopenialymphocyte subsetsregulatory T cell count

《协和医学杂志》 2026 (1)

86-97,12

国家科技部重大专项-四大慢病(2024ZD0526100) National Key Research and Development Program of China-Major Project for Four Chronic Noncommunicable Disea-ses(2024ZD0526100)

10.12290/xhyxzz.2025-0959

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