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新型冠状病毒肺炎相关急性呼吸衰竭患者T淋巴细胞亚群绝对计数的特征及预测价值:一项回顾性研究

Characteristics and Predictive Value of T-lymphocyte Subset Absolute Counts in Patients with COVID-19-associated Acute Respiratory Failure: A Retrospective Study.

作者信息

Vadi Sonali, Pednekar Ashwini, Suthar Durga, Sanwalka Neha, Ghodke Kiran, Rabade Nikhil

机构信息

Department of Intensive Care Medicine, Kokilaben Dhirubhai Ambani Hospital & Medical Research Institute, Mumbai, Maharashtra, India.

Department of Nutrition and Biostatistics, NutriCanvas, Mumbai, Maharashtra, India.

出版信息

Indian J Crit Care Med. 2022 Nov;26(11):1198-1203. doi: 10.5005/jp-journals-10071-24352.

Abstract

BACKGROUND

Of the factors influencing severity and outcomes following coronavirus disease-2019 (COVID-19), cellular immune response has a strong impact. The spectrum of response varies from over-activation to hypo-functioning. The severe infection leads to reduction in numbers and dysfunction of T-lymphocytes/subsets.

PATIENTS AND METHODS

This retrospective, single-center study aimed to analyze the expression of T-lymphocyte/subsets by flow cytometry and inflammation-related biomarker, serum ferritin in real-time polymerase chain reaction (RT-PCR) positive patients. According to oxygen requirements, patients were stratified into nonsevere (room air, nasal prongs, and face mask) and severe [nonrebreather mask (NRBM), noninvasive ventilation (NIV), high-flow nasal oxygen (HFNO), and invasive mechanical ventilation (IMV)] subgroups for analysis. Patients were classified into survivors and nonsurvivors. Mann-Whitney test was used to analyze differences in T-lymphocyte and subset values when classified according to gender, the severity of COVID, outcome, and prevalence of diabetes mellitus (DM). Cross tabulations were computed for categorical data and compared using Fisher's exact test. Spearman correlation was used to analyze the correlation of T-lymphocyte and subset values with age or serum ferritin levels. <0.05 values were considered to be statistically significant.

RESULTS

A total of 379 patients were analyzed. Significantly higher percentage of patients with DM were aged ≥61 years in both nonsevere and severe COVID groups. A significant negative correlation of CD3+, CD4+, and CD8+ was found with age. CD3+ and CD4+ absolute counts were significantly higher in females as compared to males. Patients with severe COVID had significantly lesser total lymphocyte (%), CD3+, CD4+, and CD8+ counts as compared to those with nonsevere COVID ( <0.05). T-lymphocyte subsets were reduced in patients with severe disease. A significant negative correlation of total lymphocyte (%), CD3+, CD4+, and CD8+ counts was found with serum ferritin levels.

CONCLUSIONS

T-lymphocyte/subset trends are an independent risk factor for clinical prognosis. Monitoring may help in intervening in patients with disease progression.

HOW TO CITE THIS ARTICLE

Vadi S, Pednekar A, Suthar D, Sanwalka N, Ghodke K, Rabade N. Characteristics and Predictive Value of T-lymphocyte Subset Absolute Counts in Patients with COVID-19-associated Acute Respiratory Failure: A Retrospective Study. Indian J Crit Care Med 2022;26(11):1198-1203.

摘要

背景

在影响2019冠状病毒病(COVID-19)严重程度和预后的因素中,细胞免疫反应有很大影响。反应谱从过度激活到功能减退不等。严重感染会导致T淋巴细胞/亚群数量减少和功能障碍。

患者与方法

这项回顾性单中心研究旨在通过流式细胞术分析T淋巴细胞/亚群的表达以及实时聚合酶链反应(RT-PCR)阳性患者炎症相关生物标志物血清铁蛋白的情况。根据氧气需求,将患者分为非重症组(室内空气、鼻导管和面罩)和重症组[非重复呼吸面罩(NRBM)、无创通气(NIV)、高流量鼻导管吸氧(HFNO)和创机械通气(IMV)]进行分析。患者分为存活者和非存活者。采用曼-惠特尼检验分析根据性别、COVID严重程度、预后和糖尿病(DM)患病率分类时T淋巴细胞和亚群值的差异。对分类数据计算交叉表并使用Fisher精确检验进行比较。采用Spearman相关性分析T淋巴细胞和亚群值与年龄或血清铁蛋白水平的相关性。P<0.05被认为具有统计学意义。

结果

共分析了379例患者。在非重症和重症COVID组中,糖尿病患者中年龄≥61岁的比例显著更高。发现CD3 +、CD4 +和CD8 +与年龄呈显著负相关。女性的CD3 +和CD4 +绝对计数显著高于男性。与非重症COVID患者相比,重症COVID患者的总淋巴细胞(%)、CD3 +、CD4 +和CD8 +计数显著更低(P<0.05)。重症患者的T淋巴细胞亚群减少。发现总淋巴细胞(%)、CD3 +、CD4 +和CD8 +计数与血清铁蛋白水平呈显著负相关。

结论

T淋巴细胞/亚群趋势是临床预后的独立危险因素。监测可能有助于对疾病进展的患者进行干预。

如何引用本文

Vadi S, Pednekar A, Suthar D, Sanwalka N, Ghodke K, Rabade N. COVID-19相关急性呼吸衰竭患者T淋巴细胞亚群绝对计数的特征及预测价值:一项回顾性研究。《印度重症监护医学杂志》2022;26(11):1198 - 1203。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/192c/9983653/611db0c73ad0/ijccm-26-1198-g001.jpg

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