论著

新型冠状病毒肺炎淋巴细胞亚群与严重程度的相关分析

  • 包芳 ,
  • 史尉利 ,
  • 胡静 ,
  • 张娣 ,
  • 高东晗 ,
  • 夏云霞 ,
  • 景红梅 ,
  • 克晓燕 ,
  • 葛庆岗 ,
  • 沈宁
展开
  • 1. 北京大学第三医院 血液内科
    2. 北京大学第三医院 运动医学研究所
    3. 北京大学第三医院 呼吸与危重医学科
    4. 北京大学第三医院 风湿免疫科
    5. 北京大学第三医院 危重医学科,北京 100191

收稿日期: 2020-07-16

  网络出版日期: 2020-12-13

Analysis of the correlation between lymphocyte subsets and severity of corona virus disease 19

  • Fang BAO ,
  • Wei-li SHI ,
  • Jing HU ,
  • Di ZHANG ,
  • Dong-han GAO ,
  • Yun-xia XIA ,
  • Hong-mei JING ,
  • Xiao-yan KE ,
  • Qing-gang GE ,
  • Ning SHEN
Expand
  • 1. Department of Hematology
    2. Institute of Sports Medicine
    3. Department of Respiratory and Critical Care Medicine
    4. Department of Rheumatology and Immunology
    5. Department of Critical Care Medicine, Peking University Third Hospital, Beijing 100191, China

Received date: 2020-07-16

  Online published: 2020-12-13

摘要

目的:了解不同临床亚型新型冠状病毒肺炎(corona virus disease 19, COVID-19)患者淋巴细胞亚群的差异。方法:选取2020年2月8日至3月28日在华中科技大学同济医学院附属同济医院中法新城院区由三家援鄂医疗队负责的隔离病房收治的81例COVID-19患者为研究对象。根据相关诊断标准,将患者的疾病状态分为普通型(35例)、重型(39例)、危重型(7例)。检测血常规、淋巴细胞亚群等指标,比较不同临床亚型组患者间各指标是否存在差异。结果:三组患者淋巴细胞、T淋巴细胞、CD4+T淋巴细胞、CD8+T淋巴细胞、自然杀伤(natural killer,NK)细胞绝对数等指标差异均有统计学意义(P<0.05),危重型患者上述指标均明显低于普通型及重型患者,且随疾病严重程度加重呈递减趋势。22例患者首次检测时T淋巴细胞、B淋巴细胞、CD4+T淋巴细胞、CD8+T淋巴细胞及NK细胞绝对数、CD4+/CD8+六项指标均在正常参考值范围内,59例患者上述指标存在异常,以NK细胞和CD8+T淋巴细胞绝对数减少最为常见(61%,56%)。将NK、CD8+T淋巴细胞绝对数均低于正常参考值范围患者作为一组,其余指标异常患者作为一组,前者危重型患者较多(普通型:重型:危重型分别为4:8:7 vs. 19:21:0,P=0.001),且死亡病例均在此组(6例 vs. 0例,P=0.001)。15例患者B淋巴细胞绝对数低于正常参考值范围,余64例均在正常参考值范围内,减低组与正常组普通型:重型:危重型分别为4:7:4和30:31:3,减低组危重型患者比例多于正常组,两组间差异有统计学意义(P=0.043)。结论:COVID-19患者临床亚型越危重淋巴细胞各亚群绝对数越低。

本文引用格式

包芳 , 史尉利 , 胡静 , 张娣 , 高东晗 , 夏云霞 , 景红梅 , 克晓燕 , 葛庆岗 , 沈宁 . 新型冠状病毒肺炎淋巴细胞亚群与严重程度的相关分析[J]. 北京大学学报(医学版), 2020 , 52(6) : 1075 -1081 . DOI: 10.19723/j.issn.1671-167X.2020.06.014

Abstract

Objective: To understand the differences in lymphocyte subsets in patients with different clinical classifications of corona virus disease 19 (COVID-19). Methods: Eighty-one patients with COVID-19 who were admitted to the isolation ward under the responsibility of three medical aid teams in the Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, from February 8, 2020 to March 28, 2020, were selected to collect clinical data. According to the relevant diagnostic criteria, the disease status of the patients was classified into moderate cases (n=35), severe cases (n=39) and critical cases (n=7) when lymphocyte subset testing was performed. Their blood routine tests, lymphocyte subsets and other indicators were tested to compare whether there were differences in each indicator between the patients of different clinical classification groups. Results: The differences in the absolute count of total lymphocytes, T-lymphocytes, CD4+T-lymphocytes, CD8+T-lymphocytes and natural killer (NK) cells among the three groups of patients were all statistically significant (P<0.05), and the critical cases were significantly lower than the moderate and severe cases in the above indicators, and the indicators showed a decreasing trend with the severity of the disease. In 22 patients, the six indicators of the absolute count of T-lymphocytes, B-lymphocytes, CD4+T-lymphocytes, CD8+T-lymphocytes and NK cells, CD4+/CD8+ ratio were all within the normal reference range in the first test, and 59 patients had abnormalities of the above indicators, with the absolute count of NK cells and CD8+ T lymphocytes decreasing most frequently (61%, 56%). The patients with the absolute count of NK cells and CD8+ T lymphocytes below the normal reference range were one group, and the remaining abnormal patients were the other group. There were more critical cases in the former group (moderate:severe:critical cases were 4:8:7 vs. 19:21:0, respectively, P=0.001), and all the deaths were in this group (6 cases vs. 0 case, P=0.001). The absolute B lymphocyte count was below the normal reference range in 15 patients, and the remaining 64 cases were within the normal range. The ratio of moderate, severe and critical cases in the reduced group was 4:7:4, and the ratio of critical cases was more in normal group which was 30:31:3, and the difference between the two groups was statistically significant (P=0.043). Conclusion: The more critical the clinical subtype of patients with COVID-19, the lower the absolute count of each subset of lymphocytes.

参考文献

[1] Luo Y, Xie YL, Zhang WJ, et al. Combination of lymphocyte number and function in evaluating host immunity[J]. Aging (Albany NY), 2019,11(24):12685-12707.
[2] Qin C, Zhou LQ, Hu ZW, et al. Dysregulation of immune response in patients with COVID-19 in Wuhan, China[J]. Clin Infect Dis, 2020,71(15):762-768.
[3] Zhou P, Yang XL, Wang XG, et al. A pneumonia outbreak associated with a new coronavirus of probable bat origin[J]. Nature, 2020,579(7798):270-273.
[4] Wang DW, Hu B, Hu C, et al. Clinical characteristics of 138 hospitalized patients with 2019 novel coronavirus-infected pneumonia in Wuhan, China[J]. JAMA, 2020,323(11):1061-1069.
[5] Tan L, Wang Q, Zhang DY, et al. Lymphopenia predicts disease severity of COVID-19: a descriptive and predictive study[J]. Signal Transduct Target Ther, 2020,5(1):33.
[6] 董庆鸣, 何忠平, 庄辉, 等. SARS患者外周血B淋巴细胞和自然杀伤细胞动态变化[J]. 中华流行病学杂志, 2004,25(8):695-697.
[7] He ZP, Zhao CH, Dong QM, et al. Effects of severe acute respi-ratory syndrome (SARS) coronavirus infection on peripheral blood lymphocytes and their subsets[J]. Int J Infect Dis, 2005,9(6):323-330.
[8] Chen MH, Wong VW, Wong CK, et al. Serum LD1 isoenzyme and blood lymphocyte subsets as prognostic indicators for severe acute respiratory syndrome[J]. J Inter Med, 2004,255(4):512-518.
[9] 贺莉, 丁彦青, 王蔚, 等. 免疫细胞在SARS病变组织中的表达及其作用[J]. 第一军医大学学报, 2003,23(8):774-776, 780.
[10] Glass WG, Subbarao K, Murphy B, et al. Mechanisms of host defense following severe acute respiratory syndrome-coronavirus (SARS-CoV) pulmonary infection of mice[J]. J Immunol, 2004,173(6):4030-4039.
[11] Maloir Q, Ghysen K, von Frenckell C, et al. Détresse respiratoire aiguё révélatrice d’un syndrome des antisynthétases[J]. Rev Med Liege, 2018,73(7-8):370-375.
[12] Chen J, Lau YF, Lamirande E W, et al. Cellular immune responses to severe acute respiratory syndrome coronavirus (SARS-CoV) infection in senescent BALB/c mice: CD4+ T cells are important in control of SARS-CoV infection[J]. J Virol, 2010,84(3):1289-1301.
[13] Wang F, Nie JY, Wang HZ, et al. Characteristics of peripheral lymphocyte subset alteration in COVID-19 pneumonia[J]. J Infect Dis, 2020,221(11):1762-1769.
[14] Zhang Z, Xu DP, Li YG, et al. Longitudinal alteration of circulating dendritic cell subsets and its correlation with steroid treatment in patients with severe acute respiratory syndrome[J]. Clin Immunol, 2005,116(3):225-235.
文章导航

/