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在感染性休克期间,γδ T淋巴细胞百分比和CD3表达均降低。

Both percentage of gammadelta T lymphocytes and CD3 expression are reduced during septic shock.

作者信息

Venet Fabienne, Bohé Julien, Debard Anne-Lise, Bienvenu Jacques, Lepape Alain, Monneret Guillaume

机构信息

Immunology Laboratory, Lyon-Sud University Hospital, France.

出版信息

Crit Care Med. 2005 Dec;33(12):2836-40. doi: 10.1097/01.ccm.0000189745.66585.ae.

Abstract

OBJECTIVE

The mechanisms involved during sepsis-induced immunosuppression are far from being extensively established. The objective of the present study was to investigate whether two characteristics of T cells were altered in this situation: the percentage of circulating gammadelta T lymphocytes and the level of CD3 expression on T lymphocytes.

DESIGN

Observational study.

SETTING

Adult intensive care units in a university hospital.

PATIENTS

Patients with septic shock (n = 21) and healthy individuals (n = 21).

INTERVENTIONS

None.

MEASUREMENTS AND MAIN RESULTS

In patients, we first observed the decreased percentage of gammadelta T lymphocytes in peripheral blood (1% [0.7-3.1], median [interquartile range]) in comparison with healthy individuals (3.5% [2.1-4.8]). Regarding CD3, we measured a highly significant decrease of its expression on both alphabeta and gammadelta T lymphocytes from patients (p < .005), whereas the CD3 mean fluorescence intensities ratio (gammadelta/alphabeta) was not affected: 2.2 [2.1-2.4] and 2.1 [1.9-2.3] in healthy individuals and septic patients, respectively. The magnitude in the decrease of CD3 expression was thus similar in alphabeta and gammadelta cells, suggesting a common down-regulation mechanism for both T-cell lineages.

CONCLUSIONS

Combined with a reduced percentage of monocytes expressing human leukocyte antigen-DR, a reduced CD3 expression may be involved in the failure of antigen presentation depicted after septic shock, whereas the diminished percentage of circulating gammadelta T cells could be partly responsible for the elevated incidence of secondary infections. These two observations constitute additional pieces of the complex puzzle of sepsis-induced immunosuppression.

摘要

目的

脓毒症诱导的免疫抑制所涉及的机制尚未完全明确。本研究的目的是调查在这种情况下T细胞的两个特征是否发生改变:循环γδT淋巴细胞的百分比以及T淋巴细胞上CD3的表达水平。

设计

观察性研究。

地点

大学医院的成人重症监护病房。

患者

感染性休克患者(n = 21)和健康个体(n = 21)。

干预措施

无。

测量指标及主要结果

在患者中,我们首先观察到外周血中γδT淋巴细胞的百分比降低(中位数[四分位间距]为1%[0.7 - 3.1]),而健康个体为3.5%[2.1 - 4.8]。关于CD3,我们测量到患者的αβ和γδT淋巴细胞上其表达均显著降低(p < 0.005),而CD3平均荧光强度比值(γδ/αβ)未受影响:健康个体和脓毒症患者分别为2.2[2.1 - 2.4]和2.1[1.9 - 2.3]。因此,αβ和γδ细胞中CD3表达降低的幅度相似,提示两种T细胞谱系存在共同的下调机制。

结论

与表达人类白细胞抗原-DR的单核细胞百分比降低相结合,CD3表达降低可能参与了感染性休克后所描述的抗原呈递功能障碍,而循环γδT细胞百分比降低可能部分导致继发感染发生率升高。这两个观察结果构成了脓毒症诱导的免疫抑制这一复杂谜题的额外部分。

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