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NK(CD16 + 56 +)和B细胞(CD19)受体分子的表达作为利妥昔单抗治疗下系统性红斑狼疮和类风湿关节炎患者可靠的临床反应生物标志物。

Expression of NK (CD16+56+) and B cells (CD19) Receptor Molecules as a Reliable Clinical Response Biomarkers of SLE and RA Patients Under the Rituximab Treatment.

作者信息

Zecevic Lamija, Mekic Mevludin, Subasic Djemo, Hadziabulic Majda, Isak Edmira, Subasic Emina, Selmanovic Kenan

机构信息

Department of Immunology, Clinical Center University of Sarajevo, Sarajevo, Bosnia and Herzegovina.

Department for Rheumatology, Clinic for Heart, Blood Vessel and Rheumatism, Clinical Center University of Sarajevo, Sarajevo, Bosnia and Herzegovina.

出版信息

Med Arch. 2019 Dec;73(6):374-377. doi: 10.5455/medarh.2019.73.374-377.

Abstract

INTRODUCTION

Lately, the use of biological therapy in various autoimmune diseases is increasing. The ideal marker for monitoring the effects of modern therapy is still non-existent.

AIM

To investigate early response biomarkers of SLE and RA patients under the rituximab treatment are in research phase and each new investigations offer new and original useful data.

MATERIAL AND METHODS

Immunophenotyping of cells was carried out by a standard method of sample preparation. We investigated by flow cytometric analyses expression of NK and CD19+ cells at ten SLE and five RA patients before and after treatment with rituximab, in laboratory of Department of Clinical immunology in the Clinical Centre University of Sarajevo.

RESULTS

In both cases, SLE and RA patients, reduced number of CD16+ parameter indicates lower cytotoxic activity of NK cells. Increased number of B cells indicates higher pathological activity leading to severe autoimmune disease allegation.

CONCLUSION

Determining the proportion of NK and B will be useful diagnostic tool in therapeutic strategy, and also in monitoring of effect of biological therapy.

摘要

引言

近来,生物疗法在各种自身免疫性疾病中的应用日益增加。目前仍不存在用于监测现代疗法效果的理想标志物。

目的

研究利妥昔单抗治疗下系统性红斑狼疮(SLE)和类风湿关节炎(RA)患者的早期反应生物标志物,相关研究仍处于探索阶段,每项新研究都能提供新颖且有价值的数据。

材料与方法

采用标准样本制备方法进行细胞免疫表型分析。在萨拉热窝大学临床中心临床免疫科实验室,我们通过流式细胞术分析了10例SLE患者和5例RA患者在接受利妥昔单抗治疗前后NK细胞和CD19+细胞的表达情况。

结果

在SLE和RA患者中,CD16+参数数量减少均表明NK细胞的细胞毒性活性降低。B细胞数量增加表明更高的病理活性,这会导致严重自身免疫性疾病的发生。

结论

确定NK细胞和B细胞的比例将成为治疗策略中的有用诊断工具,也有助于监测生物疗法的效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5df/7007611/8ec00a94f184/medarch-73-374-g001.jpg

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