Suppr超能文献

[血小板输注无效患者T、B淋巴细胞抗原及血小板抗体表达的研究]

[Study on the expression of T, B lymphocyte antigen and platelet antibodies in patients with platelet transfusion refractoriness].

作者信息

Du C H, Huang H T, Yuan G Y, Zhao G S, Li H X, Zhang Y, Sun Y J, Xu H M, Dong S Z

机构信息

The General Hospital of Tianjin Medical University, Tianjin 300052, China.

出版信息

Zhonghua Xue Ye Xue Za Zhi. 2016 Mar;37(3):238-41. doi: 10.3760/cma.j.issn.0253-2727.2016.03.013.

Abstract

OBJECTIVE

To explore whether T lymphocytes subgroup, B lymphocytes, platelet antigen CD41a, CD61 or platelet antibodies are involved in the platelet transfusion refractoriness.

METHODS

Forty-seven patients diagnosed as platelet transfusion refractoriness and 32 patients that achieved effective platelet therapy were ennolled in this study. Flow cytometry was performed to detect the proportion of cytotoxic T cell (CD3(+)CD4(-)CD8(+)), helper T cell (CD3(+)CD4(+)CD8(-)) and B lymphocytes (CD19 (+) ), and the expression of platelet glycoproteins, including CD41a and CD61, while platelet antibodies were also measured by solid-phase agglutination.

RESULTS

The significant lower level of helper T cell (36.60% vs 48.53%), higher level of cytotoxic T cell (53.26% vs 44.02%) and lower cytotoxic/helper T cell ratio (0.85 vs 1.31) were observed in platelet refractoriness group when compared with effective platelet therapy group (P<0.05). However, the significant difference was not observed in B lymphocytes between the two group (3.02% vs 2.85%, P>0.05). Platelet glycoproteins CD41a and CD61 and antibodies were both expressed at high levels in platelet refractoriness group (88.10% vs 51.69%, 88.36% vs 51.83%, 85.37% vs 14.82%, respectively, P<0.05).

CONCLUSIONS

Activation of cytotoxic T cells, suppression of helper T cells, higher expression level of platelet glycoproteins CD41a and CD61 as well as the development of anti-platelet antibodies are involved in the immunologic mechanism of platelet refractoriness.

摘要

目的

探讨T淋巴细胞亚群、B淋巴细胞、血小板抗原CD41a、CD61或血小板抗体是否参与血小板输注无效。

方法

本研究纳入47例诊断为血小板输注无效的患者和32例血小板治疗有效的患者。采用流式细胞术检测细胞毒性T细胞(CD3(+)CD4(-)CD8(+))、辅助性T细胞(CD3(+)CD4(+)CD8(-))和B淋巴细胞(CD19(+))的比例,以及血小板糖蛋白包括CD41a和CD61的表达,同时采用固相凝集法检测血小板抗体。

结果

与血小板治疗有效组相比,血小板输注无效组辅助性T细胞水平显著降低(36.60%对48.53%),细胞毒性T细胞水平升高(53.26%对44.02%),细胞毒性/辅助性T细胞比值降低(0.85对1.31)(P<0.05)。然而,两组间B淋巴细胞差异无统计学意义(3.02%对2.85%,P>0.05)。血小板输注无效组血小板糖蛋白CD41a和CD61及抗体均高表达(分别为88.10%对51.69%、88.36%对51.83%、85.37%对14.82%,P<0.05)。

结论

细胞毒性T细胞激活、辅助性T细胞抑制、血小板糖蛋白CD41a和CD61表达水平升高以及抗血小板抗体的产生参与了血小板输注无效的免疫机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3441/7342956/9c95ccfb9a84/cjh-37-03-238-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验