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一种新型细胞疗法治疗耐多药结核病的有效性

Effectiveness of a novel cellular therapy to treat multidrug-resistant tuberculosis.

作者信息

Skrahin Aliaksandr, Jenkins Helen E, Hurevich Henadz, Solodovnikova Varvara, Isaikina Yanina, Klimuk Dzmitri, Rohava Zoya, Skrahina Alena

机构信息

Clinical Department, Republican Research and Practical Centre for Pulmonology and TB, Minsk, Belarus; Department of Intensive Care and Anesthesiology, Belarus State Medical University, Minsk, Belarus.

Division of Global Health Equity, Brigham and Women's Hospital, Boston, USA; Harvard Medical School, Boston, USA.

出版信息

J Clin Tuberc Other Mycobact Dis. 2016 Aug;4:21-27. doi: 10.1016/j.jctube.2016.05.003.

Abstract

INTRODUCTION

We urgently need novel treatments for multidrug-resistant tuberculosis (MDR-TB). Autologous mesenchymal stromal cell (MSC) infusion is one such possibility due to its potential to repair damaged lung tissue and boost immune responses. We aimed to assess the effectiveness of MSC to improve outcomes among MDR-TB patients.

METHODS

We analyzed outcomes for 108 Belarussian MDR-TB patients receiving chemotherapy. Thirty-six patients ("cases") also had MSCs extracted, cultured and re-infused (average time from chemotherapy start to infusion was 49 days); another 36 patients were "study controls". We identified another control group: 36 patients from the Belarussian surveillance database ("surveillance controls") 1:1 matched to cases.

RESULTS

Of the cases, 81% had successful outcomes versus 42% of surveillance controls and 39% of study controls. Successful outcome odds were 6.5 (95% Confidence Interval: 1.2-36.2, p=0.032) times greater for cases than surveillance controls (age-adjusted). Radiological improvement was more likely in cases than study controls. Culture analysis prior to infusion demonstrated a poorer initial prognosis in cases, yet despite this they had better outcomes than the control groups.

CONCLUSION

MSC treatment could vastly improve outcomes for MDR-TB patients. Our findings could revolutionize therapy options and have strong implications for future directions of MDR-TB therapy research.

摘要

引言

我们迫切需要针对耐多药结核病(MDR-TB)的新型治疗方法。自体间充质基质细胞(MSC)输注是一种可能的方法,因为它有修复受损肺组织和增强免疫反应的潜力。我们旨在评估MSC对改善耐多药结核病患者治疗结果的有效性。

方法

我们分析了108名接受化疗的白俄罗斯耐多药结核病患者的治疗结果。36名患者(“病例组”)还提取、培养并重新输注了MSC(从开始化疗到输注的平均时间为49天);另外36名患者为“研究对照组”。我们确定了另一个对照组:从白俄罗斯监测数据库中选取的36名患者(“监测对照组”),与病例组进行1:1匹配。

结果

病例组中81%获得了成功的治疗结果,而监测对照组为42%,研究对照组为39%。病例组成功治疗结果的几率比监测对照组高6.5倍(95%置信区间:1.2 - 36.2,p = 0.032)(年龄调整后)。病例组比研究对照组更有可能出现影像学改善。输注前的培养分析显示病例组的初始预后较差,但尽管如此,他们的治疗结果仍优于对照组。

结论

MSC治疗可极大地改善耐多药结核病患者的治疗结果。我们的研究结果可能会彻底改变治疗选择,并对耐多药结核病治疗研究的未来方向产生重大影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4897/6850265/9d2e6d16f168/gr1.jpg

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