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印度次大陆内脏利什曼病的传播动力学——一项系统文献综述

Transmission Dynamics of Visceral Leishmaniasis in the Indian Subcontinent - A Systematic Literature Review.

作者信息

Hirve Siddhivinayak, Boelaert Marleen, Matlashewski Greg, Mondal Dinesh, Arana Byron, Kroeger Axel, Olliaro Piero

机构信息

Global Influenza Programme, World Health Organization, Geneva, Switzerland.

Epidemiology and Control of Tropical Diseases, Institute of Tropical Medicine, Antwerp, Belgium.

出版信息

PLoS Negl Trop Dis. 2016 Aug 4;10(8):e0004896. doi: 10.1371/journal.pntd.0004896. eCollection 2016 Aug.

Abstract

BACKGROUND

As Bangladesh, India and Nepal progress towards visceral leishmaniasis (VL) elimination, it is important to understand the role of asymptomatic Leishmania infection (ALI), VL treatment relapse and post kala-azar dermal leishmaniasis (PKDL) in transmission.

METHODOLOGY/ PRINCIPAL FINDING: We reviewed evidence systematically on ALI, relapse and PKDL. We searched multiple databases to include studies on burden, risk factors, biomarkers, natural history, and infectiveness of ALI, PKDL and relapse. After screening 292 papers, 98 were included covering the years 1942 through 2016. ALI, PKDL and relapse studies lacked a reference standard and appropriate biomarker. The prevalence of ALI was 4-17-fold that of VL. The risk of ALI was higher in VL case contacts. Most infections remained asymptomatic or resolved spontaneously. The proportion of ALI that progressed to VL disease within a year was 1.5-23%, and was higher amongst those with high antibody titres. The natural history of PKDL showed variability; 3.8-28.6% had no past history of VL treatment. The infectiveness of PKDL was 32-53%. The risk of VL relapse was higher with HIV co-infection. Modelling studies predicted a range of scenarios. One model predicted VL elimination was unlikely in the long term with early diagnosis. Another model estimated that ALI contributed to 82% of the overall transmission, VL to 10% and PKDL to 8%. Another model predicted that VL cases were the main driver for transmission. Different models predicted VL elimination if the sandfly density was reduced by 67% by killing the sandfly or by 79% by reducing their breeding sites, or with 4-6y of optimal IRS or 10y of sub-optimal IRS and only in low endemic setting.

CONCLUSION/ SIGNIFICANCE: There is a need for xenodiagnostic and longitudinal studies to understand the potential of ALI and PKDL as reservoirs of infection.

摘要

背景

随着孟加拉国、印度和尼泊尔朝着消除内脏利什曼病(VL)的目标迈进,了解无症状利什曼原虫感染(ALI)、VL治疗复发以及黑热病后皮肤利什曼病(PKDL)在传播中的作用至关重要。

方法/主要发现:我们系统地回顾了关于ALI、复发和PKDL的证据。我们搜索了多个数据库,纳入了关于ALI、PKDL和复发的负担、危险因素、生物标志物、自然史和传染性的研究。在筛选了292篇论文后,纳入了98篇涵盖1942年至2016年的论文。ALI、PKDL和复发研究缺乏参考标准和合适的生物标志物。ALI的患病率是VL的4至17倍。VL病例接触者中ALI的风险更高。大多数感染仍无症状或自行缓解。一年内进展为VL疾病的ALI比例为1.5%至23%,在抗体滴度高的人群中更高。PKDL的自然史显示出变异性;3.8%至28.6%的患者既往无VL治疗史。PKDL的传染性为32%至53%。HIV合并感染时VL复发的风险更高。建模研究预测了一系列情况。一个模型预测,早期诊断的情况下,长期来看VL不太可能消除。另一个模型估计,ALI占总传播的82%,VL占10%,PKDL占8%。另一个模型预测VL病例是传播的主要驱动因素。不同模型预测,如果通过杀灭白蛉将白蛉密度降低67%,或通过减少其繁殖地将白蛉密度降低79%,或进行4至6年的最佳室内滞留喷洒(IRS)或10年的次优IRS,且仅在低流行地区,VL有可能消除。

结论/意义:需要进行异种诊断和纵向研究,以了解ALI和PKDL作为感染储存库的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9b2/4973965/bab008e4ee78/pntd.0004896.g001.jpg

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