期刊论文详细信息
BMC Infectious Diseases
The combined effect of chemoprophylaxis with single dose rifampicin and immunoprophylaxis with BCG to prevent leprosy in contacts of newly diagnosed leprosy cases: a cluster randomized controlled trial (MALTALEP study)
Jan H Richardus2  Annemieke Geluk1  Sabiena G Feenstra2  David Pahan3  Khorshed Alam3  Renate A Richardus2 
[1] Department of Infectious Diseases, Leiden University Medical Center, Leiden, The Netherlands;Department of Public Health, Erasmus MC, University Medical Center Rotterdam, P.O. Box 2040, 3000, CA Rotterdam, The Netherlands;Rural Health Program, The Leprosy Mission International Bangladesh, Nilphamari, Bangladesh
关键词: Study protocol;    RCT;    Prevention;    Rifampicin;    BCG vaccine;    M. leprae;    Leprosy;   
Others  :  1145717
DOI  :  10.1186/1471-2334-13-456
 received in 2013-09-09, accepted in 2013-09-30,  发布年份 2013
PDF
【 摘 要 】

Background

Despite almost 30 years of effective chemotherapy with MDT, the global new case detection rate of leprosy has remained quite constant over the past years. New tools and methodologies are necessary to interrupt the transmission of M. leprae. Single-dose rifampicin (SDR) has been shown to prevent 57% of incident cases of leprosy in the first two years, when given to contacts of newly diagnosed cases. Immunization of contacts with BCG has been less well documented, but appears to have a preventive effect lasting up to 9 years. However, one major disadvantage is the occurrence of excess cases within the first year after immunization. The objective of this study is to examine the effect of chemoprophylaxis with SDR and immunoprophylaxis with BCG on the clinical outcome as well as on host immune responses and gene expression profiles in contacts of newly diagnosed leprosy patients. We hypothesize that the effects of both interventions may be complementary, causing the combined preventive outcome to be significant and long-lasting.

Methods/design

Through a cluster randomized controlled trial we compare immunization with BCG alone with BCG plus SDR in contacts of new leprosy cases. Contact groups of around 15 persons will be established for each of the 1300 leprosy patients included in the trial, resulting in approximately 20,000 contacts in total. BCG will be administered to the intervention group followed by SDR, 2 months later. The control group will receive BCG only. In total 10,000 contacts will be included in both intervention arms over a 2-year period. Follow-up will take place one year as well as two years after intake. The primary outcome is the occurrence of clinical leprosy within two years. Simultaneously with vaccination and SDR, blood samples for in vitro analyses will be obtained from 300 contacts participating in the trial to determine the effect of these chemo- and immunoprophylactic interventions on immune and genetic host parameters.

Discussion

Combined chemoprophylaxis and immunoprophylaxis is potentially a very powerful and innovative tool aimed at contacts of leprosy patients that could reduce the transmission of M. leprae markedly. The trial intends to substantiate this potential preventive effect. Evaluation of immune and genetic biomarker profiles will allow identification of pathogenic versus (BCG-induced) protective host biomarkers and could lead to effective prophylactic interventions for leprosy using optimized tools for identification of individuals who are most at risk of developing disease.

Trial registration

Netherlands Trial Register: NTR3087

【 授权许可】

   
2013 Richardus et al.; licensee BioMed Central Ltd.

【 预 览 】
附件列表
Files Size Format View
20150402205608250.pdf 291KB PDF download
Figure 1. 69KB Image download
【 图 表 】

Figure 1.

【 参考文献 】
  • [1]Anonymous: Global leprosy situation, 2012. Wkly Epidemiol Rec 2012, 87(34):317-328.
  • [2]Moet FJ, Schuring RP, Pahan D, Oskam L, Richardus JH: The prevalence of previously undiagnosed leprosy in the general population of northwest Bangladesh. PLoS Negl Trop Dis 2008, 2(2):e198.
  • [3]Moet FJ, Pahan D, Schuring RP, Oskam L, Richardus JH: Physical distance, genetic relationship, age, and leprosy classification are independent risk factors for leprosy in contacts of patients with leprosy. J Infect Dis 2006, 193(3):346-353.
  • [4]Richardus JH, Oskam L: Protecting people against leprosy: Chemoprophylaxis and Immunoprophylaxis (vaccination). Clin Dermatolin press
  • [5]Merle CS, Cunha SS, Rodrigues LC: BCG vaccination and leprosy protection: review of current evidence and status of BCG in leprosy control. Expert Rev Vaccines 2010, 9(2):209-222.
  • [6]Setia MS, Steinmaus C, Ho CS, Rutherford GW: The role of BCG in prevention of leprosy: a meta-analysis. Lancet Infect Dis 2006, 6(3):162-170.
  • [7]Duppre NC, Camacho LA, da Cunha SS, Struchiner CJ, Sales AM, Nery JA, Sarno EN: Effectiveness of BCG vaccination among leprosy contacts: a cohort study. Transac Royal Soc Trop Med Hyg 2008, 102(7):631-638.
  • [8]Moet FJ, Pahan D, Oskam L, Richardus JH: Effectiveness of single dose rifampicin in preventing leprosy in close contacts of patients with newly diagnosed leprosy: cluster randomised controlled trial. BMJ 2008, 336(7647):761-764.
  • [9]Schuring RP, Richardus JH, Pahan D, Oskam L: Protective effect of the combination BCG vaccination and rifampicin prophylaxis in leprosy prevention. Vaccine 2009, 27(50):7125-7128.
  • [10]Bangladesh Bureau of Statistics: Bangladesh Population & Housing Census 2011. 2011. http://www.bbs.gov.bd webcite (Accessed 9 Sep 2013)
  • [11]Anonymous: WHO Expert Committee on Leprosy. World Health Organ Tech Rep Ser 1998, 874:1-43.
  • [12]Anonymous: Global strategy for further reducing the leprosy burden and sustaining leprosy control activities 2006–2010. Operational guidelines. Lepr Rev 2006, 77(3):1-50. IX, X
  • [13]Drugs.com: Rifampin Side Effects. 2013. http://www.drugs.com/sfx/rifampin-side-effects.htm webcite (Accessed 13 Aug 2013)
  • [14]Grange JM: Complications of bacille Calmette-Guerin (BCG) vaccination and immunotherapy and their management. Commun Dis Public Health/PHLS 1998, 1(2):84-88.
  • [15]Mori T, Yamauchi Y, Shiozawa K: Lymph node swelling due to bacille Calmette-Guerin vaccination with multipuncture method. Tuber Lung Dis 1996, 77(3):269-273.
  • [16]Kroger L, Korppi M, Brander E, Kroger H, Wasz-Hockert O, Backman A, Rapola J, Launiala K, Katila ML: Osteitis caused by bacille Calmette-Guerin vaccination: a retrospective analysis of 222 cases. J Infect Dis 1995, 172(2):574-576.
  • [17]Casanova JL, Blanche S, Emile JF, Jouanguy E, Lamhamedi S, Altare F, Stephan JL, Bernaudin F, Bordigoni P, Turck D, et al.: Idiopathic disseminated bacillus Calmette-Guerin infection: a French national retrospective study. Pediatrics 1996, 98(4 Pt 1):774-778.
  • [18]Talbot EA, Perkins MD, Silva SF, Frothingham R: Disseminated bacille Calmette-Guerin disease after vaccination: case report and review. Clin Infect Dis 1997, 24(6):1139-1146.
  • [19]Cunha SS, Alexander N, Barreto ML, Pereira ES, Dourado I, Maroja Mde F, Ichihara Y, Brito S, Pereira S, Rodrigues LC: BCG revaccination does not protect against leprosy in the Brazilian Amazon: a cluster randomised trial. PLoS Negl Trop Dis 2008, 2(2):e167.
  • [20]Geluk A, Bobosha K, van der Ploeg-van Schip JJ, Spencer JS, Banu S, Martins MV, Cho SN, Franken KL, Kim HJ, Bekele Y, et al.: New biomarkers with relevance to leprosy diagnosis applicable in areas hyperendemic for leprosy. J Immunol 2012, 188(10):4782-4791.
  • [21]Corstjens PL, de Dood CJ, van der Ploeg-van Schip JJ, Wiesmeijer KC, Riuttamaki T, van Meijgaarden KE, Spencer JS, Tanke HJ, Ottenhoff TH, Geluk A: Lateral flow assay for simultaneous detection of cellular- and humoral immune responses. Clin Biochem 2011, 44(14–15):1241-1246.
  • [22]Joosten SA, Goeman JJ, Sutherland JS, Opmeer L, de Boer KG, Jacobsen M, Kaufmann SH, Finos L, Magis-Escurra C, Ota MO, et al.: Identification of biomarkers for tuberculosis disease using a novel dual-color RT-MLPA assay. Genes Immun 2012, 13(1):71-82.
  文献评价指标  
  下载次数:22次 浏览次数:35次