Inhibition of angiogenesis as a new therapeutic target in the treatment of lepromatous leprosy

Mohamed El-Khalawany1, Dalia Shaaban2, Maha Sultan1, Fatma Abd AlSalam11Departments of Dermatology, Faculty of Medicine, Al-Azhar University, Cairo, 2Department of Dermatology, Faculty of Medicine, Tanta University, Gharbia, EgyptBackground: Angiogenesis was suggested to have a significant role in t...

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Main Authors: El-Khalawany M, Shaaban D, Sultan M, Abd AlSalam F
Format: Article
Language:English
Published: Dove Medical Press 2011-12-01
Series:Clinical, Cosmetic and Investigational Dermatology
Online Access:http://www.dovepress.com/inhibition-of-angiogenesis-as-a-new-therapeutic-target-in-the-treatmen-a8963
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spelling doaj-c702e7156b154fe9857d81448416872b2020-11-24T23:52:37ZengDove Medical PressClinical, Cosmetic and Investigational Dermatology1178-70152011-12-012012default16Inhibition of angiogenesis as a new therapeutic target in the treatment of lepromatous leprosyEl-Khalawany MShaaban DSultan MAbd AlSalam FMohamed El-Khalawany1, Dalia Shaaban2, Maha Sultan1, Fatma Abd AlSalam11Departments of Dermatology, Faculty of Medicine, Al-Azhar University, Cairo, 2Department of Dermatology, Faculty of Medicine, Tanta University, Gharbia, EgyptBackground: Angiogenesis was suggested to have a significant role in the pathogenesis of leprosy. However, the benefit of inhibiting angiogenesis in lepromatous leprosy patients has not previously been studied. The purpose of this study was to evaluate angiogenesis in leprosy patients before and after treatment with multidrug therapy (MDT) with and without minocycline.Methods: A total of 40 patients with lepromatous leprosy were enrolled in this study. They were categorized into two equal groups (A and B), each formed of 20 patients. Group A received World Health Organization MDT, and Group B received MDT combined with minocycline, which has a known antiangiogenic effect. Microvascular density (MVD) in dermal granuloma was evaluated in both groups by immunostaining with CD31 and CD34 markers before and after 6 months of treatment.Results: With CD31 immunostaining, the mean MVD in Group A significantly decreased from 39.1 ± 3.1 vessels (v)/high power field (HPF) to 16.5 ± 2.7 v/HPF, and in Group B it significantly decreased from 38.3 ± 2.5 v/HPF to 7.6 ± 1.9 v/HPF. CD34 immunostaining also showed a significant decrease of MVD from 42.2 ± 3.1 v/HPF to 18.8 ± 2.4 v/HPF in Group A, and in Group B it significantly decreased from 43.7 ± 2.3 v/HPF to 11.5 ± 1.6 v/HPF. The reduction of MVD was significantly higher in Group B compared with in Group A (P < 0.0001). Moreover, there was a significant reduction in bacterial density (assessed by bacterial index) in the cutaneous lesions of in Group B (decreased from 4.9 ± 0.3 to 1.4 ± 0.2) compared with in Group A (decreased from 5.1 ± 0.4 to 2.3 ± 0.4).Conclusion: The synergistic effect of MDT and minocycline seems to be promising in the treatment of lepromatous leprosy. It significantly reduces angiogenesis and rapidly eliminates lepra bacilli from the skin that enables a rapid control and elimination of the disease.Keywords: leprosy, angiogenesis, minocyclinehttp://www.dovepress.com/inhibition-of-angiogenesis-as-a-new-therapeutic-target-in-the-treatmen-a8963
collection DOAJ
language English
format Article
sources DOAJ
author El-Khalawany M
Shaaban D
Sultan M
Abd AlSalam F
spellingShingle El-Khalawany M
Shaaban D
Sultan M
Abd AlSalam F
Inhibition of angiogenesis as a new therapeutic target in the treatment of lepromatous leprosy
Clinical, Cosmetic and Investigational Dermatology
author_facet El-Khalawany M
Shaaban D
Sultan M
Abd AlSalam F
author_sort El-Khalawany M
title Inhibition of angiogenesis as a new therapeutic target in the treatment of lepromatous leprosy
title_short Inhibition of angiogenesis as a new therapeutic target in the treatment of lepromatous leprosy
title_full Inhibition of angiogenesis as a new therapeutic target in the treatment of lepromatous leprosy
title_fullStr Inhibition of angiogenesis as a new therapeutic target in the treatment of lepromatous leprosy
title_full_unstemmed Inhibition of angiogenesis as a new therapeutic target in the treatment of lepromatous leprosy
title_sort inhibition of angiogenesis as a new therapeutic target in the treatment of lepromatous leprosy
publisher Dove Medical Press
series Clinical, Cosmetic and Investigational Dermatology
issn 1178-7015
publishDate 2011-12-01
description Mohamed El-Khalawany1, Dalia Shaaban2, Maha Sultan1, Fatma Abd AlSalam11Departments of Dermatology, Faculty of Medicine, Al-Azhar University, Cairo, 2Department of Dermatology, Faculty of Medicine, Tanta University, Gharbia, EgyptBackground: Angiogenesis was suggested to have a significant role in the pathogenesis of leprosy. However, the benefit of inhibiting angiogenesis in lepromatous leprosy patients has not previously been studied. The purpose of this study was to evaluate angiogenesis in leprosy patients before and after treatment with multidrug therapy (MDT) with and without minocycline.Methods: A total of 40 patients with lepromatous leprosy were enrolled in this study. They were categorized into two equal groups (A and B), each formed of 20 patients. Group A received World Health Organization MDT, and Group B received MDT combined with minocycline, which has a known antiangiogenic effect. Microvascular density (MVD) in dermal granuloma was evaluated in both groups by immunostaining with CD31 and CD34 markers before and after 6 months of treatment.Results: With CD31 immunostaining, the mean MVD in Group A significantly decreased from 39.1 ± 3.1 vessels (v)/high power field (HPF) to 16.5 ± 2.7 v/HPF, and in Group B it significantly decreased from 38.3 ± 2.5 v/HPF to 7.6 ± 1.9 v/HPF. CD34 immunostaining also showed a significant decrease of MVD from 42.2 ± 3.1 v/HPF to 18.8 ± 2.4 v/HPF in Group A, and in Group B it significantly decreased from 43.7 ± 2.3 v/HPF to 11.5 ± 1.6 v/HPF. The reduction of MVD was significantly higher in Group B compared with in Group A (P < 0.0001). Moreover, there was a significant reduction in bacterial density (assessed by bacterial index) in the cutaneous lesions of in Group B (decreased from 4.9 ± 0.3 to 1.4 ± 0.2) compared with in Group A (decreased from 5.1 ± 0.4 to 2.3 ± 0.4).Conclusion: The synergistic effect of MDT and minocycline seems to be promising in the treatment of lepromatous leprosy. It significantly reduces angiogenesis and rapidly eliminates lepra bacilli from the skin that enables a rapid control and elimination of the disease.Keywords: leprosy, angiogenesis, minocycline
url http://www.dovepress.com/inhibition-of-angiogenesis-as-a-new-therapeutic-target-in-the-treatmen-a8963
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AT sultanm inhibitionofangiogenesisasanewtherapeutictargetinthetreatmentoflepromatousleprosy
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