The local immune response in ulcerative lesions of Buruli disease

AE Kiszewski, E Becerril, LD Aguilar… - Clinical & …, 2006 - academic.oup.com
AE Kiszewski, E Becerril, LD Aguilar, ITA Kader, W Myers, F Portaels, R Hernandez Pando
Clinical & Experimental Immunology, 2006academic.oup.com
Buruli disease (BU) is a progressive necrotic and ulcerative disease of the skin and
subcutaneous tissue caused by Mycobacterium ulcerans. BU is considered the third most
common mycobacterial disease after tuberculosis and leprosy. Three clinical stages of the
cutaneous lesions have been described in BU: pre-ulcerative, ulcerative and healed lesions.
In this study we used immunohistochemistry and automated morphometry to determine the
percentage of macrophages and of CD4/CD8 lymphocytes and their expression of interferon …
Summary
Buruli disease (BU) is a progressive necrotic and ulcerative disease of the skin and subcutaneous tissue caused by Mycobacterium ulcerans. BU is considered the third most common mycobacterial disease after tuberculosis and leprosy. Three clinical stages of the cutaneous lesions have been described in BU: pre-ulcerative, ulcerative and healed lesions. In this study we used immunohistochemistry and automated morphometry to determine the percentage of macrophages and of CD4/CD8 lymphocytes and their expression of interferon (IFN)-γ, interleukin (IL)-10, tumour necrosis factor (TNF)-α and transforming growth factor (TGF)-β. Expression of these cytokines was correlated with the inflammatory response evaluated by histopathology. All the studied BU ulcerative cases showed extensive necrosis and chronic inflammation. The most important feature was the presence or absence of granulomas co-existing with a mixed pro-inflammatory/anti-inflammatory cytokine balance. When granulomas were present significantly higher expression of IFN-γ was seen, whereas in ulcerative lesions without granulomas there was increased expression of IL-10 and significantly higher bacillary counts. These features correlated with the chronicity of the lesions; longer-lasting lesions showed granulomas. Thus, granulomas were absent from relatively early ulcerative lesions, which contained more bacilli and little IFN-γ, suggesting that at this stage of the disease strong suppression of the protective cellular immune response facilitates proliferation of bacilli.
Oxford University Press