TY - JOUR
T1 - Immunologic determinants of disease evolution in localized cutaneous leishmaniasis due to Leishmania major
AU - Louzir, Hechmi
AU - Melby, Peter C.
AU - Salah, Afif Ben
AU - Marrakchi, Héla
AU - Aoun, Karim
AU - Ismail, Riadh Ben
AU - Dellagi, Koussay
N1 - Funding Information:
Financial support: US Agency for International Development, through NIH and the Middle East Regional Cooperation program (AI-45183 to K.D.); NIH (AI-31065 to P.C.M.). Laboratories of Immunology and of Epidemiology and Ecology of Parasitic Diseases, Pasteur Institute of Tunis, were supported by United Nations Development Programme/World Bank/WHO Special Program for Research and Training in Tropical Diseases (RSG/ID-890266) and by Aupelf-Uref Agency.
PY - 1998
Y1 - 1998
N2 - Localized cutaneous leishmaniasis caused by Leishmania major is polymorphic in its clinical presentation and evolution. Clinical and parasitologic features and disease evolution of 112 Tunisian patients was evaluated. The expression of interleukin (IL)-4, IL-6, IL-10, IL-12 (p40), interferon (IFN)-γ, and tumor necrosis factor (TNF)-α mRNA was analyzed by reverse transcription-polymerase chain reaction in 73 biopsies. Cytokine mRNA expression varied individually over a wide range; TNF-α, IL-6, and IFN-γ were detectable in >90% of lesions, IL-12 and IL-10 in 40% and 70%, respectively, and IL-4 in only 9%. Statistical analysis demonstrated positive association between the level of IL-12 and IFN-γ and the presence of parasites in the lesions. Unfavorable evolution of the lesions was positively associated with high IL-10, IL-12, and IFN-γ mRNA expression. These results indicate that an unfavorable clinical outcome was not related to an inadequate Th1 cell response and suggest that the macrophage-activating effect of IFN-γ may be inhibited by the concomitant expression of IL-10.
AB - Localized cutaneous leishmaniasis caused by Leishmania major is polymorphic in its clinical presentation and evolution. Clinical and parasitologic features and disease evolution of 112 Tunisian patients was evaluated. The expression of interleukin (IL)-4, IL-6, IL-10, IL-12 (p40), interferon (IFN)-γ, and tumor necrosis factor (TNF)-α mRNA was analyzed by reverse transcription-polymerase chain reaction in 73 biopsies. Cytokine mRNA expression varied individually over a wide range; TNF-α, IL-6, and IFN-γ were detectable in >90% of lesions, IL-12 and IL-10 in 40% and 70%, respectively, and IL-4 in only 9%. Statistical analysis demonstrated positive association between the level of IL-12 and IFN-γ and the presence of parasites in the lesions. Unfavorable evolution of the lesions was positively associated with high IL-10, IL-12, and IFN-γ mRNA expression. These results indicate that an unfavorable clinical outcome was not related to an inadequate Th1 cell response and suggest that the macrophage-activating effect of IFN-γ may be inhibited by the concomitant expression of IL-10.
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U2 - 10.1086/515297
DO - 10.1086/515297
M3 - Article
C2 - 9607850
AN - SCOPUS:0031781615
SN - 0022-1899
VL - 177
SP - 1687
EP - 1695
JO - Journal of Infectious Diseases
JF - Journal of Infectious Diseases
IS - 6
ER -