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Please use this identifier to cite or link to this item: https://saber.ucv.ve/handle/10872/4894

Title: Variations in the serum levels of soluble CD23, nitric oxide and IgE across the spectrum of American cutaneous leishmaniasis
Authors: Cabrera, Maira
Rodríguez, Orquídea
Monsalve, Iraima
Tovar, Robert
Hagel, Isabel
Keywords: cutaneous leishmaniasis
CD23
IgE
Nitric Oxide
Issue Date: Oct-2003
Publisher: Elsevier
Citation: Acta Tropica 88 (2003) 145–151
Series/Report no.: 88;
Abstract: Serum IgE levels and the expression of low affinity receptor for IgE (FcεRII/CD23) are increased in cutaneous leishmaniasis. The ligation of CD23 receptor by IgE–anti-IgE immune complexes results in nitric oxide (NO) production, which is a critical leishmanicidal factor. Human monocytes/macrophages express FcεRII/CD23 after activation with IFN- and IL-4. In the present study,we assessed the relationship between NO, total and Leishmania-specific IgE and soluble CD23 across the clinical spectrum of American cutaneous leishmaniasis (ACL). Sixty-nine ACL patients and 22 endemic controls were studied. NO concentration was estimated using the Greiss method. Soluble CD23, total IgE and anti-Leishmania IgE levels were measured using ELISA. Soluble CD23 was increased in the four patient groups (0.001 < P < 0.05) compared by the Mann–Whitney test to healthy subjects, particularly in mucocutaneous leishmaniasis (MCL) and diffuse cutaneous leishmaniasis (DCL) patients. Total IgE levels were higher inACL patients (P < 0.0001). Anti-Leishmania IgE showed a similar tendency, whereMCLand DCL patients had greater levels. All patients groups, except intermediate or chronic cutaneous leishmaniasis (ICL) patients, showed elevated levels of NO2−/NO3 − compared to healthy individuals (0.001 < P < 0.01). Interestingly, ICL patients did not produce significant levels of NO2−/NO3−. ACL patients showed a significant positive correlation between soluble CD23 and anti-Leishmania IgE. DCL patients showed a positive correlation between both parameters. Overall results suggest that sCD23, IgE and NO may play different roles across the ACL spectrum.
URI: http://hdl.handle.net/10872/4894
ISSN: 0001-706X
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