Trop Med Int Health. 1999 Dec;4(12):801-11. Unique Identifier : AIDSLINE MED/20098847
Salaiza-Suazo N; Volkow P; Tamayo R; Moll H; Gillitzer R; Perez-Torres A; Perez-Montfort R; Dominguez JD; Velasco-Castrejon O; Crippa M; Becker I; Departamento de Medicina Experimental, Faculdad de Medicina,; UNAM, Mexico.
Abstract: Two patients with diffuse cutaneous leishmaniasis caused by Leishmania mexicana were treated with two leishmanicidal drugs (pentamidine and allopurinol) combined with recombinant interferon-gamma restoring Th-1 favouring conditions in the patients. Parasites decreased dramatically in the lesions and macrophages diminished concomitantly, while IL-12-producing Langerhans cells and interferon-gamma- producing NK and CD8 + lymphocytes increased in a reciprocal manner. The CD4+/CD8 + ratio in the peripheral blood normalized. During exogenous administration of interferon-gamma the parasites' capacity to inhibit the oxidative burst of the patients' monocytes was abolished. Even though Th-1-favouring conditions were restored, both patients relapsed two months after therapy was discontinued. We conclude that the tendency to develop a disease-promoting Th-2 response in DCL patients is unaffected by, and independent of, parasite numbers. Even though intensive treatment in DCL patients induced Th-1 disease restricting conditions, the disease-promoting immunomodulation of few persistent Leishmania sufficed to revert the immune response.
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