dc.creatorBarral Netto, Manoel
dc.creatorSantos, S
dc.creatorSantos, Isis Fernandes Magalhães
dc.creatorVon Sohsten, R. L
dc.creatorBittencourt, Achilea Candida Lisboa
dc.creatorCarvalho Filho, Edgar Marcelino
dc.creatorBarral, Aldina Maria Prado
dc.creatorWaters, M
dc.date2014-03-25T13:50:54Z
dc.date2014-03-25T13:50:54Z
dc.date1999
dc.date.accessioned2023-09-26T23:19:24Z
dc.date.available2023-09-26T23:19:24Z
dc.identifierBARRAL-NETTO, M. et al. Immunochemotherapy with interferon-gamma and multidrug therapy for multibacillary leprosy. Acta Tropica, v. 72, n. 2, p. 185-201, 1999.
dc.identifier0001-706X
dc.identifierhttps://www.arca.fiocruz.br/handle/icict/7443
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/8889302
dc.descriptionTreatment for multibacillary leprosy is presently performed with a multidrug therapy (MDT) scheme maintained for 2 years. Leprosy treatment however can benefit from the reduction of length. The lack of interferon-gamma (IFN-gamma) production by lepromatous leprosy (LL) patients' lymphocytes lead us to use this cytokine in the treatment of multibacillary leprosy associated with MDT in the treatment of multibacillary leprosy, and monitor several clinical and immunological parameters during the course of treatment. A total of 20 multibacillary leprosy patients were evaluated, 10 treated with MDT alone, and 10 treated with MDT + 10 daily doses of 2 x 10(6) international units (IU) of recombinant human IFN-gamma/m2 followed by 10 daily doses of 10(7) IU IFN-gamma/m2, intramuscularly, during the first 20 days of MDT. IFN-gamma was well tolerated and did not cause any increase in the rate of leprosy reactions development during treatment. Decrease of bacillary load, fall of anti-Mycobacterium leprae IgG serum antibodies, changes of histological pattern, as well as changes in lymphocyte proliferation assay in response to mitogens (PHA or PWM), M. leprae antigen or PPD was similar in both groups of patients. Among several soluble immunological markers measured before and 30 days after beginning of treatment, levels of soluble IL-2R receptor increased in patients treated with MDT plus IFN-gamma whereas decreased in patients treated with MDT alone. Soluble ICAM-1 levels decreased in the MDT group but did not change in the MDT + IFN-gamma treated patients. Soluble CD4 and soluble CD8 markers did not change significantly in either group of patients. Neopterin, a marker of macrophage activation, increased in all but one patient treated with MDT + IFN-gamma but in none treated with MDT alone, indicating that IFN-gamma was active in vivo. Our findings indicate that despite being able to promote macrophage activation in multibacillary leprosy patients a short course of systemically administered IFN-gamma is not able to change the clinical course of a long standing disease such as leprosy.
dc.formatapplication/pdf
dc.languageeng
dc.publisherElsevier B.V
dc.rightsopen access
dc.subjectInterferon gama/uso terapêutico
dc.subjectHansenostáticos/uso terapêutico
dc.subjectHanseníase/quimioterapia
dc.subjectAnticorpos Antibacterianos/sangue
dc.subjectAdolescente
dc.subjectAdulto
dc.subjectCriança
dc.subjectClofazimina/uso terapêutico
dc.subjectDapsona/uso terapêutico
dc.subjectQuimioterapia Combinada
dc.subjectFeminino
dc.subjectHumanos
dc.subjectInterferon gama/biossíntese
dc.subjectHanseníase/imunologia
dc.subjectAtivação Linfocitária
dc.subjectMeia-Idade
dc.subjectMasculino
dc.subjectNeopterina/análise
dc.subjectProteínas Recombinantes
dc.subjectRifampina/uso terapêutico
dc.subjectPele/microbiologia
dc.titleImmunochemotherapy with interferon-gamma and multidrug therapy for multibacillary leprosy.
dc.typeArticle


Este ítem pertenece a la siguiente institución