Cytokine production in lungs and adrenal glands of high and low antibody producing mice infected with Paracoccidioides brasiliensis

References

• Franco M, Poncio-Mendes R, Moscardi-Bacchi M, Rezkallah-Iwasso MT, Montenegro MR. Paracoccidioidomycosis. Bailliere's Clin Trop Med Commun Dis 1989; 4: 185–220
   Google Scholar
• Singer-Vermes LM, Caldeira CB, Burger E, Calich VLG. Experimental murine paracoccidioidomycosis: relationship among dissemination of the infection, humoral and cellular immune responses. Clin Exp Immunol 1993; 94: 75–79
   Google Scholar
• McEwen JG, Bedoya V, Patiño MM, Salazar ME, Restrepo A. Experimental murine paracoccidioidomycosis induced by inhalation of conidia. J Med Vet Mycol 1987; 25: 165–175
   PubMedGoogle Scholar
• Defaveri J, Rezkallah-Iwasso MT, Franco MF. Experimental pulmonary paracoccidioidomycosis in mice: morphology and correlation of lesions with humoral and cellular immune response. Mycopathologia 1982; 77: 3–11
   PubMed Web of Science ®Google Scholar
• Iabuki K, Montenegro MR. Experimental paracoccidioidomycosis in the Sirian hamster: morphology, ultrastructure and correlation of the lesions with presence of specific antigens and serum levels of antibodies. Mycopathologia 1979; 67: 131–141
   PubMedGoogle Scholar
• Biozzi G, Mounton D, Stiffel C, Bouthillier Y. A major role of the macrophage in quantitative genetic regulation of immunoresponsiveness and antiinfectious immunity. Adv Immunol 1984; 36: 189–233
   PubMed Web of Science ®Google Scholar
• Ibanez OM, Mouton D, Oliveira SL, et al. Polygenic control of quantitative antibody responsiveness: restrictions of the multispecific effect related to the selection antigen. Immunogenetics 1988; 28: 6–12
   PubMed Web of Science ®Google Scholar
• Cannat A, Bousquet C, Serre A. Response of high and low antibody producers to Brucella. Ann Immunol 1988; 129C: 669–683
   Google Scholar
• Sant'anna OA, Massa S, Mouton D, et al. Salmonella typhimurium infection in high and low antibody responder mice: inverse correlation between antibody responsiveness and resistance to infection. FEMS Microbiol Immunol 1989; 47: 465–472
   Google Scholar
• Soares AMVC, Rezkallah-Iwasso MT, Oliveira SL, et al. Experimental paracoccidioidomycosis in high and low antibody responder mice of Selection IV-A. Med Mycology 2000; 38: 309–315
   Google Scholar
• Del Negro G. Lesões das supra-renais. Paracoccidioidomicose (Blastomicose Sul-americana), G Del Negro, CS Lacaz, AM Fiorillo. Sarvier–Edusp, São Paulo 1982; 195–202
   Google Scholar
• Tendrich M, De Luca V, Tourinho EK, et al. Computed tomography and ultrasonography of the adrenal glands in paracoccidioidomycosis. Comparison with cortisol and aldosterone responses to ACTH stimulation. Am J Trop Med Hyg 1991; 44: 83–92
   Google Scholar
• Swain SL, Mckenzie DT, Weinberg AD, Hancock W. Characterization of T helper 1 and 2 cell subsets in normal mice. Helper T cells responsible for IL-4 and IL-5 production are present as precursor that require priming before they developed into lymphokine-secreting cells. J Immunol 1988; 141: 3445–3455
   PubMed Web of Science ®Google Scholar
• Fiorentino DF, Bond MW, Mosmann TR. Two types of mouse helper T cell. II. Th2 cells secreted a factor that inhibits cytokines production by Th1 clones. J Exp Med 1989; 170: 2981–2989
   Google Scholar
• Calich VL, Kashino SS. Cytokines produced by susceptible and resistance mice in the course of Paracoccidioides brasiliensis infection. Braz J Med Biol Res 1998; 31: 615–623
   PubMed Web of Science ®Google Scholar
• Fava Netto C, Vegas VS, Sciannaméa IM, Guarniere DB. Antígeno polissacarídico do Paracoccidioides brasiliensis. Estudo do tempo de cultivo do P. brasiliensis necessário ao preparo do antígeno. Rev Inst Med Trop SãoPaulo 1969; 11: 177–181
   Google Scholar
• Calich VLG, Singer-Vermes LM, Siqueira AM, Burger E. Susceptibility and resistance of inbred mice to Paracoccidioides brasiliensis. Br J Exp Pathol 1985; 66: 585–594
   PubMedGoogle Scholar
• Singer-Vermes LM, Ciavaglia MC, Kashino SS, Burger E, Calich VLG. The source of the growth promoting factor(s) affects the platting efficiency of Paracoccidioides brasiliensis. J Med Vet Mycol 1992; 30: 261–263
   PubMedGoogle Scholar
• Godfrey KAM. Statistics in practice. Comparing the means of several groups. N Engl J Med 1958; 313: 450–456
   Google Scholar
• Frenkel JK. Pathogenesis of infections of the adrenal gland leading to Addison's disease in man: the role of corticoids in adrenal and generalized infection. Ann NY Acad Sci 1960; 84: 391–440
   Web of Science ®Google Scholar
• Cano LE, Wolf RG, Meltzer M, Crawford RD. Differential regulation of class II MHC determinants on macrophages by interferon-gamma and IL-4. J Immunol 1989; 143: 3524–3531
   Google Scholar
• Jain-Vora S, LeVine AM, Chroneos Z, et al. Interleukin-4 enhance pulmonary clearance of Pseudomonas aeruginosa. Infect Immun 1998; 66: 4229–4236
   PubMed Web of Science ®Google Scholar
• Calich, VLG, Arruda, C. Natural and acquired immunity in the pulmonary model of paracoccidioidomycosis. In:. 6° Encontro Internacional sobre Paracoccidioidomicose; Campos do Jordão; 1999. p.51.
   Google Scholar
• de Waal Malefyt R, Haanen J, Spits H, et al. Interleukin 10 (IL-10) and viral IL-10 strongly reduce antigen-specific human T cell proliferation by diminishing the antigen-presenting capacity of monocytes via downregulation of class II major histocompatibility complex expression. J Exp Med 1991; 174: 915–924
   PubMed Web of Science ®Google Scholar
• Mosmann TR. Properties and functions of interleukin-10. Adv Immunol 1994; 56: 1–26
   PubMed Web of Science ®Google Scholar
• Cano LE, Kashino SS, Arruda C, et al. Protective role of gamma interferon in experimental pulmonary paracoccidioidomycosis. Infect Immun 1998; 66: 800–806
   PubMed Web of Science ®Google Scholar
• Cano LE, Singer-Vermes LM, Vaz CAC, Russo M, Calich VLG. Pulmonary paracoccidioidomycosis in resistant and susceptible mice: relationship among progression of infection, bronchoalveolar cells activation, cellular immune response, and specific isotype patterns. Infect Immun 1995; 63: 1777–1783
   PubMed Web of Science ®Google Scholar
• Brummer E, Hanson LH, Restrepo A, Stevens DA. In vivo and in vitro activation of pulmonary macrophages by IFN-γ for enhanced killing of P. brasiliensis or B. dermatitides. J Immunol 1988; 140: 2786–2787
   PubMedGoogle Scholar
• Cano LE, Arango R, Salazar ME, et al. Killing of P. brasiliensis conidia by pulmonary macrophages and the effects of cytokines. J Med Vet Mycol 1992; 30: 161–168
   PubMedGoogle Scholar
• Figueiredo F, Alves LMC, Silva CL. Tumor necrosis factor production in vivo and in vitro in response to Paracoccidioides brasiliensis and the cell wall fractions thereof. Clin Exp Immunol 1993; 93: 189–194
   PubMed Web of Science ®Google Scholar
• Kindler V, Sappino AP, Grau GE, Piguet PF, Vassali P. The inducing role of tumor necrosis factor in the development of bactericidal granulomas during BCG infection. Cell 1989; 56: 731–740
   PubMed Web of Science ®Google Scholar
• Calvi SA, Peraçoli MT, Mendes RP, et al. Effect of cytokines on the in vitro fungicidal activity of monocytes from paracoccidioidomycosis patients. Microbes Infect 2003; 5: 107–113
   PubMed Web of Science ®Google Scholar
• Souto JT, Figueiredo F, Furlanetto A, et al. Interferon-γ and tumor necrosis factor-α determine resistance to Paracoccidioides brasiliensis infection in mice. Am J Pathol 2000; 156: 1811–1820
   PubMed Web of Science ®Google Scholar
• Pfeffer K, Matsuyama T, Kündig TM, et al. Mice deficient for the 55 kd tumor necrosis factor receptor are resistant to shock, yet succumb to L. monocytogenes infection. Cell 1993; 73: 457–467
   PubMed Web of Science ®Google Scholar
• Deckert-Schluter M, Bluethmann H, Rang A, Hof H, Schluter D. Crucial role of TNF receptor type 1 (p55), but not of TNF receptor type 2 (p75), in murine toxoplasmosis. J Immunol 1998; 160: 3427–3436
   PubMedGoogle Scholar