RESUMEN
The murine model of paracoccidioidomycosis, the most important South American endemic mycosis, mimics the human disease: resistance is associated with preserved cellular immunity while T-cell anergy is related with susceptibility. In the present study we asked whether a previous s.c. infection which induces strong cellular immunity would protect mice against a lethal pulmonary challenge. It was found that susceptible but not resistant mice developed immunoprotection and aseptic cure of infection. Immunoprotection led to reversal of DTH anergy, increased levels of antibodies and pulmonary IL-12, IL-2 and IL-4 indicating a balanced type 1/type 2 response. On the contrary, no marked differences in A/Sn infection and immunity were observed. Depletion experiments showed that immunoprotection required the cooperative action of CD4(+) and CD8(+) T cells in association with IFN-gamma and IL-12. Altogether, these observations demonstrated that susceptible hosts can develop sterilizing immunity and defined the main immunological requirements to control secondary paracoccidioidomycosis.
Asunto(s)
Vacunas Fúngicas/administración & dosificación , Inmunización , Enfermedades Pulmonares Fúngicas/genética , Enfermedades Pulmonares Fúngicas/prevención & control , Paracoccidioides/inmunología , Paracoccidioidomicosis/genética , Paracoccidioidomicosis/prevención & control , Animales , Anticuerpos Antifúngicos/sangre , Linfocitos T CD4-Positivos/inmunología , Linfocitos T CD8-positivos/inmunología , Susceptibilidad a Enfermedades/inmunología , Predisposición Genética a la Enfermedad , Hipersensibilidad Tardía , Inyecciones Subcutáneas , Interferón gamma/inmunología , Interleucinas/inmunología , Pulmón/inmunología , Enfermedades Pulmonares Fúngicas/sangre , Enfermedades Pulmonares Fúngicas/inmunología , Masculino , Ratones , Paracoccidioidomicosis/sangre , Paracoccidioidomicosis/inmunología , Subgrupos de Linfocitos TRESUMEN
The pathogenic fungus Paracoccidioides brasiliensis is the causative agent of paracoccidioidomycosis (PCM). This pulmonary mycosis, acquired by inhalation of airborne propagules, may disseminate to several internal organs and tissues, leading to severe disease. Adhesion to host cell components is the first step involved in dissemination of pathogens. Previous studies showed that laminin, the most abundant glycoprotein of the basement membrane, binds to P. brasiliensis yeast cells, enhancing their pathogenicity in the hamster testicle model. As PCM is primarily a pulmonary infection, we studied the influence of previous treatment of yeast cells with laminin on the course of the intratracheal infection of resistant and susceptible mice using high-virulence (Pb18) and low-virulence (Pb265) P. brasiliensis isolates. Laminin treatment did not alter fungal loads, delayed-type hypersensitivity reactions, levels of pulmonary cytokines and production of specific antibodies in any group of Pb18-infected mice. However, early in the infection, a less intense inflammatory reaction was detected in the lungs of the laminin-treated groups. In addition, laminin treatment of Pb265 resulted in a less severe infection as revealed by the lower fungal loads recovered from lungs. Antibody and cytokine levels, however, did not change after laminin treatment. Altogether, our results demonstrate that laminin binding to yeast cells diminishes P. brasiliensis pathogenicity. The lower inflammatory response observed with the virulent isolate and the decreased pulmonary fungal burden with the low-virulence isolate indicate an inhibitory effect of laminin treatment on P. brasiliensis infectivity and interaction with pulmonary host cells or extracellular matrix proteins.
Asunto(s)
Laminina/metabolismo , Enfermedades Pulmonares Fúngicas/microbiología , Paracoccidioides/patogenicidad , Paracoccidioidomicosis/microbiología , Animales , Anticuerpos Antifúngicos/sangre , Antifúngicos/metabolismo , Antifúngicos/farmacología , Recuento de Colonia Microbiana , Citocinas/análisis , Hipersensibilidad Tardía , Laminina/farmacología , Pulmón/inmunología , Pulmón/microbiología , Pulmón/patología , Enfermedades Pulmonares Fúngicas/inmunología , Enfermedades Pulmonares Fúngicas/patología , Masculino , Ratones , Paracoccidioides/efectos de los fármacos , Paracoccidioides/inmunología , Paracoccidioides/metabolismo , Paracoccidioidomicosis/inmunología , Paracoccidioidomicosis/patología , Neumonía/patología , Unión ProteicaRESUMEN
Randomly amplified polymorphic DNA (RAPD) analysis of 35 Paracoccidioides brasiliensis isolates was carried out to evaluate the correlation of RAPD profiles with the virulence degree or the type of the clinical manifestations of human paracoccidioidomycosis. The dendrogram presented two main groups sharing 64% genetic similarity. Group A included two isolates from patients with chronic paracoccidioidomycosis; group B comprised the following isolates showing 65% similarity: two non-virulent, six attenuated, five virulent, eight from patients with chronic paracoccidioidomycosis and two from patients with acute paracoccidioidomycosis. The virulent Pb18 isolate and six attenuated or non-virulent samples derived from it were genetically indistinguishable (100% of similarity). Thus, in our study, RAPD patterns could not discriminate among 35 P. brasiliensis isolates according to their differences either in the degree of virulence or in the type of the clinical manifestation of this fungal infection.
Asunto(s)
ADN de Hongos/genética , Paracoccidioides/patogenicidad , Paracoccidioidomicosis/microbiología , Polimorfismo Genético , Animales , Cartilla de ADN , ADN de Hongos/análisis , Humanos , Ratones , Paracoccidioides/genética , Paracoccidioidomicosis/fisiopatología , Técnica del ADN Polimorfo Amplificado Aleatorio , Virulencia/genéticaRESUMEN
Host resistance to paracoccidiodomycosis, the main deep mycosis in Latin America, is mainly due to cellular immunity and gamma interferon (IFN-gamma) production. To assess the role of interleukin-4 (IL-4), a Th2-inducing cytokine, pulmonary paracoccidioidomycosis was studied in IL-4-deficient (IL-4(-/-)) and wild-type (WT) C57BL/6 mice at the innate and acquired phases of immune response. Forty-eight hours after infection, equivalent numbers of viable Paracoccidioides brasiliensis yeast cells were recovered from the lungs of IL-4(-/-) and WT mice intratracheally infected with one million fungal cells. Alveolar macrophages from infected IL-4(-/-) mice controlled in vitro fungal growth more efficiently than macrophages from WT mice and secreted higher levels of nitric oxide. Compared with WT mice, IL-4(-/-) animals presented increased levels of pulmonary IFN-gamma and augmented polymorphonuclear leukocyte influx to the lungs. Decreased pulmonary fungal loads were characterized in deficient mice at week 2 postinfection, concomitant with diminished presence of IL-10. At week 8, lower numbers of yeasts were recovered from lungs and liver of IL-4(-/-) mice associated with increased production of IFN-gamma but impaired synthesis of IL-5 and IL-10. However, a clear shift to a Th1 pattern was not characterized, since IL-4(-/-) mice did not alter delayed-type hypersensitivity anergy or IL-2 levels. In addition, IL-4 deficiency resulted in significantly reduced levels of pulmonary IL-12, granulocyte-macrophage colony-stimulating factor, IL-3, monocyte chemotactic protein 1, and specific antibody isotypes. In IL-4(-/-) mice, well-organized granulomas restraining fungal cells replaced the more extensive lesions containing high numbers of fungi and inflammatory leukocytes developed by IL-4-sufficient mice. These results clearly showed that genetically determined deficiency of IL-4 can exert a protective role in pulmonary paracoccidioidomycosis.
Asunto(s)
Interleucina-4/deficiencia , Enfermedades Pulmonares Fúngicas/inmunología , Paracoccidioides/patogenicidad , Paracoccidioidomicosis/inmunología , Células Th2/patología , Animales , Anticuerpos Antifúngicos/sangre , Citocinas/metabolismo , Hipersensibilidad Tardía , Interleucina-4/genética , Interleucina-4/inmunología , Células Asesinas Naturales/inmunología , Pulmón/inmunología , Enfermedades Pulmonares Fúngicas/microbiología , Macrófagos/inmunología , Ratones , Ratones Endogámicos C57BL , Paracoccidioidomicosis/microbiología , Índice de Severidad de la Enfermedad , Células Th2/inmunologíaRESUMEN
Paracoccidioides brasiliensis is a facultative, intracellular pathogen causing the most important deep mycosis in Latin America. As the production of IFN-gamma and induction of cell-mediated immunity to P. brasiliensis is of critical importance in host defense, the immunotherapeutic effect of exogenous IL-12 administration was studied in a murine model of susceptibility to pulmonary infection. rIL-12 treatment led to a less disseminated disease, as confirmed by decreased fungal loads in liver and spleen. Administration of rIL-12 did not affect fungal growth in the lungs, although it did induce an augmented pulmonary mononuclear cell inflammation. IL-12 treatment induced an early (week 1) increase in pulmonary IFN-gamma, but decreased cytokine and specific antibody (IgG1 and IgG3) production at week 8 after infection. These results show that IL-12 administration induces a less severe infection, but the high inflammatory response detected in the lungs precludes its possible use as a new therapeutic tool for severe paracoccidioidomycosis.
Asunto(s)
Interleucina-12/farmacología , Paracoccidioidomicosis/inmunología , Animales , Anticuerpos Antifúngicos/biosíntesis , Citocinas/biosíntesis , Modelos Animales de Enfermedad , Humanos , Hipersensibilidad Tardía , Inmunoterapia , Leucocitos Mononucleares/inmunología , Leucocitos Mononucleares/patología , Pulmón/inmunología , Pulmón/microbiología , Pulmón/patología , Masculino , Ratones , Paracoccidioides/inmunología , Paracoccidioides/aislamiento & purificación , Paracoccidioidomicosis/etiología , Paracoccidioidomicosis/patología , Paracoccidioidomicosis/prevención & controlRESUMEN
Resistance to paracoccidioidomycosis, the most important endemic mycosis in Latin America, is thought to be primarily mediated by cellular immunity and the production of gamma interferon. To assess the role of interleukin-4 (IL-4), a Th2 cytokine, pulmonary paracoccidioidomycosis in IL-4-depleted susceptible (B10.A) and intermediate (C57BL/6) mice was studied. Two different protocols were used to neutralize endogenous IL-4 in B10.A mice: 1 mg of anti-IL-4 monoclonal antibody (MAb)/week and 8 mg 1 day before intratracheal infection with 10(6) Paracoccidioides brasiliensis yeast cells. Unexpectedly, both protocols enhanced pulmonary infection but did not alter the levels of pulmonary cytokines and specific antibodies. Since in a previous work it was verified that C57BL/6 mice genetically deficient in IL-4 were more resistant to P. brasiliensis infection, we also investigated the effect of IL-4 depletion in this mouse strain. Treatment with the MAb at 1 mg/week led to less severe pulmonary disease associated with impaired synthesis of Th2 cytokines in the lungs and liver of control C57BL/6 mice. Conversely, in IL-4-depleted C57BL/6 mice, increased levels of tumor necrosis factor alpha and IL-12 were found in the lungs and liver, respectively. In addition, higher levels of immunoglobulin G2a (IgG2a) and lower levels of IgG1 antibodies were produced by IL-4-depleted mice than by control mice. Lung pathologic findings were equivalent in IL-4-depleted and untreated B10.A mice. In IL-4-depleted C57BL/6 mice, however, smaller and well-organized granulomas replaced the more extensive lesions that developed in untreated mice. These results clearly showed that IL-4 can have a protective or a disease-promoting effect in pulmonary paracoccidioidomycosis depending on the genetic background of the host.
Asunto(s)
Interleucina-4/metabolismo , Enfermedades Pulmonares/microbiología , Paracoccidioidomicosis/metabolismo , Animales , Formación de Anticuerpos/inmunología , Isotipos de Inmunoglobulinas/inmunología , Pulmón/microbiología , Pulmón/patología , Enfermedades Pulmonares/inmunología , Enfermedades Pulmonares/metabolismo , Masculino , Ratones , Paracoccidioidomicosis/inmunología , Células Th2/inmunologíaRESUMEN
Natural resistance and acquired immune responses to Paracoccidioides brasiliensis infection were investigated employing resistant and susceptible inbred mice infected with Pb18, a virulent isolate. Intraperitoneally infected susceptible mice present an innefficient macrophage activation, depressed DTH reactions, high levels of specific antibodies mainly of the IgG2b and IgA isotypes, evident polyclonal activation of IgG1, IgG2b and IgG2a producing B cells and a progressive disease. Resistant mice on the contrary, present an efficient macrophage activation, adequate DTH responses, low levels of specific antibodies mainly of the IgG2a isotype and absence of polyclonal activation of B cell resulting in the resolution of the infectious process. Similar results were obtained when the intratracheal or intravenous routes of infection were used. The previous subcutaneous infection with Pb18 establishes a stable cell-mediated immunity that makes the innately susceptible B10. A mice resistant to P. brasiliensis ip infection. This murine model, which mimics the benign and severe chronic forms of the human disease, is proposed as a framework of our current knowledge of the host-parasite interactions in paracoccidioidomycosis and as a basis ofor future challenge in continuing analyses.