RESUMO
The epidithiodioxopiperazine gliotoxin is a virulence factor of Aspergillus fumigatus, the most important airborne fungal pathogen of humans. Gliotoxin suppresses innate immunity in invasive aspergillosis, particularly by compromising neutrophils, but the underlying molecular mechanisms remain elusive. Neutrophils are the first responders among innate immune cells recruited to sites of infection by the chemoattractant leukotriene (LT)B4 that is biosynthesized by 5-lipoxygenase and LTA4 hydrolase (LTA4H). Here, we identified gliotoxin as inhibitor of LTA4H that selectively abrogates LTB4 formation in human leukocytes and in distinct animal models. Gliotoxin failed to inhibit the formation of other eicosanoids and the aminopeptidase activity of the bifunctional LTA4H. Suppression of LTB4 formation by gliotoxin required the cellular environment and/or reducing conditions, and only the reduced form of gliotoxin inhibited LTA4H activity. Conclusively, gliotoxin suppresses the biosynthesis of the potent neutrophil chemoattractant LTB4 by direct interference with LTA4H thereby impairing neutrophil functions in invasive aspergillosis.
Assuntos
Aspergilose/imunologia , Aspergillus fumigatus/imunologia , Epóxido Hidrolases/imunologia , Gliotoxina/imunologia , Leucotrieno B4/imunologia , Animais , Aspergilose/microbiologia , Linhagem Celular , Feminino , Humanos , Imunidade Inata , Leucócitos/imunologia , Leucócitos/microbiologia , Masculino , Camundongos , Neutrófilos/imunologia , Neutrófilos/microbiologia , Ratos WistarRESUMO
Gliotoxin (GT) belongs to the epipolythiodioxopiperazine class of toxins secreted from certain fungi including Aspergillus fumigatus, which is the most prolific producer of this secondary metabolite. Recently, enhanced amounts of GT were found in in vitro biofilm-grown A. fumigatus mycelium. To further correlate the A. fumigatus biofilm growth phenotype with the enhanced secretion of GT, a polyclonal antibody (pAb) was produced by immunizing mice against GT. By an indirect immunofluorescent assay, pAb was then able to recognize specifically GT onto A. fumigatus Af293 biofilm formed on human pulmonary epithelial cells. Then, treating Af293 biofilms with a compound which reduces the GT disulfide bonds provoked shutdown of the GT-specific immunofluorescence (IF) signals along the hyphae. To explore the potential of GT for diagnostic use, pAb was shown to react with GT on hyphae into Aspergillus culture-positive respiratory tract specimens from patients with probable invasive aspergillosis (IA) and into tissue specimens from the lungs of patients with proven IA. As the presence of fungal hyphae in clinical specimens strongly indicates the in vivo A. fumigatus growth as a biofilm, anti-GT antibodies could be a specific and sensitive diagnostic tool for detecting A. fumigatus biofilm-associated clinical infections.
Assuntos
Aspergilose/imunologia , Aspergilose/microbiologia , Aspergillus fumigatus/fisiologia , Biofilmes/crescimento & desenvolvimento , Gliotoxina/biossíntese , Animais , Anticorpos Antifúngicos/imunologia , Especificidade de Anticorpos/imunologia , Linhagem Celular , Células Epiteliais/microbiologia , Feminino , Gliotoxina/imunologia , Humanos , Hifas , Camundongos , Ligação Proteica/imunologia , Mucosa Respiratória/microbiologiaRESUMO
Allergic fungal sinusitis (AFS) is a form of paranasal nasal disease if not managed early often involves bone destruction and extension into the orbit and anterior skull base. We present our study of patients with AFS with intracranial, exdradural extension. This study includes our experience of 26 patients with the histological and immunological diagnosis of AFS based on findings of branching septate fungi interspersed with eosinophilic mucin and Charcot-Leyden crystals without fungal invasion of soft tissue, with intracranial extension. All had erosion of bone, which was observed on computerized tomography (CT) scans, extending intracranially and eight had disease that additionally involved the lamina papyracea. The average age of patients in this study was 25 years (range 9-46). There were 20 male and 6 female patients. All patients were immunocompetent. Skin test against aspergillin showed all patients had Type 1 hypersensitivity. All patients underwent transnasal and/or transmaxillary endoscopic approaches for debridement and eight underwent orbital decompression. No patient underwent craniotomy for removal of intracranial extradural disease. No patient had a cerebrospinal fluid leak. Postoperatively, all 26 were treated with a course of corticosteroids. The follow-up period ranged from 2 to 5 years. We conclude AFS is a unique form of fungal disease that might mimic anterior skull base and paranasal sinus tumors. Most cases can be successfully managed with transnasal and/or transmaxillary endoscopic techniques.
Assuntos
Sinusite Etmoidal/microbiologia , Sinusite Frontal/microbiologia , Fungos/isolamento & purificação , Rinite Alérgica Perene/microbiologia , Rinite Alérgica Perene/cirurgia , Adolescente , Antígenos/imunologia , Doença Crônica , Eosinófilos/metabolismo , Sinusite Etmoidal/cirurgia , Feminino , Seguimentos , Sinusite Frontal/cirurgia , Fungos/imunologia , Gliotoxina/imunologia , Glicoproteínas/metabolismo , Humanos , Lisofosfolipase/metabolismo , Masculino , Mucinas/metabolismo , Obstrução Nasal/cirurgia , Rinite Alérgica Perene/metabolismo , Testes CutâneosRESUMO
Aspergillus fumigatus (AF) is a ubiquitous mold and the most common cause of invasive aspergillosis (IA) in immunocompromised patients. In stem cell transplant recipients, IA now occurs most frequently in the setting of therapy with corticosteroids, including methylprednisolone (MP). We showed previously that gliotoxin (GT), an AF-derived mycotoxin, induces apoptosis in monocytes and dendritic cells, resulting in the suppression of AF-specific T cell responses. We examined the ability of GT to induce apoptosis in polymorphonuclear leukocytes (PMN) and assessed GT effects on important neutrophil functions, including phagocytic function, degranulation, myeloperoxidase activity, and the production of reactive oxygen species (ROS). In contrast to its effects on monocytes, PMN remained resistant to GT-mediated apoptosis. Although many essential neutrophil functions were unaffected, GT inhibited phagocytosis and also induced a decrease in ROS generation by PMN. In contrast, MP therapy potentiated ROS production, suggesting a mechanism that may facilitate tissue injury in IA. Distinct from its effects on untreated PMN, GT augmented ROS production in MP-treated PMN. Our results suggest that although GT may suppress the adaptive immune response, GT may also serve to increase PMN-mediated inflammation, which is likely to play an important role in tissue destruction in the setting of IA.
Assuntos
Anti-Inflamatórios/farmacologia , Apoptose/imunologia , Aspergilose/imunologia , Aspergillus fumigatus/patogenicidade , Gliotoxina/imunologia , Metilprednisolona/farmacologia , Neutrófilos/imunologia , Anti-Inflamatórios/efeitos adversos , Anti-Inflamatórios/uso terapêutico , Apoptose/efeitos dos fármacos , Aspergilose/tratamento farmacológico , Aspergillus fumigatus/imunologia , Degranulação Celular/efeitos dos fármacos , Degranulação Celular/imunologia , Células Cultivadas , Células Dendríticas/imunologia , Células Dendríticas/patologia , Gliotoxina/farmacologia , Humanos , Hospedeiro Imunocomprometido/efeitos dos fármacos , Hospedeiro Imunocomprometido/imunologia , Inflamação/induzido quimicamente , Inflamação/imunologia , Metilprednisolona/efeitos adversos , Metilprednisolona/uso terapêutico , Monócitos/imunologia , Monócitos/patologia , Neutrófilos/patologia , Peroxidase/imunologia , Fagocitose/efeitos dos fármacos , Fagocitose/imunologia , Espécies Reativas de Oxigênio/imunologia , Transplante de Células-Tronco/efeitos adversosRESUMO
Gliotoxin is a mycotoxin having a considerable number of immuno-suppressive actions and is produced by several moulds such as Aspergillus fumigatus. In this study, we investigated its toxic effects on human neutrophils at concentrations corresponding to those found in the blood of patients with invasive aspergillosis. Incubation of the cells for 10min with 30-100ng/ml of gliotoxin inhibited phagocytosis of either zymosan or serum-opsonized zymosan without affecting superoxide production or the exocytosis of specific and azurophil granules. Gliotoxin also induced a significant re-organization of the actin cytoskeleton which collapsed around the nucleus leading to cell shrinkage and the disappearance of filopodia. This gliotoxin-induced actin phenotype was reversed by the cAMP antagonist Rp-cAMP and mimicked by pCPT-cAMP indicating that it probably resulted from the deregulation of intracellular cAMP homeostasis as previously described for gliotoxin-induced apoptosis. By contrast, gliotoxin-induced inhibition of phagocytosis was not reversed by Rp-cAMP but by arachidonic acid, another member of a known signalling pathway affected by the toxin. This suggests that gliotoxin can affect circulating neutrophils and favour the dissemination of A. fumigatus by inhibiting phagocytosis and the consequent killing of conidia.
Assuntos
Actinas/metabolismo , Aspergillus fumigatus/metabolismo , Citoesqueleto/efeitos dos fármacos , Gliotoxina/toxicidade , Neutrófilos/efeitos dos fármacos , Fagocitose/efeitos dos fármacos , Actinas/fisiologia , Ácido Araquidônico/metabolismo , Aspergilose/imunologia , Aspergilose/metabolismo , Aspergilose/microbiologia , Aspergillus fumigatus/química , Aspergillus fumigatus/imunologia , AMP Cíclico/metabolismo , Citoesqueleto/metabolismo , Gliotoxina/imunologia , Gliotoxina/isolamento & purificação , Gliotoxina/metabolismo , Humanos , NADPH Oxidases/metabolismo , Neutrófilos/enzimologia , Neutrófilos/imunologia , Neutrófilos/metabolismo , Fagocitose/imunologia , Transdução de Sinais/efeitos dos fármacosRESUMO
We have established a novel TCRalphabeta (TCRVbeta6)(+)CD4(-)CD8(-) T cell hybridoma designated B6HO3. When the B6HO3 cells were cocultured with bacterial-infected J774 macrophage-like cells, IFN-gamma production by B6HO3 cells was triggered through direct cell-cell contact with dying J774 cells infected with Listeria monocytogenes (LM), Shigella flexneri, or Salmonella typhimurium that expressed the type III secretion system, but not with intact J774 cells infected with heat-killed LM, nonhemolytic lysteriolysin O-deficient (Hly(-)) LM, plasmid-cured Shigella, or stationary-phase Salmonella. However, the triggering of B6HO3 cells for IFN-gamma production involved neither dying hepatoma cells infected with LM nor dying J774 cells caused by gliotoxin treatment or freeze thawing. Cycloheximide and Abs to H-2K(d), H-2D(d), Ia(d), CD1d, TCRVbeta6, and IL-12 did not inhibit the contact-dependent IFN-gamma response, indicating that this IFN-gamma response did not require de novo protein synthesis in bacterial-infected J774 cells and was TCR and IL-12 independent. Thus, in an as yet undefined way, B6HO3 hybridoma recognizes a specialized form of macrophage cell death resulting from bacterial infection and consequently produces IFN-gamma. Moreover, contact-dependent interaction of minor subsets of splenic alphabeta T cells, including NKT cells with dying LM-infected J774 and bone marrow-derived macrophage (BMM) cells, proved to provide an IFN-gamma-productive stimulus for these minor T cell populations, to which the parental T cell of the B6HO3 hybridoma appeared to belong. Unexpectedly, subsets of gammadelta T and NK cells similarly responded to dying LM-infected macrophage cells. These results propose that innate lymphocytes may possess a recognition system sensing macrophage cell "danger" resulting from bacterial infection.
Assuntos
Citotoxicidade Celular Dependente de Anticorpos/imunologia , Macrófagos/imunologia , Macrófagos/microbiologia , Subpopulações de Linfócitos T/imunologia , Subpopulações de Linfócitos T/microbiologia , Animais , Carcinoma Hepatocelular/microbiologia , Carcinoma Hepatocelular/patologia , Comunicação Celular/imunologia , Morte Celular/imunologia , Linhagem Celular Tumoral , Técnicas de Cocultura , Reagentes de Ligações Cruzadas/metabolismo , Apresentação Cruzada/imunologia , Congelamento , Gliotoxina/imunologia , Hibridomas , Imunofenotipagem , Interferon gama/biossíntese , Listeriose/imunologia , Listeriose/microbiologia , Linfoma de Células T/imunologia , Linfoma de Células T/microbiologia , Linfoma de Células T/patologia , Macrófagos/patologia , Camundongos , Camundongos Endogâmicos C3H , Camundongos Endogâmicos C57BL , Camundongos Endogâmicos DBA , Complexo Receptor-CD3 de Antígeno de Linfócitos T/imunologia , Complexo Receptor-CD3 de Antígeno de Linfócitos T/metabolismo , Receptores de Antígenos de Linfócitos T alfa-beta/imunologia , Receptores de Antígenos de Linfócitos T alfa-beta/metabolismo , Receptores de Antígenos de Linfócitos T gama-delta/imunologia , Receptores de Antígenos de Linfócitos T gama-delta/metabolismo , Subpopulações de Linfócitos T/metabolismoRESUMO
BACKGROUND: Microbial growth is considered one of the major causes of indoor air problems. Moulds have been associated with asthma, allergy and a wide range of diffuse indoor air-related symptoms. However, mechanisms of the adverse health effects are not well understood. OBJECTIVE: We hypothesized that the mycotoxins citrinin and gliotoxin could cause an imbalance between the secretion of the pro-inflammatory cytokines TNF-alpha and IL-6 and the anti-inflammatory cytokine IL-10. METHODS: We investigated the influence of citrinin and gliotoxin on the human monocytic cell line Mono-Mac-6 (MM6) with and without lipopolysaccharide -stimulation. The levels of IL-10, IL-6 and TNF-alpha were analysed in cell culture supernatants by ELISA. Cell viability and cell apoptosis were measured by flow cytometry. RESULTS: The strongest inhibition of cytokine secretion was found for IL-10. IL-6 levels were found to decrease in a dose-dependent manner along with reduced cell viability. TNF-alpha levels increased with low gliotoxin exposure (less than 100 ng/mL), but decreased significantly at 375 ng/mL and higher along with increased cell apoptosis and reduced cell viability. TNF-alpha levels were not reduced by citrinin exposure. CONCLUSION: We observed a cytokine imbalance with a more pronounced reduction of IL-10 concentrations compared with those of TNF-alpha and IL-6. We suggest that low exposure doses of citrinin and gliotoxin (corresponding to less than 100 ng/mL gliotoxin and less than 10 mug/mL citrinin) may inhibit IL-10 and lead to increased risk of an inflammatory response with relative overproduction of TNF-alpha and IL-6. The findings and their clinical implications must be verified by human studies. However, we speculate that the observed biological effects may be of importance as they may partly explain the occurrence of diffuse general indoor air-related symptoms as well as the worsening of asthmatic inflammatory reactions experienced in mouldy environments.
Assuntos
Citrinina/imunologia , Gliotoxina/imunologia , Interleucina-10/imunologia , Interleucina-6/imunologia , Fator de Necrose Tumoral alfa/imunologia , Poluição do Ar em Ambientes Fechados , Antibacterianos/imunologia , Apoptose/imunologia , Linhagem Celular , Sobrevivência Celular/imunologia , Relação Dose-Resposta Imunológica , Humanos , Imunossupressores/imunologia , Lipopolissacarídeos/imunologia , Monócitos/imunologia , Hipersensibilidade Respiratória/imunologiaRESUMO
Aspergillus fumigatus (AF) is a ubiquitous mold and is the most common cause of invasive aspergillosis, an important source of morbidity and mortality in immunocompromised hosts. Using cytokine flow cytometry, we assessed the magnitude of functional CD4+ and CD8+ T-cell responses following stimulation with Aspergillus antigens. Relative to those seen with cytomegalovirus (CMV) or superantigen stimulation, responses to Aspergillus antigens were near background levels. Subsequently, we confirmed that gliotoxin, the most abundant mycotoxin produced by AF, was able to suppress functional T-cell responses following CMV or staphylococcal enterotoxin B (SEB) stimulation. Additional studies demonstrated that crude AF filtrates and purified gliotoxin inhibited antigen-presenting cell function and induced the preferential death of monocytes, leading to a marked decrease in the monocyte-lymphocyte ratio. Analysis of caspase-3 activation confirmed that gliotoxin preferentially induced apoptosis of monocytes; similar effects were observed in CD83+ monocyte-derived dendritic cells. Importantly, the physiologic effects of gliotoxin in vitro were observed below concentrations recently observed in the serum of patients with invasive aspergillosis. These studies suggest that the production of gliotoxin by AF may constitute an important immunoevasive mechanism that is mediated by direct effects on antigen-presenting cells and both direct and indirect effects on T cells.
Assuntos
Antígenos de Fungos/imunologia , Apoptose/imunologia , Aspergilose/imunologia , Aspergillus fumigatus/imunologia , Gliotoxina/imunologia , Monócitos/imunologia , Antígenos CD/imunologia , Aspergilose/mortalidade , Aspergilose/patologia , Aspergillus fumigatus/química , Linfócitos T CD4-Positivos/imunologia , Linfócitos T CD4-Positivos/patologia , Linfócitos T CD8-Positivos/imunologia , Linfócitos T CD8-Positivos/patologia , Caspase 3 , Caspases/imunologia , Células Cultivadas , Citomegalovirus/imunologia , Células Dendríticas/imunologia , Células Dendríticas/patologia , Relação Dose-Resposta Imunológica , Enterotoxinas/imunologia , Gliotoxina/química , Humanos , Imunoglobulinas/imunologia , Ativação Linfocitária/imunologia , Glicoproteínas de Membrana/imunologia , Monócitos/patologia , Antígeno CD83RESUMO
Immunological detection of secreted low molecular weight toxins represents a potentially novel means of diagnosing infection by the fungus Aspergillus fumigatus. Two such metabolites, gliotoxin and helvolic acid, were selected and conjugated to thyroglobulin for antisera generation in rabbits. Gliotoxin was initially activated using N-[p-maleimidophenyl] isocyanate (PMPI) and subsequently conjugated to S-acetyl thioglycolic acid N-hydroxysuccinimide-activated thyroglobulin, whereas helvolic acid was activated with N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide (EDC) in the presence of thyroglobulin prior to immunisation. To facilitate subsequent antisera evaluation, both toxins were similarly conjugated to bovine serum albumin (BSA). Matrix-Assisted Laser Desorption Ionisation-Time Of Flight (MALDI-TOF) mass spectrometry and SDS-PAGE analysis confirmed covalent attachment of toxins to BSA in the ratios of 15 and 2.4 mol per mol BSA for gliotoxin and helvolic acid, respectively. Resultant high titer antisera were capable of detecting both BSA-conjugated toxins (inhibitory concentration (IC)(50): 4-5 microg/ml). Free toxins were also detectable by competitive immunoassay, whereby 10 microg/ml free gliotoxin (30 microM) and helvolic acid (17 microM), respectively, inhibited antibody binding to cognate toxin-BSA previously immobilised on microwells. This work confirms that sensitive and specific antisera can be raised against fungal toxins and may have an application in diagnosing fungal infection.
Assuntos
Anticorpos Antifúngicos , Aspergillus fumigatus/química , Ácido Fusídico/análogos & derivados , Ácido Fusídico/análise , Gliotoxina/análise , Micotoxinas/análise , Animais , Anticorpos Antifúngicos/biossíntese , Especificidade de Anticorpos , Aspergilose/diagnóstico , Aspergilose/microbiologia , Aspergillus fumigatus/imunologia , Aspergillus fumigatus/metabolismo , Western Blotting , Ensaio de Imunoadsorção Enzimática , Feminino , Ácido Fusídico/química , Ácido Fusídico/imunologia , Gliotoxina/antagonistas & inibidores , Gliotoxina/química , Gliotoxina/imunologia , Micotoxinas/antagonistas & inibidores , Micotoxinas/química , Micotoxinas/imunologia , Coelhos , Soroalbumina Bovina/imunologia , Tireoglobulina/antagonistas & inibidores , Tireoglobulina/imunologiaRESUMO
Gliotoxin, a potential etiologic agent which is synthesized by Aspergillus fumigatus and other pathogenic fungi, exhibits a variety of immunosuppressive activities. We have found that gliotoxin markedly inhibits both perforin-dependent and Fas ligand-dependent cytotoxic T-lymphocyte (CTL)-mediated cytotoxicity. Gliotoxin blocked granule exocytosis and the production of inositol phosphates in response to anti-CD3 stimulation. Apparently, activation signals were not efficiently received by the gliotoxin-treated CTL clone, perhaps because gliotoxin profoundly disturbed CTL cell attachment to immobilized anti-CD3. Although the expression of surface molecules of the CTL clone such as CD3 was unaffected by gliotoxin, the effector/target conjugate formation was inhibited dose-dependently by gliotoxin treatment of the effector CTL clone. These results suggest that gliotoxin prevents CTL from interacting with target cells.
Assuntos
Gliotoxina/imunologia , Imunossupressores/imunologia , Linfócitos T Citotóxicos/imunologia , Animais , Aspergillus fumigatus/metabolismo , Dissulfetos , Proteína Ligante Fas , Gliotoxina/química , Imunossupressores/química , Glicoproteínas de Membrana/imunologia , Camundongos , Estrutura Molecular , Perforina , Proteínas Citotóxicas Formadoras de PorosRESUMO
Gliotoxin , a metabolite of Aspergillus fumigatus, inhibits phagocytosis of macrophages at concentrations of 20-50 ng/ml. Pretreatment of stimulator cells in mixed lymphocyte cultures with gliotoxin (100 ng/ml) abrogates induction of alloreactive cytotoxic T cells. The presence of gliotoxin 48 hr after initiation of cytotoxic T-cell induction has no effect. Inhibition of cytotoxic T-cell induction by gliotoxin at low concentrations, acting on the stimulator cells, can be overridden by concanavalin A-activated cell supernatants. Gliotoxin does not induce immediate cell-surface antigen modification on target cells. The possible role of gliotoxin in the etiology of A. fumigatus-related diseases is discussed.