RESUMO
Schistosome infection is a major cause of global morbidity, particularly in sub-Saharan Africa. However, there is no effective vaccine for this major neglected tropical disease, and re-infection routinely occurs after chemotherapeutic treatment. Following invasion through the skin, larval schistosomula enter the circulatory system and migrate through the lung before maturing to adulthood in the mesenteric or urogenital vasculature. Eggs released from adult worms can become trapped in various tissues, with resultant inflammatory responses leading to hepato-splenic, intestinal, or urogenital disease - processes that have been extensively studied in recent years. In contrast, although lung pathology can occur in both the acute and chronic phases of schistosomiasis, the mechanisms underlying pulmonary disease are particularly poorly understood. In chronic infection, egg-mediated fibrosis and vascular destruction can lead to the formation of portosystemic shunts through which eggs can embolise to the lungs, where they can trigger granulomatous disease. Acute schistosomiasis, or Katayama syndrome, which is primarily evident in non-endemic individuals, occurs during pulmonary larval migration, maturation, and initial egg-production, often involving fever and a cough with an accompanying immune cell infiltrate into the lung. Importantly, lung migrating larvae are not just a cause of inflammation and pathology but are a key target for future vaccine design. However, vaccine efforts are hindered by a limited understanding of what constitutes a protective immune response to larvae. In this review, we explore the current understanding of pulmonary immune responses and inflammatory pathology in schistosomiasis, highlighting important unanswered questions and areas for future research.
Assuntos
Pneumopatias Parasitárias/parasitologia , Pulmão/parasitologia , Schistosoma/patogenicidade , Esquistossomose/parasitologia , Animais , Modelos Animais de Doenças , Interações Hospedeiro-Parasita , Humanos , Evasão da Resposta Imune , Pulmão/efeitos dos fármacos , Pulmão/imunologia , Pneumopatias Parasitárias/imunologia , Pneumopatias Parasitárias/prevenção & controle , Camundongos , Vacinas Protozoárias/uso terapêutico , Schistosoma/efeitos dos fármacos , Schistosoma/imunologia , Esquistossomose/imunologia , Esquistossomose/prevenção & controle , Esquistossomicidas/uso terapêuticoRESUMO
Respiratory diseases compromise the health of millions of people all over the world and are strongly linked to the immune dysfunction. CD4+FOXP3+ T regulatory cells, also known as Tregs, have a central role maintaining tissue homeostasis during immune responses. Their activity and clinical impact have been widely studied in different clinical conditions including autoimmune diseases, inflammatory conditions, and cancer, amongst others. Tregs express transcription factor forkhead box P3 (FOXP3), which allows regulation of the immune response through anti-inflammatory cytokines such as IL-10 or transforming growth factor beta (TGF-ß) and direct cell-to-cell interaction. Maintenance of immune tolerance is achieved via modulation of effector CD4+ T helper 1, 2 or 17 (Th1, Th2, Th17) cells by Tregs. This review highlights the recent progress in the understanding of Tregs in different disorders of the respiratory system.
Assuntos
Pulmão/imunologia , Linfócitos T Reguladores/imunologia , Asma/imunologia , Asma/patologia , Citocinas/metabolismo , Fatores de Transcrição Forkhead/metabolismo , Humanos , Fibrose Pulmonar Idiopática/imunologia , Fibrose Pulmonar Idiopática/patologia , Pneumopatias Parasitárias/imunologia , Pneumopatias Parasitárias/patologia , Neoplasias Pulmonares/imunologia , Neoplasias Pulmonares/patologia , Pneumonia/imunologia , Pneumonia/patologia , Doença Pulmonar Obstrutiva Crônica/imunologia , Doença Pulmonar Obstrutiva Crônica/patologia , Sarcoidose Pulmonar/imunologia , Sarcoidose Pulmonar/patologiaRESUMO
Eosinophilic lung diseases especially comprise eosinophilic pneumonia or as the more transient Löffler syndrome, which is most often due to parasitic infections. The diagnosis of eosinophilic pneumonia is based on characteristic clinical-imaging features and the demonstration of alveolar eosinophilia, defined as at least 25% eosinophils at BAL. Peripheral blood eosinophilia is common but may be absent at presentation in idiopathic acute eosinophilic pneumonia, which may be misdiagnosed as severe infectious pneumonia. All possible causes of eosinophilia, including drug, toxin, fungus related etiologies, must be thoroughly investigated. Extrathoracic manifestations should raise the suspicion of eosinophilic granulomatosis with polyangiitis.
Assuntos
Aspergilose Broncopulmonar Alérgica/diagnóstico , Síndrome de Churg-Strauss/diagnóstico , Eosinofilia/diagnóstico , Pneumopatias Parasitárias/diagnóstico , Eosinofilia Pulmonar/diagnóstico , Doença Aguda , Aspergilose Broncopulmonar Alérgica/imunologia , Aspergilose Broncopulmonar Alérgica/terapia , Asma/diagnóstico , Asma/imunologia , Asma/terapia , Lavagem Broncoalveolar , Doença Crônica , Diagnóstico Diferencial , Eosinofilia/complicações , Eosinofilia/imunologia , Humanos , Pneumopatias Parasitárias/imunologia , Pneumopatias Parasitárias/terapia , Eosinofilia Pulmonar/complicações , Eosinofilia Pulmonar/imunologia , Eosinofilia Pulmonar/terapia , FumarRESUMO
Parasitic infection caused by Trichinella spiralis provokes an early stimulation of the mucosal immune system which causes an allergic inflammatory response in the lungs. The present work was intended to characterize the kinetics of emergence of regulatory parameters in Wistar rat lungs during this early inflammatory response, between days 0 and 13p.i. The presence of regulatory cells such as regulatory T cells (Tregs) and alternatively activated macrophages (AAM) was analyzed in lung cell suspensions. Moreover, a regulatory cytokine (TGF-ß) was studied in lung tissue extracts. Considering that newborn larvae (NBL) travel along the pulmonary microvasculature, the ability of this parasite stage to modulate the activation of lung macrophages was evaluated. For this purpose, lung macrophages from non-infected or infected rats (day 6p.i.) were cultured with live or dead NBL. Arginase activity (characteristic of AAM) and nitric oxide (NO produced by iNOS, characteristic of classical activated macrophages) were measured after 48h. Our results revealed a significant increase in the percentage of Tregs on days 6 and 13p.i., arginase activity on day 13p.i. and TGF-ß levels on days 6 and 13p.i. Lung macrophages from non-infected rats cultured with live NBL showed a significant increase in arginase activity and NO levels. Live and dead NBL induced a significant increase in arginase activity in lung macrophages from infected rats. Only live NBL significantly increased NO levels in these macrophages. The present work demonstrates for the first time, the emergence of regulatory parameters in the early lung immune response during T. spiralis infection. The immumodulatory properties exerted by NBL during its passage through this organ could be the cause of such regulation. Moreover, we have shown the ability of NBL to activate macrophages from the lung parenchyma by the classical and alternative pathways.
Assuntos
Pneumopatias Parasitárias/imunologia , Pulmão/imunologia , Triquinelose/imunologia , Animais , Feminino , Inflamação/imunologia , Inflamação/parasitologia , Larva , Pneumopatias Parasitárias/parasitologia , Pneumopatias Parasitárias/patologia , Ativação de Macrófagos , Macrófagos , Ratos , Ratos Wistar , Triquinelose/patologiaRESUMO
INTRODUCTION: The aim of this study was to investigate the associations between radiological findings, blood eosinophilia, hyperimmunoglobulinemia E and G and Toxocara seropositivity in Polish children with newly diagnosed pulmonary infiltration. MATERIAL AND METHODS: We retrospectively analyzed the documentation of 119 patients, aged 1 to 18 years (mean age: 7.21 ± 4.82), who were seropositive in Toxocara sp. antibodies. In all cases, peripheral blood eosinophils and leukocyte counts, serum total IgE, IgG levels and specific IgG antibodies against excretory and secretory Toxocara sp. antigens were measured at the first presentation. After the confirmation of seropositivity, all children had a routine radiological examination. RESULTS: In the documentation of 23 children (mean age 3.58 ± 2.63 years) we found abnormalities in the radiological examination of their lungs. Fifteen children who had abnormalities in radiological findings presented clinical respiratory complaints such as chronic cough, wheezing, asthma and haemoptysis. Eight children were asymptomatic. The analysis of peripheral eosinophils and leukocyte number, the level of IgE and specific anti-Toxocara IgG presented significantly higher values in children with radiological lesions than in children who had correct radiology. The concentrations of total IgG and gamma globulins were not significantly different. In 10 patients CT showed irregular round nodules with and without halo ranging from 1 to 13 mm. The number of nodules varied from a single lesion to multiple, disseminated ones. All nodules were located in peripheral areas of the lungs. None of them were found in the central areas. In 13 patients, CT images showed ground-glass opacities with ill-defined margins. None of the CT images presented lymphadenopathy and pleural effusion. CONCLUSION: The pulmonary lesions in small children with high eosinophilia and hyperimmunoglobulinemia E could be related to toxocariasis and for this reason they are eligible to undergo therapy with prolonged observation for several months, rather than start invasive malignancy investigations.
Assuntos
Anticorpos Anti-Helmínticos/sangue , Pneumopatias Parasitárias/diagnóstico , Pulmão/patologia , Toxocara/imunologia , Toxocaríase/diagnóstico , Toxocaríase/imunologia , Adolescente , Animais , Antígenos de Helmintos/imunologia , Asma/imunologia , Asma/parasitologia , Criança , Pré-Escolar , Ensaio de Imunoadsorção Enzimática , Eosinofilia/etiologia , Feminino , Humanos , Hipergamaglobulinemia/etiologia , Imunoglobulina E/sangue , Imunoglobulina G/sangue , Lactente , Contagem de Leucócitos , Pulmão/diagnóstico por imagem , Pulmão/parasitologia , Pneumopatias Parasitárias/epidemiologia , Pneumopatias Parasitárias/imunologia , Pneumopatias Parasitárias/parasitologia , Masculino , Polônia/epidemiologia , Estudos Retrospectivos , Tomografia Computadorizada por Raios X , Toxocaríase/epidemiologia , Toxocaríase/parasitologiaRESUMO
In schistosomiasis patients, parasite eggs trapped in hepatic sinusoids become foci for CD4+ T cell-orchestrated granulomatous cellular infiltrates. Since the immune response is unable to clear the infection, the liver is subjected to ongoing cycles of focal inflammation and healing that lead to vascular obstruction and tissue fibrosis. This is mitigated by regulatory mechanisms that develop over time and which minimize the inflammatory response to newly deposited eggs. Exploring changes in the hepatic inflammatory infiltrate over time in infected mice, we found an accumulation of schistosome egg antigen-specific IgG1-secreting plasma cells during chronic infection. This population was significantly diminished by blockade of the receptor for IL-10, a cytokine implicated in plasma cell development. Strikingly, IL-10R blockade precipitated the development of portal hypertension and the accumulation of parasite eggs in the lungs and heart. This did not reflect more aggressive Th2 cell responsiveness, increased hepatic fibrosis, or the emergence of Th1 or Th17 responses. Rather, a role for antibody in the prevention of severe disease was suggested by the finding that pulmonary involvement was also apparent in mice unable to secrete class switched antibody. A major effect of anti-IL-10R treatment was the loss of a myeloid population that stained positively for surface IgG1, and which exhibited characteristics of regulatory/anti-inflammatory macrophages. This finding suggests that antibody may promote protective effects within the liver through local interactions with macrophages. In summary, our data describe a role for IL-10-dependent B cell responses in the regulation of tissue damage during a chronic helminth infection.
Assuntos
Fígado/imunologia , Pneumopatias Parasitárias/imunologia , Plasmócitos/imunologia , Receptores de Interleucina-10/antagonistas & inibidores , Schistosoma mansoni , Esquistossomose mansoni/imunologia , Animais , Anticorpos Anti-Helmínticos/genética , Anticorpos Anti-Helmínticos/imunologia , Anticorpos Anti-Helmínticos/metabolismo , Linfócitos T CD4-Positivos/imunologia , Linfócitos T CD4-Positivos/metabolismo , Linfócitos T CD4-Positivos/patologia , Doença Crônica , Imunoglobulina G/genética , Imunoglobulina G/imunologia , Imunoglobulina G/metabolismo , Interleucina-10/genética , Interleucina-10/imunologia , Interleucina-10/metabolismo , Fígado/metabolismo , Fígado/parasitologia , Fígado/patologia , Cirrose Hepática/genética , Cirrose Hepática/imunologia , Cirrose Hepática/metabolismo , Cirrose Hepática/parasitologia , Pneumopatias Parasitárias/genética , Pneumopatias Parasitárias/metabolismo , Pneumopatias Parasitárias/parasitologia , Pneumopatias Parasitárias/patologia , Camundongos , Camundongos Endogâmicos BALB C , Camundongos Knockout , Plasmócitos/metabolismo , Plasmócitos/patologia , Receptores de Interleucina-10/genética , Receptores de Interleucina-10/imunologia , Receptores de Interleucina-10/metabolismo , Esquistossomose mansoni/genética , Esquistossomose mansoni/metabolismo , Esquistossomose mansoni/patologiaRESUMO
Helminths induce potent T helper 2 (TH2)-type immune responses that can mediate worm expulsion, but the role of this response in controlling the acute tissue damage caused by migrating multicellular parasites through vital tissues remains uncertain. We used a helminth infection model in which parasitic nematode larvae migrate transiently through the lung, resulting in hemorrhage and inflammation. We found that IL-17 initially contributed to inflammation and lung damage, whereas subsequent IL-4 receptor (IL-4R) signaling reduced elevations in IL-17 mRNA levels, enhanced the expression of insulin-like growth factor 1 (IGF-1) and IL-10 and stimulated the development of M2 macrophages, all of which contributed to the rapid resolution of tissue damage. These studies indicate an essential role for TH2-type immune responses in mediating acute wound healing during helminth infection.
Assuntos
Helmintíase Animal/imunologia , Células Th2/fisiologia , Animais , Feminino , Hemorragia/imunologia , Hemorragia/parasitologia , Imunidade Celular , Inflamação/imunologia , Inflamação/parasitologia , Fator de Crescimento Insulin-Like I/fisiologia , Interleucina-17/fisiologia , Interleucina-4/fisiologia , Pulmão/irrigação sanguínea , Pulmão/imunologia , Pulmão/parasitologia , Pneumopatias Parasitárias/imunologia , Pneumopatias Parasitárias/parasitologia , Macrófagos/imunologia , Macrófagos/fisiologia , Camundongos , Camundongos Endogâmicos BALB C , Infiltração de Neutrófilos/imunologia , Neutrófilos/fisiologia , Nippostrongylus/imunologia , Infecções por Strongylida/imunologiaRESUMO
Nippostrongylus brasiliensis infections generate pulmonary pathologies that can be associated with strong T(H)2 polarization of the host's immune response. We present data demonstrating N. brasiliensis-driven airway mucus production to be dependent on smooth muscle cell interleukin 4 receptor-α (IL-4Rα) responsiveness. At days 7 and 10 post infection (PI), significant airway mucus production was found in IL-4Rα(-/lox) control mice, whereas global knockout (IL-4Rα(-/-)) and smooth muscle-specific IL-4Rα-deficient mice (SM-MHC(Cre) IL-4Rα(-/lox)) showed reduced airway mucus responses. Furthermore, interleukin (IL)-13 and IL-5 cytokine production in SM-MHC(Cre) IL-4Rα(-/lox) mice was impaired along with a transient reduction in T-cell numbers in the lung. In vitro treatment of smooth muscle cells with secreted N. brasiliensis excretory-secretory antigen (NES) induced IL-6 production. Decreased protein kinase C (PKC)-dependent smooth muscle cell proliferation associated with cell cycle arrest was found in cells stimulated with NES. Together, these data demonstrate that both IL-4Rα and NES-driven responses by smooth muscle cells make important contributions in initiating T(H)2 responses against N. brasiliensis infections.
Assuntos
Subunidade alfa de Receptor de Interleucina-4/imunologia , Pneumopatias Parasitárias/imunologia , Miócitos de Músculo Liso/imunologia , Miócitos de Músculo Liso/metabolismo , Nippostrongylus/imunologia , Infecções por Strongylida/imunologia , Células Th2/imunologia , Animais , Ciclo Celular/genética , Citometria de Fluxo , Interleucina-13/biossíntese , Interleucina-13/imunologia , Subunidade alfa de Receptor de Interleucina-4/genética , Subunidade alfa de Receptor de Interleucina-4/metabolismo , Interleucina-5/biossíntese , Interleucina-5/imunologia , Interleucina-6/biossíntese , Interleucina-6/imunologia , Pneumopatias Parasitárias/patologia , Camundongos , Camundongos Endogâmicos BALB C , Camundongos Knockout , Muco/metabolismo , Nippostrongylus/patogenicidade , Proteína Quinase C/metabolismo , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Transdução de Sinais , Infecções por Strongylida/patologiaRESUMO
Human pulmonary and subcutaneous dirofilariosis caused by Dirofilaria immitis and Dirofilaria repens are worldwide diagnosed with increasing frequency. These species are responsible for the development of benign pulmonary and subcutaneous nodules, respectively, that can be confused with lung or cutaneous cancer. The aim of the present work was to identify D. immitis and D. repens proteins differentially recognized by serum samples from individuals with human pulmonary and subcutaneous dirofilariosis, using two-dimensional electrophoresis and mass spectrometry. Twenty-three immunoreactive proteins of D. immitis and 15 of D. repens were identified. The results point to the existence of differential antigenic recognition in each species, both in the number and type of proteins recognized. Individuals with pulmonary dirofilariosis recognized, on the proteome of D. immitis, among others, different isoforms of 6 enzymes involved in glycolysis, 3 redox-related proteins with antioxidant capacity and 3 heat shock proteins. Individuals with subcutaneous dirofilariosis recognized on the proteome of D. repens only 3 glycolytic enzymes, one protein involved in redox processes and one heat shock protein. These data suggest that in cases of pulmonary dirofilariosis there exists a wider recognition of immunoreactive D. immitis proteins related to key survival processes, such as energy generation, the struggle against oxidative stress and molecular repair, than in cases of human subcutaneous dirofilariosis against D. repens. This could contribute to explain the differences described in the capacity of D. immitis and D. repens development and in the frequency of occurrence of pulmonary and subcutaneous dirofilariosis in the human host.
Assuntos
Dirofilaria immitis/imunologia , Dirofilaria/imunologia , Dirofilariose/imunologia , Proteínas de Helminto/imunologia , Soros Imunes/imunologia , Pneumopatias Parasitárias/imunologia , Animais , Anticorpos Anti-Helmínticos/sangue , Anticorpos Anti-Helmínticos/imunologia , Antígenos de Helmintos/química , Antígenos de Helmintos/imunologia , Doenças do Gato/imunologia , Gatos , Dirofilaria/classificação , Dirofilariose/parasitologia , Dirofilariose/fisiopatologia , Doenças do Cão/imunologia , Cães , Proteínas de Helminto/química , Humanos , Immunoblotting , Pneumopatias Parasitárias/parasitologia , Proteoma , Especificidade da Espécie , Espectrometria de Massas por Ionização e Dessorção a Laser Assistida por Matriz , Tela Subcutânea/imunologiaRESUMO
Retnla (Resistin-like molecule alpha/FIZZ1) is induced during Th2 cytokine immune responses. However, the role of Retnla in Th2-type immunity is unknown. Here, using Retnla(-/-) mice and three distinct helminth models, we show that Retnla functions as a negative regulator of Th2 responses. Pulmonary granuloma formation induced by the eggs of the helminth parasite Schistosoma mansoni is dependent on IL-4 and IL-13 and associated with marked increases in Retnla expression. We found that both primary and secondary pulmonary granuloma formation were exacerbated in the absence of Retlna. The number of granuloma-associated eosinophils and serum IgE titers were also enhanced. Moreover, when chronically infected with S. mansoni cercariae, Retnla(-/-) mice displayed significant increases in granulomatous inflammation in the liver and the development of fibrosis and progression to hepatosplenic disease was markedly augmented. Finally, Retnla(-/-) mice infected with the gastrointestinal (GI) parasite Nippostrongylus brasiliensis had intensified lung pathology to migrating larvae, reduced fecundity, and accelerated expulsion of adult worms from the intestine, suggesting Th2 immunity was enhanced. When their immune responses were compared, helminth infected Retnla(-/-) mice developed stronger Th2 responses, which could be reversed by exogenous rRelmalpha treatment. Studies with several cytokine knockout mice showed that expression of Retnla was dependent on IL-4 and IL-13 and inhibited by IFN-gamma, while tissue localization and cell isolation experiments indicated that eosinophils and epithelial cells were the primary producers of Retnla in the liver and lung, respectively. Thus, the Th2-inducible gene Retnla suppresses resistance to GI nematode infection, pulmonary granulomatous inflammation, and fibrosis by negatively regulating Th2-dependent responses.
Assuntos
Peptídeos e Proteínas de Sinalização Intercelular/fisiologia , Esquistossomose mansoni/imunologia , Infecções por Strongylida/imunologia , Células Th2/imunologia , Animais , Eosinófilos/metabolismo , Granuloma/metabolismo , Imunidade Inata , Peptídeos e Proteínas de Sinalização Intercelular/uso terapêutico , Interferon gama/fisiologia , Interleucina-13/fisiologia , Interleucina-4/fisiologia , Pneumopatias Parasitárias/tratamento farmacológico , Pneumopatias Parasitárias/imunologia , Camundongos , Camundongos Endogâmicos C57BL , Nippostrongylus/imunologia , Fibrose Pulmonar/parasitologia , Schistosoma mansoni/imunologia , Esquistossomose mansoni/tratamento farmacológico , Infecções por Strongylida/tratamento farmacológicoRESUMO
Lung disease during active human visceral leishmaniasis is frequently reported. As such, studies have associated pulmonary symptoms to interstitial pneumonitis with a mononuclear infiltrate. However, the immune response in this condition has never been described before. The aim of this study was to determine the immunophenotypic pattern and cytokine profile of lung involvement (IPL) in human visceral leishmaniasis. Quantitative methods of analysis were performed using immunohistochemistry, and were compared with a control group of normal lung. Interstitial macrophages and cd8 cells were increased in IPL, and IL-4 as well as TNF-alpha displayed increased expression when compared to the control group. This inflammatory process with a Th2 pattern, as suggested by increased IL-4 and low IFN-gamma expression, is consistent with the immune response in other organs of visceral leishmaniasis. The microenvironment of the immune response in this condition is associated with lung disease in patients with interstitial pneumonitis related to visceral leishmaniasis, increasing the chance of bacterial infection.
Assuntos
Leishmaniose Visceral/imunologia , Doenças Pulmonares Intersticiais/imunologia , Pneumopatias Parasitárias/imunologia , Linfócitos T CD8-Positivos/imunologia , Proliferação de Células , Humanos , Imuno-Histoquímica , Interferon gama/biossíntese , Interleucina-4/biossíntese , Leishmaniose Visceral/complicações , Doenças Pulmonares Intersticiais/parasitologia , Pneumopatias Parasitárias/etiologia , Macrófagos/imunologia , Fator de Necrose Tumoral alfa/biossínteseRESUMO
This study describes the immunohistochemical and histochemical phenotypes of inflammatory cells in sheep lungs infected with lungworms. A total of 20 naturally infected sheep lungs were used. Protostrongylus spp., Muellerius capillaris, Neostrongylus linearis, and Cystocaulus ocreatus were the chief organisms determined from such lesions, which were of a chronic nature. All the lungs had many developmental stages of the parasites and a similar inflammatory response, which included numerous mast cells, eosinophils, T cells, B cells, dendritic cells, and macrophages. In the bronchial and interstitial tissues, the inflammatory cells were dominated by MHCII, CD1, CD4, CD5, CD14, CD21, IgM, and CD172a positive cells, whereas CD2 and WC1 positive cells were detected less. The data provided additional evidence that subsets of inflammatory cells were included within ovine lungs infected with lungworms; however, understanding the entire immune-response process and development of resistance to lungworms in sheep remain to be clearly elucidated.
Assuntos
Pneumopatias Parasitárias/veterinária , Ativação Linfocitária/imunologia , Doenças dos Ovinos/imunologia , Infecções por Strongylida/veterinária , Strongyloidea/imunologia , Matadouros , Animais , Estudos de Casos e Controles , Interações Hospedeiro-Parasita , Imuno-Histoquímica/veterinária , Estágios do Ciclo de Vida , Pneumopatias Parasitárias/imunologia , Pneumopatias Parasitárias/patologia , Ovinos , Doenças dos Ovinos/patologia , Infecções por Strongylida/imunologia , Infecções por Strongylida/patologiaAssuntos
Carcinoma de Células Escamosas/diagnóstico , Carcinoma de Células Escamosas/secundário , Pneumopatias Parasitárias/diagnóstico , Neoplasias Pulmonares/complicações , Neoplasias Pulmonares/diagnóstico , Estrongiloidíase/diagnóstico , Superinfecção/diagnóstico , Idoso , Protocolos de Quimioterapia Combinada Antineoplásica/efeitos adversos , Líquido da Lavagem Broncoalveolar/parasitologia , Carcinoma de Células Escamosas/complicações , Carcinoma de Células Escamosas/tratamento farmacológico , Cisplatino/administração & dosagem , Desoxicitidina/administração & dosagem , Desoxicitidina/análogos & derivados , Dexametasona/administração & dosagem , Diagnóstico Diferencial , Difosfonatos/administração & dosagem , Humanos , Imidazóis/administração & dosagem , Hospedeiro Imunocomprometido , Pneumopatias Parasitárias/imunologia , Neoplasias Pulmonares/tratamento farmacológico , Masculino , Estrongiloidíase/imunologia , Superinfecção/imunologia , Ácido Zoledrônico , GencitabinaRESUMO
AIMS: To determine whether, in view of the massive inflammatory cell infiltration and the rounded rather than wedge-shaped character of pulmonary lesions in dirofilariasis, the inflammatory response against the worm contributes to the coagulative necrosis, in addition to an ischaemic process. METHODS AND RESULTS: The histopathological features of 13 resected dirofilariasis cases with well-defined nodules ranged from 10 to 30 mm were analysed. On routine histology and using immunohistochemistry, the peripheral encapsulating wall showed mild to severe infiltration of eosinophils, lymphocytes and plasma cells and a histiocytic reaction in all cases, often with necrotic eosinophils seen within the necrosis (84.6%) and inflammatory changes in the adjacent lung (38.5%). The CD4+ lymphocyte count (80.8 +/- 33.4) was greater than that of CD8+ lymphocytes (24.5 +/- 16.9) in the central necrosis and vice versa in the wall. In the necrotic regions, disruption of the pulmonary artery (61.5%) and extravasation of the torn worm (23.1%) could be seen. CONCLUSIONS: These findings indicate that an allergic inflammatory reaction, mediated by eosinophils and lymphocytes, is involved in the formation of the dirofilarial necrotizing granuloma rather than infarction caused simply by embolism.
Assuntos
Dirofilariose/patologia , Hipersensibilidade/patologia , Hipersensibilidade/parasitologia , Pneumopatias Parasitárias/patologia , Pulmão/patologia , Pulmão/parasitologia , Adulto , Idoso , Animais , Dirofilaria/patogenicidade , Dirofilariose/complicações , Dirofilariose/imunologia , Eosinófilos/patologia , Feminino , Histiócitos/patologia , Humanos , Hipersensibilidade/imunologia , Pulmão/imunologia , Pneumopatias Parasitárias/complicações , Pneumopatias Parasitárias/imunologia , Linfócitos/patologia , Masculino , Pessoa de Meia-Idade , NecroseRESUMO
Interleukin (IL) 31Ralpha (glycoprotein 130-like monocyte receptor and glycoprotein 130-like receptor) heterodimerizes with oncostatin M receptor beta to bind IL-31, a cytokine expressed preferentially by CD4(+) T helper type 2 (Th2) cells. However, the functions of IL-31-IL-31R signaling in immune regulation remain unknown. Here, we identify a novel role for IL-31R in limiting type 2 inflammation in the lung. After intravenous injection of Schistosoma mansoni eggs, IL-31Ralpha(-/-) mice developed severe pulmonary inflammation, characterized by an increase in the area of granulomatous inflammation, increased numbers of resistin-like molecule alpha(+) cells, and enhanced collagen deposition compared to WT counterparts. In vitro, macrophages generated from IL-31Ralpha(-/-) mice promoted enhanced ovalbumin-specific CD4(+) T cell proliferation and purified naive CD4(+) T cells from IL-31Ralpha(-/-) mice exhibited enhanced proliferation and expression of Th2 cytokines, identifying a T cell- and macrophage-intrinsic regulatory function for IL-31R signaling. In contrast, the generation of CD4(+) T cell-mediated Th1 responses were normal in IL-31Ralpha(-/-) mice, suggesting that the regulatory role of IL-31R signaling is limited to type 2 responses. Together, these data implicate IL-31R signaling as a novel negative regulatory pathway that specifically limits type 2 inflammation.
Assuntos
Regulação para Baixo/imunologia , Mediadores da Inflamação/metabolismo , Interleucinas/metabolismo , Pneumopatias Parasitárias/imunologia , Pneumopatias Parasitárias/patologia , Receptores de Interleucina/metabolismo , Células Th2/imunologia , Células Th2/patologia , Doença Aguda , Animais , Células Cultivadas , Técnicas de Cocultura , Regulação para Baixo/genética , Mediadores da Inflamação/fisiologia , Pneumopatias Parasitárias/prevenção & controle , Camundongos , Camundongos Endogâmicos C57BL , Camundongos Knockout , Camundongos Transgênicos , Receptores de Interleucina/genética , Receptores de Interleucina/fisiologia , Esquistossomose mansoni/genética , Esquistossomose mansoni/imunologia , Esquistossomose mansoni/patologiaRESUMO
In the present study we investigated whether the pathological changes induced by Cryptosporidium in the lungs are mediated through the activation of COX-2, and whether the pathway employed for this activation involves NF-kB. 70 albino rats were submitted for this work. They were categorized into 3 groups: 30 immunocompetent (IC) rats infected with Cryptosporidium oocysts, 30 immunosuppressed (IS) rats infected with Cryptosporidium oocysts, and 10 IC, non-infected rats. Immunohistochemical expression of COX2 and NF-kB in lung tissues of the rats was examined. 43.3% of IC rats showed chronic pneumonia and fibrosis, 40% COX2 positivity, and 36.67% NF-kB positivity. 96.7% of IS rats showed chronic pneumonia and fibrosis, 56.7% non-caseating granuloma with Cryptosporidium oocysts, and 66.7% positivity for both COX2 and NF-kB. Density of inflammatory infiltration was statistically correlated with quickscore of both COX2 and NF-kB in both IC and IS groups. An association between quickscores of COX2 and NF-kB was found in our studied material. These data could demonstrate that Cryptosporidium infection induces upregulation of COX2 possibly through the NF-kB pathway, which suggests the events that contribute to the pathogenesis of Cryptosporidium. These findings could indicate potential therapeutic pharmacological target-mediating treatment of lesions caused by Cryptosporidium.
Assuntos
Criptosporidiose/imunologia , Criptosporidiose/metabolismo , Cryptosporidium , Ciclo-Oxigenase 2/fisiologia , Hospedeiro Imunocomprometido , Pneumopatias Parasitárias/imunologia , Pneumopatias Parasitárias/metabolismo , NF-kappa B/fisiologia , Animais , Criptosporidiose/patologia , Ciclo-Oxigenase 2/metabolismo , Dexametasona/efeitos adversos , Feminino , Fibrose/patologia , Granuloma/patologia , Imunocompetência , Imuno-Histoquímica , Pulmão/metabolismo , Pneumopatias Parasitárias/patologia , NF-kappa B/metabolismo , Pneumonia/patologia , Ratos , Regulação para CimaRESUMO
CCR4 is purported to be a Th type 2 (Th2) cell-biased receptor but its functional role is unclear. Recent studies suggest that chemokine receptor expression and function are more complex in vivo and raise doubts regarding restricted CCR4 expression by Th2 cells. To address these issues, we analyzed the role of CCR4 in highly polarized models of Th type 1 (Th1) and Th2 cell-mediated pulmonary granulomas, respectively, elicited by i.v. challenge of primed mice with either mycobacterial purified protein derivative or schistosomal egg Ag-coated beads. CCR4 agonists were expressed during both responses, correlating with a shift of CCR4+ CD4+ T cells from blood to lungs. CCL22 dominated in draining nodes during the Th1 response. Analysis of CD4+ effector T cells revealed CCR4 expression and CCR4-mediated chemotaxis by both IFN-gamma and IL-4 producers. Studies of CCR4 knockout (CCR4(-/-)) mice showed partial impairment of the local type-2 cytokine response and surprisingly strong impairment of the Th1 response with abrogated IFN-gamma production during secondary but not primary challenge. Adoptive transfer indicated CCR4(-/-)CD4+ Th1 cell function was defective but this could not be reconstituted with wild-type (CCR4(+/+)) CD4+ T cells indicating involvement of another CCR4+ population. Coculture of CCR4(+/+)CD4+ T cells and CCR4(-/-) dendritic cells revealed intact IL-2 but impaired IFN-gamma production, pointing to a role for CCR4+ dendritic cells in effector cell expression. Therefore, CCR4 is not Th2-restricted and was required for sustenance and expression of the Th1 effector/memory response to mycobacterial Ags.
Assuntos
Granuloma do Sistema Respiratório/imunologia , Memória Imunológica , Mycobacterium bovis/imunologia , Esquistossomose mansoni/imunologia , Células Th1/imunologia , Células Th2/imunologia , Fatores de Transcrição/fisiologia , Animais , Células Cultivadas , Granuloma do Sistema Respiratório/genética , Granuloma do Sistema Respiratório/microbiologia , Granuloma do Sistema Respiratório/parasitologia , Pneumopatias Parasitárias/genética , Pneumopatias Parasitárias/imunologia , Camundongos , Camundongos Endogâmicos C57BL , Camundongos Endogâmicos CBA , Camundongos Knockout , Receptores CCR4 , Receptores de Quimiocinas , Esquistossomose mansoni/genética , Esquistossomose mansoni/parasitologia , Células Th1/microbiologia , Células Th2/parasitologia , Fatores de Transcrição/deficiência , Fatores de Transcrição/genética , Tuberculose Pulmonar/genética , Tuberculose Pulmonar/imunologia , Tuberculose Pulmonar/microbiologiaRESUMO
In rodents and in humans, Strongyloides infection induces an immune response which is predominantly Th2 in nature. In an attempt to understand the role of the IL-4R/STAT6 signaling pathway, the pathway activated by the Th2 cytokines IL-4 and IL-13, in the induction of protection during Strongyloides venezuelensis infection, we have carried out experiments in mice lacking the IL-4Ralpha chain. Experiments were also carried out in STAT6 (STAT6(-/-)) and IL-12-deficient (IL-12(-/-)) mice for comparison. There was enhancement of IL-13 and abolition of IFN-gamma production in the small intestine of 7 day-infected IL-12(-/-) animals but worm elimination proceeded with very similar kinetics to those of wild-type mice. In IL-4Ralpha- or STAT6-deficient mice, there was a delay in parasite elimination and a large number of S. venezuelensis adult worms was still present in the small intestine 14 days after infection. Moreover, IgE production was completely abolished in IL-4Ralpha- or STAT6-deficient mice but tissue eosinophilia was normally induced by the parasite infection in deficient mice. Bone marrow transfer experiments showed that worm elimination occurred when a functional IL-4 receptor was present only in non-bone marrow-derived cells but not when IL-4R was only expressed in bone marrow cells. The induction of IL-4, but not IL-13, occurred independently of IL-4R. We believe these results are the first direct evidence that the mechanism responsible for the timely elimination of S. venezuelensis is dependent on the activation of IL-4R and STAT6. Moreover, a functional protective response is dependent on the expression of IL-4Ralpha on non-bone marrow-derived cells.
Assuntos
Enteropatias Parasitárias/imunologia , Pneumopatias Parasitárias/imunologia , Receptores de Interleucina-4/metabolismo , Strongyloides , Estrongiloidíase/imunologia , Animais , Biomarcadores/análise , Células da Medula Óssea/imunologia , Eosinofilia , Interações Hospedeiro-Parasita , Interferon gama/imunologia , Interleucina-10/imunologia , Interleucina-12/genética , Interleucina-12/metabolismo , Interleucina-4/biossíntese , Intestinos/imunologia , Camundongos , Camundongos Endogâmicos BALB C , Camundongos Endogâmicos C57BL , Camundongos Knockout , Contagem de Ovos de Parasitas , Receptores de Interleucina-4/genética , Fator de Transcrição STAT6/genética , Fator de Transcrição STAT6/metabolismo , Transdução de Sinais/fisiologia , Células Th2 , Fatores de Tempo , Fator de Necrose Tumoral alfa/imunologiaAssuntos
Febre/etiologia , Pneumopatias Parasitárias/complicações , Transplante de Pulmão/efeitos adversos , Pneumonia/etiologia , Toxoplasma/isolamento & purificação , Toxoplasmose/complicações , Adulto , Animais , Biópsia , Feminino , Febre/diagnóstico , Humanos , Hospedeiro Imunocomprometido , Pulmão/parasitologia , Pulmão/patologia , Pneumopatias Parasitárias/diagnóstico , Pneumopatias Parasitárias/imunologia , Transplante de Pulmão/imunologia , Pneumonia/imunologia , Pneumonia/patologia , Testes Sorológicos , Toxoplasma/fisiologia , Toxoplasmose/imunologia , Toxoplasmose/patologiaRESUMO
Pulmonary Cryptococcus neoformans infection of C57BL/6 mice is an established model of a chronic pulmonary fungal infection accompanied by an "allergic" response (T2) to the infection, i.e., a model of an allergic bronchopulmonary mycosis. Our objective was to determine whether IFN-gamma plays a role in regulating the pulmonary T2 immune response in C. neoformans-infected C57BL/6 mice. Long-term pulmonary fungistasis was lost in IFN-gamma knockout (KO) mice, resulting in an increased pulmonary burden of fungi at wk 3. IFN-gamma was required for the early influx of leukocytes into the lungs but was not required later in the infection. By wk 3, eosinophil and macrophage numbers were elevated in the absence of IFN-gamma. The inducible NO synthase to arginase ratio was lower in the lungs of IFN-gamma KO mice and the macrophages had increased numbers of intracellular cryptococci and YM1 crystals, indicative of alternatively activated macrophages in these mice. There was evidence of pulmonary fibrosis in both wild-type and IFN-gamma KO mice by 5 wk postinfection. IFN-gamma production was not required for the development of T2 cytokine (IL-4, IL-5, IL-13) producing cells in the lungs and lung-associated lymph nodes or induction of an IgE response. At a number of time points, T2 cytokine production was enhanced in IFN-gamma KO mice. Thus, in the absence of IFN-gamma, C57BL/6 mice develop an augmented allergic response to C. neoformans, including enhanced generation of alternatively activated macrophages, which is accompanied by a switch from a chronic to a progressive pulmonary cryptococcal infection.