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1.
Braz. oral res. (Online) ; 33: e093, 2019. tab
Article in English | LILACS | ID: biblio-1039302

ABSTRACT

Abstract Cytokines and chemokines have a fundamental role in the maintenance of inflammation and bone response, which culminate in the development of chronic periapical lesions. Regulatory (Treg) and Th17 cytokines play a key role in regulating the immune response involved in this process. The aim of this study was to investigate the role of Treg and Th17 cells in chronic inflammatory periapical disease, by comparing the expression of the immunoregulatory mediators TGF-β, IL-10, CCL4, and the proinflammatory IL-17 and CCL20 in the periapical tissue of teeth with pulp necrosis, with and without associated chronic lesions. Eighty-six periapical tissue samples were obtained from human teeth. The samples were divided into three groups: pulp necrosis with a periapical lesion (n=26); pulp necrosis without a periapical lesion (n=30), and control (n=30). All samples were submitted to histopathological analysis and cytokine and chemokine measurement through ELISA. Statistical analyses were done with Kruskal-Wallis and Mann-Whitney tests and Spearman correlation. The group with pulp necrosis and a periapical lesion showed a higher expression of CCL4 and TGF-β in comparison with pulp necrosis without a lesion. CCL20 was higher in the group with a periapical lesion when compared to the control. In all groups there was a weak positive correlation between IL-17/CCL20, IL-10/CCL4, and IL-17/TGF-β. Both types of cytokines, pro-inflammatory and immunoregulatory, occur simultaneously in periapical tissue. However, a rise in immunosuppressive cytokines and chemokines (CCL4 and TGF-β) in periapical lesions suggests a role of these cytokines in stable periapical disease.


Subject(s)
Humans , Adult , Young Adult , Periapical Periodontitis/pathology , Transforming Growth Factor beta/analysis , Interleukins/analysis , T-Lymphocytes, Regulatory/immunology , Chemokines, CC/analysis , Th17 Cells/immunology , Periapical Periodontitis/immunology , Reference Values , Case-Control Studies , Chronic Disease , Transforming Growth Factor beta/immunology , Interleukins/immunology , Statistics, Nonparametric , Dental Pulp Necrosis/immunology , Dental Pulp Necrosis/pathology , Chemokines, CC/immunology , Middle Aged
2.
Mem. Inst. Oswaldo Cruz ; 110(8): 945-955, Dec. 2015. graf
Article in English | LILACS | ID: lil-769829

ABSTRACT

Asymptomatic Plasmodium infection carriers represent a major threat to malaria control worldwide as they are silent natural reservoirs and do not seek medical care. There are no standard criteria for asymptomaticPlasmodium infection; therefore, its diagnosis relies on the presence of the parasite during a specific period of symptomless infection. The antiparasitic immune response can result in reducedPlasmodium sp. load with control of disease manifestations, which leads to asymptomatic infection. Both the innate and adaptive immune responses seem to play major roles in asymptomatic Plasmodiuminfection; T regulatory cell activity (through the production of interleukin-10 and transforming growth factor-β) and B-cells (with a broad antibody response) both play prominent roles. Furthermore, molecules involved in the haem detoxification pathway (such as haptoglobin and haeme oxygenase-1) and iron metabolism (ferritin and activated c-Jun N-terminal kinase) have emerged in recent years as potential biomarkers and thus are helping to unravel the immune response underlying asymptomatic Plasmodium infection. The acquisition of large data sets and the use of robust statistical tools, including network analysis, associated with well-designed malaria studies will likely help elucidate the immune mechanisms responsible for asymptomatic infection.


Subject(s)
Humans , Asymptomatic Infections , Antigens, Protozoan/immunology , Carrier State/immunology , Malaria, Falciparum/immunology , Malaria, Vivax/immunology , Plasmodium/immunology , Adaptive Immunity/physiology , Biomarkers , Carrier State/parasitology , Disease Reservoirs/parasitology , Ferritins/immunology , Haptoglobins/immunology , Heme Oxygenase-1/immunology , Immunity, Innate/physiology , /immunology , JNK Mitogen-Activated Protein Kinases/immunology , Malaria, Falciparum/prevention & control , Malaria, Vivax/prevention & control , Parasitemia/immunology , Plasmodium/isolation & purification , Transforming Growth Factor beta/immunology
3.
Cad. saúde pública ; 31(3): 633-646, 03/2015. tab
Article in English | LILACS | ID: lil-744824

ABSTRACT

Agricultural workers represent a population that is highly vulnerable to the toxic effects of pesticide exposure. This cross sectional study aimed to describe the health conditions of terrestrial pesticide applicators in Córdoba Province, Argentina, their work practices and socio-demographic characteristics, by means of a standardized self-administered questionnaire (n = 880). A descriptive analysis reported a high prevalence of occasional or frequent symptoms: 47.4% had symptoms of irritation, 35.5% fatigue, 40.4% headache and 27.6% nervousness or depression. Using logistic regression models, risk and protective factors were found for symptoms of irritation, medical consultation and hospitalization. Among the occupational exposure variables, marital status, length of time in the job, low level of protection with regard to the use of personal protective equipment, combined use of different pesticides and the application of the insecticide endosulfan, were associated with a higher frequency of reported symptoms and higher consultation rates and hospitalization.


Los trabajadores agrícolas son una población altamente vulnerable a los efectos tóxicos de la exposición a plaguicidas. Con el objetivo de describir las condiciones de salud de agroaplicadores terrestres de plaguicidas de la Provincia de Córdoba, Argentina, sus prácticas laborales y características sociodemográficas, se realizó un estudio transversal, mediante cuestionario (n = 880). Un análisis descriptivo reportó alta prevalencia de sintomatología ocasional o frecuente: 47,4% síntomas irritativos, 35,5% cansancio, 40,4% cefalea y 27,6% ansiedad o depresión. Mediante modelos logísticos se detectaron factores protectores y de riesgo que explican la presencia de síntomas irritativos, la consulta médica y la hospitalización. El estado civil, la antigüedad en la tarea, el nivel de protección considerando uso de equipo de protección personal, la exposición múltiple a plaguicidas y la aplicación del insecticida endosulfán, se asociaron a mayor frecuencia de reporte de síntomas, consultas médicas y hospitalizaciones por causas relacionadas con la exposición a plaguicidas.


Os trabalhadores agrícolas são uma população altamente vulnerável aos efeitos tóxicos da exposição a pesticidas. Este estudo transversal teve o objetivo de descrever as condições de saúde de aplicadores terrestres de pesticidas da Província de Córdoba, Argentina, suas práticas de trabalho e características sociodemográficas, por meio de um questionário padronizado autoadministrado (n = 880). A análise descritiva relatou alta prevalência de sintomas ocasionais ou frequentes: 47,4% sintomas irritativos, 35,5% fadiga, 40,4% dor de cabeça e 27,6% ansiedade ou depressão. Mediante modelos logísticos foram detectados os fatores protetores e do risco que explicam a presença de sintomas irritativos, consulta médica e hospitalização. O estado civil, anos de trabalho, o nível de proteção considerando o uso de equipamentos de proteção individual, a exposição a vários pesticidas e aplicação do inseticida endosulfan, foram associados com maior frequência de sintomas, consultas médicas e hospitalização por causas relacionadas à exposição ao agrotóxico.


Subject(s)
Animals , Cats , Humans , Mice , Asthma , Epitopes/immunology , Immune Tolerance/immunology , /immunology , Peptides , Allergens/immunology , Asthma/immunology , Asthma/therapy , Bronchial Hyperreactivity/immunology , Desensitization, Immunologic , Disease Models, Animal , Double-Blind Method , Forkhead Transcription Factors/immunology , Genes, MHC Class II , Glycoproteins/genetics , Glycoproteins/immunology , HLA-DR1 Antigen/immunology , Lung/cytology , Lung/immunology , Lung/pathology , Mice, Transgenic , Placebos , Peptides/immunology , Peptides/therapeutic use , Randomized Controlled Trials as Topic , /immunology , /immunology , Transforming Growth Factor beta/immunology
4.
Article in English | IMSEAR | ID: sea-144792

ABSTRACT

Background & objectives: Replication of influenza A virus in the respiratory tract leads to cell damage and liberation of cytokines and chemokines. The in vivo cytokine induction and modulation by recombinant transforming growth factor- β1 (rTGF-β1) has not been studied. Therefore, in the present study the effect of rTGF-β1, a potent immunomodulatory cytokine which has anti-inflammatory properties and downregulates the release of inflammatory molecules, against influenza-virus infection in the airway of mice was investigated. Methods: rTGF-β1 was administered intravenously to mice with concomitant intranasal infection of influenza A/Udorn/317/72 (H3N2) virus, and the survival rate, virus titre, histopathological changes and levels of factors regulating inflammation in the airway fluid were analysed. Result: The immune response to influenza A virus was characterized by an influx of both macrophages and lymphocytes into the lungs of the infected host. rTGF-β1 significantly suppressed virus multiplication and improved the survival rate of mice. rTGF-β1 downregulated infiltration of neutrophils and the release of inflammatory molecules, such as interferon-gamma (IFN-γ), interleukin-1 β (IL-1β) and stimulated release of IL-10 that potentiates anti-inflammatory response into airway. Interpretation & conclusions: A generalized pulmonary inflammation does not contribute to viral clearance but represents an immunological background within which antiviral immunity operates. Treatment with rTGF-β1 reduced macrophage count and neutrophils influx in lungs of infected mice.


Subject(s)
Immune System Phenomena , Influenza A virus/growth & development , Influenza A virus/immunology , Influenza A virus/pathogenicity , Respiratory Tract Infections , Transforming Growth Factor beta/genetics , Transforming Growth Factor beta/immunology
5.
Braz. j. med. biol. res ; 44(2): 84-90, Feb. 2011. ilus
Article in English | LILACS | ID: lil-573659

ABSTRACT

Infection with the protozoan parasite Trypanosoma cruzi leads to Chagas disease, which affects millions of people in Latin America. Infection with T. cruzi cannot be eliminated by the immune system. A better understanding of immune evasion mechanisms is required in order to develop more effective vaccines. During the acute phase, parasites replicate extensively and release immunomodulatory molecules that delay parasite-specific responses mediated by T cells. This immune evasion allows the parasite to spread in the host. In the chronic phase, parasite evasion relies on its replication strategy of hijacking the TGF-β signaling pathway involved in inflammation and tissue regeneration. In this article, the mechanisms of immune evasion described for T. cruzi are reviewed.


Subject(s)
Humans , Chagas Disease/immunology , Immune Evasion/immunology , T-Lymphocytes/immunology , Transforming Growth Factor beta/immunology , Trypanosoma cruzi/immunology , Acute Disease , Antigens, Protozoan/immunology , Chronic Disease , Chagas Disease/parasitology , Host-Parasite Interactions/immunology
6.
Journal of Veterinary Science ; : 299-301, 2011.
Article in English | WPRIM | ID: wpr-108421

ABSTRACT

We analyzed the expression level and cellular localization of pro- and anti-inflammatory cytokines and histopathologically characterized canine traumatic brain injury (TBI). Canine TBI brains revealed subarachnoid and cerebral cortical hemorrhage, neutrophilic infiltration, neuronal necrosis, astrocytosis, and vasogenic edema. Immunohistochemical evaluations suggested that both pro-inflammatory cytokines [interleukin (IL)-1beta, IL-6, and tumor necrosis factor-alpha] and anti-inflammatory cytokines [IL-10 and transforming growth factor-beta (TGF-beta)] were highly expressed in neurons and neutrophils. In particular, the highest magnitude of expression was identified for IL-1beta and TGF-beta. This data helps describe the pathologic characteristics of canine TBI, and may help in the design of potential therapeutic approaches to control secondary damage by inflammatory cytokines.


Subject(s)
Animals , Dogs , Humans , Brain/immunology , Brain Injuries/immunology , Interleukin-10/immunology , Interleukin-1beta/immunology , Interleukin-6/immunology , Transforming Growth Factor beta/immunology , Tumor Necrosis Factor-alpha/immunology
7.
Mem. Inst. Oswaldo Cruz ; 104(2): 273-280, Mar. 2009. tab, ilus
Article in English | LILACS | ID: lil-533517

ABSTRACT

Toxoplasmosis and ascaridiasis evoke polar Th-1 and Th-2 host immune responses, respectively. A study to investigate the specific cytokine profile production by in vitro cultures of peripheral blood mononuclear cells from individuals living under precarious sanitary conditions in a highly endemic area for the parasites Toxoplasma gondii and Ascaris lumbricoides was conducted. High levels of both IFN-³ (Th-1) and IL-13 (Th-2) were observed in groups of co-infected individuals presenting toxoplasmic ocular lesions. Significantly lower IL-10 and TGF-² levels were produced by co-infected individuals in comparison with groups of individuals not infected with A. lumbricoides and either positive or negative for T. gondii living under good sanitary conditions (control groups). The possible influence of co-parasitism on the clinical presentation of ocular toxoplasmosis is discussed.


Subject(s)
Adult , Animals , Female , Humans , Male , Ascariasis/immunology , Ascaris lumbricoides/immunology , Cytokines/immunology , Leukocytes, Mononuclear/parasitology , Toxoplasma/immunology , Toxoplasmosis, Ocular/immunology , Ascariasis/complications , Cytokines/blood , Enzyme-Linked Immunosorbent Assay , Flow Cytometry , Interferon-gamma/blood , Interferon-gamma/immunology , /blood , /immunology , /blood , /immunology , Leukocytes, Mononuclear/immunology , Toxoplasmosis, Ocular/complications , Transforming Growth Factor beta/blood , Transforming Growth Factor beta/immunology
9.
Uberlândia; s.n; 1995. 83 p. ilus.
Thesis in Portuguese | LILACS | ID: lil-165339

ABSTRACT

Foram realizados estudos imunohistoquímicos para avaliar a presença e a distribuiçäo do polipeptídeo TGF-ß1, citocina com atividade supressora sobre macrófagos, em biópsias de pele de 41 pacientes com diferentes formas clínicas de hanseníase. Neste estudo foi utilizado um anticorpo policlonal anti-TGF-ß1 e o método Avidina-Biotina-peroxidase (complexo-ABC). Os resultados demonstram que as lesöes das formas lepromatosas e boderline-lepromatosa apresentam intensa marcaçäo para o TGF-ß1 nas células do infiltrado dérmico. A marcaçäo das células dos granulomas dos casos boderline-boderline foi de intensidade moderada, enquanto no pólo tuberculóide e boderline-tuberculóide näo houve imunorreaçäo detectável nas células dos granulomas. Considerando que no pólo lepromatoso da hanseníase o M.leprae multiplica-se no citoplasma dos macrófagos e as lesöes säo difusas e constituídas de células com indiferenciaçäo morfológica e inatividade funcional, acreditamos que essas alteraçöes poderiam ser explicadas, pelo menos em parte, pela presença de TGF-ß1 no infiltrado dérmico, contribuindo para a näo formaçäo de lesäo granulomatosa e impedindo a atividade microbicida dos macrófagos. Sua produçäo poderia ser induzida pela própria presença do bacilo e seus constituintes, determinando um mecanismo de evasäo do parasita na forma boderline-lepromatosa e lepromatosa. Da mesma forma, a ausência de TGF-ß1 na hanseníase tuberculóide e boderline-tuberculóide, poderia explicar a exacerbaçäo da resposta imunocelular específica contra o M. leprae, determinando intensa diferenciaçäo das células macrofágicas com formaçäo de granulomas epitelióides das células macrofágicas com formaçäo de granulomas epitelióides bem definidos, capazes de eliminar a grande maioria dos bacilos


Subject(s)
Humans , Skin/pathology , Transforming Growth Factor beta/immunology , Leprosy/immunology , Macrophages/immunology , Biopsy , Immunohistochemistry , Sensitivity and Specificity , Leprosy/pathology
10.
Braz. j. med. biol. res ; 27(1): 1-9, jan. 1994.
Article in English | LILACS | ID: lil-136486

ABSTRACT

1. The course of infection with the protozoan parasite Leishmania is determined in part by its early replication in macrophages, the exclusive host cells for these organisms. Resistance to and recovery from leishmanial infection is related to cell-mediated immune responses in all forms of human and murine leishmaniasis. 2. Factors contributing to the early inhibition or proliferation of Leishmania are poorly understood, but cytokines such as IFNÔ, IL-10 or transforming growth factor ß (TGF-ß) are known to influence the replication of Leishmania in macrophages. 3. TGF-ß is a multipotential cytokine with diverse effects on cells of the immune system, including down-regulation of certain macrophage functions. Infection of murine or human macrophages by Leishmania induces the production of active TGF-ß. Recombinant TGF-ß added to murine or human macrophage cultures leads to increased intracellular replication of Leishmania. Exogenous TGF-ß administered in vivo promotes enhancement of infection, whereas its neutralization by monoclonal antibodies decreases the level of in vitro infection, and protects susceptible mice. 4. Susceptible animals treated with anti-TGF-ß monoclonal antibodies change their immune response, not increasing the expression of IL-4 while increasing the expression of IFNÔ mRNA in their draining lymph nodes. Resistant animals treated with TGF-ß also change their pattern of immune response as indicated by an increase of the important Th2 cytokine IL-10 mRNA in the draining lymph node. 5. TGF-ß has profound effects on the host response to Leishmania in both mouse and man, and probably is an important parasite escape mechanism


Subject(s)
Humans , Animals , Mice , Leishmaniasis, Cutaneous/metabolism , Transforming Growth Factor beta/metabolism , Antibodies, Monoclonal , Wound Healing , Cytokines/immunology , Cytokines/pharmacology , Leishmania/drug effects , Leishmania/growth & development , Leishmaniasis, Cutaneous/immunology , Macrophages/immunology , Transforming Growth Factor beta/immunology , Transforming Growth Factor beta/pharmacology
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