43 resultados para îlot de Langerhans
em Scielo Saúde Pública - SP
Resumo:
Células de Langerhans (CL) são um tipo de células dendríticas que têm funções que envolvem apresentação de antígeno e a estimulação de resposta T dependente. Elas representam aproximadamente 4% das células do epitélio laríngeo. OBJETIVO: Identificar a presença de CL no epitélio das pregas vocais, comparar suas subpopulações, bem com comparar a capacidade de quatro marcadores imunoistoquímicos. FORMA DE ESTUDO: Experimental. CASUÍSTICA E MÉTODO: Seis cadáveres, 3 homens e 3 mulheres foram estudados. Foram analisadas amostras de pele e das pregas vocais coradas e imunomarcadas para vimentina, proteína S-100, CD-68 e fascina. Após análise histológica, foi realizado o teste t de Student e análise de variância no estudo estatístico. RESULTADOS E CONCLUSÕES: Foi possível identificar a presença de CL no epitélio das pregas vocais de humanos não fumantes de ambos os sexos. A fascina, a vimentina o CD-68 mostraram-se bons marcadores das CL, enquanto a proteína S-100 teve estatisticamente menor poder de marcação tanto na prega vocal (p=0,01) como na pele (p=0,02). Foi possível identificar três diferentes subpopulações de CL presentes tanto na prega vocal como na pele destes indivíduos, contudo apenas na pele observarmos maior quantidade estatisticamente significante na camada basal do epitélio.
Resumo:
This work analyzed the histopathology and epidermal Langerhans cells (LC) of Montenegro skin test (MST) in patients with American tegumentary leishmaniasis (ATL) in order to in situ characterize and compare the immunological reaction of the two major clinical forms of ATL, localized cutaneous leishmaniasis (LCL) and mucocutaneous leishmaniasis (MCL). MST histopathology of both LCL and MCL showed superficial and deep perivascular inflammatory infiltrate composed mainly of lymphocytes and histiocytes. Epidermal LC population was higher in MST biopsies taken from LCL patients when compared to MCL group, at 48 and 72 hours after antigen inoculation. Increased number of epidermal LC displayed in MST biopsies of LCL patients represents specific cellular immunity against parasites. The decrease of LC in MST biopsies of MCL patients does not necessarily indicate a worse specific cellular immunity in this clinical form of leishmaniasis.
Resumo:
OBJETIVO: Caracterizar, por meio da tomografia computadorizada de alta resolução, as principais alterações pulmonares da histiocitose de células de Langerhans. MATERIAIS E MÉTODOS: Foram avaliadas, retrospectivamente, as tomografias computadorizadas de alta resolução de oito pacientes com diagnóstico comprovado da doença a partir de biópsia pulmonar a céu aberto, biópsia transbrônquica, estudos de imuno-histoquímica e/ou lesões extrapulmonares associadas. RESULTADOS: Pequenas lesões císticas, arredondadas e de paredes finas foram observadas em todos os pacientes. Nódulos, com distribuição predominantemente periférica no parênquima pulmonar, estavam presentes em 75% dos exames estudados. As lesões apresentaram distribuição difusa, com predomínio nos terços superior e médio dos pulmões em todos os casos, mas acometimento dos recessos costofrênicos foi observado em 25% dos pacientes. CONCLUSÃO: A comparação das tomografias computadorizadas de alta resolução com radiografias de tórax mostrou que cistos de paredes finas e pequenos nódulos não podem ser avaliados satisfatoriamente por radiografias convencionais. A tomografia computadorizada de alta resolução, por sua capacidade de detectar e caracterizar cistos e nódulos pulmonares, permite o diagnóstico de histiocitose de células de Langerhans pulmonar com alta probabilidade.
Resumo:
A histiocitose de células de Langerhans é uma doença rara caracterizada proliferação de células de Langerhans. Neste artigo descrevemos um caso de histiocitose de células de Langerhans em um paciente de 63 anos, com uma lesão expansiva periorbital como primeiro sintoma e cuja tomografia computadorizada revelou acometimento pulmonar característico da doença. A condução do caso, os achados radiológicos e os resultados são apresentados.
Resumo:
OBJETIVOS: estudar a relação dos fatores biocomportamentais (idade, menarca, número de gestações e precocidade sexual) com alterações das células de Langerhans em mulheres com captura híbrida negativa para HPV. MÉTODOS: foram estudadas 30 mulheres com alterações citológicas ou lesão no colo uterino que foram submetidas aos exames de colposcopia, biópsia dirigida e histopatologia. As células de Langerhans foram identificadas pela reação de imuno-histoquímica com uso de antígenos anti-S100. As células visualizadas em marron foram contadas utilizando o software Cytoviewer. Para análise estatística utilizou-se o teste não-paramétrico de soma das ordens de Wilcoxon. RESULTADOS: o número de células de Langerhans em mulheres com menarca após os 13 anos apresentou diferença significante (173,34 cels/mm²) comparado ao grupo com menarca antes de 12 anos (271,41 cel/mm²). A precocidade sexual associou-se ao baixo número de células de Langerhans com 127,15 cels/mm² e 250,14 cels/mm², respectivamente, para início da atividade até 17 anos e após 17 anos (p=0,03). Cauterizações anteriores do colo uterino foram relacionadas com o menor número de células de Langerhans, no epitélio com a média 120,30 cels/mm² e 236,06 cels/mm² para aquelas que nunca haviam sido submetidas a esse procedimento (p=0,05). Outros fatores como idade da paciente e número de gestações não foram relacionadas a alteração na densidade de células de Langerhans. CONCLUSÕES: o presente estudo observou associação de fatores biocomportamentais sobre o número das células de Langerhans.
Resumo:
OBJETIVO: avaliar a ação de drogas anti-retrovirais sobre o metabolismo glicídico e sobre o pâncreas de ratas Wistar prenhes. MÉTODOS: estudo com ratas prenhes adultas da raça Wistar, pesando entre 200-230 g. Foram testadas a azidotimidina, lamivudina e o nelfinavir, em doses 10 vezes superiores à dose utilizada em gestantes. Foram avaliados sete grupos, contendo 10 ratas por grupo, incluindo o controle. O sacrifício foi realizado no 21º dia de prenhez. Procederam-se a dosagens de glicemia, insulina, glucagon, ácidos graxos livres (AGL) e glicogênio hepático. Para avaliação de lesão pancreática, optou-se pela contagem direta do número de células produtoras de insulina e glucagon marcadas por imuno-histoquímica. Os dados foram analisados pelo teste t de Student, sendo comparados os animais dos grupos controle e tratados. RESULTADOS: após 21 dias de prenhez houve elevação dos níveis séricos de glucagon (grupo controle: 88,2 pg/ml; grupos tratados: 99,7 a 120,7 pg/ml ) e redução dos níveis de insulina (grupo controle: 6,2 miUI/ml; grupos tratados: 2,1 a 2,7 miUI/ml) em todos os grupos tratados com anti-retrovirais. Não houve diferenças significativas nos valores plasmáticos de glicemia, AGL e valores de glicogênio hepático ao final dos 21 dias de prenhez. Não houve diferença quanto ao número de células pancreáticas produtoras de insulina e glucagon entre os grupos tratados e o grupo controle ao final dos 21 dias de prenhez. CONCLUSÕES: os fármacos anti-retrovirais utilizados durante a prenhez de ratas não infectadas alteram o metabolismo glicídico materno em grau leve causando queda de insulina e elevação do glucagon, com índices glicêmicos normais e número de células pancreáticas inalterado.
Resumo:
OBJETIVO: estudar a influência do uso de anticoncepcionais orais (AO) sobre o número de células de Langerhans em mulheres sem infecção cervical por papilomavírus humano (HPV). MÉTODOS: foram incluídas trinta mulheres com alterações citológicas e biópsia dirigida pela colposcopia com amostras de colo uterino sem sinais de infecção por HPV. A ausência de DNA de HPV foi confirmada pela captura híbrida. As células de Langerhans foram identificadas pela reação de imuno-histoquímica com uso de antígenos anti-S100. As células visualizadas em microscopia de luz foram contadas utilizando o software Cytoviewer. Para análise estatística utilizou-se o teste não paramétrico de soma das ordens de Wilcoxon. RESULTADOS: a média do número de células de Langerhans em mulheres usuárias de AO foi de 320,7/mm² e em não usuárias 190,7/mm², não sendo esta diferença significante. Na camada intermediária do epitélio cervical observou-se tendência ao aumento dessas células, com as médias 192,1/mm² para usuárias e 93,4/mm² para não usuárias de AO (p=0,05). CONCLUSÕES: no presente estudo não se observou diferença significativa no total de células de Langerhans entre as usuárias e não usuárias de AO, porém, na camada intermediária do epitélio observou-se tendência ao aumento no número dessas células entre as usuárias de AO. Este resultado sugere que os AO podem induzir alterações no número das células de Langerhans, considerando porém o limitado número de casos, este achado não pode ser confirmado.
Resumo:
Nitric oxide synthase activity was measured in Langerhans islets isolated from control and streptozotocin diabetic rats. The activity of the enzyme was linear up to 150 µg of protein from control rats and was optimal at 0.1 µM calcium, when it was measured after 45 min of incubation at 37oC in the presence of 200 µM arginine. Specific activity of the enzyme was 25 x 10-4 nmol [3H]citrulline 45 min-1 mg protein-1. Streptozotocin diabetic rats exhibited less enzyme activity both in total pancreas homogenate and in isolated Langerhans islets when compared to control animals. Nitric oxide synthase activity measured in control and diabetic rats 15 days after the last streptozotocin injection in the second group of animals corresponded only to a constitutive enzyme since it was not inhibited by aminoguanidine in any of the mentioned groups. Hyperglycemia in diabetic rats may be the consequence of impaired insulin release caused at least in part by reduced positive modulation mediated by constitutive nitric oxide synthase activity, which was dramatically reduced in islets severely damaged after streptozotocin treatment.
Resumo:
Symptomatic involvement of the gastrointestinal (GI) tract as a prominent symptom in Langerhans' cell histiocytosis (LCH) is uncommon, occurring in less than 1 to 5% of all cases, even when the disease is in its disseminated form. Up to now, there have been reports of 18 cases of LCH with GI manifestations, including our 2 cases, with diarrhea (77.7%), protein-losing enteropathy (33.3%) and bloody stool being the most frequent findings. The authors present two patients with severe diarrhea and refractory hypoalbuminemia, and with the protein-losing enteropathy documented by Cr51-labeled albumin studies. A review of the literature indicated that the presence of GI symptoms is often associated with systemic disease as well as with poor prognosis, mainly under 2 years of age. Radioisotopes are useful for documenting protein loss in several diseases with high specificity and sensitivity, and their utilization in the cases reviewed here permitted diagnoses in 6 children, as well as improved therapeutic management.
Resumo:
Dysregulation of the skin immune system (SIS) could explain the high prevalence of skin disorders in HIV+ individuals. The present study was carried out to determine whether alterations in the cell population of SIS and epidermal immunoactivation occur in the normal skin of HIV+ individuals. Forty-five biopsies were taken from the normal upper arm skin of 45 HIV+ patients and of 15 healthy controls. HIV+ individuals were divided into three categories according to their CD4 cell blood count (<200, 200-499 and ³500/µl). Hematoxylin-eosin was used to stain tissue sections for morphological analysis and immunohistochemistry was used for the evaluation of the frequency of macrophages, Langerhans cells, and CD lymphocyte subsets. In addition, semiquantitative analysis of LFA-1, ICAM-1 and HLA-DR was determined in epidermal cells. Macrophages, Langerhans cells, and CD lymphocyte subsets did not differ significantly between any of the patient categories and the control group. When all HIV+ individuals were compared as a group to the control group, a significant increase in dermal CD8+ T lymphocytes (P < 0.01) and lower CD4-CD8 ratios (P < 0.01) were observed in the HIV+ individuals. Epidermal ICAM-1 and HLA-DR expression was negative in both HIV+ and normal skin biopsies. No evidence of a depletion of the SIS population or of epidermal immunoactivation in normal skin from HIV+ individuals was demonstrable, suggesting that alterations in the central immune system are not necessarily reflected in the SIS of HIV-infected patients.
Resumo:
OBJECTIVE: To compare the immunogenicity of three yellow fever vaccines from WHO-17D and Brazilian 17DD substrains (different seed-lots). METHODS: An equivalence trial was carried out involving 1,087 adults in Rio de Janeiro. Vaccines produced by Bio-Manguinhos, Fiocruz (Rio de Janeiro, Brazil) were administered following standardized procedures adapted to allow blocked randomized allocation of participants to coded vaccine types (double-blind). Neutralizing yellow fever antibody titters were compared in pre- and post-immunization serum samples. Equivalence was defined as a difference of no more than five percentage points in seroconversion rates, and ratio between Geometric Mean Titters (GMT) higher than 0.67. RESULTS: Seroconversion rates were 98% or higher among subjects previously seronegative, and 90% or more of the total cohort of vaccinees, including those previously seropositive. Differences in seroconversion ranged from -0.05% to -3.02%. The intensity of the immune response was also very similar across vaccines: 14.5 to 18.6 IU/mL. GMT ratios ranged from 0.78 to 0.93. Taking the placebo group into account, the vaccines explained 93% of seroconversion. Viremia was detected in 2.7% of vaccinated subjects from Day 3 to Day 7. CONCLUSIONS: The equivalent immunogenicity of yellow fever vaccines from the 17D and 17DD substrains was demonstrated for the first time in placebo-controlled double-blind randomized trial. The study completed the clinical validation process of a new vaccine seed-lot, provided evidence for use of alternative attenuated virus substrains in vaccine production for a major manufacturer, and for the utilization of the 17DD vaccine in other countries.
Resumo:
ABSTRACT OBJECTIVE To examine whether the level of complexity of the services structure and sociodemographic and clinical characteristics of patients in hemodialysis are associated with the prevalence of poor health self-assessment. METHODS In this cross-sectional study, we evaluated 1,621 patients with chronic terminal kidney disease on hemodialysis accompanied in 81 dialysis services in the Brazilian Unified Health System in 2007. Sampling was performed by conglomerate in two stages and a structured questionnaire was applied to participants. Multilevel multiple logistic regression was used for data analysis. RESULTS The prevalence of poor health self-assessment was of 54.5%, and in multivariable analysis it was associated with the following variables: increasing age (OR = 1.02; 95%CI 1.01–1.02), separated or divorced marital status (OR = 0.62; 95%CI 0.34–0.88), having 12 years or more of study (OR = 0.51; 95%CI 0.37–0.71), spending more than 60 minutes in commuting between home and the dialysis service (OR = 1.80; 95%CI 1.29–2.51), having three or more self-referred diseases (OR = 2.20; 95%CI 1.33–3.62), and reporting some (OR = 2.17; 95%CI 1.66–2.84) or a lot of (OR = 2.74; 95%CI 2.04–3.68) trouble falling asleep. Individuals in treatment in dialysis services with the highest level of complexity in the structure presented less chance of performing a self-assessment of their health as bad (OR = 0.59; 95%CI 0.42–0.84). CONCLUSIONS We showed poor health self-assessment is associated with age, years of formal education, marital status, home commuting time to the dialysis service, number of self-referred diseases, report of trouble sleeping, and also with the level of complexity of the structure of health services. Acknowledging these factors can contribute to the development of strategies to improve the health of patients in hemodialysis in the Brazilian Unified Health System.
Resumo:
Calf serum and fetal bovine serum present great variability as to its growth promoting efficiency (GPE). As supplement of culture media to cultivate cells of animal origin they stimulate the "in vitro" multiplication and maintain cell viability. When fourteen lots of calf sera of variable GPE had the total protein contents as well as the percentages of serum fractions determined, no significant differences that could possibly explain the variability of the GPE were observed. Evaluation of the antiproteolytic activity of nineteen lots of calf serum and eighteen serum lots of younger calves showed that the former exhibited lower antiproteolytic titers (1:40 to 1:80) than the latter (1:80 to 1:160). Twelve lots of fetal bovine serum studied in parallel, showed the highest concentration of antiproteolytic factors, with titers equal to 1:320. Sera of bovine origin, but not fetal sera, are usually heat-inactivated, what was demonstrated to be responsible for the decrease of the antiproteolytic activity of 75% of the lots tested. This could explain the inability of certain heat-inactivated sera in promoting multiplication of some cells "in vitro", as verified with primary monkey kidney cells. The results obtained in this study indicated the convenience of submiting each lot of serum to be introduced in cell culture to previous determination of its characteristics, such as growth promoting efficiency, antiproteolytic activity and also toxicity, absence of extraneous agents, etc., in order to minimize the possibility of using serum lots of questionable quality, thus preventing not only the loss of cell lines, but also undesirable and sometimes expensive delays.
Resumo:
A serologic study was undertaken in a group of 43 patients with active paracoccidioidomycosis who were treated in the same form (ketoconazole), for identical periods of time (6 months), and folio wed-up for various periods posttherapy. The tests employed were agar gel immunodiffusion (AGID) and complement fixation (FC). Also studied were 50 sera from patients with proven histoplasmosis and pulmonary aspergilloma, 30 patients with culturaly proven tuberculosis as well as 92 specimens from healthy individuals, residents in the endemic area for paracoccidioidomycosis. A single lot of yeast filtrate antigen was used throughout the study. The value of each test was measured according to GALEN and GAMBINO6. Both tests were highly sensitive, 89 and 93% respectively. Regarding their specificity, the AGID was totally specific while the CF exhibited 96.6% and 97% specificity in front of tuberculosis patients and healthy individuals respectively and 82% in comparison with patients with other mycoses. The concept of predictive value, that is, the certainty one has in accepting a positive test as diagnostic of paracoccidioidomycosis, favored the AGID procedure (100%) over the CF test. The latter could sort out with 93% certainty a patient with paracoccidioidomycosis among a group of healthy individuals and with 97.5% in the case of TB patients; when the group in question was composed by individuals with other deep mycoses, such certainty was lower (81%). The above results indicate that both the AGID and the CF tests furnish results of high confidence; one should not relay, however, in the CF alone as a means to establish the specific diagnosis of paracoccidioidomycosis.
Resumo:
The hamster check pouch is an invagination of oral mucosa, characterized histologically as skin-like. In this paper we describe anatomical, histological and embriological features of the pouch and coment on the pouch as an immunologically privileged site since it lacks lymphatic drainage and has few Langerhans cells. We present the review from literature and our observations after inoculation in the pouch of mycobacteriae (BCG, Mycobacterium tuberculosis and Mycobacterium leprae) and a fungus (Paracoccidioides brasiliensis). Lesions in the pouch were granulomatous but smaller and long lasting; even granulomatous, the reaction was inefficient to control the proliferation of agents compared with inoculation in other sites, except for BCG. Appearance of immunity was also delayed or absent and, when it was detected, a sharp decrease in number of agents in pouch lesions was observed. These observations make the pouch an interesting site for the study of the role of immune system in infeccious diseases and in granuloma formation.