210 resultados para CD4 cell count


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The aim of this study was to evaluate the serum protein concentration in newborns fed with colostrum derived from healthy cows (n = 10), cows with subclinical mastitis (n = 10) and cows with clinical mastitis (n = 10). 30 Holstein cows were assigned to their respective groups according to macroscopic examination of colostral secretion, somatic cell count, CMT and presence of bacteria in colostrum samples. Blood samples of the calves were collected immediately after birth, at 24 and 48 hours after ingestion of colostrum. The total protein was measured by the biuret method and the concentrations of immunoglobulin A (IgA), immunoglobulin G (IgG), transferrin, albumin and haptoglobin was determined by sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE). No differences were obser- ved amongst groups in the concentrations of albumin, total protein and IgA. In animals from cows with subclinical and clinical mastitis haptoglobin concentrations were higher than those of healthy animals. The concentrations of IgG and transferrin were significantly lower in calves from cows with mastitis. We concluded that the ingestion of colostrum from infected and uninfected glands from cows with mastitis (GII e GIII) is unlikely to be an important contributor to the high rate of failure of passive transfer of immunoglobulins in calves.

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Coordenao de Aperfeioamento de Pessoal de Nvel Superior (CAPES)

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Fundao de Amparo Pesquisa do Estado de So Paulo (FAPESP)

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Coordenao de Aperfeioamento de Pessoal de Nvel Superior (CAPES)

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Ps-graduao em Medicina Veterinria - FCAV

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Ps-graduao em Medicina Veterinria - FCAV

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The concentrations of acute phase proteins are correlated with the severity of the surgical trauma, being elevated when severe tissue injury is produced. The aim of this study was to evaluate the leukogram and the acute phase proteins concentrations in healthy female dogs submitted to minimally invasive ovariohysterectomy, with the use of nylon cable ties (G1), and conventional (laparotomy) ovariohysterectomy, with the use of nylon suture (G2), as methods to ligate the ovarian pedicles and uterine body, respectively. Blood samples from 30 adult healthy female dogs (15 for each group) were obtained before surgery, and at 24 and 48 h and 7 days after surgery. Serum protein fractions were determined by means of sodium dodecyl sulfate polyacrylamide gel electrophoresis. Neutrophilia was observed 24 h after both surgical procedures but did not differ (P0.05) between the groups. In G1, the estimated concentration of ceruloplasmin increased (P0.05) 48 h after the surgical procedure. The estimated ceruloplasmin concentration was significantly higher in G1 (P0.05) when compared to G2 48 h postoperatively, and the estimated haptoglobin concentration was also significantly greater in G1 (P0.05) than in G2 from 24 h to 7 days after surgery. Through the ceruloplasmin and haptoglobin estimated concentrations, we conclude that the minimally invasive ovariohysterectomy caused a more intense inflammatory response, which was not reflected in the white blood cell count.

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Mastits is considered uncommon disease in mares. Streptococcus equi, Staphylococcus sp., Corynebacterium sp., Actinobacillus sp., Nocardia sp. and enterobacterias are major microorganisms involved in equine mammary infections. The disease is commonly related to traumatic lesions in mammary glands and teats. Edema, fibrosis, masses to palpation of glands, and viscous to seropurulent milk are mainly clinical signs observed in affected animals. The diagnosis is based on clinical exam of mammary glands and microbiological culture of the milk. There are no standard to use of indirect exams on diagnosis, including California Mastits Test and Somatic Cell Count. Systemic antimicrobials are recommended in therapy, based on previous in vitro susceptibility microbiological test. No specific control measures are indicated in equine mastits. The present study reviewed the mastits in mares, with emphasis to etiology, epidemiology findings, clinical manifestation, diagnosis, treatment and control aspects.

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Vitamin A (vitA) is an essential nutrient that acts as an endocrine regulator of several metabolic pathways, modulating normal growth and health status of animals. Although the importance of vitA for normal haematology and immune response is well documented for higher vertebrates, there is limited information on the physiological effects of vitA on fish. Therefore, we designed a 130-day feeding trial to evaluate the effect of vitA supplementation on growth, haematology, immune function and resistance to experimental infection with Aeromonas hydrophila and cold-induced stress. A group of 320 Nile tilapia fingerlings 7.49 0.19 g weight (mean SD) were randomly stocked into 40 250 L-aquaria and fed practical diets containing graded levels of vitA (0, 0.06, 0.12, 0.24, 0.48, 0.96, 1.92, 3.84 mg retinol (ROH) kg1 diet. Growth, haematology, plasma protein profile and immune response were significantly affected by vitA supplementation; however, no clear protective effect of vitA supplementation on disease and cold stress resistance were observed in this study. Clinical signs of vitA deficiency were: resting and abnormal swimming behaviour, exophthalmia, haemorrhages at the base of fins and on skin, serous fluids in abdominal cavity, neutropenia, reduction in red blood cell count, haematocrit and haemoglobin evolving to high mortality rates in a short period of time. A dietary level of vitA around 1.2 mg ROH kg1 may be required to prevent gross deficiency signs and promote proper growth and health status of Nile tilapia. VitA does not seem to have a pronounced effect on leucocyte differentiation, but clearly plays an important role on maintaining normal erythropoiesis.

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Foram avaliados dezesseis doentes portadores de pnfigo foliceo endmico, dez com a forma localizada da doena (Grupo G1) e seis com a forma disseminada (Grupo G2), com os objetivos de correlacionar o quadro clnico e laboratorial desses pacientes com o perfil imunolgico dos mesmos, e verificar a relao dos ttulos dos anticorpos antiepiderme circulantes, identificados pela imunofluorescncia indireta, com intensidade da leso e com a evoluo das leses em tratamento. Foram realizados: hemograma completo, quantificao de subpopulao de clulas mononucleares por anticorpos monoclonais e estudo da transformao blstica de linfcitos e quantificao de anticorpos circulantes por meio da reao de imunofluorescncia indireta. Observou-se leucocitose principalmente no grupo G2, diminuio dos valores relativos das subpopulaes de linfcitos CD3+ e CD4+ e tendncia diminuio dos valores relativos da subpopulao CD8+ nos doentes (Grupos G1 e G2). Os ndices de transformao blstica de linfcitos frente fitohemaglutinina revelaram nveis mais elevados nos doentes (Grupos G1 + G2), que nos controles. A reao de imunofluorescncia indireta foi positiva em 100% dos doentes do grupo G2 e em 80% do grupo G1 A mediana dos valores dos ttulos foi maior no grupo G2, quando comparado com o grupo G1. A anlise global dos resultados permite concluir que a imunidade celular est preservada, e que existe uma relao entre os ttulos de anticorpos obtidos reao de imunofluorescncia indireta e extenso da leso cutnea.

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Este estudo se reporta s funes de clulas natural killer (NK), como adeso, lise e citotoxicidade e de subpopulaes de clulas T em uma famlia com alta prevalncia de pacientes com cncer e que apresentaram: glioblastoma, leucemia mielide crnica, osteoblastoma, melanoma e carcinomas gstrico, pancretico e clon retal. Quinze membros dessa famlia foram estudados, sendo 13 sadios, acompanhados por 5 anos e dois com cncer: glioblastoma e leucemia mielide crnica. Duas pessoas sadias, no momento da avaliao, desenvolveram posteriormente osteoblastoma mandibular ou melanoma maligno. Como controle, foram avaliados 19 indivduos saudveis de faixa etria equivalente. A determinao de linfcitos T CD3+ e de suas subpopulaes CD4+ e CD8+ foi realizada empregando-se anticorpos monoclonais e a atividade citotxica de clulas NK, avaliada pelo teste de single-cell contra clulas alvo da linhagem eritroleucmica K562. Os resultados mostraram que as percentagens de clulas T totais (CD3+), da subpopulao CD4+ e da relao CD4/CD8 foram significativamente menores nos indivduos da famlia estudada em comparao aos valores observados no grupo controle. em todos os membros dessa famlia a percentagem de formao de conjugados entre clulas NK-clulas alvo foi inferior ao valor mnimo observado nos controles. Essa alterao poderia estar relacionada a defeito na expresso de molculas de adeso, presentes na membrana de clulas NK, como provvel causa das alteraes funcionais dessas clulas. A herana dos mecanismos determinantes desta deficincia pode ser um fator de risco, com valor prognstico para o desenvolvimento de cancer.

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Subcutaneous heat-coagulated egg white implants (EWI) induce chronic, intense local eosinophilia in mice, followed by asthma-like responses to airway ovalbumin challenge. Our goal was to define the mechanisms of selective eosinophil accumulation in the EWI model. EWI carriers were challenged i.p. with ovalbumin and the contributions of cellular immunity and inflammatory mediators to the resulting leukocyte accumulation were defined through cell transfer and pharmacological inhibition protocols. Eosinophil recruitment required Major Histocompatibility Complex Class It expression, and was abolished by the leukotriene B4 (LTB4) receptor antagonist CP 105.696, the 5-lipoxygenase inhibitor BWA4C and the 5-lipoxygenase activating protein inhibitor MK886. Eosinophil recruitment in EWI carriers followed transfer of: a) CD4(+) (but not CD4(-)) cells, harvested from EWI donors and restimulated ex vivo; b) their cell-free supernatants, containing LTB4. Restimulation in the presence of MK886 was ineffective. CC chemokine receptor ligand (CCL)5 and CCL2 were induced by ovalbumin challenge in vivo. mRNA for CCL17 and CCL11 was induced in ovalbumin-restimulated CD4(+) cells ex vivo. MK886 blocked induction of CCL17 Pretreatment of EWI carriers with MK886 eliminated the effectiveness of exogenously administered CCL11, CCL2 and CCL5. In conclusion, chemokine-producing, ovalburnin-restimulated CD4(+) cells initiate eosinophil recruitment which is strictly dependent on LTB4 production. (C) 2008 Elsevier B.V. All rights reserved.

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Ethnopharmacological relevance: Uncaria tomentosa (Willd.) DC (Rubiaceae) is a species native to the Amazon rainforest and surrounding tropical areas that is endowed with immunomodulatory properties and widely used around the world. In this study we investigated the immunomodulatory potential of Uncaria tomentosa (UT) aqueous-ethanol extract on the progression of immune-mediated diabetes.Materials and methods: C57BL/6 male mice were injected with MLDS (40 mg/kg) and orally treated with UT at 10-400 mg/kg during 21 days. Control groups received MLDS alone or the respective dilution vehicle. Pancreatic mononuclear infiltrate and beta-cell insulin content were analyzed by HE and immunohistochemical staining, respectively, and measured by digital morphometry. Lymphocyte immunophenotyping and cytokine production were determined by flow cytometry analysis.Results: Treating the animals with 50-400 mg/kg of UT caused a significant reduction in the glycemic levels, as well as in the incidence of diabetes. The morphometric analysis of insulitis revealed a clear protective effect. Animals treated with UT at 400 mg/kg presented a higher number of intact islets and a significant inhibition of destructive insulitis. Furthermore, a significant protection against the loss of insulin-secreting presented beta-cells was achieved, as observed by a careful immunohistochemical evaluation. The phenotypic analysis indicated that the groups treated with higher doses (100-400 mg/kg) presented CD4(+) and CD8(+) T-cell values similar to those observed in healthy animals. These same higher doses also increased the number of CD4(+)CD25(+)Foxp3(+) regulatory T-cells. Moreover, the extract modulated the production of Th1 and Th2, with increased levels of IL-4 and IL-5.Conclusions: The extract was effective to prevent the progression of immune-mediated diabetes by distinct pathways. (C) 2011 Elsevier B.V. All rights reserved.

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OBJETIVO: O objetivo deste estudo foi determinar o perfil da deficincia imune em um grupo bem definido de epilepsia: crianas com sndrome de West (SW) e seus padres EEG de evoluo, idade-dependentes, como os complexos onda-aguda- onda lenta generalizadas da sndrome de Lenox-Gastaut (SLG) e as pontas multifocais independentes (PMI). MTODO: Um grupo de 50 crianas, 33 com SW, 10 com SLG, 7 com PMI e 20 crianas sadias (controle) foram avaliadas em relao aos seguintes parmetros:determinao de subpopulaes de linfcitos T (CD1, CD3, CD4 e CD8), relao CD4/CD8 e resposta proliferativa de linfcitos frente a fitohemaglutinina (PHA), na presena de plasma autlogo ou de plasma AB (homlogo). A prova cutnea de sensibilizao ao Dinitroclorobenzeno (DNCB) foi realizada apenas nos pacientes. Os nveis sricos de IgG, IgA e IgM foram comparados aos valores normais em crianas Brasileiras, em diferentes faixas etrias. RESULTADOS: A resposta ao DNCB foi ausente ou fracamente reativa em 76% dos pacientes. Nveis sricos elevados de IgG (45,7%) e de IgM (61,4%) e baixos de IgA (23,9%) foram detectados nos pacientes. A determinao das subpopulaes de linfcitos T em sangue perifrico mostrou: deficincia nas propores de clulas CD3+ (p<0,05) e de CD4+ (p<0,05), aumento de CD8+ (p<0,01) e diminuio da relao CD4 / CD8 (p<0,001). A proporo de clulas CD1+ no grupo controle manteve-se menor que 3%, enquanto que em 18% dos pacientes esses nveis variaram entre 3 e 11%. A resposta proliferativa de linfcitos frente a PHA revelou ndices blastognicos significativamente mais baixos apenas quando clulas dos pacientes foram cultivadas na presena do prprio plasma (plasma autlogo). Quando estas clulas foram cultivadas na presena de plasma AB, no se evidenciou diferena significativa em relao ao grupo controle. CONCLUSO: A imunodeficincia na SW caracterizou-se por: anergia, alterao de imunidade mediada por clulas e dos nveis de imunoglobulinas, presena de timcitos imaturos na circulao perifrica e deficincia funcional de linfcitos T induzida por fatores plasmticos inibidores. Discutem-se as principais evidncias de disfuno imune como imunodeficincia e autoimunidade.