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1.
J Clin Immunol ; 31(5): 784-91, 2011 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-21744182

RESUMO

Patients with common variable immunodeficiency disorders (CVIDs) who developed B cell lymphoproliferation of indeterminate malignant potential are described in order to raise a discussion of the relationship between infection and lymphoproliferation in infection prone patients. Those with CVID are at risk of developing either polyclonal or monoclonal lymphoproliferation in part due to the dysregulation of their adaptive immune systems. The aetiologies of the lymphoproliferations are unknown but intriguing; the relevance of infection being particularly problematic. The patients described here demonstrate variability in preceding infection, age at presentation, response to antibiotics and other types of therapy as well as outcome. The question of treatment is also controversial; issues include whether antibiotics or chemotherapy are the first line of therapy in all patients and whether transformation to aggressive B cell malignancy is inevitable or depends on other factors and if so, the length of time for such progression.


Assuntos
Aspergilose/diagnóstico , Aspergillus fumigatus/imunologia , Linfócitos B/patologia , Imunodeficiência de Variável Comum/diagnóstico , Infecções por Vírus Epstein-Barr/diagnóstico , Herpesvirus Humano 4/imunologia , Neoplasias Pulmonares/diagnóstico , Pulmão/patologia , Linfoma de Zona Marginal Tipo Células B/diagnóstico , Lesões Pré-Cancerosas/patologia , Pele/patologia , Adulto , Idoso , Aspergilose/etiologia , Aspergilose/imunologia , Aspergilose/patologia , Aspergilose/fisiopatologia , Aspergillus fumigatus/patogenicidade , Autoimunidade , Linfócitos B/imunologia , Linfócitos B/microbiologia , Linfócitos B/virologia , Transformação Celular Neoplásica , Transformação Celular Viral , Imunodeficiência de Variável Comum/complicações , Imunodeficiência de Variável Comum/imunologia , Imunodeficiência de Variável Comum/patologia , Imunodeficiência de Variável Comum/fisiopatologia , Diagnóstico Diferencial , Infecções por Vírus Epstein-Barr/etiologia , Infecções por Vírus Epstein-Barr/imunologia , Infecções por Vírus Epstein-Barr/patologia , Infecções por Vírus Epstein-Barr/fisiopatologia , Evolução Fatal , Feminino , Herpesvirus Humano 4/patogenicidade , Humanos , Pulmão/imunologia , Pulmão/microbiologia , Pulmão/virologia , Neoplasias Pulmonares/imunologia , Neoplasias Pulmonares/patologia , Neoplasias Pulmonares/fisiopatologia , Linfoma de Zona Marginal Tipo Células B/imunologia , Linfoma de Zona Marginal Tipo Células B/patologia , Linfoma de Zona Marginal Tipo Células B/fisiopatologia , Transtornos Linfoproliferativos , Masculino , Pessoa de Meia-Idade , Remissão Espontânea , Pele/imunologia , Pele/microbiologia , Pele/virologia
2.
Carbohydr Polym ; 244: 116448, 2020 Sep 15.
Artigo em Inglês | MEDLINE | ID: mdl-32536383

RESUMO

Myrtenol has gained wide interest because of its pharmacological profiles, mainly for treatment of chronic diseases. To improve the solubility of myrtenol, the formation of inclusion complexes with ß-cyclodextrin was performed by physical mixture, kneading process or slurry complexation (SC) methods and characterized using thermal analysis, XRD, SEM and NMR. From these results, myrtenol complexed by SC was successfully complexed into ß-cyclodextrin cavity. The interaction between myrtenol and ß-cyclodextrin was confirmed by molecular docking. Hence, the SC ß-cyclodextrin-myrtenol complex was evaluate for its anti-hyperalgesic, anxiolytic and antioxidant activity in a fibromyalgia model. Results show that myrtenol and ß-cyclodextrin form a stable complex and have anti-hyperalgesic effect, improve the cognitive impairment caused and have an anxiolytic-like effect. Furthermore, the ß-cyclodextrin/myrtenol complex decrease lipoperoxidation, increased catalase activity and a reduce SOD/CAT ratio. Therefore, ß-cyclodextrin/myrtenol complex reduce painful behavior, improves motor skills and emotional behavior and decreases oxidative stress in a fibromyalgia model.


Assuntos
Monoterpenos Bicíclicos/uso terapêutico , Disfunção Cognitiva/tratamento farmacológico , Fibromialgia/tratamento farmacológico , Hiperalgesia/tratamento farmacológico , Dor Musculoesquelética/tratamento farmacológico , Dor Nociceptiva/tratamento farmacológico , beta-Ciclodextrinas/uso terapêutico , Animais , Antioxidantes/uso terapêutico , Dor Crônica/tratamento farmacológico , Masculino , Camundongos
3.
Lancet Infect Dis ; 19(10): 1138-1147, 2019 10.
Artigo em Inglês | MEDLINE | ID: mdl-31559967

RESUMO

BACKGROUND: Zika virus infections and suspected microcephaly cases have been reported in Angola since late 2016, but no data are available about the origins, epidemiology, and diversity of the virus. We aimed to investigate the emergence and circulation of Zika virus in Angola. METHODS: Diagnostic samples collected by the Angolan Ministry of Health as part of routine arboviral surveillance were tested by real-time reverse transcription PCR by the Instituto Nacional de Investigação em Saúde (Ministry of Health, Luanda, Angola). To identify further samples positive for Zika virus and appropriate for genomic sequencing, we also tested samples from a 2017 study of people with HIV in Luanda. Portable sequencing was used to generate Angolan Zika virus genome sequences from three people positive for Zika virus infection by real-time reverse transcription PCR, including one neonate with microcephaly. Genetic and mobility data were analysed to investigate the date of introduction and geographical origin of Zika virus in Angola. Brain CT and MRI, and serological assays were done on a child with microcephaly to confirm microcephaly and assess previous Zika virus infection. FINDINGS: Serum samples from 54 people with suspected acute Zika virus infection, 76 infants with suspected microcephaly, 24 mothers of infants with suspected microcephaly, 336 patients with suspected dengue virus or chikungunya virus infection, and 349 samples from the HIV study were tested by real-time reverse transcription PCR. Four cases identified between December, 2016, and June, 2017, tested positive for Zika virus. Analyses of viral genomic and human mobility data suggest that Zika virus was probably introduced to Angola from Brazil between July, 2015, and June, 2016. This introduction probably initiated local circulation of Zika virus in Angola that continued until at least June, 2017. The infant with microcephaly in whom CT and MRI were done had brain abnormalities consistent with congenital Zika syndrome and serological evidence for Zika virus infection. INTERPRETATION: Our analyses show that autochthonous transmission of the Asian lineage of Zika virus has taken place in Africa. Zika virus surveillance and surveillance of associated cases of microcephaly throughout the continent is crucial. FUNDING: Royal Society, Wellcome Trust, Global Challenges Research Fund (UK Research and Innovation), Africa Oxford, John Fell Fund, Oxford Martin School, European Research Council, Departamento de Ciência e Tecnologia/Ministério da Saúde/National Council for Scientific and Technological Development, and Ministério da Educação/Coordenação de Aperfeicoamento de Pessoal de Nível Superior.


Assuntos
Surtos de Doenças , Transmissão Vertical de Doenças Infecciosas , Filogenia , Complicações Infecciosas na Gravidez/virologia , Infecção por Zika virus/epidemiologia , Infecção por Zika virus/transmissão , Zika virus/genética , Angola/epidemiologia , Sequência de Bases , Feminino , Genoma Viral/genética , Genótipo , Humanos , Lactente , Recém-Nascido , Masculino , Microcefalia/sangue , Microcefalia/etiologia , Microcefalia/virologia , Mães , Gravidez , RNA Viral/genética , Infecção por Zika virus/complicações , Infecção por Zika virus/virologia
4.
Arch Gerontol Geriatr ; 75: 158-164, 2018.
Artigo em Inglês | MEDLINE | ID: mdl-29306767

RESUMO

INTRODUCTION: Metabolic syndrome is highly prevalent among older adults. Concurrent training comprises muscle strengthening and aerobic exercise. OBJECTIVE: Determine the effects of a concurrent training program on muscle strength, walking function, metabolic profile, cardiovascular risk, use of medications and quality of life among older adults with metabolic syndrome. METHODS: A randomised, controlled, blind, clinical trial was conducted in the city of Santos, state of São Paulo, Brazil, involving 41 male and female older adults. The participants were randomly allocated to a control group (n = 18) and intervention group (n = 23) and were submitted to the following evaluations: strength - 1 maximum repetition (1MR) for 12 muscle groups; the Six-Minute Walk Test (6MWT); blood concentrations of cholesterol and glucose; the use of medications; and the administration of the SF-36 questionnaire. The intervention was conducted twice a week over a total of 24 sessions of concurrent training: 50 min of strength exercises (40-70% 1MR) and 40 min of walking exercises (70-85% maximum heart rate). RESULTS: Increases in muscle strength were found in the upper and lower limbs in the inter-group analysis and a greater distance travelled on the 6MWT was found in the intervention group (p = 0.001). The intervention group demonstrated a reduction in the consumption of biguanides (p = 0.002). No changes were found regarding metabolic profile, cardiovascular risk or self-perceived quality of life. CONCLUSION: The findings of this clinical trial can be used for the prescription of concurrent training for older adults with metabolic syndrome for gains in muscle strength and walking distance as well as a reduction in the use of biguanides.


Assuntos
Terapia por Exercício , Síndrome Metabólica/fisiopatologia , Síndrome Metabólica/terapia , Força Muscular/fisiologia , Treinamento Resistido , Idoso , Biguanidas/uso terapêutico , Método Duplo-Cego , Feminino , Humanos , Hipoglicemiantes/uso terapêutico , Masculino , Teste de Caminhada
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