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1.
Blood Cancer J ; 11(7): 136, 2021 07 30.
Artigo em Inglês | MEDLINE | ID: mdl-34330895

RESUMO

B-cell chronic lymphocytic leukaemia (CLL) is associated with immunosuppression and patients are at increased clinical risk following SARS-CoV-2 infection. Covid-19 vaccines offer the potential for protection against severe infection but relatively little is known regarding the profile of the antibody response following first or second vaccination. We studied spike-specific antibody responses following first and/or second Covid-19 vaccination in 299 patients with CLL compared with healthy donors. 286 patients underwent extended interval (10-12 week) vaccination. 154 patients received the BNT162b2 mRNA vaccine and 145 patients received ChAdOx1. Blood samples were taken either by venepuncture or as dried blood spots on filter paper. Spike-specific antibody responses were detectable in 34% of patients with CLL after one vaccine (n = 267) compared to 94% in healthy donors with antibody titres 104-fold lower in the patient group. Antibody responses increased to 75% after second vaccine (n = 55), compared to 100% in healthy donors, although titres remained lower. Multivariate analysis showed that current treatment with BTK inhibitors or IgA deficiency were independently associated with failure to generate an antibody response after the second vaccine. This work supports the need for optimisation of vaccination strategy in patients with CLL including the potential utility of booster vaccines.


Assuntos
Anticorpos Antivirais , Formação de Anticorpos/efeitos dos fármacos , Vacinas contra COVID-19 , COVID-19 , Imunização Secundária , Leucemia Linfocítica Crônica de Células B , Adulto , Idoso , Idoso de 80 Anos ou mais , Anticorpos Antivirais/sangue , Anticorpos Antivirais/imunologia , Vacina BNT162 , COVID-19/sangue , COVID-19/imunologia , COVID-19/prevenção & controle , Vacinas contra COVID-19/administração & dosagem , Vacinas contra COVID-19/imunologia , Feminino , Humanos , Leucemia Linfocítica Crônica de Células B/sangue , Leucemia Linfocítica Crônica de Células B/imunologia , Masculino , Pessoa de Meia-Idade
2.
Diabetologia ; 54(8): 2143-51, 2011 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-21538175

RESUMO

AIMS/HYPOTHESIS: Obesity is a major risk factor for development of insulin resistance, a proximal cause of type 2 diabetes and is also associated with an increased relative risk of Alzheimer's disease. We therefore investigated the susceptibility of transgenic mice carrying human mutated transgenes for amyloid precursor protein (APP (SWE)) and presenilin 1 (PSEN1 (A246E)) (APP/PSEN1), or PSEN1 (A246E) alone, which are well-characterised animal models of Alzheimer's disease, to develop obesity, glucose intolerance and insulin resistance, and whether this was age- and/or diet-dependent. METHODS: We analysed the effects of age and/or diet on body weight of wild-type, PSEN1 and APP/PSEN1 mice. We also analysed the effects of diet on glucose homeostasis and insulin signalling in these mice. RESULTS: While there were no body weight differences between 16-17- and 20-21-month-old PSEN1 mice, APP/PSEN1 mice and their wild-type controls on standard, low-fat, chow diet, the APP/PSEN1 mice still exhibited impaired glucose homeostasis, as investigated by glucose tolerance tests. This was associated with increased brain protein tyrosine phosphatase 1B protein levels in APP/PSEN1 mice. Interestingly, short-term high-fat diet (HFD) feeding of wild-type, PSEN1 and APP/PSEN1 mice for a period of 8 weeks led to higher body weight gain in APP/PSEN1 than in PSEN1 mice and wild-type controls. In addition, HFD-feeding caused fasting hyperglycaemia and worsening of glucose maintenance in PSEN1 mice, the former being further exacerbated in APP/PSEN1 mice. The mechanism(s) behind this glucose intolerance in PSEN1 and APP/PSEN1 mice appeared to involve increased levels of brain retinol-binding protein 4 and basal phosphorylation of S6 ribosomal protein, and decreased insulin-stimulated phosphorylation of Akt/protein kinase B and extracellular signal-regulated kinase 1/2 in the brain. CONCLUSIONS/INTERPRETATION: Our results indicate that Alzheimer's disease increases susceptibility to body weight gain induced by HFD, and to the associated glucose intolerance and insulin resistance.


Assuntos
Doença de Alzheimer/metabolismo , Precursor de Proteína beta-Amiloide/metabolismo , Intolerância à Glucose/fisiopatologia , Obesidade/metabolismo , Presenilina-1/metabolismo , Proteína Tirosina Fosfatase não Receptora Tipo 1/metabolismo , Proteínas Plasmáticas de Ligação ao Retinol/metabolismo , Proteína S6 Ribossômica/metabolismo , Doença de Alzheimer/genética , Precursor de Proteína beta-Amiloide/genética , Animais , Peso Corporal/genética , Peso Corporal/fisiologia , Encéfalo/metabolismo , Modelos Animais de Doenças , Eletroforese em Gel de Poliacrilamida , Humanos , Immunoblotting , Camundongos , Camundongos Transgênicos , Obesidade/induzido quimicamente , Fosforilação , Presenilina-1/genética
4.
Hosp Health Netw ; 73(11): 36-3, 40, 42-4, 1999 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-10633768

RESUMO

Cost control, customer service and collaboration among health care sectors rank as top concerns with panelists in H&HN's annual Leadership Report. Efforts to improve community health are a priority, too, but are often frustrated by financial and other constraints. The 16 panelists represent managed care, physicians, and hospitals and health systems.


Assuntos
Atitude do Pessoal de Saúde , Liderança , Serviços de Saúde Comunitária , Comportamento do Consumidor , Comportamento Cooperativo , Controle de Custos , Prática de Grupo/organização & administração , Administração Hospitalar , Administradores Hospitalares , Humanos , Programas de Assistência Gerenciada/organização & administração , Diretores Médicos , Estados Unidos
6.
Compens Rev ; 15(4): 15-31, 1983.
Artigo em Inglês | MEDLINE | ID: mdl-10310260

RESUMO

Benefits administrators--and their employers--can no longer ignore the skyrocketing costs of health care. The wide range of measures explored here for controlling these costs include negotiating with providers, analyzing medical claims, enlisting the aid of employee/patients, structuring benefit programs to eliminate excesses, and setting up wellness programs to alter the lifestyles--smoking, drinking, poor nutrition--that result in crippling, even fatal diseases.


Assuntos
Controle de Custos/tendências , Planos de Assistência de Saúde para Empregados/organização & administração , Seguro Saúde/organização & administração , Gastos em Saúde/tendências , Estados Unidos
7.
Appl Microbiol ; 24(3): 358-62, 1972 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-4562474

RESUMO

In a paired, double-blind study, the modified ("Beckford tube") R-B system was compared with conventional bacteriological procedures for the identification of members of the family Enterobacteriaceae from clinical isolates and stock cultures. The tests in the R-B system yielding positive reactions comparable to those predicted by Ewing's taxonomic classification of Enterobacteriaceae were production of hydrogen sulfide and presence of lysine and ornithine decarboxylasè activities. The test reactions in the R-B system found to be comparable to those in the conventional method were fermentation of glucose, hydrogen sulfide production, and lysine and ornithine decarboxylase activities. The production of gas from glucose was positive in the R-B system more often than in the conventional method; however, the motility test and the production of indole were positive less often in the R-B system. Adequate preliminary identification of the Enterobacteriaceae with the R-B system is enhanced if Simmons' citrate and Christensen's urea tests are used concomitantly. These findings emphasize the manufacturer's instructions that, in interpretation of results, colonial morphology and biochemical reactions must be used concurrently to make an accurate identification.


Assuntos
Técnicas Bacteriológicas , Enterobacteriaceae/classificação , Carboxiliases/metabolismo , Citratos/metabolismo , Ensaios Clínicos como Assunto , Meios de Cultura , Enterobacteriaceae/enzimologia , Enterobacteriaceae/crescimento & desenvolvimento , Enterobacteriaceae/metabolismo , Estudos de Avaliação como Assunto , Fermentação , Gases/biossíntese , Glucose/metabolismo , Sulfeto de Hidrogênio/biossíntese , Indóis/biossíntese , Lactose/metabolismo , Lisina , Ornitina , Ureia/metabolismo
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