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1.
Blood Cancer J ; 11(7): 136, 2021 07 30.
Artículo en Inglés | MEDLINE | ID: mdl-34330895

RESUMEN

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.


Asunto(s)
Anticuerpos Antivirales , Formación de Anticuerpos/efectos de los fármacos , Vacunas contra la COVID-19 , COVID-19 , Inmunización Secundaria , Leucemia Linfocítica Crónica de Células B , Adulto , Anciano , Anciano de 80 o más Años , Anticuerpos Antivirales/sangre , Anticuerpos Antivirales/inmunología , Vacuna BNT162 , COVID-19/sangre , COVID-19/inmunología , COVID-19/prevención & control , Vacunas contra la COVID-19/administración & dosificación , Vacunas contra la COVID-19/inmunología , Femenino , Humanos , Leucemia Linfocítica Crónica de Células B/sangre , Leucemia Linfocítica Crónica de Células B/inmunología , Masculino , Persona de Mediana Edad
2.
Diabetologia ; 54(8): 2143-51, 2011 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-21538175

RESUMEN

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.


Asunto(s)
Enfermedad de Alzheimer/metabolismo , Precursor de Proteína beta-Amiloide/metabolismo , Intolerancia a la Glucosa/fisiopatología , Obesidad/metabolismo , Presenilina-1/metabolismo , Proteína Tirosina Fosfatasa no Receptora Tipo 1/metabolismo , Proteínas Plasmáticas de Unión al Retinol/metabolismo , Proteína S6 Ribosómica/metabolismo , Enfermedad de Alzheimer/genética , Precursor de Proteína beta-Amiloide/genética , Animales , Peso Corporal/genética , Peso Corporal/fisiología , Encéfalo/metabolismo , Modelos Animales de Enfermedad , Electroforesis en Gel de Poliacrilamida , Humanos , Immunoblotting , Ratones , Ratones Transgénicos , Obesidad/inducido químicamente , Fosforilación , Presenilina-1/genética
4.
Hosp Health Netw ; 73(11): 36-3, 40, 42-4, 1999 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-10633768

RESUMEN

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.


Asunto(s)
Actitud del Personal de Salud , Liderazgo , Servicios de Salud Comunitaria , Comportamiento del Consumidor , Conducta Cooperativa , Control de Costos , Práctica de Grupo/organización & administración , Administración Hospitalaria , Administradores de Hospital , Humanos , Programas Controlados de Atención en Salud/organización & administración , Ejecutivos Médicos , Estados Unidos
6.
Compens Rev ; 15(4): 15-31, 1983.
Artículo en Inglés | MEDLINE | ID: mdl-10310260

RESUMEN

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.


Asunto(s)
Control de Costos/tendencias , Planes de Asistencia Médica para Empleados/organización & administración , Seguro de Salud/organización & administración , Gastos en Salud/tendencias , Estados Unidos
7.
Appl Microbiol ; 24(3): 358-62, 1972 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-4562474

RESUMEN

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.


Asunto(s)
Técnicas Bacteriológicas , Enterobacteriaceae/clasificación , Carboxiliasas/metabolismo , Citratos/metabolismo , Ensayos Clínicos como Asunto , Medios de Cultivo , Enterobacteriaceae/enzimología , Enterobacteriaceae/crecimiento & desarrollo , Enterobacteriaceae/metabolismo , Estudios de Evaluación como Asunto , Fermentación , Gases/biosíntesis , Glucosa/metabolismo , Sulfuro de Hidrógeno/biosíntesis , Indoles/biosíntesis , Lactosa/metabolismo , Lisina , Ornitina , Urea/metabolismo
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