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1.
J Infect Dis ; 229(4): 1035-1040, 2024 Apr 12.
Artículo en Inglés | MEDLINE | ID: mdl-37962870

RESUMEN

BACKGROUND: Published studies on mRNA coronavirus disease 2019 (COVID-19) vaccine effects focus on younger individuals, comprising the majority of the workforce. Studies in elderly adults are sparse. METHODS: In total, 107 subjects were recruited (median age 78; interquartile range [IQR], 58.5-90.5; range, 35-105 years). Factors associated with antibody titer after the third mRNA COVID-19 vaccination were compared between 49 elderly (age ≥80; median, 94; IQR, 86-97; range, 80-105 years) and 58 younger (age ≤79; median, 61; IQR, 46-71; range, 35-79 years) adults. RESULTS: Among body mass index (BMI) categories, the group of underweight elderly adults had a lower antibody titer compared to those with normal weight (P < .01 after 1, 3, and 5 months). Elderly adults were less likely to maintain effective antibody titer (≥4160 AU/mL) compared to younger adults: 76% versus 98%, P < .001 after 1 month, and 45% versus 78%, P < .001 after 3 months. Elderly adults who maintained effective antibody titer for 5 months had a higher BMI (22.9 kg/m2 vs 20.1 kg/m2, P = .02), and were less likely to have underweight BMI (0% vs 31%, P = .02) compared to the subjects who failed to maintain effective antibody titer. CONCLUSIONS: These results highlight the impact of nutritional status and the deleterious effect of underweight BMI on antibody titer and its maintenance among elderly adults following booster mRNA COVID-19 vaccination.


Asunto(s)
COVID-19 , Estado Nutricional , Adulto , Anciano , Humanos , Vacunas contra la COVID-19 , Japón/epidemiología , Delgadez , COVID-19/prevención & control , ARN Mensajero , Anticuerpos Antivirales
2.
Intern Med ; 60(20): 3245-3249, 2021 Oct 15.
Artículo en Inglés | MEDLINE | ID: mdl-33776015

RESUMEN

Drug-induced lupus (DIL) is a drug-mediated immune reaction with the same symptoms as that of lupus erythematosus. We herein report the first case of tocilizumab-induced lupus syndrome presenting with cardiac tamponade. A 65-year-old man presented with cough, exertional dyspnea, and chest pain after 2 months of tocilizumab therapy for rheumatoid arthritis. Echocardiography revealed marked pericardial effusion. Antinuclear antibodies and anti-double-stranded deoxyribonucleic acid antibodies were positive. The diagnosis of cardiac tamponade due to tocilizumab-induced lupus syndrome was made. He had no recurrence of pericardial effusion after tocilizumab discontinuation. Clinicians should be alert for lupus syndrome in patients receiving tocilizumab.


Asunto(s)
Artritis Reumatoide , Taponamiento Cardíaco , Lupus Eritematoso Sistémico , Anciano , Anticuerpos Monoclonales Humanizados/efectos adversos , Artritis Reumatoide/tratamiento farmacológico , Taponamiento Cardíaco/inducido químicamente , Taponamiento Cardíaco/diagnóstico , Humanos , Lupus Eritematoso Sistémico/inducido químicamente , Lupus Eritematoso Sistémico/diagnóstico , Lupus Eritematoso Sistémico/tratamiento farmacológico , Masculino
5.
Oncol Rep ; 10(3): 665-9, 2003.
Artículo en Inglés | MEDLINE | ID: mdl-12684641

RESUMEN

Thymidine kinase (TK) is a protein closely associated with DNA replication. Here we show that, in contrast with the variation of TK activity, which changed parallel with S phase cell distribution during asynchronous culture of rat hepatoma JB1 cells, the serine residues of cytosolic TK protein was phosphorylated continuously in response to increasing G0/G1 phase cell distribution. The shifting of phosphorylation of TK protein during different cell growth conditions was further confirmed with the examination of the elution profile of cytosolic TK activity by anion-exchange high performance liquid chromatography (HPLC). HPLC analysis revealed that the rapid proliferating (62 h after asynchronous culture) rat hepatoma JB1 cells showed only the hyperphosphorylated form of cytosolic TK activity, while synchronously M phase-arrested JB1 cells showed hypo- and hyper-phosphorylated forms of cytosolic TK activity. These results suggested that the modulation of phosphorylation of cytosolic TK protein was cell cycle-dependent, and that the phosphorylation of cytosolic TK protein might be involved in the negative regulation of TK activity in vivo.


Asunto(s)
Citosol/enzimología , Neoplasias Hepáticas Experimentales/patología , Timidina Quinasa/metabolismo , Animales , Western Blotting , Ciclo Celular , División Celular , Cromatografía Líquida de Alta Presión , Inhibidores Enzimáticos/farmacología , Regulación Enzimológica de la Expresión Génica , Neoplasias Hepáticas Experimentales/enzimología , Mitosis , Fosforilación , Pruebas de Precipitina , Ratas , Células Tumorales Cultivadas
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