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1.
Ann Clin Lab Sci ; 51(6): 827-836, 2021 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-34921036

RESUMEN

OBJECTIVE: CD8+ T cells can participate in immune action by secreting various cytokines, which have a killing effect on certain viruses, tumor cells, and other antigenic substances. However, in studies such as chronic viral infections and some parasitic infections, CD8+ T lymphocyte showed functional depletion, and its immune dysfunction was an important reason for the persistence of infection. Tim-3 has been shown to be a negative regulator of CD8+ T cell function, causing depletion of CD8+ T cells in cancer and chronic infection. However, the relationship between Tim-3 and CD8+ T cells in Echinococcus multilocularis infection is not clear. METHODS: In this study, we analyzed peripheral blood CD8+ T cells from 62 alveolar echinococcosis (AE) patients and 30 healthy controls. RESULTS: Compared with the healthy control group, the proportion of CD8+ T cells in the peripheral blood of AE patients increased significantly, while the levels of perforin, granzyme B and IFN-γ in peripheral blood CD8+ T cell related factors of metabolically active alveolar echinococcosis (MAAE) patients decreased significantly. Later detection revealed that the expression of Tim-3 on CD8+ T cells in the peripheral blood of MAAE patients was significantly higher than that of metabolically inactive alveolar echinococcosis (MIAE) patients and healthy controls. The expression levels of function-related factors perforin, granzyme B and IFN-γ in CD8+ Tim-3+ T cell were significantly lower in the CD8+Tim-3- T cells of AE patients. In vitro, the secretion of CD8+ T cell-associated factors was significantly restored by inhibiting Tim-3 expression. CONCLUSION: Therefore, the depletion of CD8+ T lymphocyte in patients with alveolar echinococcosis disease is considered to be related to the high expression of Tim-3 on the surface.


Asunto(s)
Linfocitos T CD8-positivos , Equinococosis , Granzimas/metabolismo , Receptor 2 Celular del Virus de la Hepatitis A/metabolismo , Interferón gamma/metabolismo , Perforina/metabolismo , Animales , Linfocitos T CD8-positivos/parasitología , Linfocitos T CD8-positivos/fisiología , Equinococosis/sangre , Equinococosis/inmunología , Equinococosis/metabolismo , Echinococcus multilocularis/aislamiento & purificación , Echinococcus multilocularis/metabolismo , Femenino , Perfilación de la Expresión Génica/métodos , Humanos , Inmunocompetencia , Masculino , Monitorización Inmunológica/métodos , Gravedad del Paciente , Receptores Virales
2.
Clin Chim Acta ; 510: 665-670, 2020 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-32828732

RESUMEN

OBJECTIVE: Acute pancreatitis (AP) is an inflammatory disease with rapid progression. In severe cases, it can cause systemic inflammatory response syndrome (SIRS), multiple organ failure (POF) and even death. The study aimed to investigate the diagnostic value of C-reactive protein (CRP), procalcitonin (PCT), interleukin-6 (IL-6) and lactate dehydrogenase (LDH) in patients with severe AP. METHODS: AP patients (n = 153) divided into mild AP patients (n = 81) and severe AP patients (n = 72) were selected from June 2014 to June 2016. The demographic information (age, sex) and the hematological parameters (WBC, PLT, CRP, PCT, IL-6, LDH and so on) were analyzed. RESULTS: Significant differences were found out of CRP, PCT, IL-6 and LDH values between AP patients and controls (P < 0.05), even those results had significant difference between MAP group and SAP group (P < 0.05). In SAP group, the cut-off values of CRP, PCT, IL-6 and LDH were 16.62, 2.29, 16.66, 273.04; sensitivity 55.6%, 77.8%, 80.2%, 82.7%; specificity 73%, 94%, 85%, 96% and AUC 0.637, 0.929, 0.886, 0.919, respectively. The AUC of combined detection of CRP, PCT, IL-6 and LDH was 0.989 (95%CI). CONCLUSION: The combined detection of CRP, PCT, IL-6 and LDH has a high diagnostic value for judging the severity of AP.


Asunto(s)
Interleucina-6 , Pancreatitis , Enfermedad Aguda , Biomarcadores , Proteína C-Reactiva/análisis , Humanos , L-Lactato Deshidrogenasa , Pancreatitis/diagnóstico , Polipéptido alfa Relacionado con Calcitonina
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