RNF43 p.G659fs 通过 PI3K/AKT/mTOR 信号通路和 HLA-E 上调导致 MSI-high 结直肠癌中 NK 细胞功能障碍
RNF43 p.G659fs leads to natural killer cell dysfunction in MSI-high colorectal cancer through PI3K/AKT/mTOR signaling and HLA-E up-regulation.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Association of serum vitamin B(12) with immuno-hematological parameters in treatment-naive HIV positive cases.
Association of serum vitamin B(12) with immuno-hematological parameters in treatment-naive HIV positive cases.
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在早期阶段,快速分裂的免疫细胞导致微量营养素消耗增加,进而造成维生素 B12 缺乏。
人类免疫缺陷病毒(HIV)感染的表现与维生素B12缺乏症存在重叠,因此早期诊断和干预非常重要。本研究旨在确定新确诊HIV阳性患者的血清维生素B12水平,并分析其与CD4和CD8计数、临床分期以及血液和生化状态的关系。
研究纳入55例18岁以上确诊HIV患者及55例年龄和性别匹配的健康对照。使用流式细胞仪检测CD4和CD8计数,并测定全血细胞计数、血清维生素B12、叶酸、铁蛋白和C反应蛋白(CRP)。
HIV阳性患者血清维生素B12显著低于健康对照,均值分别为240.62±56.75 pg/mL和317.57±52.56 pg/mL。HIV阳性患者CD4计数降低,铁蛋白和CRP水平升高。亚组分析显示,维生素B12水平与CD4计数呈正相关。CD8计数也与血清B12水平显著相关,但其变化与B12缺乏程度并不成比例。近三分之一HIV阳性患者存在维生素B12缺乏。
感染早期,快速分裂的免疫细胞会增加微量营养素消耗,导致维生素B12缺乏;这会造成甲基化障碍,影响免疫功能和NK细胞活性,并导致CD8细胞数量增加。因此,维生素B12可能是HIV感染的一种有益免疫调节因子,在资源受限环境中也可能产生重要影响。
The manifestations of human immunodeficiency virus (HIV) infection and vitamin B 12 deficiency overlap each other, so early diagnosis and intervention is important. The study aims to find out serum vitamin B 12 level and its association with CD4 and CD8 count, clinical-staging, and hemato-biochemical status in newly diagnosed HIV positive cases. METHODOLOGY: Fifty-five confirmed HIV cases above 18 years of age and equal number of age and sex matched controls were recruited for the study. CD4 and CD8 counts were analyzed by Flow cytometer. Complete Blood Count, Serum vitamin B 12 , Folic acid, ferritin, and C-Reactive Protein (CRP) concentration were done.
Serum vitamin B 12 was observed to be significantly low in HIV positive cases than healthy controls with a mean value of 240.62 56.75 pg/ml and 317.57 52.56 pg/ml, respectively. Decreased CD4 counts with elevated levels of ferritin and CRP was seen in HIV positive individuals. The subgroup analysis based on the levels of vitamin B 12 was directly proportional to CD4 counts. CD8 counts also registered a significant association with serum B 12 level, yet the response is not proportionate with the level of vitamin B 12 deficiency. Nearly one-third of HIV positive cases revealed vitamin B 12 deficiency.
During the early stage, fast dividing immune cells cause increased consumption of micronutrients contributing toward vitamin B 12 deficiency. It contributes to disorders in methylation affecting the immune function and NK Cell activity which increases the number of CD8 cells. Hence, vitamin B 12 is a beneficial immunological modulator of HIV infection and can be a potent game changer in resource constrained set up.
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