循环细胞因子和血液学特征:hiv / aids疾病进展的可能生物标志物

J. Mugwe, M. Gicheru, J. Mwatha
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The study group composed of male and female of different ages ranging from 7-72 years.  Hematology auto analyzer system was used to analyze hematological parameters and indices.  Types and concentrations of cytokines were determined using multiplex cytokine immunoassay by flow cytometry using Becton and Dickinsonfluorescence activated cell sorter (BD FACS) count.  Descriptive statistics were applied and a p- value < 0.05 was considered statistically significant. Results: This study found a significant difference in mean Interleukin 12p70 (p<0.001), Tumor Necrosis Factor (p<0.05), Interleukin 10 (p<0.05), Interleukin 6 (p<0.005) and interleukin 1β (p<0.05) between HIV negative patients, treatment naive HIV patients and HIV patients on highly active antiretroviral therapy (HAART). 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引用次数: 0

摘要

本研究旨在确定新诊断的HIV患者血浆中可测量的循环细胞因子和血液学特征,作为可能预测急性HIV感染过程中HIV和AIDS疾病进展的生物标志物。方法:采用前瞻性横断面研究设计,在肯尼亚纳库鲁省总医院招募参与者。研究小组包括那些在开始治疗之前和之后HIV呈阳性的人以及HIV呈阴性的人。研究组由7-72岁的男女组成。血液学自动分析系统用于血液学参数和指标的分析。采用Becton和dickinson荧光活化细胞分选仪(BD FACS)计数,流式细胞术采用多重细胞因子免疫分析法测定细胞因子的类型和浓度。采用描述性统计,p值< 0.05为差异有统计学意义。结果:本研究发现,在HIV阴性患者、初治HIV患者和接受高效抗逆转录病毒治疗(HAART)的HIV患者中,白细胞介素12p70 (p<0.001)、肿瘤坏死因子(p<0.05)、白细胞介素10 (p<0.05)、白细胞介素6 (p<0.005)和白细胞介素1β (p<0.05)的平均值均有显著差异。在接受治疗的初治HIV患者中,IL-12p70与HGB有显著相关性(p<0.05);TNF与MPV之间的差异(p<0.001);IL-10与PDW差异有统计学意义(p<0.005);IL-6与Gran#之间存在差异(p-0.05);IL-1β与PDW之间存在差异(p<0.005)。结论:HIV感染早期具有较高的循环细胞因子水平,可作为HIV感染早期免疫激活的生物标志物和指标。本研究结果还表明,急性HIV感染引起多种血液学变化,涉及所有血液参数和指标,其中一些可能作为HIV/AIDS疾病进展的指标。文章DOI: https://dx.doi.org/10.20319/lijhls.2019.51.105118本作品遵循知识共享署名-非商业4.0国际许可协议。要查看本许可协议的副本,请访问http://creativecommons.org/licenses/by-nc/4.0/或致函美国山景城CA 94042邮政信箱1866号创用cc。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
CIRCULATORY CYTOKINES AND HEMATOLOGICAL PROFILES: POSSIBLE BIOMARKERS OF HIV/AIDS DISEASE PROGRESSION
Introduction: This study sought to identify circulatory cytokines and hematological profiles measureable in blood plasma in newly diagnosed HIV patients as possible biomarkers that could predict the progression of HIV and AIDS disease in the course of acute HIV infection. Methodology: A prospective cross sectional study design was used to recruit the participants at the Nakuru Provincial General hospital in Kenya.  The study group included those who were HIV positive before and after commencing therapy and those who were HIV negative. The study group composed of male and female of different ages ranging from 7-72 years.  Hematology auto analyzer system was used to analyze hematological parameters and indices.  Types and concentrations of cytokines were determined using multiplex cytokine immunoassay by flow cytometry using Becton and Dickinsonfluorescence activated cell sorter (BD FACS) count.  Descriptive statistics were applied and a p- value < 0.05 was considered statistically significant. Results: This study found a significant difference in mean Interleukin 12p70 (p<0.001), Tumor Necrosis Factor (p<0.05), Interleukin 10 (p<0.05), Interleukin 6 (p<0.005) and interleukin 1β (p<0.05) between HIV negative patients, treatment naive HIV patients and HIV patients on highly active antiretroviral therapy (HAART). Among the treatment naive HIV patients, significant associations were observed between IL-12p70 and HGB (p<0.05); between TNF and MPV (p<0.001); between IL-10 and PDW (p<0.005); between IL-6 and Gran# (p-0.05); between IL-1β and PDW (p<0.005). Conclusion: The early period of infection with HIV is characterized by high circulatory cytokines levels and could be useful biomarkers and indicators of early immune activation of HIV infection. The results from this study also showed that acute HIV infection induces several hematological changes, involving all the blood parameters and indices, some of which may act as indicators of HIV/AIDS disease progression. Article DOI: https://dx.doi.org/10.20319/lijhls.2019.51.105118 This work is licensed under the Creative Commons Attribution-Non-commercial 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc/4.0/ or send a letter to Creative Commons, PO Box 1866, Mountain View, CA 94042, USA.
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