摩洛哥儿童淋巴细胞的年龄分层参考值。

Q3 Medicine
Aicha El Allam, Sara El Fakihi, Hicham Tahoune, Karima Sahmoudi, Houria Bousserhane, Youssef Bakri, Naima El Hafidi, Fouad Seghrouchni
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引用次数: 2

摘要

在许多疾病中,循环淋巴细胞的数量发生改变,包括增加(淋巴细胞增多)或减少(淋巴细胞减少)。因此,评估血液淋巴细胞总数和淋巴细胞亚群的相对分布是临床诊断包括儿科疾病和障碍在内的许多疾病的关键一线工具。然而,对这些数据的解释需要将患者的结果与可靠的参考值进行比较。血液淋巴细胞亚群数量也受遗传多态性、免疫原性和环境因素的影响,在人群之间差异很大。虽然最佳做法参考值应在当地健康受试者的代表性人群中确定,但由于缺乏土著参考值,迄今为止,摩洛哥使用的是高加索参考值。高加索人与摩洛哥人之间血液淋巴细胞亚群参考值的潜在差异可能对儿科和儿童疾病的诊断产生不利影响,如摩洛哥原发性免疫缺陷(PID)。目的:本研究的目的是为摩洛哥儿童建立按年龄分层的血淋巴细胞亚群正常参考值。方法:采用流式细胞术检测83名摩洛哥健康受试者淋巴细胞亚群浓度,将其分为0-1、1-2、2-6、6-12和> 12-18(成人)5个年龄组。结果:测量了t细胞、B细胞和自然杀伤(NK)细胞的主要淋巴细胞亚群的绝对和相对数量,并与先前描述的喀麦隆、土耳其、美国和荷兰人群的参考值进行了比较。此外,我们还观察到,在我们的研究组中,淋巴细胞亚群的绝对种群大小与年龄相关。随着年龄的增长,CD3+CD4+辅助性T淋巴细胞的相对比例下降,到12 -成年时,CD3+CD4+辅助性T淋巴细胞和CD3+CD8+细胞毒性T淋巴细胞以及CD3- cd19 + B淋巴细胞的比例也下降。最后,我们将摩洛哥研究组的中位数和范围与喀麦隆、土耳其、美国和荷兰发表的结果进行了比较,发现淋巴细胞亚群绝对数量和相对比例的中位数和平均值存在显著差异,特别是在0-1岁和1-2岁年龄组。在12岁以上,摩洛哥的数值较低。对于NK细胞,摩洛哥值也较低。结论:这项研究的结果对提高参考区间的阈值具有重大影响,这些阈值通常用于诊断儿科疾病,例如在摩洛哥人口中诊断aids或母婴传播艾滋病毒。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Age-stratified pediatric reference values of lymphocytes in the Moroccan population.

The number of circulating lymphocytes is altered in a number of diseases including either increase (lymphocytosis) or decrease (lymphocytopenia). Therefore, the assessment of total blood lymphocyte numbers and the relative distribution of lymphocyte subsets is a critical front-line tool in the clinical diagnosis of a number of diseases, including pediatric diseases and disorders. However, the interpretation of this data requires comparison of patient's results to reliable reference values. Blood lymphocyte subpopulation numbers are also subject to genetic polymorphisms, immunogenic and environmental factors and vary greatly between populations. While the best practice reference values should be established within local representative populations of healthy subjects, to date, Caucasian reference values are used in Morocco due to the absence of indigenous reference values. Potential differences in blood lymphocyte subpopulation reference values between Caucasian versus Moroccan populations can adversely affect the diagnosis of pediatric and childhood diseases and disorders such as primary immunodeficiency (PID) in Morocco.

Objective: The aim of this study was to establish the age-stratified normal reference values of blood lymphocyte subsets for the pediatric Moroccan population.

Methods: We measured the concentration of lymphocyte subpopulations by flow cytometry from 83 Moroccan healthy subjects stratified into 5 age groups of 0-1, 1-2, 2-6, 6-12 and > 12-18 (adult).

Results: The absolute and relative amounts of the main lymphocyte subsets of T-cells, B cells and Natural Killer (NK) cells were measured and compared to previously described reference values from Cameroonian, Turkish, American and Dutch populations. Additionally, we also observed an age-related decline in the absolute population sizes of lymphocyte subsets within our study group. Relative proportions of CD3+CD4+ helper T lymphocytes decreased with increasing age and by 12 years-adult age, both proportions of CD3+CD4+ helper T lymphocytes and CD3+CD8+ cytotoxic T lymphocytes, as well as CD3-CD19+ B lymphocytes were also decreased. Finally, we compared the median values and range of our Moroccan study group with that of published results from Cameroon, Turkey, USA and Netherlands and observed significant differences in median and mean values of absolute number and relative proportions of lymphocyte subsets especially at 0-1 years and 1-2 years age groups. Above age 12 years, the Moroccan values were lower. For NK cells, the Moroccan values are also lower.

Conclusions: The results of this study have a significant impact in improving the threshold values of the references intervals routinely used in the diagnosis of paediatric diseases such as PIDs or mother-to-child transmitted HIV within the Moroccan population.

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来源期刊
Human Antibodies
Human Antibodies Medicine-Immunology and Allergy
CiteScore
3.50
自引率
0.00%
发文量
27
期刊介绍: Human Antibodies is an international journal designed to bring together all aspects of human hybridomas and antibody technology under a single, cohesive theme. This includes fundamental research, applied science and clinical applications. Emphasis in the published articles is on antisera, monoclonal antibodies, fusion partners, EBV transformation, transfections, in vitro immunization, defined antigens, tissue reactivity, scale-up production, chimeric antibodies, autoimmunity, natural antibodies/immune response, anti-idiotypes, and hybridomas secreting interesting growth factors. Immunoregulatory molecules, including T cell hybridomas, will also be featured.
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