Kflc Index Evaluation to Assess Immunoglobulin Intrathecal Synthesis

M. Pieri, R. Zenobi, M. Dessi
{"title":"Kflc Index Evaluation to Assess Immunoglobulin Intrathecal Synthesis","authors":"M. Pieri, R. Zenobi, M. Dessi","doi":"10.4172/2155-9899.1000515","DOIUrl":null,"url":null,"abstract":"Multiple sclerosis (MS), where intrathecal synthesis is present, is one of the most common neurological diseases of the young adults in CNS, and it often causes deficits since its early stage. Clinically isolated syndrome (CIS) is a central nervous system demyelinating event isolated in time and it is compatible with the possible future development of multiple sclerosis (MS). Early risk stratification for conversion to MS helps with treatment decisions [3]. Currently it is possible to identify the presence of antibodies by the detection of oligoclonal immunoglobulin bands (OCBs) in cerebrospinal fluid (CSF) [4,5]. It is necessary to differentiate the origin of immunoglobulin (Ig) in the CSF before intrathecal immunoglobulin synthesis can be diagnosed [6]. Immunoglobulin light chains that are circulating in serum in a free state are called Free Light Chains (FLCs). These can be both kappa (kFLCs) and lambda type (λFLCs). We examined 80 CSF/serum pairs from patients of the neurological clinic who underwent analysis of OCBs during their diagnostic workup. We analysed the correlation between OCBs test and the FLCs nephelometric assay [1] and we assessed the diagnostic accuracy of a nephelometric assay for k free light chain determination in cerebrospinal fluid and serum. The correlation between the two methods was very good, but the method to determine OCBs is timeconsuming, not quantitative, and also relatively insensitive and operator depending. [1,2,7-9]. On the contrary, the nephelometric determination of FLCs in serum and CSF is a quantitative method and it might be a sensitive alternative to the above-mentioned approach.","PeriodicalId":15473,"journal":{"name":"Journal of clinical & cellular immunology","volume":"68 1","pages":"1-2"},"PeriodicalIF":0.0000,"publicationDate":"2017-08-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of clinical & cellular immunology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4172/2155-9899.1000515","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Multiple sclerosis (MS), where intrathecal synthesis is present, is one of the most common neurological diseases of the young adults in CNS, and it often causes deficits since its early stage. Clinically isolated syndrome (CIS) is a central nervous system demyelinating event isolated in time and it is compatible with the possible future development of multiple sclerosis (MS). Early risk stratification for conversion to MS helps with treatment decisions [3]. Currently it is possible to identify the presence of antibodies by the detection of oligoclonal immunoglobulin bands (OCBs) in cerebrospinal fluid (CSF) [4,5]. It is necessary to differentiate the origin of immunoglobulin (Ig) in the CSF before intrathecal immunoglobulin synthesis can be diagnosed [6]. Immunoglobulin light chains that are circulating in serum in a free state are called Free Light Chains (FLCs). These can be both kappa (kFLCs) and lambda type (λFLCs). We examined 80 CSF/serum pairs from patients of the neurological clinic who underwent analysis of OCBs during their diagnostic workup. We analysed the correlation between OCBs test and the FLCs nephelometric assay [1] and we assessed the diagnostic accuracy of a nephelometric assay for k free light chain determination in cerebrospinal fluid and serum. The correlation between the two methods was very good, but the method to determine OCBs is timeconsuming, not quantitative, and also relatively insensitive and operator depending. [1,2,7-9]. On the contrary, the nephelometric determination of FLCs in serum and CSF is a quantitative method and it might be a sensitive alternative to the above-mentioned approach.
评价免疫球蛋白鞘内合成的Kflc指数
存在鞘内合成的多发性硬化症(MS)是年轻成人中枢神经系统中最常见的神经系统疾病之一,从早期开始就经常导致缺陷。临床孤立综合征(CIS)是一种及时分离的中枢神经系统脱髓鞘事件,与多发性硬化症(MS)未来可能的发展相适应。早期转化为多发性硬化症的风险分层有助于制定治疗决策[3]。目前,可以通过检测脑脊液(CSF)中的寡克隆免疫球蛋白带(ocb)来识别抗体的存在[4,5]。在诊断鞘内免疫球蛋白合成前,有必要鉴别脑脊液中免疫球蛋白(Ig)的来源[6]。在血清中以游离状态循环的免疫球蛋白轻链称为游离轻链(FLCs)。它们可以是kappa型(kFLCs)和λ型(λFLCs)。我们检查了80对脑脊液/血清,这些患者在诊断过程中接受了ocb分析。我们分析了OCBs试验和FLCs浊度测定法之间的相关性[1],并评估了浊度测定法在脑脊液和血清中游离轻链k的诊断准确性。两种方法之间的相关性非常好,但确定ocb的方法耗时,非定量,并且相对不敏感和依赖于操作员。(1、2、7 - 9)。相反,浊度法测定血清和脑脊液中的FLCs是一种定量方法,可能是上述方法的一种敏感的替代方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信