Clinical manifestations and expression of CD18 to guide the diagnosis of leukocyte adhesion deficiency type 1: Mexico experience

IF 2.5 4区 医学 Q3 ALLERGY Allergologia et immunopathologia Pub Date : 2023-11-01 DOI:10.15586/v51i6.914
Elma Isela Fuentes-Lara, Gabriel Emmanuel Arce-Estrada, Abner Bojalil-Cabildo, Marco Antonio Yamazaki-Nakashimada, Sara Elva Espinosa-Padilla, Luisa Berenise Gamez-Gonzalez, Rosa Mar�a Nideshda Ramirez-Uribe, Omar Josue Saucedo-Ramirez, Laura Berron-Ruiza
{"title":"Clinical manifestations and expression of CD18 to guide the diagnosis of leukocyte adhesion deficiency type 1: Mexico experience","authors":"Elma Isela Fuentes-Lara, Gabriel Emmanuel Arce-Estrada, Abner Bojalil-Cabildo, Marco Antonio Yamazaki-Nakashimada, Sara Elva Espinosa-Padilla, Luisa Berenise Gamez-Gonzalez, Rosa Mar�a Nideshda Ramirez-Uribe, Omar Josue Saucedo-Ramirez, Laura Berron-Ruiza","doi":"10.15586/v51i6.914","DOIUrl":null,"url":null,"abstract":"Background: Leukocyte adhesion deficiency type 1 (LAD-1) is an inborn error of immunity characterized by a defect in leukocyte trafficking. Methods: Patients with clinical suspicion of LAD-1 were referred to our institution. Complete blood count and flow cytometric analysis, to identify the expression of CD18, CD11b, and the lymphocyte population phenotyping, were performed, and statistical analysis was completed. Results: We report clinical manifestations and immunological findings of six Mexican patients diagnosed with LAD-1. The diagnosis was based on typical clinical presentation, combined with laboratory demonstration of leukocytosis, and significant reduction or near absence of CD18 and its associated molecules CD11a, CD11b, and CD11c on leukocytes. We found atypical manifestations, not described in other countries, such as early-onset autoimmunity or infections caused by certain microorganisms. Conclusions: Patients with LAD-1 may present with atypical manifestations, making flow cytometry an indispensable tool to confirm the diagnosis. We present the first report of LAD-1 patients in a Latin American country.","PeriodicalId":7536,"journal":{"name":"Allergologia et immunopathologia","volume":null,"pages":null},"PeriodicalIF":2.5000,"publicationDate":"2023-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Allergologia et immunopathologia","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.15586/v51i6.914","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"ALLERGY","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Leukocyte adhesion deficiency type 1 (LAD-1) is an inborn error of immunity characterized by a defect in leukocyte trafficking. Methods: Patients with clinical suspicion of LAD-1 were referred to our institution. Complete blood count and flow cytometric analysis, to identify the expression of CD18, CD11b, and the lymphocyte population phenotyping, were performed, and statistical analysis was completed. Results: We report clinical manifestations and immunological findings of six Mexican patients diagnosed with LAD-1. The diagnosis was based on typical clinical presentation, combined with laboratory demonstration of leukocytosis, and significant reduction or near absence of CD18 and its associated molecules CD11a, CD11b, and CD11c on leukocytes. We found atypical manifestations, not described in other countries, such as early-onset autoimmunity or infections caused by certain microorganisms. Conclusions: Patients with LAD-1 may present with atypical manifestations, making flow cytometry an indispensable tool to confirm the diagnosis. We present the first report of LAD-1 patients in a Latin American country.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
CD18的临床表现及表达指导1型白细胞粘附缺乏症的诊断:墨西哥经验
背景:白细胞粘附缺陷1型(LAD-1)是一种以白细胞运输缺陷为特征的先天性免疫错误。方法:对临床怀疑为lad1的患者进行转诊。进行全血细胞计数和流式细胞术分析,以确定CD18、CD11b的表达和淋巴细胞群体表型,并完成统计分析。结果:我们报告了6例诊断为lad1的墨西哥患者的临床表现和免疫学结果。诊断基于典型的临床表现,结合白细胞增多的实验室证明,以及白细胞上CD18及其相关分子CD11a, CD11b和CD11c的明显减少或几乎缺失。我们发现了其他国家未描述的非典型表现,如早发性自身免疫或某些微生物引起的感染。结论:lad1患者可能表现不典型,流式细胞术是诊断lad1不可缺少的工具。我们提出了拉丁美洲国家的第一份lad1患者报告。
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 去求助
来源期刊
CiteScore
3.70
自引率
0.00%
发文量
131
审稿时长
6-12 weeks
期刊介绍: Founded in 1972 by Professor A. Oehling, Allergologia et Immunopathologia is a forum for those working in the field of pediatric asthma, allergy and immunology. Manuscripts related to clinical, epidemiological and experimental allergy and immunopathology related to childhood will be considered for publication. Allergologia et Immunopathologia is the official journal of the Spanish Society of Pediatric Allergy and Clinical Immunology (SEICAP) and also of the Latin American Society of Immunodeficiencies (LASID). It has and independent international Editorial Committee which submits received papers for peer-reviewing by international experts. The journal accepts original and review articles from all over the world, together with consensus statements from the aforementioned societies. Occasionally, the opinion of an expert on a burning topic is published in the "Point of View" section. Letters to the Editor on previously published papers are welcomed. Allergologia et Immunopathologia publishes 6 issues per year and is included in the major databases such as Pubmed, Scopus, Web of Knowledge, etc.
期刊最新文献
Immune response regulation by transduced mesenchymal stem cells with decorin gene on bleomycin-induced lung injury, fibrosis, and inflammation. Jolkinolide B attenuates allergic airway inflammation and airway remodeling in asthmatic mice. Knockdown of GNL3 inhibits LUAD cell growth by regulating Wnt-β-catenin pathway. Methotrexate might become the sole treatment option for leukemia following the occurrence of Stevens-Johnson syndrome. Overexpression of USP8 inhibits inflammation and ferroptosis in chronic obstructive pulmonary disease by regulating the OTUB1/SLC7A11 signaling pathway.
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1