1型戈谢病患者及其携带者外周血T滤泡辅助细胞(TFH)的特征

IF 2.1 4区 医学 Q3 HEMATOLOGY Blood Cells Molecules and Diseases Pub Date : 2023-05-01 DOI:10.1016/j.bcmd.2023.102728
Ramazan Uzen , Fahri Bayram , Huseyin Dursun , Fatih Kardas , Mustafa Cakir , Nurhan Cucer , Ahmet Eken , Hamiyet Donmez-Altuntas
{"title":"1型戈谢病患者及其携带者外周血T滤泡辅助细胞(TFH)的特征","authors":"Ramazan Uzen ,&nbsp;Fahri Bayram ,&nbsp;Huseyin Dursun ,&nbsp;Fatih Kardas ,&nbsp;Mustafa Cakir ,&nbsp;Nurhan Cucer ,&nbsp;Ahmet Eken ,&nbsp;Hamiyet Donmez-Altuntas","doi":"10.1016/j.bcmd.2023.102728","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><p>Gaucher disease<span><span><span> (GD) is the most common autosomal recessive </span>lipid storage disease. In this study, the changes in </span>TFH cells and IL-4 and IL-21 cytokines in blood samples of GD patients, carriers and healthy volunteers were investigated.</span></p></div><div><h3>Methods</h3><p>Two pretreatment type 1 GD patients, 20 currently treated type 1 GD patients, 6 carriers, and 27 healthy volunteers were enrolled in the study. TFH cell (CD45RA<sup>−</sup>CD4<sup>+</sup><span>CXCR5</span><sup>+</sup><span>) number, phenotype (PD1, ICOS expression), and cytokine production (IL-21, IL-4) were assessed via flow cytometric assays.</span></p></div><div><h3>Results</h3><p>No significant differences were found between the groups with respect to the number, frequency and PD1 or ICOS expression of TFH cells between healthy controls, patients and carriers. However, IL-4<sup>+</sup> TFH cells were significantly reduced both in percent and number in the treated GD patients compared with healthy controls (<em>p</em> &lt; 0.05). Interestingly, the IL-21<sup>+</sup><span> TFH cell number was increased in treated GD patients. When TFH cells were examined based on CXCR3 expression, the frequency of the PD1</span><sup>+</sup>Th17-Th2-like fraction (CXCR3<sup>−</sup>) was found to be significantly increased in treated GD patients.</p></div><div><h3>Conclusion</h3><p>To our knowledge, this is the first study to assess TFH cells in GD patients, and to show that the production of IL-4 and IL-21 by TFH cells and their subsets may be altered in type 1 GD patients.</p></div>","PeriodicalId":8972,"journal":{"name":"Blood Cells Molecules and Diseases","volume":"100 ","pages":"Article 102728"},"PeriodicalIF":2.1000,"publicationDate":"2023-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Characterization of peripheral blood T follicular helper (TFH) cells in patients with type 1 Gaucher disease and carriers\",\"authors\":\"Ramazan Uzen ,&nbsp;Fahri Bayram ,&nbsp;Huseyin Dursun ,&nbsp;Fatih Kardas ,&nbsp;Mustafa Cakir ,&nbsp;Nurhan Cucer ,&nbsp;Ahmet Eken ,&nbsp;Hamiyet Donmez-Altuntas\",\"doi\":\"10.1016/j.bcmd.2023.102728\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background</h3><p>Gaucher disease<span><span><span> (GD) is the most common autosomal recessive </span>lipid storage disease. In this study, the changes in </span>TFH cells and IL-4 and IL-21 cytokines in blood samples of GD patients, carriers and healthy volunteers were investigated.</span></p></div><div><h3>Methods</h3><p>Two pretreatment type 1 GD patients, 20 currently treated type 1 GD patients, 6 carriers, and 27 healthy volunteers were enrolled in the study. TFH cell (CD45RA<sup>−</sup>CD4<sup>+</sup><span>CXCR5</span><sup>+</sup><span>) number, phenotype (PD1, ICOS expression), and cytokine production (IL-21, IL-4) were assessed via flow cytometric assays.</span></p></div><div><h3>Results</h3><p>No significant differences were found between the groups with respect to the number, frequency and PD1 or ICOS expression of TFH cells between healthy controls, patients and carriers. However, IL-4<sup>+</sup> TFH cells were significantly reduced both in percent and number in the treated GD patients compared with healthy controls (<em>p</em> &lt; 0.05). Interestingly, the IL-21<sup>+</sup><span> TFH cell number was increased in treated GD patients. When TFH cells were examined based on CXCR3 expression, the frequency of the PD1</span><sup>+</sup>Th17-Th2-like fraction (CXCR3<sup>−</sup>) was found to be significantly increased in treated GD patients.</p></div><div><h3>Conclusion</h3><p>To our knowledge, this is the first study to assess TFH cells in GD patients, and to show that the production of IL-4 and IL-21 by TFH cells and their subsets may be altered in type 1 GD patients.</p></div>\",\"PeriodicalId\":8972,\"journal\":{\"name\":\"Blood Cells Molecules and Diseases\",\"volume\":\"100 \",\"pages\":\"Article 102728\"},\"PeriodicalIF\":2.1000,\"publicationDate\":\"2023-05-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Blood Cells Molecules and Diseases\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1079979623000050\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"HEMATOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Blood Cells Molecules and Diseases","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1079979623000050","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"HEMATOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

背景戈谢病(GD)是最常见的常染色体隐性遗传性脂质储存病。在本研究中,研究了GD患者、携带者和健康志愿者血液样本中TFH细胞以及IL-4和IL-21细胞因子的变化。方法2例治疗前1型GD患者、20例目前治疗的1型GD病人、6例携带者和27名健康志愿者参与研究。TFH细胞(CD45RA−CD4+CXCR5+)数量、表型(PD1、ICOS表达)和细胞因子产生(IL-21、IL-4)通过流式细胞仪测定进行评估。结果健康对照组、患者组和携带者组TFH细胞的数量、频率、PD1或ICOS表达均无显著差异。然而,与健康对照组相比,接受治疗的GD患者的IL-4+TFH细胞在百分比和数量上均显著减少(p<0.05)。有趣的是,接受治疗GD患者的IL-21+TFH细胞数量增加。当基于CXCR3表达检测TFH细胞时,发现在治疗的GD患者中PD1+Th17-Th2样部分(CXCR3-)的频率显著增加。结论据我们所知,这是首次评估1型GD患者TFH细胞及其亚群产生IL-4和IL-21的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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
Characterization of peripheral blood T follicular helper (TFH) cells in patients with type 1 Gaucher disease and carriers

Background

Gaucher disease (GD) is the most common autosomal recessive lipid storage disease. In this study, the changes in TFH cells and IL-4 and IL-21 cytokines in blood samples of GD patients, carriers and healthy volunteers were investigated.

Methods

Two pretreatment type 1 GD patients, 20 currently treated type 1 GD patients, 6 carriers, and 27 healthy volunteers were enrolled in the study. TFH cell (CD45RACD4+CXCR5+) number, phenotype (PD1, ICOS expression), and cytokine production (IL-21, IL-4) were assessed via flow cytometric assays.

Results

No significant differences were found between the groups with respect to the number, frequency and PD1 or ICOS expression of TFH cells between healthy controls, patients and carriers. However, IL-4+ TFH cells were significantly reduced both in percent and number in the treated GD patients compared with healthy controls (p < 0.05). Interestingly, the IL-21+ TFH cell number was increased in treated GD patients. When TFH cells were examined based on CXCR3 expression, the frequency of the PD1+Th17-Th2-like fraction (CXCR3) was found to be significantly increased in treated GD patients.

Conclusion

To our knowledge, this is the first study to assess TFH cells in GD patients, and to show that the production of IL-4 and IL-21 by TFH cells and their subsets may be altered in type 1 GD patients.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
4.90
自引率
0.00%
发文量
42
审稿时长
14 days
期刊介绍: Blood Cells, Molecules & Diseases emphasizes not only blood cells, but also covers the molecular basis of hematologic disease and studies of the diseases themselves. This is an invaluable resource to all those interested in the study of hematology, cell biology, immunology, and human genetics.
期刊最新文献
Immunodeficiency in children with Diamond Blackfan and Diamond Blackfan like anemia Hereditary disorders of ineffective erythropoiesis Red blood cell pyruvate kinase properties in Townes and Berkeley sickle cell disease mouse models – Of mice and men Short- and long-term alterations of hematopoietic cell lineages in rats with congenital iron deficiency Editorial Board
×
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