Evaluation of the relationship between de‐novo DSA development and CXCR5+PD‐1+CD8+ T cells and PD‐1/PD‐L1 mRNA expression in kidney transplant recipients

医学 CD8型 细胞毒性T细胞 PD-L1 流式细胞术 内科学 肾移植 移植 T细胞 免疫学 免疫系统 生物 免疫疗法 生物化学 体外
作者
Nurten Sayin Ekinci,V.T. Yılmaz,Yahya Kilinc,Hüseyin Koçak,Şule Darbaş,Abdullah Kısaoğlu,Bülent Aydınlı,Sezin Yakut,Fahri Uçar
出处
期刊:Clinical transplantation [Wiley]
卷期号:37 (11)
标识
DOI:10.1111/ctr.15104
摘要

The relationship between the Follicular Cytotoxic T cell subgroup and expression levels of PD1/PD-L1 genes and the development of donor specific antibody (DSA) is unknown. In this study, we aimed to examine CD8+CXCR5+PD-1+ follicular cytotoxic T cell levels and expression levels of PD1/PD-L1 genes in peripheral blood lymphocytes in de-novo DSA positive and negative kidney transplant recipients (KTR).In our study, expression of PD-1/ PD-L1 genes by Real-Time Quantitative PCR method and CD8+CXCR5+PD-1+ T cell expression levels by flow cytometric method were obtained from peripheral blood samples. 63 participants were included in the study (de-novo DSA positive recipients (n = 22, group 1), de-novo DSA negative recipients (n = 20, group 2) and healthy control (n = 21, group 3). All patients had negative PRA before kidney transplantation. Expression (%) levels of target cells were evaluated by flow cytometry method. IBM SPSS Statistics for Windows Version 22 and R.3.3.2 software were used to evaluate the data.The demographic data of the groups were similar. PD-1 mRNA expression was higher in de-novo DSA positive KTR than negative (respectively, 1.03 ± .29/.82 ± .15, p: .001). CD8+CXCR5+PD-1+ T cell expression levels were found to be higher in the de-novo DSA positive group than in the negative group and similar to the healthy group (respectively, 3.06 ± 1.98/.52 ± .40, p:.001, 3.06 ± 1.98/2.78 ± .59, p:.62). The percentage of CD8+CXCR5+PD-1+ expressing T cells was significantly lower in the HLA-Class II+ group than other groups (HLA CI/II/ I+II, respectively, 3.63 ± 2.72/1.65 ± .50/3.68 ± 1.67, p: .04).In our study, a significant relationship was found between DSA formation and PD-1 mRNA level and CD8+CXCR5+PD-1+ follicular cytotoxic T cell in KTR.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
PDF的下载单位、IP信息已删除 (2025-6-4)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
nuannuan发布了新的文献求助10
1秒前
帅气男孩应助Coco采纳,获得10
2秒前
量子星尘发布了新的文献求助10
3秒前
加一完成签到,获得积分10
4秒前
熊蔓蔓完成签到,获得积分10
6秒前
dingyi601完成签到,获得积分10
6秒前
tt123完成签到,获得积分10
6秒前
7秒前
糟糕的学姐完成签到,获得积分10
8秒前
yookia应助vbbbj采纳,获得10
8秒前
今后应助124cndhaP采纳,获得30
9秒前
meng完成签到 ,获得积分10
10秒前
HHHZZZ完成签到,获得积分10
10秒前
香蕉沧海发布了新的文献求助10
11秒前
高挑的梦芝完成签到,获得积分10
12秒前
婷123发布了新的文献求助20
12秒前
13秒前
我不爱池鱼应助Torment采纳,获得10
13秒前
小阮完成签到,获得积分10
13秒前
13秒前
迷人问兰发布了新的文献求助30
14秒前
vovoking完成签到 ,获得积分10
14秒前
15秒前
Jasper应助nuannuan采纳,获得10
15秒前
hzwyyds应助栗子采纳,获得10
17秒前
李希发布了新的文献求助50
17秒前
英俊的铭应助元宝采纳,获得10
18秒前
ZJHYNL应助111采纳,获得20
18秒前
早睡早起发布了新的文献求助10
19秒前
鳗鱼焦完成签到 ,获得积分10
19秒前
新威宝贝发布了新的文献求助10
20秒前
Jocd完成签到,获得积分10
25秒前
小二郎应助SAOKA采纳,获得10
27秒前
农夫果园完成签到,获得积分10
29秒前
31秒前
加二完成签到,获得积分10
32秒前
33秒前
辞忧完成签到,获得积分10
33秒前
无情的豆芽完成签到 ,获得积分10
36秒前
ASDS发布了新的文献求助10
36秒前
高分求助中
The Mother of All Tableaux Order, Equivalence, and Geometry in the Large-scale Structure of Optimality Theory 2400
Ophthalmic Equipment Market by Devices(surgical: vitreorentinal,IOLs,OVDs,contact lens,RGP lens,backflush,diagnostic&monitoring:OCT,actorefractor,keratometer,tonometer,ophthalmoscpe,OVD), End User,Buying Criteria-Global Forecast to2029 2000
Optimal Transport: A Comprehensive Introduction to Modeling, Analysis, Simulation, Applications 800
Official Methods of Analysis of AOAC INTERNATIONAL 600
ACSM’s Guidelines for Exercise Testing and Prescription, 12th edition 588
A new approach to the extrapolation of accelerated life test data 500
T/CIET 1202-2025 可吸收再生氧化纤维素止血材料 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 遗传学 基因 物理化学 催化作用 冶金 细胞生物学 免疫学
热门帖子
关注 科研通微信公众号,转发送积分 3954469
求助须知:如何正确求助?哪些是违规求助? 3500461
关于积分的说明 11099572
捐赠科研通 3230989
什么是DOI,文献DOI怎么找? 1786217
邀请新用户注册赠送积分活动 869884
科研通“疑难数据库(出版商)”最低求助积分说明 801713