• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

20例大颗粒淋巴细胞增殖症中血小板型凝血酶受体的分析。

Analysis of the platelet-type thrombin receptor in 20 cases of large granular lymphocyte proliferations.

作者信息

Macey M G, Howells G L, Stone S R, Newland A C

机构信息

Department of Haematology, Royal London Hospital, Whitechapel, UK.

出版信息

Leukemia. 1996 Apr;10(4):687-92.

PMID:8618448
Abstract

The platelet-type thrombin receptor was expressed by large granular lymphocytes (LGLs) in a variety of proliferative diseases. Twenty patients with LGL proliferative disease were examined, including five T cell clones and a variety of polyclonal proliferations, some secondary to rheumatoid arthritis and Felty's syndrome; 17/20 showed high number of CD3+, CD8+, and CD57+ lymphocytes and 9/20 also had high numbers of CD16+ or CD 56+ positive lymphocytes. The thrombin receptor was present on more than 20% of the LGLs in 13/20 patients. The clonal T cell expansions showed the highest receptor expression with greater than 75% cells positive. Regression analysis of all 20 cases showed striking and highly statistically significant positive Spearman rank correlation between the proportion of thrombin receptor and CD57-positive LGLs (r = 0.56, P = 0.009). A negative correlation with CD56 was also found (r = -0.46, P= 0.043). Dual antibody flow cytometry showed the receptor was more often co-expressed with CD57 (64%) than with CD16 (19%) or CD56 (11%). The expression of the platelet-type thrombin receptor by LGLs of this phenotype raises the possibility of a functional role for thrombin in the pathogenesis of LGL proliferative diseases.

摘要

血小板型凝血酶受体在多种增殖性疾病的大颗粒淋巴细胞(LGL)中表达。对20例LGL增殖性疾病患者进行了检查,包括5个T细胞克隆和多种多克隆增殖,其中一些继发于类风湿关节炎和费尔蒂综合征;20例中有17例显示CD3 +、CD8 +和CD57 +淋巴细胞数量较高,20例中有9例CD16 +或CD56 +阳性淋巴细胞数量也较高。20例患者中有13例LGL上的凝血酶受体存在率超过20%。克隆性T细胞扩增显示受体表达最高,超过75%的细胞呈阳性。对所有20例病例的回归分析显示,凝血酶受体比例与CD57阳性LGL比例之间存在显著且具有高度统计学意义的正Spearman等级相关性(r = 0.56,P = 0.009)。还发现与CD56呈负相关(r = -0.46,P = 0.043)。双抗体流式细胞术显示,该受体与CD57共表达的情况更常见(64%),而与CD16(19%)或CD56(11%)共表达的情况较少。这种表型的LGL表达血小板型凝血酶受体增加了凝血酶在LGL增殖性疾病发病机制中发挥功能作用的可能性。

相似文献

1
Analysis of the platelet-type thrombin receptor in 20 cases of large granular lymphocyte proliferations.20例大颗粒淋巴细胞增殖症中血小板型凝血酶受体的分析。
Leukemia. 1996 Apr;10(4):687-92.
2
Lymphoproliferative disorder of granular lymphocytes: nine cases including one with features of CD56 (NKH1)-positive aggressive natural killer cell lymphoma.颗粒淋巴细胞增殖性疾病:9例报告,其中1例具有CD56(NKH1)阳性侵袭性自然杀伤细胞淋巴瘤特征
Mod Pathol. 1994 Oct;7(8):819-24.
3
Characteristic expansion of CD45RA CD27 CD28 CCR7 lymphocytes with stable natural killer (NK) receptor expression in NK- and T-cell type lymphoproliferative disease of granular lymphocytes.颗粒淋巴细胞NK和T细胞型淋巴增殖性疾病中,CD45RA CD27 CD28 CCR7淋巴细胞特征性扩增,自然杀伤(NK)受体表达稳定。
Br J Haematol. 2004 Jul;126(1):55-62. doi: 10.1111/j.1365-2141.2004.05005.x.
4
[Proliferation of large granular lymphocytes in patients with systemic lupus erythematosus].系统性红斑狼疮患者大颗粒淋巴细胞的增殖
Rev Clin Esp. 1995 Jun;195(6):373-9.
5
Thrombin receptor expression and function in large granular lymphocyte proliferative disorders.凝血酶受体在大颗粒淋巴细胞增殖性疾病中的表达及功能
Br J Haematol. 1994 Oct;88(2):383-8. doi: 10.1111/j.1365-2141.1994.tb05034.x.
6
Lymphoproliferative disorder of granular lymphocytes. A heterogeneous disease.颗粒淋巴细胞增殖性疾病。一种异质性疾病。
Arch Pathol Lab Med. 1992 Mar;116(3):242-8.
7
Analysis of lymphocyte phenotype and T cell receptor genotype in Felty's syndrome.费尔蒂综合征中淋巴细胞表型和T细胞受体基因型分析。
J Rheumatol. 1992 Jul;19(7):1058-64.
8
Flow cytometric characterization of human umbilical cord blood lymphocytes: immunophenotypic features.人脐带血淋巴细胞的流式细胞术特征:免疫表型特征
Haematologica. 1998 Mar;83(3):197-203.
9
CD3+, CD4-, CD8-, TCR alpha beta-, TCR gamma delta+ granular lymphocyte proliferative disorder without lymphocytosis and clinical symptoms.CD3阳性、CD4阴性、CD8阴性、TCRαβ阴性、TCRγδ阳性的颗粒淋巴细胞增殖性疾病,无淋巴细胞增多及临床症状。
Acta Haematol. 2000;104(1):54-6. doi: 10.1159/000041073.
10
CD8+, CD57+ T cells from healthy elderly subjects suppress neutrophil development in vitro: implications for the neutropenia of Felty's and large granular lymphocyte syndromes.健康老年受试者的CD8 +、CD57 + T细胞在体外抑制中性粒细胞发育:对费尔蒂综合征和大颗粒淋巴细胞综合征中性粒细胞减少症的影响。
Arthritis Rheum. 2000 Apr;43(4):834-43. doi: 10.1002/1529-0131(200004)43:4<834::AID-ANR14>3.0.CO;2-H.