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本文引用的文献

1
Increased circulating Ia-antigen-bearing T cells in type I diabetes mellitus.I型糖尿病中循环中携带Ia抗原的T细胞增加。
N Engl J Med. 1982 Apr 1;306(13):785-8. doi: 10.1056/NEJM198204013061305.
2
B-cell function in vitro during rubella infection.风疹感染期间B细胞的体外功能。
Infect Immun. 1984 Feb;43(2):589-92. doi: 10.1128/iai.43.2.589-592.1984.
3
Characterization of immunoregulatory T cells in EBV-induced infectious mononucleosis by monoclonal antibodies.通过单克隆抗体对EB病毒诱导的传染性单核细胞增多症中免疫调节性T细胞的特征分析。
N Engl J Med. 1981 Feb 19;304(8):460-2. doi: 10.1056/NEJM198102193040804.
4
Analysis of T lymphocyte subsets in cytomegalovirus mononucleosis.巨细胞病毒单核细胞增多症中T淋巴细胞亚群的分析
J Immunol. 1981 Jun;126(6):2114-6.
5
Characterization of human lymphocyte subpopulations: alloreactive cytotoxic T-lymphocyte precursor and effector cells are phenotypically distinct from Leu 2+ suppressor cells.人类淋巴细胞亚群的特征:同种异体反应性细胞毒性T淋巴细胞前体和效应细胞在表型上与Leu 2+抑制细胞不同。
J Clin Immunol. 1984 Sep;4(5):395-402. doi: 10.1007/BF00917143.
6
Peripheral blood T-cell subsets studied by monoclonal antibodies in type 1 (insulin-dependent) diabetes: effect of blood glucose control.
Diabetologia. 1984 Jul;27 Suppl:136-8. doi: 10.1007/BF00275671.
7
Lymphocyte subpopulations at the onset of type 1 (insulin-dependent) diabetes.
Diabetologia. 1984 Jul;27 Suppl:106-8. doi: 10.1007/BF00275661.
8
Alterations in lymphocyte subpopulations in type 1 (insulin-dependent) diabetes mellitus: exploration of possible mechanisms and relationships to autoimmune phenomena.1型(胰岛素依赖型)糖尿病患者淋巴细胞亚群的改变:可能机制的探索及其与自身免疫现象的关系。
Diabetologia. 1984 Jul;27 Suppl:102-5. doi: 10.1007/BF00275660.
9
Immunoregulatory T-lymphocyte subset deficiency in newly diagnosed type 1 (insulin-dependent) diabetes mellitus.新诊断的1型(胰岛素依赖型)糖尿病患者免疫调节性T淋巴细胞亚群缺乏
Diabetologia. 1984 Jun;26(6):426-30. doi: 10.1007/BF00262214.
10
Characterization of a phenotypically distinct subpopulation of Leu-2+ cells that suppresses T cell proliferative responses.对抑制T细胞增殖反应的Leu-2+细胞表型不同亚群的特征描述。
J Immunol. 1983 Dec;131(6):2757-61.

1型(胰岛素依赖型)糖尿病患者CD4和CD8 T淋巴细胞亚群的异常。

Abnormalities within CD4 and CD8 T lymphocytes subsets in type 1 (insulin-dependent) diabetes.

作者信息

Ilonen J, Surcel H M, Käär M L

机构信息

Department of Medical Microbiology, University of Oulu, Finland.

出版信息

Clin Exp Immunol. 1991 Aug;85(2):278-81. doi: 10.1111/j.1365-2249.1991.tb05718.x.

DOI:10.1111/j.1365-2249.1991.tb05718.x
PMID:1677834
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1535750/
Abstract

Abnormalities in the proportions of various T lymphocyte subpopulations have been found in a number of autoimmune diseases. Monoclonal antibodies labelled with various fluorochromes were used here to define the percentages of subsets, and especially to divide CD4+ (helper/inducer) and CD8+ (suppressor/cytotoxic) cells into phenotypic subgroups. Blood samples were analysed from 25 patients (age 10.1 +/- 3.7 years) with recently diagnosed insulin-dependent diabetes mellitus (IDDM) and 25 age- and sex-matched control subjects. The percentages of CD4+ cells and CD4+CD45RA+ cells described as naive T helper cells or suppressor/inducers were increased in the IDDM patients (P less than 0.05 and P less than 0.05. Student's t-test, respectively), whereas the percentage of CD4+CD45RA- cells (memory T-helper cells, helper/inducers) was similar in the patients and controls. The percentage of CD8+CD11b+ cells containing suppressor/effector lymphocytes was decreased in the IDDM patients as compared with the controls (P less than 0.01) but no significant difference was seen in total CD8+ cells. The percentages of CD3+ cells and the proportions of these simultaneously positive for HLA-DR antigen (activated T cells) were also increased in the recent IDDM patients (P less than 0.001 and P less than 0.05, respectively), while the proportion of CD20+ B cells was decreased (P less than 0.05). The findings support the view that disturbed immune regulation occurs in IDDM and indicate that further division of T cell subpopulations may clarify our understanding of the disease process.

摘要

在许多自身免疫性疾病中均发现了各种T淋巴细胞亚群比例异常的情况。在此使用用各种荧光染料标记的单克隆抗体来确定亚群的百分比,尤其是将CD4 +(辅助/诱导)和CD8 +(抑制/细胞毒性)细胞分为表型亚组。对25例近期诊断为胰岛素依赖型糖尿病(IDDM)的患者(年龄10.1±3.7岁)和25名年龄及性别匹配的对照受试者的血样进行了分析。IDDM患者中被描述为初始T辅助细胞或抑制/诱导细胞的CD4 +细胞和CD4 + CD45RA +细胞的百分比增加(分别为P <0.05和P <0.05,学生t检验),而患者和对照中CD4 + CD45RA-细胞(记忆T辅助细胞,辅助/诱导细胞)的百分比相似。与对照组相比,IDDM患者中含有抑制/效应淋巴细胞的CD8 + CD11b +细胞的百分比降低(P <0.01),但总CD8 +细胞未见明显差异。近期IDDM患者中CD3 +细胞的百分比以及同时对HLA-DR抗原呈阳性的这些细胞的比例(活化T细胞)也增加(分别为P <0.001和P <0.05),而CD20 + B细胞的比例降低(P <0.05)。这些发现支持了IDDM中发生免疫调节紊乱的观点,并表明T细胞亚群的进一步划分可能会阐明我们对疾病过程的理解。