Suppr超能文献

B细胞慢性淋巴细胞白血病和良性B淋巴细胞增多症患者血清中辅助因子(IL-1α、IL-1β和IL-6)、T细胞产物(sCD4和sCD8)、可溶性白细胞介素-2受体和β2-微球蛋白的水平。

Serum levels of helper factors (IL-1 alpha, IL-1 beta and IL-6), T-cell products (sCD4 and sCD8), sIL-2R and beta 2-microglobulin in patients with B-CLL and benign B lymphocytosis.

作者信息

Aguilar-Santelises M, Loftenius A, Ljungh C, Svenson S B, Andersson B, Mellstedt H, Jondal M

机构信息

Department of Immunology, Karolinska Institute, Stockholm, Sweden.

出版信息

Leuk Res. 1992 Jun-Jul;16(6-7):607-13. doi: 10.1016/0145-2126(92)90009-v.

Abstract

Chronic B-lymphocytic leukemia (B-CLL) cells may be regulated by immune functions. In an attempt to analyze such functions, helper factors (IL-1 alpha, IL-1 beta and IL-6), T-cell products (sCD4 and sCD8) and sIL-2R and beta 2-microglobulin were measured in serum of patients at different stages of the disease. Patients were classified as having monoclonal lymphocytosis of undetermined significance (MLUS), stable or progressive B-CLL respectively. A significant, but modest, increase of IL-1 alpha was found in B-CLL as well as in MLUS patients whereas IL-6 levels were increased in MLUS only. sCD8 levels were increased both in MLUS and B-CLL but augmented sCD4 concentrations were found statistically significant only in progressive B-CLL. beta 2-microglobulin and sIL-2R were related to the extent of the monoclonal B-cell fraction. The data indicate an increased T-suppressor activity in both MLUS and B-CLL patients and a selective increase of helper T-cell activity in progressive B-CLL. A possible immunoregulatory influence of helper T cells on disease progression is discussed.

摘要

慢性B淋巴细胞白血病(B-CLL)细胞可能受免疫功能调节。为分析此类功能,对处于疾病不同阶段患者血清中的辅助因子(IL-1α、IL-1β和IL-6)、T细胞产物(sCD4和sCD8)以及sIL-2R和β2-微球蛋白进行了检测。患者分别被归类为意义未明的单克隆淋巴细胞增多症(MLUS)、稳定型或进展型B-CLL。在B-CLL患者以及MLUS患者中均发现IL-1α有显著但适度的升高,而IL-6水平仅在MLUS中升高。sCD8水平在MLUS和B-CLL中均升高,但sCD4浓度升高仅在进展型B-CLL中具有统计学意义。β2-微球蛋白和sIL-2R与单克隆B细胞比例程度相关。数据表明MLUS和B-CLL患者中T抑制活性均增加,且进展型B-CLL中辅助性T细胞活性选择性增加。讨论了辅助性T细胞对疾病进展可能的免疫调节影响。

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