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系统性红斑狼疮中I型蛋白激酶A T细胞缺陷的高患病率。

High prevalence of T cell type I protein kinase A deficiency in systemic lupus erythematosus.

作者信息

Kammer G M

机构信息

Department of Internal Medicine, Wake Forest University School of Medicine, Winston-Salem, North Carolina 27157, USA.

出版信息

Arthritis Rheum. 1999 Jul;42(7):1458-65. doi: 10.1002/1529-0131(199907)42:7<1458::AID-ANR20>3.0.CO;2-P.

DOI:10.1002/1529-0131(199907)42:7<1458::AID-ANR20>3.0.CO;2-P
PMID:10403274
Abstract

OBJECTIVE

To estimate the prevalence of protein kinase A type I isozyme (PKA-I) deficiency in a cohort of systemic lupus erythematosus (SLE) patients, and to establish whether the isozyme deficiency is associated with SLE disease activity.

METHODS

Thirty-five SLE patients and 35 age-, sex-, and race-matched normal controls were studied. Fifteen subjects were restudied on at least 3 occasions over a 4-year interval. Clinical disease activity was estimated by the Systemic Lupus Erythematosus Disease Activity Index (SLEDAI), and the T cell activation markers CD25+ and HLA-DR+ were quantified by flow cytometry. PKA-I isozyme activities were quantified in enriched T cells. Statistical analyses were performed by Student's t-test, Mann Whitney U test, and Pearson product moment test.

RESULTS

The mean PKA-I activity in SLE T cells (540 pmoles/minute/mg of protein) was significantly lower than that in control T cells (1,578 pmoles/ minute/mg of protein) (P<0.001). The prevalence of isozyme deficiency in this cohort was 80%. During a 4-year interval, PKA-I activities remained significantly reduced, whereas SLEDAI scores significantly improved. There was no relationship between deficient PKA-I activity and either SLEDAI scores or the proportion of T cells bearing CD25+ or HLA-DR+ activation markers.

CONCLUSION

There is a high prevalence of deficient T cell PKA-I isozyme activity in SLE that persists over time and is independent of SLE disease activity.

摘要

目的

评估系统性红斑狼疮(SLE)患者队列中蛋白激酶A I型同工酶(PKA-I)缺乏的患病率,并确定该同工酶缺乏是否与SLE疾病活动相关。

方法

研究了35例SLE患者和35例年龄、性别及种族匹配的正常对照。15名受试者在4年的时间间隔内至少接受了3次重新研究。通过系统性红斑狼疮疾病活动指数(SLEDAI)评估临床疾病活动度,并通过流式细胞术对T细胞活化标志物CD25+和HLA-DR+进行定量。在富集的T细胞中对PKA-I同工酶活性进行定量。采用学生t检验、曼-惠特尼U检验和皮尔逊积矩检验进行统计分析。

结果

SLE患者T细胞中的平均PKA-I活性(540皮摩尔/分钟/毫克蛋白)显著低于对照T细胞中的活性(1578皮摩尔/分钟/毫克蛋白)(P<0.001)。该队列中同工酶缺乏的患病率为80%。在4年的时间间隔内,PKA-I活性仍显著降低,而SLEDAI评分显著改善。PKA-I活性缺乏与SLEDAI评分或携带CD25+或HLA-DR+活化标志物的T细胞比例均无关联。

结论

SLE患者中T细胞PKA-I同工酶活性缺乏的患病率较高,且这种情况随时间持续存在,与SLE疾病活动无关。

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