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口服IPD - 1151T治疗期间出现的间质性膀胱炎症状及问题的改善情况。

Improvement of interstitial cystitis symptoms and problems that developed during treatment with oral IPD-1151T.

作者信息

Ueda T, Tamaki M, Ogawa O, Yamauchi T, Yoshimura N

机构信息

Department of Urology, Kouga Public Hospital, Shiga, Japan.

出版信息

J Urol. 2000 Dec;164(6):1917-20.

Abstract

PURPOSE

We examined the efficacy of Suplatast Tosilatedouble dagger (IPD-1151T), a new immunoregulator that suppresses helper T cell mediated allergic responses, including IgE production and eosinophilic inflammation for treating patients with interstitial cystitis.

MATERIALS AND METHODS

A total of 14 women (average age 43.7 years) with interstitial cystitis, which was nonulcerative in 13 and ulcerative in 1, were treated with 300 mg. IPD-1151T orally daily for 12 months. All patients received laboratory assessments, including hematology (eosinophils and CD20 positive cells) and serum chemistry (IgE, and interleukin-4 (IL-4) and 5, and immunohistochemical analyses of urine leukocytes (CD45RO positive cells as a T cell marker) before treatment. These parameters were also measured 4 and 12 months after continuous treatment. The voiding chart, and interstitial cystitis symptom and problem indexes were evaluated before and after IPD-1151T treatment.

RESULTS

IPD-1151T treatment for 1 year resulted in a significantly increased bladder capacity and decreased symptoms, such as urinary urgency, frequency and lower abdominal pain, in patients with nonulcerative interstitial cystitis. These effects also correlated with a reduction in blood eosinophils, CD20 positive cells and IgE, and urine CD45RO positive memory T cells. No major side effects were observed.

CONCLUSIONS

Our study suggests that immunological responses are involved in the development of interstitial cystitis symptoms. IPD-1151T could be a new oral agent for treatment of voiding symptoms and bladder pain in patients with interstitial cystitis.

摘要

目的

我们研究了新型免疫调节剂托西酸舒拉他定(IPD-1151T)治疗间质性膀胱炎患者的疗效,该药物可抑制辅助性T细胞介导的过敏反应,包括IgE产生和嗜酸性粒细胞炎症。

材料与方法

总共14名间质性膀胱炎女性患者(平均年龄43.7岁)接受治疗,其中13例为非溃疡性,1例为溃疡性。患者口服300mg IPD-1151T,每日一次,持续12个月。所有患者在治疗前均接受实验室评估,包括血液学检查(嗜酸性粒细胞和CD20阳性细胞)和血清化学检查(IgE、白细胞介素-4(IL-4)和5),并对尿白细胞进行免疫组化分析(以CD45RO阳性细胞作为T细胞标志物)。在持续治疗4个月和12个月后也测量这些参数。在IPD-1151T治疗前后评估排尿图表以及间质性膀胱炎症状和问题指数。

结果

IPD-1151T治疗1年可使非溃疡性间质性膀胱炎患者的膀胱容量显著增加,并使尿急、尿频和下腹痛等症状减轻。这些效果还与血液嗜酸性粒细胞、CD20阳性细胞和IgE以及尿CD45RO阳性记忆T细胞的减少相关。未观察到重大副作用。

结论

我们的研究表明免疫反应参与了间质性膀胱炎症状的发生发展。IPD-1151T可能是一种治疗间质性膀胱炎患者排尿症状和膀胱疼痛的新型口服药物。

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