病例系列:多克隆静脉注射免疫球蛋白治疗难治性艰难梭菌感染的疗效。

IF 3 Q3 IMMUNOLOGY Antibodies Pub Date : 2024-04-01 DOI:10.3390/antib13020026
Sophie A Ragan, Caitlin Doyle, Neha Datta, Heather Abdic, Mark H Wilcox, Ros Montgomery, Shanika A Crusz, Yashwant R Mahida, Tanya M Monaghan
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引用次数: 0

摘要

背景:治疗艰难梭菌感染(CDI)的静脉注射免疫球蛋白(IVIg)已不再列入治疗指南。然而,一些临床医生仍在对严重或复发性 CDI(rCDI)病例使用 IVIg。本研究的主要目的是探讨IVIg的疗效,并确定CDI患者使用IVIg后疾病缓解的可能预测因素:这项回顾性观察队列研究于 2018 年 4 月至 2023 年 3 月期间在英国一家大型三甲医院进行,研究对象为住院治疗的≥2 岁重症、复发性或 rCDI 患者,这些患者均接受过 IVIg 治疗。通过扫描患者入院电子记录和临床报告系统收集相关数据:在为期5年的研究中,共有20/978名确诊为CDI的患者接受了IVIg治疗。其中 12 例(60%)是在医院发病的 CDI 患者。20名患者中有11名(55%)对治疗有反应,平均8.6天(标准差10.7天)疾病缓解。16名患者(80%)接受了重症CDI治疗,4名患者(20%)接受了rCDI(3人)和复发性CDI(1人)治疗。两组患者在使用 IVIg 后疾病缓解的可能独立预测因素方面没有明显的统计学差异。确诊后平均 6.2(4.9)天开始使用 IVIg,应答者与非应答者之间无差异(P = 0.88),其他指标也无明显差异。四名应答者(36%)有免疫抑制,而无应答者中仅有一人(11%)有免疫抑制(p = 0.15)。六名应答者(两名复发性 CDI 患者和四名重症 CDI 患者)的病情在两天内迅速好转,其中三人患有免疫抑制:结论:我们观察到 50%以上的难治性 CDI 患者在接受 IVIg 治疗后病情得到缓解。我们的数据还证明,IVIg 对免疫抑制患者的作用可能会增强。因此,IVIg 在 CDI 治疗中的作用,尤其是在免疫抑制人群中的作用,值得在未来开展病例对照研究,并进行机理调查,以改善对这一持续存在的重大医疗相关感染的治疗。
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Case Series: Efficacy of Polyclonal Intravenous Immunoglobulin for Refractory Clostridioides difficile Infection.

Background: Intravenous immunoglobulin (IVIg) for Clostridioides difficile infection (CDI) no longer features in treatment guidelines. However, IVIg is still used by some clinicians for severe or recurrent CDI (rCDI) cases. The main objective of this study was to investigate the efficacy of IVIg and to identify possible predictors of disease resolution post IVIg administration for patients with CDI.

Methods: This retrospective observational cohort study of patients ≥2 years old hospitalised with severe, relapsing, or rCDI treated with IVIg therapy was performed in a large UK tertiary hospital between April 2018 and March 2023. Scanned electronic notes from patient admissions and clinical reporting systems were used to collect relevant data.

Results: In total, 20/978 patients diagnosed with CDI over the 5-year study were treated with IVIg. Twelve (60%) had hospital-onset CDI. Eleven of the twenty patients (55%) responded to treatment, with a mean of 8.6 (SD 10.7) days to disease resolution. Sixteen (80%) patients were treated for severe CDI and four (20%) for rCDI (n = 3) and relapsing CDI (n = 1). There were no statistically significant differences in possible independent predictors of disease resolution post IVIg administration between groups. There was an average of 6.2 (4.9) days to IVIg administration after diagnosis with no difference between responders and non-responders (p = 0.88) and no further significant difference in additional indicators. Four (36%) of the responders were immunosuppressed compared to just one (11%) of the non-responders (p = 0.15). Six of the responders (two with recurrent and four with severe CDI) improved rapidly within 2 days, and three of these were immunosuppressed.

Conclusion: We observed disease resolution post IVIg therapy in over 50% of patients with refractory CDI. Our data also support a potential enhanced effect of IVIg in immunosuppressed individuals. Thus, the role of IVIg for CDI treatment, particularly in the immunosuppressed, warrants future case-control studies coupled to mechanistic investigations to improve care for this ongoing significant healthcare-associated infection.

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来源期刊
Antibodies
Antibodies IMMUNOLOGY-
CiteScore
7.10
自引率
6.40%
发文量
68
审稿时长
11 weeks
期刊介绍: Antibodies (ISSN 2073-4468), an international, peer-reviewed open access journal which provides an advanced forum for studies related to antibodies and antigens. It publishes reviews, research articles, communications and short notes. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. There is no restriction on the length of the papers. Full experimental and/or methodical details must be provided. Electronic files or software regarding the full details of the calculation and experimental procedure - if unable to be published in a normal way - can be deposited as supplementary material. This journal covers all topics related to antibodies and antigens, topics of interest include (but are not limited to): antibody-producing cells (including B cells), antibody structure and function, antibody-antigen interactions, Fc receptors, antibody manufacturing antibody engineering, antibody therapy, immunoassays, antibody diagnosis, tissue antigens, exogenous antigens, endogenous antigens, autoantigens, monoclonal antibodies, natural antibodies, humoral immune responses, immunoregulatory molecules.
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