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与多糖疫苗相比,肺炎球菌结合疫苗在克罗恩病患者中的抗体持久性 - 一年随访。

Persistence of antibodies to pneumococcal conjugate vaccine compared to polysaccharide vaccine in patients with Crohn's disease - one year follow up.

机构信息

a Department of Virus & Microbiological Special Diagnostics, Statens Serum Institut , Copenhagen , Denmark.

b Department of Gastroenterology, Copenhagen University Hospital Hvidovre , Copenhagen , Denmark.

出版信息

Infect Dis (Lond). 2019 Sep;51(9):651-658. doi: 10.1080/23744235.2019.1638519. Epub 2019 Jul 10.

Abstract

Patients suffering from Crohn's disease (CD) are at increased risk of infectious diseases, such as pneumococcal infection. The risk increases with immunotherapy. Pneumococcal infection can be prevented by vaccination. We conducted a randomized trial of the 23-valent pneumococcal polysaccharide vaccine (PPV23) and the 13-valent pneumococcal conjugated vaccine (PCV13) in groups of CD patients treated with immunosuppressive (IS) drugs in the form of thiopurines (PPV23  = 28, PCV13  = 28) alone or in combination with TNF-α antagonists (PPV23  = 13, PCV13  = 13) and CD patients not treated with any of these drugs (untreated) (PPV23  = 30, PCV13  = 24). In this article, we report the immunogenicity of PPC23 and PCV13 one year after vaccination. No overall differences in vaccine-induced serotype-specific immunoglobulin G (IgG) antibodies or functional antibodies (opsonophagocytic activity (OPA)) were found between the two vaccines. PCV13 induced a higher concentration of IgG antibodies for serotype 9V than PPV23 in untreated patients. In contrast, PPV23 induced higher OPA for serotypes 6B and 19F than PCV13 in IS treated patients. Untreated patients showed generally higher IgG and OPA antibody levels than patients treated with IS and TNF-α antagonists. In conclusion, we found no general differences in the persistence of induced antibodies when comparing PPV23 with PCV13 regardless of treatment and also within treatment groups (IS, IS + TNF-α and untreated). This was demonstrated for both serotype-specific IgG antibodies and as functional antibodies (OPA). Patients treated with thiopurines in combination with TNF-α inhibitors have an impaired immune response against both PPV23 and PCV13, as compared to untreated patients. This study has been registered in the European Clinical Trials Database (EudraCT, record no 2012-002867-86) and ClinicalTrials.gov (record no. NCT01947010).

摘要

患有克罗恩病(CD)的患者感染肺炎球菌等传染病的风险增加。这种风险随着免疫治疗而增加。肺炎球菌感染可以通过疫苗接种来预防。我们在接受免疫抑制(IS)药物治疗的 CD 患者中(硫嘌呤单药治疗组:PPV23 28 例,PCV13 28 例;联合 TNF-α 拮抗剂治疗组:PPV23 13 例,PCV13 13 例)以及未接受此类药物治疗的 CD 患者(未治疗组:PPV23 30 例,PCV13 24 例)中进行了 23 价肺炎球菌多糖疫苗(PPV23)和 13 价肺炎球菌结合疫苗(PCV13)的随机试验。在本文中,我们报告了接种疫苗一年后 PPC23 和 PCV13 的免疫原性。在两种疫苗之间,未发现疫苗诱导的血清型特异性免疫球蛋白 G(IgG)抗体或功能性抗体(调理吞噬活性(OPA))存在总体差异。与 PPV23 相比,未治疗患者中 PCV13 诱导的血清型 9V 的 IgG 抗体浓度更高。相比之下,在接受 IS 治疗的患者中,PPV23 诱导的血清型 6B 和 19F 的 OPA 高于 PCV13。未治疗患者的 IgG 和 OPA 抗体水平普遍高于接受 IS 和 TNF-α 拮抗剂治疗的患者。总之,无论治疗与否,与 PPV23 相比,我们在比较 PCV13 时并未发现诱导抗体的持续存在存在总体差异,并且在治疗组内(IS、IS+TNF-α和未治疗)也未发现差异。这在血清型特异性 IgG 抗体和功能性抗体(OPA)中均得到了证明。与未治疗患者相比,接受硫嘌呤联合 TNF-α 抑制剂治疗的患者对 PPV23 和 PCV13 的免疫反应受损。本研究已在欧洲临床试验数据库(EudraCT,记录号 2012-002867-86)和 ClinicalTrials.gov(记录号 NCT01947010)注册。

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