减毒带状疱疹活疫苗对系统性红斑狼疮患者的长期免疫原性

IF 4.5 3区 医学 Q2 IMMUNOLOGY
Chi Chiu Mok, Kar Li Chan, Sau Mei Tse
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引用次数: 0

摘要

目的研究带状疱疹减毒活疫苗对系统性红斑狼疮(SLE)的5年免疫原性。方法:本研究是一项扩展观察性研究,研究HZ活疫苗(Zostavax)对参加安慰剂(PBO)对照随机对照试验(RCT)的成年稳定SLE (SLEDAI <;6和免疫抑制治疗≥6个月)患者的免疫原性。重新评估5年后体液(抗vzv IgG反应性)和细胞介导(vzv刺激的IFN-γ酶联ELISPOT测定)对HZ的反应。在最初的RCT的90例患者中,70例患者同意这项研究(32例接受疫苗治疗;PBO组38例;年龄51.9±15.5 vs 50.0±13.2;p = 0.59;91% vs 97%的女性;p = 0.33)。从第6周到第5年,疫苗组抗vzv IgG反应性变化为- 14.5% (p = 0.06), PBO组为- 10.1% (p = 0.02)。在调整基线值后,接种疫苗的5年抗vzv IgG反应性显著高于接受pbo治疗的患者(3.61±1.56 vs 2.94±1.03;p = 0.01)。接种疫苗的患者分泌IFN-γ的t细胞斑点数量(每5 × 105个细胞)增加(+ 65.5%;p = 0.23),但pbo治疗的患者在第6周至第5年下降(- 5.3%;p = 0.83)。经基线值调整后,疫苗组患者第5年的t细胞斑点数高于PBO组患者(58.1±71.5 vs 24.9±23.2;p = 0.06)。t细胞斑点数量减少≥20%的患者比例在疫苗组(30.8%)显著低于PBO组(61.1%)(p = 0.046)。在接种疫苗的患者中,在t细胞或体液HZ反应降低≥20%的患者中,观察到累积泼尼松龙增加的趋势,非糖皮质激素免疫抑制药物的新添加或剂量增加的趋势。1名接种疫苗的患者(3.1%)和3名pbo治疗的患者(7.9%)经历了HZ再激活,但差异无统计学意义(p = 0.62)。结论安定型SLE患者5年免疫原性基本保持。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Long-term immunogenicity of a live attenuated herpes zoster vaccine in patients with systemic lupus erythematosus

Objectives

To study the 5-year immunogenicity of a live attenuated herpes zoster (HZ) vaccine in systemic lupus erythematosus (SLE).

Method

This is an extended observational study of the immunogenicity of a live HZ vaccine (Zostavax) in adult patients with stable SLE (SLEDAI <6 and immunosuppressive treatment for ≥6 months) who participated in a placebo (PBO)-controlled randomized controlled trial (RCT). Humoral (anti-VZV IgG reactivity) and cell-mediated (VZV-stimulated IFN-γ enzyme-linked ELISPOT assay) responses to HZ at 5 years were reassessed.

Results

Of the 90 patients in the original RCT, 70 patients consented for this study (32 treated with vaccine; 38 treated with PBO; age 51.9 ± 15.5 vs 50.0 ± 13.2 years; p = 0.59; 91 % vs 97 % women; p = 0.33). The change in anti-VZV IgG reactivity from week 6 to year 5 was −14.5 % (p = 0.06) in the vaccine and − 10.1 % (p = 0.02) in the PBO group, respectively. The anti-VZV IgG reactivity at year 5 was significantly higher in vaccinated than PBO-treated patients, after adjustment for baseline values (3.61 ± 1.56 vs 2.94 ± 1.03; p = 0.01). The number of IFN-γ secreting T-cell spots (per 5 × 105 cells) increased in vaccinated patients (+65.5 %; p = 0.23) from week 6 to year 5 but decreased in PBO-treated patients (−5.3 %; p = 0.83). The T-cell spots number at year 5 was higher in vaccine than PBO treated patients after adjustment for baseline values (58.1 ± 71.5 vs 24.9 ± 23.2; p = 0.06). The proportion of patients who had a reduction in T-cell spots number by ≥20 % was significantly lower in the vaccine (30.8 %) than PBO (61.1 %) groups (p = 0.046). Among vaccinated patients, a trend of higher cumulative prednisolone, more new addition or dosage increase of non-glucocorticoid immunosuppressive drugs was observed in those who had reduction in T-cell or humoral HZ responses by ≥20 %. One vaccinated patient (3.1 %) and three PBO-treated patients (7.9 %) experienced HZ reactivation, but the difference was not significant (p = 0.62).

Conclusions

Immunogenicity of Zostavax in stable SLE patients is largely retained at 5 years.
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来源期刊
Vaccine
Vaccine 医学-免疫学
CiteScore
8.70
自引率
5.50%
发文量
992
审稿时长
131 days
期刊介绍: Vaccine is unique in publishing the highest quality science across all disciplines relevant to the field of vaccinology - all original article submissions across basic and clinical research, vaccine manufacturing, history, public policy, behavioral science and ethics, social sciences, safety, and many other related areas are welcomed. The submission categories as given in the Guide for Authors indicate where we receive the most papers. Papers outside these major areas are also welcome and authors are encouraged to contact us with specific questions.
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