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大流行 H1N1 流感无佐剂疫苗接种后类风湿关节炎患者的血清保护作用降低:对临床实践的影响。

Reduced seroprotection after pandemic H1N1 influenza adjuvant-free vaccination in patients with rheumatoid arthritis: implications for clinical practice.

机构信息

Division of Rheumatology, Faculdade de Medicina da Universidade de São Paulo, Brazil.

出版信息

Ann Rheum Dis. 2011 Dec;70(12):2144-7. doi: 10.1136/ard.2011.152983. Epub 2011 Aug 22.

Abstract

BACKGROUND

Reduced response to pandemic (2009) H1N1 (pH1N1) vaccine in patients with rheumatoid arthritis (RA) was recently reported.

OBJECTIVES

To evaluate the contribution of age, disease activity, medication and previous antibody levels to this reduced response.

METHODS

340 adult RA patients and 234 healthy controls were assessed before and 21 days after adjuvant-free influenza A/California/7/2009 (pH1N1) vaccine. Disease activity (DAS28), current treatment and pH1N1 antibody titres were collected. Seroprotection, seroconversion and factor increase in geometric mean titre (GMT) were calculated and adverse events registered.

RESULTS

RA and controls showed similar (p>0.05) prevaccination GMT (8.0 vs 9.3) and seroprotection (10.8% vs 11.5%). After vaccination a significant reduction (p<0.001) was observed in all endpoints: GMT and factor increase in GMT, seroprotection and seroconversion rates. Disease activity did not preclude seroconversion or seroprotection and remained unchanged in 97.4% of patients. Methotrexate was the only disease-modifying antirheumatic drug associated with reduced responses (p=0.001). Vaccination was well tolerated.

CONCLUSIONS

The data confirmed both short-term anti-pH1N1 vaccine safety and, different from most studies with seasonal influenza, reduced seroprotection in RA patients, unrelated to disease activity and to most medications (except methotrexate). Extrapolation of immune responses from one vaccine to another may therefore not be possible and specific immunisation strategies (possibly booster) may be needed. Clinicaltrials.gov no NCT01151644.

摘要

背景

最近有报道称,类风湿关节炎(RA)患者对大流行(2009 年)H1N1(pH1N1)疫苗的反应降低。

目的

评估年龄、疾病活动度、药物和先前抗体水平对此种低反应的影响。

方法

340 例成年 RA 患者和 234 例健康对照者在接受无佐剂流感 A/加利福尼亚/7/2009(pH1N1)疫苗接种前后 21 天进行评估。收集疾病活动度(DAS28)、当前治疗方案和 pH1N1 抗体滴度。计算血清保护率、血清转化率和几何平均滴度(GMT)的增长率,并登记不良反应。

结果

RA 患者和对照组在接种前的 GMT(8.0 对 9.3)和血清保护率(10.8%对 11.5%)相似(p>0.05)。接种后,所有终点均显著降低(p<0.001):GMT 和 GMT 的增长率、血清保护率和血清转化率。疾病活动度并不妨碍血清转化或血清保护,97.4%的患者疾病活动度无变化。甲氨蝶呤是唯一与低反应相关的疾病修饰抗风湿药物(p=0.001)。疫苗接种耐受性良好。

结论

数据证实了短期抗 pH1N1 疫苗的安全性,与大多数季节性流感研究不同,RA 患者的血清保护率降低,与疾病活动度和大多数药物(除甲氨蝶呤外)无关。因此,从一种疫苗到另一种疫苗的免疫反应可能无法推断,可能需要特定的免疫接种策略(可能需要加强免疫)。临床试验.gov 编号 NCT01151644。

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