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Response to 2009 pandemic influenza a (H1N1) vaccine in HIV-infected patients and the influence of prior seasonal influenza vaccination

机译:HIV感染患者对2009年甲型H1N1大流行性流感疫苗的反应以及以前的季节性流感疫苗接种的影响

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textabstractBackground: The immunogenicity of 2009 pandemic influenza A(H1N1) (pH1N1) vaccines and the effect of previous influenza vaccination is a matter of current interest and debate. We measured the immune response to pH1N1 vaccine in HIV-infected patients and in healthy controls. In addition we tested whether recent vaccination with seasonal trivalent inactivated vaccine (TIV) induced cross-reactive antibodies to pH1N1. (clinicaltrials.gov Identifier:NCT01066169) Methods and Findings: In this single-center prospective cohort study MF59-adjuvanted pH1N1 vaccine (Focetria®, Novartis) was administered twice to 58 adult HIV-infected patients and 44 healthy controls in November 2009 (day 0 and day 21). Antibody responses were measured at baseline, day 21 and day 56 with hemagglutination-inhibition (HI) assay. The seroprotection rate (defined as HI titers ≥1:40) for HIV-infected patients was 88% after the first and 91% after the second vaccination. These rates were comparable to those in healthy controls. Post-vaccination GMT, a sensitive marker of the immune competence of a group, was lower in HIV-infected patients. We found a high seroprotection rate at baseline (31%). Seroprotective titers at baseline were much more common in those who had received 2009-2010 seasonal TIV three weeks prior to the first dose of pH1N1 vaccine. Using stored serum samples of 51 HIV-infected participants we measured the pH1N1 specific response to 2009-2010 seasonal TIV. The seroprotection rate to pH1N1 increased from 22% to 49% after vaccination with 2009-2010 seasonal TIV. Seasonal TIV induced higher levels of antibodies to pH1N1 in older than in younger subjects. Conclusion: In HIV-infected patients on combination antiretroviral therapy, with a median CD4+ T-lymphocyte count above 500 cells/mm3, one dose of MF59-adjuvanted pH1N1 vaccine induced a high seroprotection rate comparable to that in healthy controls. A second dose had a modest additional effect. Furthermore, seasonal TIV induced cross-reactive antibodies to pH1N1 and this effect was more pronounced in older subjects.
机译:背景:2009年大流行性流感A(H1N1)(pH1​​N1)疫苗的免疫原性和以前的流感疫苗接种的影响是当前引起人们关注和辩论的问题。我们测量了HIV感染患者和健康对照者对pH1N1疫苗的免疫反应。此外,我们测试了近期的季节性三价灭活疫苗(TIV)疫苗接种是否引起针对pH1N1的交叉反应抗体。 (clinicaltrials.gov标识符:NCT01066169)方法和调查结果:在这一单中心前瞻性队列研究中,2009年11月(日),对58例成人HIV感染患者和44例健康对照进行了MF59佐剂的pH1N1疫苗(Focetria®,诺华)。 0和第21天)。在基线,第21天和第56天用血凝抑制(HI)测定法测量抗体应答。第一次接种后,HIV感染患者的血清保护率(HI滴度≥1:40)为88%,第二次接种后为91%。这些比率与健康对照者相当。艾滋病毒感染患者的疫苗接种后格林尼治标准时间(GMT)是一组患者免疫能力的敏感指标,其水平较低。我们发现基线时有很高的血清保护率(31%)。在首次接种pH1N1疫苗前三周接受2009-2010季节性TIV的人群中,基线时的血清保护性滴度更​​为常见。使用存储的51名HIV感染者的血清样本,我们测量了对2009-2010季节性TIV的pH1N1特异性反应。在接种2009-2010季节性TIV疫苗后,对pH1N1的血清保护率从22%增加到49%。与年轻受试者相比,季节性TIV在年龄较大的人中诱导更高的针对pH1N1的抗体。结论:在接受HIV联合抗逆转录病毒治疗的患者中,CD4 + T淋巴细胞的中位数超过500个细胞/ mm3,一剂MF59佐剂的pH1N1疫苗诱导的血清保护率与健康对照组相当。第二剂具有适度的附加作用。此外,季节性TIV诱导了针对pH1N1的交叉反应抗体,这种作用在老年受试者中更为明显。

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