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在乙型肝炎病毒基因型 D 中,富含乙型肝炎表面抗原疫苗逃逸突变的复杂乙型肝炎病毒变异体的循环呈意外上升:对乙型肝炎表面抗原检测/定量和疫苗接种策略的潜在影响。

Unexpected rise in the circulation of complex HBV variants enriched of HBsAg vaccine-escape mutations in HBV genotype-D: potential impact on HBsAg detection/quantification and vaccination strategies.

机构信息

Department of Biology, Tor Vergata University, Rome, Italy.

Department of Experimental Medicine, Tor Vergata University, Rome, Italy.

出版信息

Emerg Microbes Infect. 2023 Dec;12(1):2219347. doi: 10.1080/22221751.2023.2219347.

Abstract

Specific HBsAg mutations are known to hamper HBsAg recognition by neutralizing antibodies thus challenging HBV-vaccination efficacy. Nevertheless, information on their impact and spreading over time is limited. Here, we characterize the circulation of vaccine-escape mutations from 2005 to 2019 and their correlation with virological parameters in a large cohort of patients infected with HBV genotype-D ( = 947), dominant in Europe. Overall, 17.7% of patients harbours ≥1 vaccine-escape mutation with the highest prevalence in subgenotype-D3. Notably, complex profiles (characterized by ≥2 vaccine-escape mutations) are revealed in 3.1% of patients with a prevalence rising from 0.4% in 2005-2009 to 3.0% in 2010-2014 and 5.1% in 2015-2019 ( = 0.007) (OR[95%CI]:11.04[1.42-85.58],  = 0.02, by multivariable-analysis). The presence of complex profiles correlates with lower HBsAg-levels (median[IQR]:40[0-2905]IU/mL for complex profiles vs 2078[115-6037]IU/ml and 1881[410-7622]IU/mL for single or no vaccine-escape mutation [ < 0.02]). Even more, the presence of complex profiles correlates with HBsAg-negativity despite HBV-DNA positivity (HBsAg-negativity in 34.8% with ≥2 vaccine-escape mutations vs 6.7% and 2.3% with a single or no vaccine-escape mutation,  < 0.007). These in-vivo findings are in keeping with our in-vitro results showing the ability of these mutations in hampering HBsAg secretion or HBsAg recognition by diagnostic antibodies. In conclusion, vaccine-escape mutations, single or in complex profiles, circulate in a not negligible fraction of HBV genotype-D infected patients with an increasing temporal trend, suggesting a progressive enrichment in the circulation of variants able to evade humoral responses. This should be considered for a proper clinical interpretation of HBsAg-results and for the development of novel vaccine formulations for prophylactic and therapeutic purposes.

摘要

已知特定的 HBsAg 突变会阻碍中和抗体对 HBsAg 的识别,从而影响乙肝疫苗的疗效。然而,关于这些突变的影响及其随时间传播的信息是有限的。在这里,我们描述了 2005 年至 2019 年期间,在欧洲主要流行的乙肝病毒基因型-D( = 947)感染患者中,疫苗逃逸突变的循环及其与病毒学参数的相关性。总的来说,17.7%的患者携带至少 1 种疫苗逃逸突变,其中亚基因型-D3 的发生率最高。值得注意的是,在 3.1%的患者中发现了复杂的(至少有 2 种疫苗逃逸突变)突变谱,其发生率从 2005-2009 年的 0.4%上升到 2010-2014 年的 3.0%和 2015-2019 年的 5.1%( = 0.007)(OR[95%CI]:11.04[1.42-85.58], = 0.02,多变量分析)。复杂谱的存在与较低的 HBsAg 水平相关(复杂谱的中位数[四分位数间距]:40[0-2905]IU/ml,而单一或无疫苗逃逸突变的中位数[四分位数间距]为 2078[115-6037]IU/ml 和 1881[410-7622]IU/ml, < 0.02)。此外,即使在 HBV-DNA 阳性的情况下,复杂谱的存在也与 HBsAg 阴性相关(有≥2 种疫苗逃逸突变的患者中 HBsAg 阴性率为 34.8%,而单一或无疫苗逃逸突变的患者中 HBsAg 阴性率为 6.7%和 2.3%, < 0.007)。这些体内发现与我们的体外结果一致,表明这些突变能够阻碍 HBsAg 的分泌或诊断抗体对 HBsAg 的识别。总之,在感染乙肝病毒基因型-D 的患者中,存在单一或复杂的疫苗逃逸突变,且具有随时间增加的趋势,这表明能够逃避体液免疫反应的变异体在循环中逐渐富集。在对 HBsAg 结果进行临床解释时,以及在预防性和治疗性疫苗制剂的开发方面,都应考虑这一点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f55e/10251786/078c568ecdd0/TEMI_A_2219347_F0001_OB.jpg

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