Sberna Giuseppe, Minosse Claudia, Mija Cosmina, Specchiarello Eliana, Spezia Pietro Giorgio, Belladonna Sara, Berno Giulia, Fabeni Lavinia, Matusali Giulia, Meschi Silvia, Focosi Daniele, Maggi Fabrizio
Laboratory of Virology and Biosafety Laboratories, National Institute for Infectious Diseases Lazzaro Spallanzani-IRCCS, 00149 Rome, Italy.
North-Western Tuscany Blood Bank, Pisa University Hospital, 56100 Pisa, Italy.
Int J Mol Sci. 2025 Jul 7;26(13):6542. doi: 10.3390/ijms26136542.
Torquetenovirus (TTV) is a ubiquitous, non-pathogenic DNA virus that has been suggested as a biomarker of immune competence, with the viral load correlating with the level of immunosuppression. However, by detecting non-intact viral particles, standard PCR-based quantification may overestimate the TTV viremia. To improve the clinical relevance of TTV quantification, in this study, we investigated the use of PMAxx™, a virion viability dye that selectively blocks the amplification of compromised virions. Serum samples from 10 Hepatitis C Virus-positive (HCV+) individuals, 81 liver transplant recipients (LTRs), and 40 people with HIV (PWH) were treated with PMAxx™ and analyzed for TTV DNA loads by digital droplet PCR (ddPCR). Furthermore, anti-SARS-CoV-2 IgG levels and neutralizing antibody (nAbs) titers were measured post-COVID-19 vaccination. Using ddPCR, the PMAxx™ treatment significantly reduced the TTV DNA levels in all the groups (mean reduction: 0.66 Log copies/mL), indicating the abundant presence of non-intact, circulating viral genomes. However, correlations between TTV DNA and SARS-CoV-2 IgG or nAbs were weak or absent in both PMAxx™-treated and untreated samples. These findings suggest that while PMAxx™ enhanced the specificity of TTV quantification, it did not improve the predictive value of TTV viremia at assessing vaccine-induced humoral responses.
细小病毒(TTV)是一种普遍存在的非致病性DNA病毒,有人认为它是免疫能力的生物标志物,病毒载量与免疫抑制水平相关。然而,通过检测不完整的病毒颗粒,基于标准PCR的定量方法可能会高估TTV病毒血症。为了提高TTV定量的临床相关性,在本研究中,我们研究了使用PMAxx™,一种病毒体活力染料,它能选择性地阻断受损病毒体的扩增。对10名丙型肝炎病毒阳性(HCV+)个体、81名肝移植受者(LTR)和40名艾滋病毒感染者(PWH)的血清样本进行PMAxx™处理,并通过数字液滴PCR(ddPCR)分析TTV DNA载量。此外,在接种COVID-19疫苗后测量抗SARS-CoV-2 IgG水平和中和抗体(nAbs)滴度。使用ddPCR,PMAxx™处理显著降低了所有组中的TTV DNA水平(平均降低:0.66 Log拷贝/mL),表明存在大量不完整的循环病毒基因组。然而,在PMAxx™处理和未处理的样本中,TTV DNA与SARS-CoV-2 IgG或nAbs之间的相关性都很弱或不存在。这些发现表明,虽然PMAxx™提高了TTV定量的特异性,但在评估疫苗诱导的体液反应时,它并没有提高TTV病毒血症的预测价值。