Guzman Efrain, Khoo Cheen, O'Connor Deirdre, Devarajan Gayathri, Iqball Sharifah, Souberbielle Bernard, Mitrophanous Kyriacos, Lad Yatish
Oxford Biomedica (UK) Limited, Oxford, United Kingdom.
Exp Biol Med (Maywood). 2025 Apr 25;250:10422. doi: 10.3389/ebm.2025.10422. eCollection 2025.
Viral vector-based therapies are effective therapeutics for the correction of several disorders, both in mouse models and in humans. Several pre-clinical studies have demonstrated differences in transduction efficiencies and therapeutic effect between male and female mice dosed with AAV-based gene therapy product candidates. Here, we report gender-specific transduction and transgene expression differences in mice dosed systemically with lentiviral vectors (LVV). Male mice systemically dosed with LVV carrying the reporter gene luciferase showed at least a 12-fold higher expression of luciferase and a higher vector copy number (VCN) in their livers compared with female mice. Lastly, PAH male mice dosed with a LVV carrying the human phenylalanine hydroxylase (PAH) transgene were observed to have a higher VCN than their female littermates. These findings suggest that sex-based differences initially observed in AAV-mediated therapies also apply to LVV, but the exact mechanism remains to be determined.
基于病毒载体的疗法在小鼠模型和人类中都是治疗多种疾病的有效方法。多项临床前研究表明,用基于腺相关病毒(AAV)的基因治疗候选产品给药的雄性和雌性小鼠在转导效率和治疗效果上存在差异。在此,我们报告了全身注射慢病毒载体(LVV)的小鼠中存在性别特异性转导和转基因表达差异。全身注射携带报告基因荧光素酶的LVV的雄性小鼠,其肝脏中荧光素酶的表达至少比雌性小鼠高12倍,且载体拷贝数(VCN)更高。最后,观察到注射携带人苯丙氨酸羟化酶(PAH)转基因的LVV的PAH雄性小鼠比其雌性同窝小鼠具有更高的VCN。这些发现表明,最初在AAV介导的疗法中观察到的基于性别的差异也适用于LVV,但确切机制仍有待确定。