Department of Biochemistry & Molecular Biology, University of Georgia, Athens, Georgia, 30602, USA.
Center for Molecular Medicine, University of Georgia, Athens, Georgia, 30602, USA.
Pharm Res. 2020 Nov 2;37(12):236. doi: 10.1007/s11095-020-02960-3.
Streptococcus pneumoniae (Spn) serotype 3 (Spn3) is considered one of the most virulent serotypes with resistance to conventional vaccine and treatment regimens. Pn3Pase is a glycoside hydrolase that we have previously shown to be highly effective in degrading the capsular polysaccharide of type 3 Spn, sensitizing it to host immune clearance. To begin assessing the value and safety of this enzyme for future clinical studies, we investigated the effects of high doses of Pn3Pase on host cells and immune system.
We assessed the enzyme's catalytic activity following administration in mice, and performed septic infection models to determine if prior administration of the enzyme inhibited repeat treatments of Spn3-challenged mice. We assessed immune populations in mouse tissues following administration of the enzyme, and tested Pn3Pase toxicity on other mammalian cell types in vitro.
Repeated administration of the enzyme in vivo does not prevent efficacy of the enzyme in promoting bacterial clearance following bacterial challenge, with insignificant antibody response generated against the enzyme. Immune homeostasis is maintained following high-dose treatment with Pn3Pase, and no cytotoxic effects were observed against mammalian cells.
These data indicate that Pn3Pase has potential as a therapy against Spn3. Further development as a drug product could overcome a great hurdle of pneumococcal infections.
肺炎链球菌(Spn)血清型 3(Spn3)被认为是最具毒力的血清型之一,对常规疫苗和治疗方案具有耐药性。Pn3Pase 是一种糖苷水解酶,我们之前已经证明它在降解 3 型 Spn 的荚膜多糖方面非常有效,使它对宿主免疫清除敏感。为了开始评估这种酶在未来临床研究中的价值和安全性,我们研究了高剂量 Pn3Pase 对宿主细胞和免疫系统的影响。
我们在小鼠中评估了酶给药后的催化活性,并进行了败血病感染模型,以确定酶的预先给药是否抑制了 Spn3 挑战小鼠的重复治疗。我们在给药后评估了小鼠组织中的免疫群体,并在体外测试了 Pn3Pase 对其他哺乳动物细胞类型的毒性。
体内重复给药不会阻止酶在细菌挑战后促进细菌清除的功效,对酶产生的抗体反应微不足道。高剂量 Pn3Pase 治疗后维持免疫稳态,对哺乳动物细胞没有细胞毒性作用。
这些数据表明 Pn3Pase 有作为 Spn3 治疗的潜力。进一步开发为药物产品可以克服肺炎球菌感染的一个巨大障碍。