Department of Neurology, Graduate School of Medicine, Osaka University, Suita, Osaka, Japan.
Department of Health Development and Medicine, Graduate School of Medicine, Osaka University, Suita, Osaka, Japan.
Sci Rep. 2021 Jun 1;11(1):11472. doi: 10.1038/s41598-021-91153-y.
In post-stroke patients, a decreased adherence to antiplatelet drugs is a major challenge in the prevention of recurrent stroke. Previously, we reported an antiplatelet vaccine against S100A9 in mice, but the use of Freund's adjuvant and the difference in amino acid sequences in epitopes between mice and humans were problematic for clinical use. Here, we redesigned the S100A9 vaccine for the common sequence in both humans and monkeys and examined its effects in cynomolgus monkeys with Alum adjuvant. First, we assessed several candidate epitopes and selected 102 to 112 amino acids as the suitable epitope, which could produce antibodies. When this peptide vaccine was intradermally injected into 4 cynomolgus monkeys with Alum, the antibody against human S100A9 was successfully produced. Anti-thrombotic effects were shown in two monkeys in a mixture of vaccinated serum and fresh whole blood from another cynomolgus monkey. Additionally, the anti-thrombotic effects were partially inhibited by the epitope peptide, indicating the feasibility of neutralizing anti-thrombotic effects of produced antibodies. Prolongation of bleeding time was not observed in vaccinated monkeys. Although further studies on increasing the effect of vaccine and safety are necessary, this vaccine will be a promising approach to improve adherence to antiplatelet drugs in clinical settings.
在脑卒中患者中,抗血小板药物的依从性降低是预防中风复发的主要挑战。此前,我们在小鼠中报告了一种针对 S100A9 的抗血小板疫苗,但由于 Freund 佐剂的使用以及小鼠和人类表位氨基酸序列的差异,该疫苗在临床应用中存在问题。在这里,我们针对人类和猴子共有的序列重新设计了 S100A9 疫苗,并使用 Alum 佐剂在食蟹猴中检查了其效果。首先,我们评估了几个候选表位,并选择了 102 到 112 个氨基酸作为合适的表位,该表位可以产生抗体。当这种肽疫苗用 Alum 皮内注射到 4 只食蟹猴中时,成功地产生了针对人 S100A9 的抗体。在混合了接种血清和来自另一只食蟹猴的新鲜全血的两只猴子中显示出抗血栓作用。此外,抗血栓作用部分被表位肽抑制,表明产生的抗体的中和抗血栓作用是可行的。接种猴子未观察到出血时间延长。尽管需要进一步研究增加疫苗效果和安全性的方法,但这种疫苗将是改善临床环境中抗血小板药物依从性的一种有前途的方法。