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Development of anti-thrombotic vaccine against human S100A9 in rhesus monkey. | LitMetric

Development of anti-thrombotic vaccine against human S100A9 in rhesus monkey.

Sci Rep

Department of Clinical Gene Therapy, Graduate School of Medicine, Center of Medical Innovation and Translational Research, Osaka University, 6th floor, Room 0611B, 2-2 Yamada-oka, Suita, Osaka, 565-0871, Japan.

Published: June 2021

AI Article Synopsis

Article Abstract

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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8169762PMC
http://dx.doi.org/10.1038/s41598-021-91153-yDOI Listing

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