整形外科インプラントを安全にするバイオマテリアルワクチン(Biomaterial Vaccines to Make Implanted Orthopedic Devices Safer)

ad

2025-11-03 ハーバード大学

ハーバード大学ジョン・A・ポールソン工学・応用科学部とワイス研究所の研究チームは、整形外科用インプラント感染を防ぐ新しいバイオマテリアルワクチンを開発した。ゆっくり生分解する注射型足場素材に、免疫細胞を誘導する分子と黄色ブドウ球菌特異的抗原を組み込み、強力かつ持続的な免疫応答を誘発。マウス実験では従来ワクチンの約100倍の感染抑制効果を示した。メチシリン感受性菌(MSSA)由来抗原でも耐性菌(MRSA)に有効で、整形外科手術向けの汎用ワクチン開発が期待される。研究は個別菌株に基づくパーソナライズドワクチンへの応用も視野に入れており、人工関節やペースメーカーなど医療機器の安全性向上につながる成果として注目されている。

<関連情報>

整形外科用器具感染予防のためのスキャフォールドワクチン接種 Scaffold vaccination for prevention of orthopedic device infection

Alexander M. Tatara, Shanda Lightbown, Shawn Kang, +5 , and David J. Mooney
Proceedings of the National Academy of Sciences  Published:November 3, 2025
DOI:https://doi.org/10.1073/pnas.2409562122

整形外科インプラントを安全にするバイオマテリアルワクチン(Biomaterial Vaccines to Make Implanted Orthopedic Devices Safer)

Significance

Infections of orthopedic devices are difficult to treat and require additional surgery and long antimicrobial treatment courses. Preventative strategies, such as vaccination, are attractive given that most infections are caused by staphylococci. Conventional vaccine technologies have failed in preclinical studies and clinical trials to prevent surgical site infection by Staphylococcus aureus. We developed an alternative strategy using a biomaterial-based vaccine consisting of a biodegradable scaffold system to increase vaccine efficacy. This injectable scaffold system improved cell-mediated immunity and decreased bacterial burden in a murine model of orthopedic device infection against different clinically relevant strains of S. aureus.

Abstract

Staphylococcus aureus is the leading cause of global bacterial mortality. While S. aureus can cause a variety of diseases, orthopedic device infections are particularly challenging due to the need for additional surgeries with associated morbidity. Conventional vaccine technology has failed to prevent S. aureus orthopedic device infection in animal models and clinical trials. In this study, injectable scaffold vaccines are presented as a modality to augment host immunity and mitigate orthopedic device infection. These scaffold vaccines increased cytokine production, antigen-specific cell-mediated immune responses, and humoral responses. When loaded with a pool of antigens collected via an engineered human opsonin, these scaffold vaccines decreased the bacterial burden against methicillin-susceptible and methicillin-resistant S. aureus (MRSA) strains in a murine model of orthopedic device infection. Scaffold vaccination was ~100× more effective in decreasing S. aureus burden compared to prior published immunotherapy attempts in murine models of orthopedic device infection. Scaffold vaccination was also effective when using a monovalent protein-based antigen. Scaffold vaccination is an alternative strategy to facilitate more robust immunity in scenarios where conventional bolus vaccines have not been effective.

有機化学・薬学
ad
ad
Follow
ad
タイトルとURLをコピーしました