Key result
Biomaterial-loaded extracellular vesicles enhance LVEF ~39% over EV monotherapy in preclinical heart failure.
Systematic Review
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Heart failure, a pervasive global health burden, necessitates innovative therapeutic strategies. Extracellular vesicles (EVs) have emerged as promising contenders for cardiac repair, owing to their profound influence on fibrosis and inflammation. Merging EVs with biomaterials holds the potential for a synergistic leap in therapeutic efficacy. In this review, the impact of combining EVs with biomaterials in preclinical heart failure models is scrutinized. Fifteen studies, predominantly employing mesenchymal stromal cell-derived EVs along with hyaluronic acid or peptides in coronary ligation models, meet these stringent criteria. The amalgamation of EVs and biomaterials consistently enhances cardiac ejection fraction (1.39; 95% CI: 0.68, 2.11; p = 0.0001) and fractional shortening (1.46, 95% CI: 0.70, 2.22; p = 0.0002) compared to EV monotherapy. Secondary outcomes similarly showcased improvement in the combined treatment group. Although the number of studies analyzed is modest, no indications of publication bias surface. In summary, combination therapy with EVs and biomaterials enhances therapeutic benefit in preclinical heart failure models. The consistent improvement observed across diverse EV sources, biomaterials, and animal models underscores the exciting potential of this synergistic approach.
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Malhotra et al. (2023) conducted a systematic review in Heart Failure with Reduced Ejection Fraction. Extracellular vesicles combined with biomaterials (predominantly mesenchymal stromal cell-derived EVs with hyaluronic acid or peptides) vs. Extracellular vesicle monotherapy was evaluated on Cardiac ejection fraction and fractional shortening (1.39, 95% CI 0.68-2.11, p=0.0001). Combining extracellular vesicles with biomaterials enhanced cardiac ejection fraction compared to EV monotherapy in preclinical heart failure models (1.39; 95% CI 0.68-2.11; p=0.0001).
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