Stealth mRNA nanovaccines to control lymph node trafficking

mRNA-based vaccines symbolize a new paradigm shift in personalized medicine for the treatment of infectious and non-infectious diseases. However, the reactogenicity associated with the currently approved formulations limits their applicability in autoinflammatory disorders, such as tumour therapeutics. In this study, we present a delivery system showing controlled immunogenicity and minimal non-specific inflammation, allowing for selective delivery of mRNA to antigen presenting cells (APCs) within the medullary region of the lymph nodes. Our platform offers precise control over the trafficking of nanoparticles within the lymph nodes by optimizing stealth and targeting properties, as well as the subsequent opsonization process. By targeting specific cells, we observed a potent adaptive and humoral immune response, which holds promise for preventive and therapeutic anti-tumoral vaccines. Through spatial programming of nanoparticle distribution, we can promote robust immunization, thus improving and expanding the utilization of mRNA vaccines. This innovative approach signifies a remarkable step forward in the field of targeted nanomedicine.

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Publication Details

Journal
Journal of Controlled Release
Published
2024-08-22
DOI
https://doi.org/10.1016/j.jconrel.2024.08.018
Citations
13
Primary Topic
Immunotherapy and Immune Responses
Type
article
Field-Weighted Citation Impact
3.13

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article

Stealth mRNA nanovaccines to control lymph node trafficking

Salvador Borrós, Coral García-Fernández, Tommaso Virgilio, Marta Guerra‐Rebollo et al.
13 citations
Journal of Controlled Release
Immunotherapy and Immune Responses
3.13
article

Stealth mRNA nanovaccines to control lymph node trafficking

Salvador Borrós, Coral García-Fernández, Tommaso Virgilio, Marta Guerra‐Rebollo, Santiago González, Cristina Fornaguera, Irene Latino
article en
13 citations

Abstract

mRNA-based vaccines symbolize a new paradigm shift in personalized medicine for the treatment of infectious and non-infectious diseases. However, the reactogenicity associated with the currently approved formulations limits their applicability in autoinflammatory disorders, such as tumour therapeutics. In this study, we present a delivery system showing controlled immunogenicity and minimal non-specific inflammation, allowing for selective delivery of mRNA to antigen presenting cells (APCs) within the medullary region of the lymph nodes. Our platform offers precise control over the trafficking of nanoparticles within the lymph nodes by optimizing stealth and targeting properties, as well as the subsequent opsonization process. By targeting specific cells, we observed a potent adaptive and humoral immune response, which holds promise for preventive and therapeutic anti-tumoral vaccines. Through spatial programming of nanoparticle distribution, we can promote robust immunization, thus improving and expanding the utilization of mRNA vaccines. This innovative approach signifies a remarkable step forward in the field of targeted nanomedicine.

Journal of Controlled ReleaseVol. 374
Institut Químic de Sarrià (ES), Università della Svizzera italiana (CH)
Fundación Científica Asociación Española Contra el Cáncer, Agència de Gestió d'Ajuts Universitaris i de Recerca, Instituto de Salud Carlos III, Agencia Estatal de Investigación
Good health and well-being
Openalex Percentile: Top 8%
Immunotherapy and Immune Responses
3.13
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