TY - JOUR
T1 - Stealth mRNA nanovaccines to control lymph node trafficking
AU - García-Fernández, Coral
AU - Virgilio, Tommaso
AU - Latino, Irene
AU - Guerra-Rebollo, Marta
AU - F. Gonzalez, Santiago
AU - Borrós, Salvador
AU - Fornaguera, Cristina
N1 - Publisher Copyright:
© 2024
PY - 2024/10
Y1 - 2024/10
N2 - 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.
AB - 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.
KW - Cancer
KW - Delivery systems
KW - Nanoparticles
KW - Reactogenicity)
KW - mRNA
UR - http://www.scopus.com/inward/record.url?scp=85201592881&partnerID=8YFLogxK
UR - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=pure_univeritat_ramon_llull&SrcAuth=WosAPI&KeyUT=WOS:001301222600001&DestLinkType=FullRecord&DestApp=WOS_CPL
U2 - 10.1016/j.jconrel.2024.08.018
DO - 10.1016/j.jconrel.2024.08.018
M3 - Article
C2 - 39154934
AN - SCOPUS:85201592881
SN - 0168-3659
VL - 374
SP - 325
EP - 336
JO - Journal of Controlled Release
JF - Journal of Controlled Release
ER -