Maria Jesus Garrido Cid

Dr. Maria Jesus Garrido Cid

orcid

Research Focus & Metrics

Academic Career Length

32Years (1995-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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19 September 2022 in Journal of Controlled Release
Verified
Journal Article
Closed access
SZSara Zalba
Sara Zalba
THTimo L.M. Ten Hagen
Timo L.M. Ten Hagen
CBCarmen Burgui
Carmen Burgui
MCMaria Jesus Garrido Cid
Maria Jesus Garrido Cid

1 October 1999 in Journal of Pharmacological and Toxicological Methods
Verified
Journal Article
Closed access
MCMaria Jesus Garrido Cid
Maria Jesus Garrido Cid
José Ignacio de TrocónizJosé Ignacio de Trocóniz
José Ignacio de Trocóniz

1 July 2015 in Journal of Controlled Release
Verified
Journal Article
Closed access
SZSara Zalba
Sara Zalba
ACAna Contreras-Sandoval
Ana Contreras-Sandoval
AHAzadeh Haeri
Azadeh Haeri
THTimo L.M. Ten Hagen
Timo L.M. Ten Hagen
INIñigo Navarro-Blasco
Iñigo Navarro-Blasco
MCMaria Jesus Garrido Cid
Maria Jesus Garrido Cid

1 April 2018 in Journal of Controlled Release
Verified
Journal Article
Closed access
MMMaría Merino
María Merino
SZSara Zalba
Sara Zalba
MCMaria Jesus Garrido Cid
Maria Jesus Garrido Cid

19 July 2024 in Journal of Hematology & Oncology
Verified
Journal Article
Open access
PDF file
ZCZiyun Cheng
Ziyun Cheng
Seth-Frerich FobianSeth-Frerich Fobian
Seth-Frerich Fobian
EGElena Gurrieri
Elena Gurrieri
MAMohamadreza Amin
Mohamadreza Amin
VDVito Giuseppe D'Agostino
Vito Giuseppe D'Agostino
THTimo L. M. Ten Hagen
Timo L. M. Ten Hagen
Immunotherapy has become an important part of the oncotherapy arsenal. Its applicability in various cancer types is impressive, as well as its use of endogenous mechanisms to achieve desired ends. However, off-target or on-target-off-tumor toxicity, limited activity, lack of control in combination treatments and, especially for solid tumors, low local accumulation, have collectively limited clinical use thereof. These limitations are partially alleviated by delivery systems. Lipid-based nanoparticles (NPs) have emerged as revolutionary carriers due to favorable physicochemical characteristics, with specific applications and strengths particularly useful in immunotherapeutic agent delivery. The aim of this review is to highlight the challenges faced by immunotherapy and how lipid-based NPs have been, and may be further utilized to address such challenges. We discuss recent fundamental and clinical applications of NPs in a range of areas and provide a detailed discussion of the main obstacles in immune checkpoint inhibition therapies, adoptive cellular therapies, and cytokine therapies. We highlight how lipid-based nanosystems could address these through either delivery, direct modulation of the immune system, or targeting of the immunosuppressive tumor microenvironment. We explore advanced and emerging liposomal and lipid nanoparticle (LNP) systems for nucleic acid delivery, intrinsic and extrinsic stimulus-responsive formulations, and biomimetic lipid-based nanosystems in immunotherapy. Finally, we discuss the key challenges relating to the clinical use of lipid-based NP immunotherapies, suggesting future research directions for the near term to realize the potential of these innovative lipid-based nanosystems, as they become the crucial steppingstone towards the necessary enhancement of the efficacy of immunotherapy. Graphical abstract

1 February 2019 in International Journal of Pharmaceutics
Verified
Journal Article
Closed access
Krassimira YonchevaKrassimira Yoncheva
Krassimira Yoncheva
MMMaria Merino
Maria Merino
ASAslihan Shenol
Aslihan Shenol
NDNikolay T. Daskalov
Nikolay T. Daskalov
PPPetko Petkov
Petko Petkov
MCMaria Jesus Garrido Cid
Maria Jesus Garrido Cid