The DOI matches its Crossref record; 92 of the 92 references it cites were found in a registry or an index.
Cationic lipids activate intracellular signaling pathways
Abstract
Cationic liposomes are commonly used as a transfection reagent for DNA, RNA or proteins and as a co-adjuvant of antigens for vaccination trials. A high density of positive charges close to cell surface is likely to be recognized as a signal of danger by cells or contribute to trigger cascades that are classically activated by endogenous cationic compounds. The present review provides evidence that cationic liposomes activate several cellular pathways like pro-apoptotic and pro-inflammatory cascades. An improved knowledge of the relationship between the cationic lipid properties (nature of the lipid hydrophilic moieties, hydrocarbon tail, mode of organization) and the activation of these pathways opens the way to the use and design of cationic tailored for a specific application (e.g. for gene transport or as adjuvants).
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Cationic lipids have been associated with the activation of several cellular pathways like pro-apoptotic and pro-inflammatory cascades [65]”
From The dawn of mRNA vaccines: the COVID-19 case (2021) · cites this paper as [65]
Citations
Cites
Boussif, O., Lezoualc’h, F., Zanta, M. A., Djavaheri‐Mergny, M., Scherman, D., DEMENEIX, B. A., & Behr, J. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.16.7297 · Cited by 6,256
Human CD14dim Monocytes Patrol and Sense Nucleic Acids and Viruses via TLR7 and TLR8 Receptors
Cros, J. F., Cagnard, N., Woollard, K. J., Patey, N., Zhang, S., Sénéchal, B., Puel, A., Biswas, S. K., Moshous, D., Pïcard, C., et al. (2010) · Immunity · doi:10.1016/j.immuni.2010.08.012 · Cited by 1,320
Uptake Pathways and Subsequent Intracellular Trafficking in Nonviral Gene Delivery
Khalil, I. A., Kogure, K., Akita, H., & Harashima, H. (2006) · Pharmacological Reviews · doi:10.1124/pr.58.1.8 · Cited by 1,263
Mechanism of DNA Release from Cationic Liposome/DNA Complexes Used in Cell Transfection,
Xu, Y., & Szoka, F. C. (1996) · Biochemistry · doi:10.1021/bi9602019 · Cited by 1,136
CD14 Controls the LPS-Induced Endocytosis of Toll-like Receptor 4
Zanoni, I., Ostuni, R., Marek, L. R., Barresi, S., Barbalat, R., Barton, G. M., Granucci, F., & Kagan, J. C. (2011) · Cell · doi:10.1016/j.cell.2011.09.051 · Cited by 997
The Vaccine Adjuvant Monophosphoryl Lipid A as a TRIF-Biased Agonist of TLR4
Mata‐Haro, V., Cekic, C., Martin, M., Chilton, P. M., Casella, C. R., & Mitchell, T. C. (2007) · Science · doi:10.1126/science.1138963 · Cited by 901
Progress in developing cationic vectors for non-viral systemic gene therapy against cancer
Morille, M., Passirani, C., Vonarbourg, A., Clavreul, A., & Benoît, J. (2008) · Biomaterials · doi:10.1016/j.biomaterials.2008.04.036 · Cited by 786
The inflammasome: an integrated view
Gross, O., Thomas, C. J., Guarda, G., & Tschopp, J. (2011) · Immunological Reviews · doi:10.1111/j.1600-065x.2011.01046.x · Cited by 778
CD14 is required for MyD88-independent LPS signaling
Jiang, Z., Georgel, P., Du, X., Shamel, L., Sovath, S., Mudd, S., Huber, M., Kalis, C., Keck, S., Galanos, C., et al. (2005) · Nature Immunology · doi:10.1038/ni1207 · Cited by 683
Gringhuis, S. I., Kaptein, T. M., Wevers, B. A., Theelen, B., van der Vlist, M., Boekhout, T., & Geijtenbeek, T. B. H. (2012) · Nature Immunology · doi:10.1038/ni.2222 · Cited by 628
Cationic lipids, lipoplexes and intracellular delivery of genes
Wasungu, L., & Hoekstra, D. (2006) · Journal of Controlled Release · doi:10.1016/j.jconrel.2006.06.024 · Cited by 616
Recent Advances in Nonviral Vectors for Gene Delivery
Guo, X., & Huang, L. (2011) · Accounts of Chemical Research · doi:10.1021/ar200151m · Cited by 585
Kedmi, R., Ben-Arie, N., & Peer, D. (2010) · Biomaterials · doi:10.1016/j.biomaterials.2010.05.027 · Cited by 546 · cited 2×
“Finally, the fact that insertion of DOTAP into neutral liposomes lead to a larger cytokine release as compared to DOTAP alone [48,50,57] suggests that the modification of the cationic liposomes composition, by inserting cationic lipids into neutral liposomes, could be a way to regulate their immunostimulatory properti…”
BackgroundFormation and Intracellular Trafficking of Lipoplexes and Polyplexes
Elouahabi, A., & Ruysschaert, J. (2005) · Molecular Therapy · doi:10.1016/j.ymthe.2004.12.006 · Cited by 464
Self-citationFilion, M. C., & Phillips, N. C. (1997) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/s0005-2736(97)00126-0 · Cited by 428
Cationic lipids and polymers mediated vectors for delivery of siRNA
Zhang, S., Zhao, B., Jiang, H., Wang, B., & Ma, B. (2007) · Journal of Controlled Release · doi:10.1016/j.jconrel.2007.07.016 · Cited by 426
Kaiser, W. J., & Offermann, M. K. (2005) · The Journal of Immunology · doi:10.4049/jimmunol.174.8.4942 · Cited by 378
Stimulation of Toll-like receptor 3 and 4 induces interleukin-1β maturation by caspase-8
Maelfait, J., Vercammen, E., Janssens, S., Schotte, P., Haegman, M., Magez, S., & Beyaert, R. (2008) · The Journal of Experimental Medicine · doi:10.1084/jem.20071632 · Cited by 335
Cationic compounds used in lipoplexes and polyplexes for gene delivery
Zhang, S., Xu, Y., Wang, B., Qiao, W., Liu, D., & Li, Z. (2004) · Journal of Controlled Release · doi:10.1016/j.jconrel.2004.08.019 · Cited by 320
CD14 regulates the dendritic cell life cycle after LPS exposure through NFAT activation
Zanoni, I., Ostuni, R., Capuano, G., Collini, M., Caccia, M., Ronchi, A. E., Rocchetti, M., Mingozzi, F., Foti, M., Chirico, G. G., et al. (2009) · Nature · doi:10.1038/nature08118 · Cited by 319
The Design of Cationic Lipids for Gene Delivery
Martin, B., Sainlos, M., Aissaoui, A., Oudrhiri, N., Hauchecorne, M., VIGNERON, J. ‐., Lehn, J., & Lehn, P. (2005) · Current Pharmaceutical Design · doi:10.2174/1381612053382133 · Cited by 304
Karmali, P. P., & Chaudhuri, A. (2006) · Medicinal Research Reviews · doi:10.1002/med.20090 · Cited by 289
Sensing damage by the NLRP3 inflammasome
Leemans, J. C., Cassel, S. L., & Sutterwala, F. S. (2011) · Immunological Reviews · doi:10.1111/j.1600-065x.2011.01043.x · Cited by 281
Crystal Structure of CD14 and Its Implications for Lipopolysaccharide Signaling
Kim, J.-I., Lee, C. J., Jin, M. S., Lee, C.-H., Paik, S., Lee, H., & Lee, J. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m414607200 · Cited by 278
Mitochondrial ROS fuel the inflammasome
Sorbara, M. T., & Girardin, S. E. (2011) · Cell Research · doi:10.1038/cr.2011.20 · Cited by 274
Cationic liposomes as vaccine adjuvants
Christensen, D., Korsholm, K. S., Andersen, P. L., & Agger, E. M. (2011) · Expert Review of Vaccines · doi:10.1586/erv.11.17 · Cited by 262
Calcium and Mitochondrial Reactive Oxygen Species Generation: How to Read the Facts
Ádám‐Vizi, V., & Starkov, A. A. (2010) · Journal of Alzheimer s Disease · doi:10.3233/jad-2010-100465 · Cited by 253
Erridge, C., Kennedy, S., Spickett, C. M., & Webb, D. J. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m800352200 · Cited by 234
Lipopolysaccharide binding protein and soluble CD14 catalyze exchange of phospholipids.
Yu, B., Hailman, E., & Wright, S. D. (1997) · Journal of Clinical Investigation · doi:10.1172/jci119160 · Cited by 225
CD14 is a coreceptor of Toll-like receptors 7 and 9
Baumann, C., Aspalter, I. M., Sharif, O., Pichlmair, A., Blüml, S., Grebien, F., Brückner, M., Pasierbek, P., Aumayr, K., Planyavsky, M., et al. (2010) · The Journal of Experimental Medicine · doi:10.1084/jem.20101111 · Cited by 220
Intracellular Delivery of Proteins with a New Lipid-mediated Delivery System
Zelphati, O., Wang, Y., Kitada, S., Reed, J. C., Felgner, P. L., & Corbeil, J. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m104920200 · Cited by 214
Cationic liposomal lipids: From gene carriers to cell signaling
Lonez, C., Vandenbranden, M., & Ruysschaert, J. (2008) · Progress in Lipid Research · doi:10.1016/j.plipres.2008.03.002 · Cited by 208
Self-citationThe adjuvant mechanism of cationic dimethyldioctadecylammonium liposomes
Korsholm, K. S., Agger, E. M., Foged, C., Christensen, D., Dietrich, J., Andersen, C. S., Geisler, C., & Andersen, P. L. (2007) · Immunology · doi:10.1111/j.1365-2567.2007.02560.x · Cited by 188
Gene delivery by cationic lipids: in and out of an endosome
Hoekstra, D., Rejman, J., Wasungu, L., Shi, F., & Zuhorn, I. S. (2007) · Biochemical Society Transactions · doi:10.1042/bst0350068 · Cited by 186
Immunostimulation of dendritic cells by cationic liposomes
Vangasseri, D. P., Cui, Z., Chen, W., Hokey, D. A., Falo, L. D., & Huang, L. (2006) · Molecular Membrane Biology · doi:10.1080/09687860600790537 · Cited by 183
Yan, W., Chen, W., & Huang, L. (2007) · Molecular Immunology · doi:10.1016/j.molimm.2007.04.009 · Cited by 178
Therapeutic targeting of innate immunity with Toll-like receptor 4 (TLR4) antagonists
Peri, F., & Piazza, M. (2011) · Biotechnology Advances · doi:10.1016/j.biotechadv.2011.05.014 · Cited by 164
Deciphering the complexity of Toll-like receptor signaling
Ostuni, R., Zanoni, I., & Granucci, F. (2010) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-010-0464-x · Cited by 162
Zuhorn, I. S., & Hoekstra, D. (2002) · The Journal of Membrane Biology · doi:10.1007/s00232-002-1015-7 · Cited by 156
Major limitations in the use of cationic liposomes for DNA delivery
Filion, M. C., & Phillips, N. C. (1998) · International Journal of Pharmaceutics · doi:10.1016/s0378-5173(97)00423-7 · Cited by 155
Altering the immune response with lipid-based nanoparticles
Landesman‐Milo, D., & Peer, D. (2011) · Journal of Controlled Release · doi:10.1016/j.jconrel.2011.12.034 · Cited by 141
Cationic liposomes as vaccine adjuvants
Christensen, D., Korsholm, K. S., Rosenkrands, I., Lindenstrøm, T., Andersen, P. L., & Agger, E. M. (2007) · Expert Review of Vaccines · doi:10.1586/14760584.6.5.785 · Cited by 138
Two Faces of Protein Kinase Cδ: The Contrasting Roles of PKCδ in Cell Survival and Cell Death
Basu, A., & Pal, D. (2010) · The Scientific World JOURNAL · doi:10.1100/tsw.2010.214 · Cited by 132
Montier, T., Benvegnu, T. J., Jaffrès, P., Yaouanc, J., & Lehn, P. (2008) · Current Gene Therapy · doi:10.2174/156652308786070989 · Cited by 129
A simple but effective cancer vaccine consisting of an antigen and a cationic lipid
Chen, W., Yan, W., & Huang, L. (2007) · Cancer Immunology Immunotherapy · doi:10.1007/s00262-007-0390-4 · Cited by 126
Yan, W., Chen, W., & Huang, L. (2008) · Journal of Controlled Release · doi:10.1016/j.jconrel.2008.05.005 · Cited by 125
Redox regulation of calcium ion channels: Chemical and physiological aspects
Bogeski, I., Kappl, R., Kummerow, C., Gulaboski, R., Hoth, M., & Niemeyer, B. A. (2011) · Cell Calcium · doi:10.1016/j.ceca.2011.07.006 · Cited by 123
DiC14‐amidine cationic liposomes stimulate myeloid dendritic cells through Toll‐like receptor 4
Tanaka, T., Legat, A., Adam, E., Steuve, J., Gatot, J., Vandenbranden, M., Ulianov, L., Lonez, C., Ruysschaert, J., Muraille, É., et al. (2008) · European Journal of Immunology · doi:10.1002/eji.200737998 · Cited by 98
Self-citationCationic lipid-mediated nucleic acid delivery: beyond being cationic
Rao, N. M. (2010) · Chemistry and Physics of Lipids · doi:10.1016/j.chemphyslip.2010.01.001 · Cited by 98
Induction of apoptosis in macrophages by cationic liposomes
Aramaki, Y., Takano, S., & Tsuchiya, S. (1999) · FEBS Letters · doi:10.1016/s0014-5793(99)01386-1 · Cited by 97
Complex Formation with Plasmid DNA Increases the Cytotoxicity of Cationic Liposomes
Nguyen, L. T., Atobe, K., Barichello, J. M., Ishida, T., & Kiwada, H. (2007) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.30.751 · Cited by 92
Iwaoka, S., Nakamura, T., Takano, S., Tsuchiya, S., & Aramaki, Y. (2005) · Journal of Leukocyte Biology · doi:10.1189/jlb.0405181 · Cited by 91
Takano, S., Aramaki, Y., & Tsuchiya, S. (2003) · Pharmaceutical Research · doi:10.1023/a:1024441702398 · Cited by 87
Regen, T., van Rossum, D., Scheffel, J., Kastriti, M. E., Revelo, N. H., Prinz, M., Brück, W., & Hanisch, U. (2010) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2010.10.009 · Cited by 70
Interactions between Cationic Vesicles and Cultured Mammalian Cells
Carmona‐Ribeiro, A. M., Ortis, F., Schumacher, R. I., & Armelin, M. C. S. (1997) · Langmuir · doi:10.1021/la960759h · Cited by 67
Piazza, M., Rossini, C., Fiorentina, S. D., Pozzi, C., Comelli, F., Bettoni, I., Fusi, P. A., Costa, B., & Peri, F. (2009) · Journal of Medicinal Chemistry · doi:10.1021/jm801333m · Cited by 66
Weber, C., Müller, C., Podszuweit, A., Montino, C., Vollmer, J., & Forsbach, A. (2012) · Immunology · doi:10.1111/j.1365-2567.2012.03559.x · Cited by 60
Cationic Liposomes Induce Macrophage Apoptosis through Mitochondrial Pathway
Aramaki, Y., Takano, S., & Tsuchiya, S. (2001) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.2001.2458 · Cited by 58
L-Arginine and Atherothrombosis
Loscalzo, J. (2004) · Journal of Nutrition · doi:10.1093/jn/134.10.2798s · Cited by 55
Evidence of a Specific Interaction between New Synthetic Antisepsis Agents and CD14
Piazza, M., Yu, L. P., Teghanemt, A., Gioannini, T. L., Weiss, J. P., & Peri, F. (2009) · Biochemistry · doi:10.1021/bi901601b · Cited by 55
CD14 but not MD2 transmit signals from DAMP
Chun, K., & Seong, S. (2009) · International Immunopharmacology · doi:10.1016/j.intimp.2009.10.002 · Cited by 54
Induction of Apoptosis in WEHI 231 Cells by Cationic Liposomes
Aramaki, Y., Takano, S., Arima, H., & Tsuchiya, S. (2000) · Pharmaceutical Research · doi:10.1023/a:1007552529280 · Cited by 45
Caspase-containing complexes in the regulation of cell death and inflammation
Festjens, N., Cornelis, S., Lamkanfi, M., & Vandenabeele, P. (2006) · Biological Chemistry · doi:10.1515/bc.2006.124 · Cited by 45
David, S. A., Bechtel, B., Cariappa, A., Mathan, V. I., & Balaram, P. (1994) · Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism · doi:10.1016/0005-2760(94)90250-x · Cited by 42
Polyamine effects on cell function: Possible central role of plasma membrane PI(4,5)P2
Coburn, R. F. (2009) · Journal of Cellular Physiology · doi:10.1002/jcp.21899 · Cited by 42
Kongkaneramit, L., Sarisuta, N., Azad, N., Lu, Y., Iyer, A. K. V., Wang, L., & Rojanasakul, Y. (2008) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.107.136077 · Cited by 42
Gregory, C. D., & Devitt, A. (1999) · APOPTOSIS · doi:10.1023/a:1009673914340 · Cited by 40
Adhesion Receptors Mediate Efficient Non-viral Gene Delivery
Zuhorn, I. S., Kalicharan, D., Robillard, G. T., & Hoekstra, D. (2007) · Molecular Therapy · doi:10.1038/mt.sj.6300139 · Cited by 40
Interaction of Cationic Colloids at the Surface of J774 Cells: A Kinetic Analysis
Chenevier, P., Veyret, B., Roux, D., & Henry, N. (2000) · Biophysical Journal · doi:10.1016/s0006-3495(00)76383-1 · Cited by 39
Kusumoto, K.-I., & Ishikawa, T. (2010) · Journal of Controlled Release · doi:10.1016/j.jconrel.2010.07.114 · Cited by 36
Dalkara, D., Chandrashekhar, C., & Zuber, G. (2006) · Journal of Controlled Release · doi:10.1016/j.jconrel.2006.10.005 · Cited by 32
Piazza, M., Calabrese, V., Baruffa, C., Gioannini, T. L., Weiss, J. P., & Peri, F. (2010) · Biochemical Pharmacology · doi:10.1016/j.bcp.2010.06.019 · Cited by 32
Polycationic lipids inhibit the pro-inflammatory response to LPS
Leon‐Ponte, M., Kirchhof, M. G., Sun, T., Stephens, T. A., Singh, B., Sandhu, S., & Madrenas, J. (2004) · Immunology Letters · doi:10.1016/j.imlet.2004.07.019 · Cited by 31
Interactions between cationic liposomes and drugs or biomolecules
Carmona‐Ribeiro, A. M. (2000) · Anais da Academia Brasileira de Ciências · doi:10.1590/s0001-37652000000100005 · Cited by 31
Asai, Y., Makimura, Y., Kawabata, A., & Ogawa, T. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.179.11.7674 · Cited by 31
Cationic Type I Amphiphiles As Modulators of Membrane Curvature Elastic Stress in Vivo
Dymond, M. K., & Attard, G. S. (2008) · Langmuir · doi:10.1021/la8017612 · Cited by 29
Arisaka, M., Nakamura, T., Yamada, A., Negishi, Y., & Aramaki, Y. (2010) · FEBS Letters · doi:10.1016/j.febslet.2010.01.055 · Cited by 28
Polyamines protect against radiation-induced oxidative stress.
von Deutsch, A. W., Mitchell, C. D., Williams, C. E., Dutt, K., Silvestrov, N. A., Klement, B. J., Abukhalaf, I. K., & von Deutsch, D. A. (2005) · PubMed · Cited by 26
Spermine, a Molecular Switch Regulating EGFR, Integrin β3, Src, and FAK Scaffolding
Ray, R., Li, C.-Y., Bhattacharya, S., Naren, A., & Johnson, L. (2011) · Cellular Signalling · doi:10.1016/j.cellsig.2011.12.016 · Cited by 24
Cationic lipids activate cellular cascades. Which receptors are involved?
Lonez, C., Lensink, M. F., Vandenbranden, M., & Ruysschaert, J. (2009) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2009.02.015 · Cited by 24
Self-citationWilmar, A., Lonez, C., Vermeersch, M., Andrianne, M., Pérez-Morga, D. L., Ruysschaert, J., Vandenbranden, M., Léo, O., & Temmerman, S. T. (2011) · Vaccine · doi:10.1016/j.vaccine.2011.10.071 · Cited by 24
Self-citationJacquet, A., Vanderschrick, J.-F., Vandenbranden, M., Elouahabi, A., Magi, M., Garcia, L., & Ruysschaert, J. (2005) · Molecular Therapy · doi:10.1016/j.ymthe.2004.12.024 · Cited by 23
Self-citationTagami, T., Hirose, K., Barichello, J. M., Ishida, T., & Kiwada, H. (2008) · Pharmaceutical Research · doi:10.1007/s11095-008-9663-7 · Cited by 22
Lipoxygenase May Be Involved in Cationic Liposome-Induced Macrophage Apoptosis
Takano, S., Aramaki, Y., & Tsuchiya, S. (2001) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.2001.5731 · Cited by 21
Lysine triggers apoptosis through a NADPH oxidase‐dependent mechanism in human renal tubular cells
Verzola, D., Famà, A., Villaggio, B., Rocco, M. D., Simonato, A., D’Amato, E., Gianiorio, F., & Garibotto, G. (2012) · Journal of Inherited Metabolic Disease · doi:10.1007/s10545-012-9468-z · Cited by 20
Efficient Protein Transduction Method Using Cationic Peptides and Lipids
Yamaguchi, K., Inoue, M., & Goshima, N. (2011) · BioMed Research International · doi:10.1155/2011/872065 · Cited by 15
Cationic lipids involved in gene transfer mobilize intracellular calcium
Ouali, M., Ruysschaert, J., Lonez, C., & Vandenbranden, M. (2007) · Molecular Membrane Biology · doi:10.1080/09687860601108911 · Cited by 14
Self-citationInvolvement of lipid rafts in macrophage apoptosis induced by cationic liposomes
Arisaka, M., Takano, K., Negishi, Y., Arima, H., & Aramaki, Y. (2011) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2011.02.003 · Cited by 13
Involvement of actin cytoskeleton in macrophage apoptosis induced by cationic liposomes
Takano, K., Sato, K., Negishi, Y., & Aramaki, Y. (2011) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2011.12.009 · Cited by 11
Phosphatidyl inositol-3-phosphate kinase mediates CD14 dependent signaling
O’Toole, T. G., & Peppelenbosch, M. P. (2006) · Molecular Immunology · doi:10.1016/j.molimm.2006.10.010 · Cited by 9
Arima, H., Aramaki, Y., & Tsuchiya, S. (1997) · Journal of Pharmaceutical Sciences · doi:10.1021/js960530m · Cited by 9
Toxicogenomics of Nonviral Cationic Gene Delivery Nanosystems
Omidi, Y., Kafil, V., & Barar, J. (2011) · InTech eBooks · doi:10.5772/19035 · Cited by 4
Flagged first, then by citations
Cited by
Sorted by citations
mRNA vaccines for infectious diseases: principles, delivery and clinical translation
Chaudhary, N., Weissman, D., & Whitehead, K. A. (2021) · Nature Reviews Drug Discovery · doi:10.1038/s41573-021-00283-5 · Cited by 1,555
Ndeupen, S., Qin, Z., Jacobsen, S., Bouteau, A., Estanbouli, H., & Igyártó, B. Z. (2021) · iScience · doi:10.1016/j.isci.2021.103479 · Cited by 678
Lipids and Lipid Derivatives for RNA Delivery
Zhang, Y., Sun, C., Wang, C., Jankovic, K. E., & Dong, Y. (2021) · Chemical Reviews · doi:10.1021/acs.chemrev.1c00244 · Cited by 649
Liposomes as vaccine delivery systems: a review of the recent advances
Schwendener, R. A. (2014) · Therapeutic Advances in Vaccines · doi:10.1177/2051013614541440 · Cited by 524
The dawn of mRNA vaccines: the COVID-19 case
Verbeke, R., Lentacker, I., De Smedt, S. C., & Dewitte, H. (2021) · Journal of Controlled Release · doi:10.1016/j.jconrel.2021.03.043 · Cited by 504
Metadata
- Authors
- Lonez, C., Vandenbranden, M., & Ruysschaert, J.-M.
- Affiliations
- Université Libre de Bruxelles (BE)
- Corresponding author
- Lonez, Caroline
- ORCID
- Lonez, Caroline
- Venue
- Advanced Drug Delivery Reviews
- Publisher
- Elsevier BV
- Published
- 2012-12
- Volume
- 64
- Issue
- 15
- Pages
- 1749-1758
- ISSN
- 0169-409X (ISSN-L)
- OpenAlex
- W2055351480
- Cited by
- 221
- References
- 92
- Citations by year
- 2026: 7 · 2025: 13 · 2024: 20 · 2023: 18 · 2022: 21 · 2021: 21 · 2020: 14 · 2019: 10 · 2018: 11 · 2017: 14 · 2016: 16 · 2015: 20 · 2014: 19 · 2013: 12 · 2012: 4
- FWCI
- 1.60
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Advanced Drug Delivery Reviews (publishedVersion)
- PubMed (publishedVersion)
- Dépôt institutionnel de l'Université libre de Bruxelles (Université Libre de Bruxelles) (submittedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Interference and Gene Delivery
- Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
- Physical Sciences › Materials Science › Biomaterials › Nanoparticle-Based Drug Delivery
- Keywords
- cationic liposomes, cationic lipids, intracellular signaling, apoptosis, inflammation, liposome transfection, vaccine adjuvants, gene delivery, lipid structure
- MeSH terms
- Adjuvants, Immunologic, Animals, Antigens, Cations, Humans, Inflammation, Lipids, Liposomes, Transfection, Vaccines, Drug Design, Signal Transduction, Apoptosis
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review