Archaeosomes as self-adjuvanting delivery systems for cancer vaccines.

Abstract:

:Archaeal ether glycerolipid vesicles (archaeosomes) efficiently deliver exogenous antigen for induction of humoral and cell-mediated immunity. Because induction of CD8 cytotoxic T cells is critical for protective vaccination against tumors, we compared the ability of various archaeosome lipid compositions to evoke a strong CD8 CTL response to entrapped antigen. Subcutaneous immunization of mice with ovalbumin (OVA) entrapped in all archaeosome lipid compositions evoked a primary (day 10) splenic CTL response indicating processing for MHC class I presentation. Interestingly, several polar lipid compositions from halophilic archaea were very potent to adjuvant this early CTL response. Despite this, the lytic units reduced substantially by weeks 6-7. More importantly, at >50 weeks, only Methanobrevibacter smithii and Thermoplasma acidophilum both rich in bipolar membrane-spanning caldarchaeols, demonstrated recall memory CTLs. Immunization of mice with OVA entrapped in M. smithii, Halobacterium salinarum or T. acidophilum vesicles provided prophylactic protection against challenge with OVA-expressing solid tumors at 6 weeks. Even a dose of 3 microg OVA in archaeosomes significantly delayed tumor growth. Tumor protection was also noted in a therapeutic design wherein OVA-archaeosomes were injected concurrent with the tumor challenge. Interestingly, antigen-free T. acidophilum but not antigen-free H. salinarum archaeosomes provided innate therapeutic protection. Vaccination with a CTL peptide epitope from the melanoma differentiation antigen, tyrosinase-related protein 2, in archaeosomes induced a protective CD8 response against B16OVA metastasis, indicating potential for targeting self, tumor antigens. Thus, lipid structural properties of archaea may differentially modulate primary, long-term and/or innate immunity, impacting adjuvant choice for vaccine design.

journal_name

J Drug Target

authors

Krishnan L,Dennis Sprott G,Institute for Biological Sciences, National Research Council of Canada.

doi

10.1080/10611860410001670044

keywords:

subject

Has Abstract

pub_date

2003-01-01 00:00:00

pages

515-24

issue

8-10

eissn

1061-186X

issn

1029-2330

pii

PTRA16U7BD82YHXE

journal_volume

11

pub_type

杂志文章
  • Potentiation of pro-inflammatory cytokine suppression and survival by microencapsulated dexamethasone in the treatment of experimental sepsis.

    abstract::Cytokine inhibiting drugs are much more effective when delivered intracellularly to phagocytic cells in the microencapsulated form. Dexamethasone is a powerful inhibitor of TNF-α cytokine through inhibition of NF-κB which is a gene regulator of multiple pro-inflammatory cytokines. We have determined the effect of micr...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/1061186X.2011.561856

    authors: Uddin MN,Siddiq A,Oettinger CW,D'Souza MJ

    更新日期:2011-11-01 00:00:00

  • Perceptive solutions to anti-filarial chemotherapy of lymphatic filariasis from the plethora of nanomedical sciences.

    abstract:INTRODUCTION:Growing interest in the application of nanotechnology to treat lymphatic filariasis (LF) implies that the imminent medical arsenal of this interesting technology is attractive for health authorities. Currently, they are completely dependent on friendly oral mass drug (anti-filarials) administration to elim...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章,评审

    doi:10.3109/1061186X.2013.832766

    authors: Ali M,Afzal M,Kaushik U,Bhattacharya SM,Ahmad FJ,Dinda AK

    更新日期:2014-01-01 00:00:00

  • Inhibitory effect of small interfering RNA specific for a novel candidate target in PB1 gene of influenza A virus.

    abstract::Influenza, mainly caused by influenza virus, is becoming one of the major concerns in the world. Limitation in vaccines necessitates the urgent development of new therapeutic options against this virus. In the present study, we designed small interfering RNA (siRNA) targeting overlapping gene of PB1 and PB1-F2 gene of...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/10611860802473048

    authors: Cheng C,Yao L,Chen A,Jia R,Huan L,Guo J,Bo H,Shu Y,Zhang Z

    更新日期:2009-02-01 00:00:00

  • PEG-modified GoldMag nanoparticles (PGMNs) combined with the magnetic field for local drug delivery.

    abstract::Polyethylene glycol-modified GoldMag nanoparticles (PGMNs) were synthesized and characterized by several analysis including transmission electron microscopy, dynamic light scattering, Fourier transform infrared spectroscopy, and vibrating sample magnetometer. Here, we showed that the composite nanoparticles have a sat...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/10611861003801842

    authors: Chao X,Guo L,Zhao Y,Hua K,Peng M,Chen C,Cui Y

    更新日期:2011-04-01 00:00:00

  • Role of therapeutic agents on repolarisation of tumour-associated macrophage to halt lung cancer progression.

    abstract::Tumour-associated macrophages (TAMs) represent as much as 50% of the solid mass in different types of human solid tumours including lung, breast, ovarian and pancreatic adenocarcinomas. The tumour microenvironment (TME) plays an important role in the polarisation of macrophages into the M1 phenotype, which is tumour-s...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/1061186X.2019.1648478

    authors: Aldawsari HM,Gorain B,Alhakamy NA,Md S

    更新日期:2020-02-01 00:00:00

  • Brain-targeted delivery of paclitaxel using glutathione-coated nanoparticles for brain cancers.

    abstract::Paclitaxel is not effective for treatment of brain cancers because it cannot cross the blood-brain barrier (BBB) due to efflux by P-glycoprotein (P-gp). In this work, glutathione-coated poly-(lactide-co-glycolide) (PLGA) nanoparticles (NPs) of paclitaxel were developed for brain targeting for treatment of brain cancer...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/1061186X.2011.589435

    authors: Geldenhuys W,Mbimba T,Bui T,Harrison K,Sutariya V

    更新日期:2011-11-01 00:00:00

  • Preliminary evaluation of [18F]AlF-NOTA-MAL-Cys39-exendin-4 in insulinoma with PET.

    abstract:BACKGROUND:High expression of glucagon-like peptide-1 receptor (GLP-1R) in insulinoma supplies a potential drug target for tumor imaging. Exendin-4 can specifically bind to GLP-1R as an agonist and its analogs are extensively used in receptor imaging studies. PURPOSE:A new GLP-1R imaging agent, [(18)F]AlF-NOTA-MAL-Cys...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/1061186X.2015.1020808

    authors: Xu Q,Zhu C,Xu Y,Pan D,Liu P,Yang R,Wang L,Chen F,Sun X,Luo S,Yang M

    更新日期:2015-01-01 00:00:00

  • Cell-penetrating peptide-doxorubicin conjugate loaded NGR-modified nanobubbles for ultrasound triggered drug delivery.

    abstract::A new drug-targeting system for CD13(+) tumors has been developed, based on ultrasound-sensitive nanobubbles (NBs) and cell-permeable peptides (CPPs). Here, the CPP-doxorubicin conjugate (CPP-DOX) was entrapped in the asparagine-glycine-arginine (NGR) peptide modified NB (CPP-DOX/NGR-NB) and the penetration of CPP-DOX...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/1061186X.2015.1058802

    authors: Lin W,Xie X,Deng J,Liu H,Chen Y,Fu X,Liu H,Yang Y

    更新日期:2016-01-01 00:00:00

  • Enhanced efficacy of diclofenac sodium-loaded lipogelosome formulation in intra-articular treatment of rheumatoid arthritis.

    abstract::Recent research into the complex and varied components of rheumatoid arthritis (RA) is leading to the development of more effective targets for pharmaceutical approach than even before. Current treatment of RA frequently includes the use of nonsteroidal anti-inflammatory drugs, such as Diclofenac sodium (DFNa) in spit...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/10611860701725191

    authors: Türker S,Erdoğan S,Ozer YA,Bilgili H,Deveci S

    更新日期:2008-01-01 00:00:00

  • Pharmacokinetics and targeting property of TFu-loaded liposomes with different sizes after intravenous and oral administration.

    abstract::The purpose of the study was to develop the liposomal formulations of TFu for oral and intravenous (i.v.) administration, clarify the biodistribution characteristics and in vivo pharmacokinetic behaviors of TFu-loaded liposomes. Four TFu-loaded liposomes of different sizes were prepared and characterized. The pharmaco...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/10611860801927598

    authors: Sun W,Zou W,Huang G,Li A,Zhang N

    更新日期:2008-06-01 00:00:00

  • Single-walled carbon nanotube-loaded doxorubicin and Gd-DTPA for targeted drug delivery and magnetic resonance imaging.

    abstract::An aspargine-glycine-arginine (NGR) peptide modified single-walled carbon nanotubes (SWCNTs) system, developed by a simple non-covalent approach, could be loaded with the anticancer drug doxorubicin (DOX) and magnetic resonance imaging (MRI) contrast agent gadolinium-diethylenetriamine pentaacetic acid (Gd-DTPA). This...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/1061186X.2016.1221958

    authors: Yan C,Chen C,Hou L,Zhang H,Che Y,Qi Y,Zhang X,Cheng J,Zhang Z

    更新日期:2017-02-01 00:00:00

  • Effect of cationic lipid in cationic liposomes on siRNA delivery into the lung by intravenous injection of cationic lipoplex.

    abstract::Cationic liposomes composed of dialkyl cationic lipid such as 1,2-dioleoyl-3-trimethylammonium-propane (DOTAP) can efficiently deliver siRNA to the lungs following the intravenous injection of cationic liposome/siRNA complexes (lipoplexes). In this study, we examined the effect of cationic lipid of cationic liposomes ...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/1061186X.2018.1502775

    authors: Hattori Y,Nakamura M,Takeuchi N,Tamaki K,Shimizu S,Yoshiike Y,Taguchi M,Ohno H,Ozaki KI,Onishi H

    更新日期:2019-02-01 00:00:00

  • Insulin micropiles comprising biodegradable polymers for production of a long-term hypoglycemic effect.

    abstract::As a percutaneous sustained-release preparation, insulin micropiles (MPs) were prepared with biodegradable polymers poly(lactic acid) (PLA), poly(ϵ-caprolactone) (PCL) and poly(lactic-co-glycolic acid) (PLGA) as the base. The obtained PLA, PCL, and PLGA MPs of which the insulin:polymer ratio was 1:2 were administered ...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/1061186X.2010.492521

    authors: Fukushima K,Ito Y,Ishihata M,Sugioka N,Takada K

    更新日期:2011-04-01 00:00:00

  • Pharmacotherapy in COVID-19 patients: a review of ACE2-raising drugs and their clinical safety.

    abstract::The COVID-19 pandemic is caused by the severe acute-respiratory-syndrome-coronavirus-2 that uses ACE2 as its receptor. Drugs that raise serum/tissue ACE2 levels include ACE inhibitors (ACEIs) and angiotensin-II receptor blockers (ARBs) that are commonly used in patients with hypertension, cardiovascular disease and/or...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章,评审

    doi:10.1080/1061186X.2020.1797754

    authors: Akhtar S,Benter IF,Danjuma MI,Doi SAR,Hasan SS,Habib AM

    更新日期:2020-08-01 00:00:00

  • Different transfers of N-acetyl-p-aminobenzoic acid and p-aminobenzoic acid across the placenta and the small intestine in rats.

    abstract::The aim of the present study was to evaluate the transfer of N-acetyl-p-aminobenzoic acid (AcPABA) across the rat term placenta and the rat small intestine and to compare it with that of its parent drug p-aminobenzoic acid (PABA). Umbilical perfusion of the rat term placenta was used to determine the materno-fetal tra...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/10611869808995875

    authors: Staud F,Fendrich Z,Hartl J,Jindrova O,Láznícek M

    更新日期:1998-01-01 00:00:00

  • α-Tocopherol as functional excipient for resveratrol and coenzyme Q10-loaded SNEDDS for improved bioavailability and prophylaxis of breast cancer.

    abstract::The present study evaluates the prophylactic efficacy of α-tocopherol (α-TOH), resveratrol (RES), and coenzyme Q10 (CoQ10) co-loaded self-nanoemulsifying drug delivery system (α-TOH-RES-CoQ10 SNEDDS) in 7,12-Dimethylbenz[a]anthracene (DMBA) induced breast cancer model. SNEDDS formulation components were rationally sel...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/1061186X.2017.1298603

    authors: Jain S,Garg T,Kushwah V,Thanki K,Agrawal AK,Dora CP

    更新日期:2017-07-01 00:00:00

  • Liposomes and niosomes as potential carriers for dermal delivery of minoxidil.

    abstract::The aim of this work was to formulate minoxidil loaded liposome and niosome formulations to improve skin drug delivery. Multilamellar liposomes were prepared using soy phosphatidylcholine at different purity degrees (Phospholipon 90, 90% purity, soy lecithin (SL), 75% purity) and cholesterol (Chol), whereas niosomes w...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/10611860600991993

    authors: Mura S,Pirot F,Manconi M,Falson F,Fadda AM

    更新日期:2007-02-01 00:00:00

  • Similar efficiency of DNA-liposome complexes and retrovirus-producing cells for HSV-tk suicide gene therapy of peritoneal carcinomatosis.

    abstract::Several experimental approaches have been tested for suicide gene delivery into tumor cells, including viral and non-viral vectors. In this study, we compared the efficiency of Herpes Simplex Virus type 1 thymidine kinase gene (HSV-tk) delivery by retrovirus-producing cells and DNA/liposome complexes for the treatment...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/10611860008996854

    authors: Princen F,Lechanteur C,Lopez M,Gielen J,Bours V,Merville MP

    更新日期:2000-01-01 00:00:00

  • Synthesis, characterization and in vitro evaluation of dimethyl-beta-cyclodextrin-4-biphenylylacetic acid conjugate.

    abstract::Biphenylylacetic acid (BPAA) was linked to the free hydroxyl group of 2,6-di-O-methyl-beta-Cyclodextrin (DM-beta-CyD) through an ester linkage to obtain the site specific release of the drug to the colon. The conjugate at 1:1 mole ratio was separated from the reaction mixture by semipreparative reverse-phase HPLC and ...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/10611860310001615965

    authors: Ventura CA,Paolino D,Pedotti S,Pistarà V,Corsaro A,Puglisi G

    更新日期:2003-05-01 00:00:00

  • A new method to isolate polyalkylcyanoacrylate nanoparticle preparations.

    abstract::A simple method for the separation of polyalkylcyanoacrylate nanoparticles was developed using polyisohexylcyanoacrylate (PIHCA) as a model. Fluorescein isothiocyanate dextran 70 was used to label the nanoparticles. Ultracentrifugation onto a performed sucrose gradient allowed the easy elimination of the dextran and o...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/10611869509059216

    authors: Pinto-Alphandary H,Balland O,Couvreur P

    更新日期:1995-01-01 00:00:00

  • Effect of iontophoretic patterns on in vivo antidiuretic response to desmopressin acetate administered transdermally.

    abstract::The effects of concentration, amperage and duration on the antidiuretic response induced by iontophoretic delivery of desmopressin acetate (DDAVP) were examined using a diabetes insipidus model in rats. A higher current density brought about a larger and longer antidiuretic response. Prolonged iontophoretic duration c...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/10611869509015918

    authors: Nakakura M,Terajima M,Kato Y,Hayakawa E,Ito K,Kuroda T

    更新日期:1995-01-01 00:00:00

  • Lactose-modified DNA tile nanostructures as drug carriers.

    abstract:BACKGROUND:DNA hybridization allows the preparation of nanoscale DNA structures with desired shape and size. DNA structures using simple base pairing can be used for the delivery of drug molecules into the cells. Since DNA carries multiple negative charges, their cellular uptake efficiency is low. Thus, the modificatio...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/1061186X.2016.1144059

    authors: Akkus Sut P,Tunc CU,Culha M

    更新日期:2016-09-01 00:00:00

  • Muco-adhesive multivesicular liposomes as an effective carrier for transmucosal insulin delivery.

    abstract::Considering limitations of conventional insulin therapies, the present study characterizes usefulness of novel mucoadhesive multivesicular liposomes as a mucoadhesive sustained release carrier of insulin via nasal and ocular routes, thus attempts to develop non-invasive carrier system for the controlled release of bio...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/10611860701453653

    authors: Jain AK,Chalasani KB,Khar RK,Ahmed FJ,Diwan PV

    更新日期:2007-07-01 00:00:00

  • Biphasic interactions between a cationic dendrimer and actin.

    abstract::Gene delivery systems face the problem not only of the route toward the cell and tissues in question, but also of the molecularly crowded environment of both the cytoplasm and the nucleus itself. One of the physical barriers in the cytoplasm for diffusing nanoparticles is an actin network. Here, we describe the findin...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/1061186X.2010.521159

    authors: Ruenraroengsak P,Florence AT

    更新日期:2010-12-01 00:00:00

  • Prostate cancer cell-specific VEGF siRNA delivery system using cell targeting peptide conjugated polyplexes.

    abstract::A polymeric gene carrier was developed to deliver vascular endothelial growth factor (VEGF) small interfering RNA (siRNA) for prostate cancer cells in a target-specific manner. Prostate cancer-binding peptide (PCP) was conjugated with polyethylenimine (PEI) via a poly(ethylene glycol) (PEG) linker (PEI-PEG-PCP). The P...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/10611860902767232

    authors: Kim SH,Lee SH,Tian H,Chen X,Park TG

    更新日期:2009-05-01 00:00:00

  • Mitochondria-targeted antioxidant SkQT1 decreases trauma-induced neurological deficit in rat and prevents amyloid-β-induced impairment of long-term potentiation in rat hippocampal slices.

    abstract::This study assesses a protective effect of a mitochondria-targeted antioxidant SkQT1 (a mixture of 10-(6'-toluquinonyl) decyltriphenylphosphonium and 10-(5'-toluquinonyl) decyltriphenylphosphonium in proportion of 1.4:1), using an open focal trauma model of the rat brain sensorimotor cortex and a model of amyloid-beta...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/1061186X.2014.997736

    authors: Genrikhs EE,Stelmashook EV,Popova OV,Kapay NA,Korshunova GA,Sumbatyan NV,Skrebitsky VG,Skulachev VP,Isaev NK

    更新日期:2015-05-01 00:00:00

  • Bioefficacy of budesonide loaded crosslinked polyelectrolyte microparticles in rat model of induced colitis.

    abstract::A targeted delivery system for inflammatory bowel diseases, chitosan-Ca-alginate microparticles efficiently loaded with budesonide (BDS), were designed using one-step spray-drying process. They were eudragit-coated and examined for in vivo efficacy. Experimental colitis was induced by rectal instillation of 2,4,6-trin...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.3109/10611860903161310

    authors: Crcarevska MS,Dodov MG,Petrusevska G,Gjorgoski I,Goracinova K

    更新日期:2009-12-01 00:00:00

  • The role of chitosan on oral delivery of peptide-loaded nanoparticle formulation.

    abstract::Therapeutic peptides are conventionally administered via subcutaneous injection. Chitosan-based nanoparticles are gaining increased attention for their ability to serve as a carrier for oral delivery of peptides and vaccination. They offered superior biocompatibiltiy, controlled drug release profile and facilitated ga...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章,评审

    doi:10.1080/1061186X.2017.1400552

    authors: Wong CY,Al-Salami H,Dass CR

    更新日期:2018-08-01 00:00:00

  • Sulpiride gastro-retentive floating microsponges; analytical study, in vitro optimization and in vivo characterization.

    abstract::Sulpiride (SUL), anti-dopaminergic drug, has a specific site for absorption located in the upper portion of the gastrointestinal tract hence, its oral delivery represents a challenge regarding SUL absorption and bioavailability. So, a gastro-retentive oral platform of SUL was developed to increase its gastric residenc...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章

    doi:10.1080/1061186X.2019.1663526

    authors: Younis MA,El-Zahry MR,Tallat MA,Tawfeek HM

    更新日期:2020-04-01 00:00:00

  • Application of titanium dioxide (TiO2) nanoparticles in cancer therapies.

    abstract::Cancer is one of the most common diseases all over the world; many people suffer from diverse types of cancer. However, currently there is no exact cure or therapy developed for cancer. On the other hand, nanoparticles are defined as microscopic particles that have dimensions less than 100 nm and they are known for th...

    journal_title:Journal of drug targeting

    pub_type: 杂志文章,评审

    doi:10.1080/1061186X.2018.1527338

    authors: Çeşmeli S,Biray Avci C

    更新日期:2019-08-01 00:00:00