(Q42863719)

English

Antigen delivery to dendritic cells by poly(propylene sulfide) nanoparticles with disulfide conjugated peptides: Cross-presentation and T cell activation

scientific article published on 8 October 2010

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scholarly article

1 reference

Europe PubMed Central

8 November 2017

Antigen delivery to dendritic cells by poly(propylene sulfide) nanoparticles with disulfide conjugated peptides: Cross-presentation and T cell activation (English)

1 reference

Europe PubMed Central

8 November 2017

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1 reference

based on heuristic

inferred from title

Jeffrey A. Hubbell

object named as

Jeffrey A Hubbell

4

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author name string

Sachiko Hirosue

1

1 reference

Europe PubMed Central

8 November 2017

Iraklis C Kourtis

2

1 reference

Europe PubMed Central

8 November 2017

André J van der Vlies

3

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Europe PubMed Central

8 November 2017

Melody A Swartz

5

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Europe PubMed Central

8 November 2017

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publication date

8 October 2010

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Europe PubMed Central

8 November 2017

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10

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Europe PubMed Central

8 November 2017

28

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Europe PubMed Central

8 November 2017

50

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Europe PubMed Central

8 November 2017

7897-7906

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Europe PubMed Central

8 November 2017

Effector and memory CTL differentiation

1 reference

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Virosomal adjuvanted antigen delivery systems

1 reference

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In vivo targeting of dendritic cells in lymph nodes with poly(propylene sulfide) nanoparticles.

1 reference

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Exploiting lymphatic transport and complement activation in nanoparticle vaccines

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Activation of lysosomal function during dendritic cell maturation

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Targeting proteins to distinct subcellular compartments reveals unique requirements for MHC class I and II presentation

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Characterization of poly(D,L-lactic-co-glycolic acid) based nanoparticulate system for enhanced delivery of antigens to dendritic cells

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Short peptide sequences containing MHC class I and/or class II epitopes linked to nano-beads induce strong immunity and inhibition of growth of antigen-specific tumour challenge in mice

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Concomitant delivery of a CTL-restricted peptide antigen and CpG ODN by PLGA microparticles induces cellular immune response

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Acid-degradable particles for protein-based vaccines: enhanced survival rate for tumor-challenged mice using ovalbumin model

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A phagosome-to-cytosol pathway for exogenous antigens presented on MHC class I molecules

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Selective transport of internalized antigens to the cytosol for MHC class I presentation in dendritic cells.

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Enhanced and prolonged cross-presentation following endosomal escape of exogenous antigens encapsulated in biodegradable nanoparticles

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PEG-SS-PPS: reduction-sensitive disulfide block copolymer vesicles for intracellular drug delivery.

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Reduction-sensitive polymers and bioconjugates for biomedical applications

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Formulation of highly soluble poly(ethylene glycol)-peptide DNA condensates

1 reference

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Antibody-maytansinoid conjugates are activated in targeted cancer cells by lysosomal degradation and linker-dependent intracellular processing.

1 reference

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Tumor delivery and in vivo processing of disulfide-linked and thioether-linked antibody-maytansinoid conjugates

1 reference

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Synthesis of pyridyl disulfide-functionalized nanoparticles for conjugating thiol-containing small molecules, peptides, and proteins

1 reference

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An advanced culture method for generating large quantities of highly pure dendritic cells from mouse bone marrow

1 reference

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Oxidation-sensitive polymeric nanoparticles.

1 reference

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Selective loading of high-affinity peptides onto major histocompatibility complex class I molecules by the tapasin-ERp57 heterodimer

1 reference

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Dynasore, a cell-permeable inhibitor of dynamin

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Filipin-dependent inhibition of cholera toxin: evidence for toxin internalization and activation through caveolae-like domains

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Bafilomycins: a class of inhibitors of membrane ATPases from microorganisms, animal cells, and plant cells

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A role for phosphoinositide 3-kinase in the completion of macropinocytosis and phagocytosis by macrophages

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Distinct endocytotic pathways in epidermal growth factor-stimulated human carcinoma A431 cells

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Constitutive macropinocytosis allows TAP-dependent major histocompatibility complex class I presentation of exogenous soluble antigen by bone marrow-derived dendritic cells.

1 reference

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7 January 2021

Post-proteasomal antigen processing for major histocompatibility complex class I presentation

1 reference

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PAProC: a prediction algorithm for proteasomal cleavages available on the WWW.

1 reference

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An IFN-gamma-induced aminopeptidase in the ER, ERAP1, trims precursors to MHC class I-presented peptides

1 reference

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7 January 2021

MHC class II molecules on the move for successful antigen presentation

1 reference

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NOX2 Controls Phagosomal pH to Regulate Antigen Processing during Crosspresentation by Dendritic Cells

1 reference

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In vivo cross-priming of MHC class I-restricted antigens requires the TAP transporter.

1 reference

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Oxidized redox state of glutathione in the endoplasmic reticulum

1 reference

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Generation of major histocompatibility complex class I antigens: functional interplay between proteasomes and TPPII.

1 reference

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The ER aminopeptidase ERAP1 enhances or limits antigen presentation by trimming epitopes to 8-9 residues

1 reference

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Dendritic cells process antigens encapsulated in a biodegradable polymer, poly(D,L-lactide-co-glycolide), via an alternate class I MHC processing pathway

1 reference

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ISCOMATRIX adjuvant induces efficient cross-presentation of tumor antigen by dendritic cells via rapid cytosolic antigen delivery and processing via tripeptidyl peptidase II.

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Early phagosomes in dendritic cells form a cellular compartment sufficient for cross presentation of exogenous antigens

1 reference

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ER-phagosome fusion defines an MHC class I cross-presentation compartment in dendritic cells

1 reference

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Antigen loading of MHC class I molecules in the endocytic tract

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Enzymatic reduction of disulfide bonds in lysosomes: characterization of a gamma-interferon-inducible lysosomal thiol reductase (GILT)

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IRAP identifies an endosomal compartment required for MHC class I cross-presentation

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Identifiers

10.1016/J.VACCINE.2010.09.077

1 reference

Europe PubMed Central

8 November 2017

1 reference

Europe PubMed Central

8 November 2017

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