| scholarly article | Q13442814 |
| P50 | author | Alan Sher | Q88390533 |
| P2093 | author name string | Ira Mellman | |
| Isabelle Coppens | |||
| Romina S Goldszmid | |||
| Pat Caspar | |||
| Avital Lev | |||
| P2860 | cites work | ER-phagosome fusion defines an MHC class I cross-presentation compartment in dendritic cells | Q28506676 |
| Phagosomes are competent organelles for antigen cross-presentation | Q28591811 | ||
| Dual regulation of resistance against Toxoplasma gondii infection by Lyt-2+ and Lyt-1+, L3T4+ T cells in mice | Q68093960 | ||
| Sequential protein secretion from three distinct organelles of Toxoplasma gondii accompanies invasion of human fibroblasts | Q73478363 | ||
| Localization, quantitation, and in situ detection of specific peptide-MHC class I complexes using a monoclonal antibody | Q73479961 | ||
| Intracellular fate of vacuoles containing Toxoplasma gondii is determined at the time of formation and depends on the mechanism of entry | Q73900290 | ||
| Biogenesis of phagolysosomes: the 'kiss and run' hypothesis | Q75292504 | ||
| Phospholipid synthesis in a membrane fraction associated with mitochondria | Q28647511 | ||
| Dendritic cells: specialized and regulated antigen processing machines | Q29617085 | ||
| The role of phospholipase in host cell penetration by Toxoplasma gondii. | Q30461287 | ||
| Export of antigenic peptides from the endoplasmic reticulum intersects with retrograde protein translocation through the Sec61p channel | Q33912882 | ||
| Cell biology of antigen processing in vitro and in vivo | Q33985828 | ||
| A unique mitochondria-associated membrane fraction from rat liver has a high capacity for lipid synthesis and contains pre-Golgi secretory proteins including nascent lipoproteins | Q34325693 | ||
| A secreted serine-threonine kinase determines virulence in the eukaryotic pathogen Toxoplasma gondii | Q34591236 | ||
| Toxoplasma gondii scavenges host-derived lipoic acid despite its de novo synthesis in the apicoplast | Q34767686 | ||
| The parasitophorous vacuole membrane surrounding intracellular Toxoplasma gondii functions as a molecular sieve | Q34980590 | ||
| CD40 induces macrophage anti-Toxoplasma gondii activity by triggering autophagy-dependent fusion of pathogen-containing vacuoles and lysosomes | Q35009488 | ||
| Mycobacterium tuberculosis-specific CD8+ T cells and their role in immunity | Q35099713 | ||
| Biochemical characterization and protein kinase C dependency of monokine-inducing activities of Toxoplasma gondii | Q35495758 | ||
| Rapid elimination of Toxoplasma gondii by gamma interferon-primed mouse macrophages is independent of CD40 signaling | Q36097323 | ||
| Dissection of the Golgi complex. I. Monensin inhibits the transport of viral membrane proteins from medial to trans Golgi cisternae in baby hamster kidney cells infected with Semliki Forest virus | Q36207090 | ||
| Vacuolar and plasma membrane stripping and autophagic elimination of Toxoplasma gondii in primed effector macrophages | Q36228861 | ||
| TAP-1 indirectly regulates CD4+ T cell priming in Toxoplasma gondii infection by controlling NK cell IFN-gamma production | Q36229095 | ||
| Presentation of Toxoplasma gondii antigens via the endogenous major histocompatibility complex class I pathway in nonprofessional and professional antigen-presenting cells | Q36313784 | ||
| Fcgamma receptor-mediated induction of dendritic cell maturation and major histocompatibility complex class I-restricted antigen presentation after immune complex internalization | Q36367948 | ||
| ToxoDB: an integrated Toxoplasma gondii database resource | Q36454249 | ||
| Parasite stage-specific recognition of endogenous Toxoplasma gondii-derived CD8+ T cell epitopes | Q36633085 | ||
| Early phagosomes in dendritic cells form a cellular compartment sufficient for cross presentation of exogenous antigens | Q36689895 | ||
| The Toxoplasma gondii parasitophorous vacuole membrane: transactions across the border | Q36735713 | ||
| Kiss and spit: the dual roles of Toxoplasma rhoptries | Q37024471 | ||
| Toxoplasma co-opts host gene expression by injection of a polymorphic kinase homologue | Q37087502 | ||
| Polymorphic secreted kinases are key virulence factors in toxoplasmosis | Q37105671 | ||
| Immunodominant, protective response to the parasite Toxoplasma gondii requires antigen processing in the endoplasmic reticulum. | Q37158031 | ||
| Association of host cell endoplasmic reticulum and mitochondria with the Toxoplasma gondii parasitophorous vacuole membrane: a high affinity interaction | Q38342669 | ||
| Toxoplasma evacuoles: a two-step process of secretion and fusion forms the parasitophorous vacuole | Q39735086 | ||
| Toxoplasma gondii sequesters lysosomes from mammalian hosts in the vacuolar space | Q40289140 | ||
| On the biogenesis of lipid bodies in ancient eukaryotes: synthesis of triacylglycerols by a Toxoplasma DGAT1-related enzyme | Q40500782 | ||
| Dendritic cells charged with apoptotic tumor cells induce long-lived protective CD4+ and CD8+ T cell immunity against B16 melanoma | Q40614114 | ||
| Quantitating protein synthesis, degradation, and endogenous antigen processing | Q40662419 | ||
| Class I major histocompatibility complex presentation of antigens that escape from the parasitophorous vacuole of Toxoplasma gondii | Q40997338 | ||
| Synergistic role of CD4+ and CD8+ T lymphocytes in IFN-gamma production and protective immunity induced by an attenuated Toxoplasma gondii vaccine | Q41133376 | ||
| Toxoplasma gondii: fusion competence of parasitophorous vacuoles in Fc receptor-transfected fibroblasts | Q41725157 | ||
| Leishmania antigens are presented to CD8+ T cells by a transporter associated with antigen processing-independent pathway in vitro and in vivo | Q41944679 | ||
| Toxoplasma gondii resides in a vacuole that avoids fusion with host cell endocytic and exocytic vesicular trafficking pathways | Q42814484 | ||
| Efficient development of plasmodium liver stage-specific memory CD8+ T cells during the course of blood-stage malarial infection | Q44139710 | ||
| Selective disruption of phosphatidylcholine metabolism of the intracellular parasite Toxoplasma gondii arrests its growth | Q45263588 | ||
| Quantitative and dynamic assessment of the contribution of the ER to phagosome formation | Q45345589 | ||
| A role for the endoplasmic reticulum protein retrotranslocation machinery during crosspresentation by dendritic cells | Q45345591 | ||
| Spatial and mechanistic separation of cross-presentation and endogenous antigen presentation | Q46674193 | ||
| CD8+ T cells are required for primary immunity in C57BL/6 mice following low-dose, intradermal challenge with Leishmania major. | Q53974457 | ||
| P433 | issue | 2 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | vacuole | Q127702 |
| Toxoplasma gondii | Q131003 | ||
| dendritic cell | Q506253 | ||
| P304 | page(s) | 399-410 | |
| P577 | publication date | 2009-01-19 | |
| P1433 | published in | Journal of Experimental Medicine | Q3186912 |
| P1476 | title | Host ER-parasitophorous vacuole interaction provides a route of entry for antigen cross-presentation in Toxoplasma gondii-infected dendritic cells | |
| P478 | volume | 206 |
| Q37903403 | A modular and combinatorial view of the antigen cross-presentation pathway in dendritic cells. |
| Q35102296 | ATF6beta is a host cellular target of the Toxoplasma gondii virulence factor ROP18. |
| Q37791159 | Advances in imaging the innate and adaptive immune response to Toxoplasma gondii. |
| Q36609991 | An aspartyl protease defines a novel pathway for export of Toxoplasma proteins into the host cell |
| Q34040311 | Analysis of phagosomal proteomes: From latex‐bead to bacterial phagosomes |
| Q34026260 | Antigen export during liver infection of the malaria parasite augments protective immunity |
| Q38869705 | Autophagy proteins in antigen processing for presentation on MHC molecules |
| Q36986107 | Avirulent Toxoplasma gondii generates therapeutic antitumor immunity by reversing immunosuppression in the ovarian cancer microenvironment |
| Q34119416 | Avirulent uracil auxotrophs based on disruption of orotidine-5'-monophosphate decarboxylase elicit protective immunity to Toxoplasma gondii |
| Q38298375 | Bacteria, the endoplasmic reticulum and the unfolded protein response: friends or foes? |
| Q35097001 | Beta-catenin signaling drives differentiation and proinflammatory function of IRF8-dependent dendritic cells |
| Q37698282 | CD8(+) T Cell Responses to Plasmodium and Intracellular Parasites |
| Q37635978 | Cathepsin proteases in Toxoplasma gondii |
| Q37846879 | Cell biology and immunology of malaria |
| Q24614550 | Coordinated loading of IRG resistance GTPases on to the Toxoplasma gondii parasitophorous vacuole |
| Q39787236 | Critical role for the immunoproteasome subunit LMP7 in the resistance of mice to Toxoplasma gondii infection |
| Q38008346 | Cross-presentation: how to get there - or how to get the ER. |
| Q40144211 | Culling of APCs by inflammatory cell death pathways restricts TIM3 and PD-1 expression and promotes the survival of primed CD8 T cells |
| Q40700979 | Delivery of Exogenous Antigens to Induce Cytotoxic CD8+ T Lymphocyte Responses |
| Q34693251 | Dendritic cells and hepatocytes use distinct pathways to process protective antigen from plasmodium in vivo |
| Q35088720 | Differential induction of TLR3-dependent innate immune signaling by closely related parasite species |
| Q47727944 | Differential requirement of Rab22a for the recruitment of ER-derived proteins to phagosomes and endosomes in dendritic cells. |
| Q27316619 | Dynamic Imaging of CD8(+) T cells and dendritic cells during infection with Toxoplasma gondii |
| Q38269405 | Dynamic two-photon imaging of the immune response to Toxoplasma gondii infection |
| Q30541235 | Dynamics of T cell, antigen-presenting cell, and pathogen interactions during recall responses in the lymph node |
| Q54108260 | Encephalitis is mediated by ROP18 of Toxoplasma gondii, a severe pathogen in AIDS patients. |
| Q38008357 | Escape from the Phagosome: The Explanation for MHC-I Processing of Mycobacterial Antigens? |
| Q35191818 | Evidence for host cells as the major contributor of lipids in the intravacuolar network of Toxoplasma-infected cells |
| Q40991779 | Flt3 Ligand Is Essential for Survival and Protective Immune Responses during Toxoplasmosis |
| Q26825487 | Host Organelle Hijackers: a similar modus operandi for Toxoplasma gondii and Chlamydia trachomatis: co-infection model as a tool to investigate pathogenesis |
| Q54968611 | Hostile intruder: Toxoplasma holds host organelles captive. |
| Q24612341 | Immune response and immunopathology during toxoplasmosis |
| Q38256670 | Immune surveillance of the central nervous system in multiple sclerosis--relevance for therapy and experimental models. |
| Q33756823 | Impact of regulated secretion on antiparasitic CD8 T cell responses |
| Q37437538 | Increased translocation of antigens to endosomes and TLR4 mediated endosomal recruitment of TAP contribute to nicotine augmented cross-presentation |
| Q54533471 | Inhibition of ATF6β-dependent host adaptive immune response by a Toxoplasma virulence factor ROP18. |
| Q38181331 | Innate immunity to Toxoplasma gondii infection |
| Q42183323 | Intracellular events regulating cross-presentation |
| Q39700988 | Leishmania parasitophorous vacuoles interact continuously with the host cell's endoplasmic reticulum; parasitophorous vacuoles are hybrid compartments |
| Q38608424 | Lipid peroxidation causes endosomal antigen release for cross-presentation |
| Q34789311 | Location of the CD8 T cell epitope within the antigenic precursor determines immunogenicity and protection against the Toxoplasma gondii parasite. |
| Q38784040 | MHC I presentation of Toxoplasma gondii immunodominant antigen does not require Sec22b and is regulated by antigen orientation at the vacuole membrane. |
| Q37790648 | MHC presentation via autophagy and how viruses escape from it |
| Q26772968 | Membrane contact sites between pathogen-containing compartments and host organelles |
| Q36455241 | Memory CD8 T cells specific for plasmodia liver-stage antigens maintain protracted protection against malaria |
| Q38202729 | Memory T cells maintain protracted protection against malaria. |
| Q35439431 | Nonreplicating, cyst-defective type II Toxoplasma gondii vaccine strains stimulate protective immunity against acute and chronic infection |
| Q36053611 | Parasite Manipulation of the Invariant Chain and the Peptide Editor H2-DM Affects Major Histocompatibility Complex Class II Antigen Presentation during Toxoplasma gondii Infection |
| Q35145091 | Parasite fate and involvement of infected cells in the induction of CD4+ and CD8+ T cell responses to Toxoplasma gondii |
| Q36514286 | Presentation of phagocytosed antigens by MHC class I and II. |
| Q33856032 | Processing and presentation of antigens derived from intracellular protozoan parasites |
| Q42020778 | RNA granules present only in extracellular toxoplasma gondii increase parasite viability |
| Q45161599 | Rab22a controls MHC-I intracellular trafficking and antigen cross-presentation by dendritic cells. |
| Q61807977 | Regulation of Antigen Export to the Cytosol During Cross-Presentation |
| Q34108177 | Regulation of CD8+ T cell responses to infection with parasitic protozoa |
| Q51410365 | Regulation of the Cell Biology of Antigen Cross-Presentation. |
| Q38637651 | Review on the identification and role of Toxoplasma gondii antigenic epitopes |
| Q90290829 | Rhoptry and Dense Granule Secreted Effectors Regulate CD8+ T Cell Recognition of Toxoplasma gondii Infected Host Cells |
| Q34335032 | Secreted Immunodominant Mycobacterium tuberculosis Antigens Are Processed by the Cytosolic Pathway |
| Q37119146 | Secretion of Rhoptry and Dense Granule Effector Proteins by Nonreplicating Toxoplasma gondii Uracil Auxotrophs Controls the Development of Antitumor Immunity |
| Q33988110 | Subcellular antigen location influences T-cell activation during acute infection with Toxoplasma gondii |
| Q34314006 | Subversion of host cellular functions by the apicomplexan parasites |
| Q41910735 | Suggestive evidence for Darwinian Selection against asparagine-linked glycans of Plasmodium falciparum and Toxoplasma gondii |
| Q39104926 | The Biology and Underlying Mechanisms of Cross-Presentation of Exogenous Antigens on MHC-I Molecules |
| Q90206046 | The Leishmania Parasitophorous Vacuole Membrane at the Parasite-Host Interface |
| Q33598006 | The Mycobacterium bovis bacille Calmette-Guerin phagosome proteome |
| Q54337107 | The human C-type lectin-like receptor CLEC-1 is upregulated by TGF-β and primarily localized in the endoplasmic membrane compartment. |
| Q90558438 | The invasive cell coat at the microsporidian Trachipleistophora hominis-host cell interface contains secreted hexokinases |
| Q38772920 | The ongoing saga of the mechanism(s) of MHC class I-restricted cross-presentation |
| Q37792329 | Topological journey of parasite-derived antigens for presentation by MHC class I molecules |
| Q35434828 | Toxoplasma gondii effectors are master regulators of the inflammatory response |
| Q34165483 | Toxoplasma gondii ingests and digests host cytosolic proteins |
| Q36642187 | Toxoplasma gondii peptide ligands open the gate of the HLA class I binding groove |
| Q41895162 | Toxoplasma gondii-skeletal muscle cells interaction increases lipid droplet biogenesis and positively modulates the production of IL-12, IFN-g and PGE2. |
| Q40130950 | Transcription factor Batf3 is important for development of CD8+ T-cell response against a phagosomal bacterium regardless of the location of antigen |
| Q92320646 | Translocation of Dense Granule Effectors across the Parasitophorous Vacuole Membrane in Toxoplasma-Infected Cells Requires the Activity of ROP17, a Rhoptry Protein Kinase |
| Q27313711 | UNC93B1 mediates host resistance to infection with Toxoplasma gondii |
| Q26852870 | Use and abuse of dendritic cells by Toxoplasma gondii |
| Q37846863 | Views of immunology: effector T cells |
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