Dendritic cells and hepatocytes use distinct pathways to process protective antigen from plasmodium in vivo
about
Immune mechanisms in malaria: new insights in vaccine developmentThe Use of Synthetic Carriers in Malaria Vaccine DesignTissue signatures influence the activation of intrahepatic CD8(+) T cells against malaria sporozoitesLymph-node resident CD8α+ dendritic cells capture antigens from migratory malaria sporozoites and induce CD8+ T cell responsesThe Plasmodium translocon of exported proteins (PTEX) component thioredoxin-2 is important for maintaining normal blood-stage growthProtective immunity to liver-stage malariaPlasmodium cellular effector mechanisms and the hepatic microenvironmentLiver-specific protein 2: a Plasmodium protein exported to the hepatocyte cytoplasm and required for merozoite formationCD8+ T cells specific for a malaria cytoplasmic antigen form clusters around infected hepatocytes and are protective at the liver stage of infection.Engineering of Genetically Arrested Parasites (GAPs) For a Precision Malaria VaccineMalaria immunity in man and mosquito: insights into unsolved mysteries of a deadly infectious disease.Antigen export during liver infection of the malaria parasite augments protective immunityThe chemokine receptor CXCR6 is required for the maintenance of liver memory CD8⁺ T cells specific for infectious pathogens.A nonintegrative lentiviral vector-based vaccine provides long-term sterile protection against malariaCSP--a model for in vivo presentation of Plasmodium berghei sporozoite antigens by hepatocytesDynamics of the major histocompatibility complex class I processing and presentation pathway in the course of malaria parasite development in human hepatocytes: implications for vaccine development.Antigen-driven focal inflammatory death of malaria liver stagesMalaria and the liver: immunological hide-and-seek or subversion of immunity from within?Requirement of UNC93B1 reveals a critical role for TLR7 in host resistance to primary infection with Trypanosoma cruzi.Studying the effect of chloroquine on sporozoite-induced protection and immune responses in Plasmodium berghei malariaP. falciparum and P. vivax Epitope-Focused VLPs Elicit Sterile Immunity to Blood Stage Infections.Proteolytic Cleavage of the Plasmodium falciparum Circumsporozoite Protein Is a Target of Protective Antibodies.Protective antibody and CD8+ T-cell responses to the Plasmodium falciparum circumsporozoite protein induced by a nanoparticle vaccineMemory CD8 T cells specific for plasmodia liver-stage antigens maintain protracted protection against malaria.Skin-draining lymph node priming is sufficient to induce sterile immunity against pre-erythrocytic malaria.UNC93B1 and nucleic acid-sensing Toll-like receptors mediate host resistance to infection with Leishmania majorDiscriminating Protective from Nonprotective Plasmodium-Specific CD8+ T Cell ResponsesDevelopment of a chimeric Plasmodium berghei strain expressing the repeat region of the P. vivax circumsporozoite protein for in vivo evaluation of vaccine efficacy.Unique transcriptional profile of liver-resident memory CD8+ T cells induced by immunization with malaria sporozoitesSystemic toll-like receptor ligation and selective killing of dendritic cell subsets fail to dissect priming pathways for anti-vaccinia virus CD8⁺ T cellsAngiotensin II type-1 receptor (AT1R) regulates expansion, differentiation, and functional capacity of antigen-specific CD8(+) T cells.Malaria parasite pre-erythrocytic infection: preparation meets opportunity.The Threshold of Protection from Liver-Stage Malaria Relies on a Fine Balance between the Number of Infected Hepatocytes and Effector CD8+ T Cells Present in the LiverCD8+ T cells eliminate liver-stage Plasmodium berghei parasites without detectable bystander effect.Induction and maintenance of protective CD8+ T cells against malaria liver stages: implications for vaccine development.Dendritic cells and the malaria pre-erythrocytic stage.The skin: where malaria infection and the host immune response beginFeeling at home from arrival to departure: protein export and host cell remodelling during Plasmodium liver stage and gametocyte maturation.Do you see what I see: Recognition of protozoan parasites by Toll-like receptors.From the draining lymph node to the liver: the induction and effector mechanisms of malaria-specific CD8+ T cells.
P2860
Q21032484-26AE9C27-2B44-4B7E-B4B0-53857C393A3AQ26777053-C2BC34E5-651E-439E-90A7-8DC82F1DE1E5Q27026412-081EC09E-E434-4BB5-9A79-41B52472A73AQ27321397-53988065-25FD-414E-A674-C6776640FFF0Q27973421-FE723C71-7864-4B9D-82EB-33CF048FE035Q28068626-1357D78E-75D6-4FE8-B445-B11981CBD33BQ28081143-806D361E-3B52-4180-906C-560BA1D0F0A5Q30043150-02413645-9CF2-4407-8E24-1526A428A5B0Q30555356-705613D3-DB03-49F8-8894-A815539DE213Q33744460-796F8097-615C-4F7D-A844-A9B10ECD4E7AQ33821137-913C2A14-AF8B-4640-9922-319B34D7AB70Q34026260-4AC15DB0-F0D0-4E3D-BD04-999AB63A3FE7Q34396077-E466CED5-1200-4824-BF3C-92C0DF6F3DB1Q34469817-6619D067-2CE3-4AA1-AE4D-B7EB9195033FQ34525775-5A1A37AD-93BE-4DCF-A34D-2A25904968F4Q35005560-20804FED-196B-4E7A-80FD-1C37C0285ECDQ35048008-E898AFAD-92AF-4B82-92AB-C899CA713BB9Q35094560-4F1BE7BF-731A-468F-993E-ED4BDFAA6E45Q35147723-15FEFAAC-DBA4-425D-ABD5-5D48DF17891FQ35314263-E9B62D18-3B69-4F4B-AF65-A40BCE9832F2Q35561160-E7F08EFE-0884-4D3E-91A8-FB343F3229A7Q36024455-8B56D258-38F9-4836-91A4-1EEC68AA59F0Q36353548-AFD7680E-88C3-4A43-859C-5F1610A2EA8FQ36455241-5165180D-72A4-427B-B493-D7DF657E205DQ36602130-F2916B04-798B-4546-B6D8-B5718425113BQ36666215-6C8D867B-B257-4035-8C78-A3B6C15C9766Q36905568-6B36078C-6B8C-42A7-89E8-919FED05AFA9Q37036065-84497B8A-5C5B-4959-BB38-A8D23CEF923FQ37042838-B87B320C-4E23-43AD-B021-7C641A4EDA15Q37254348-076C71A1-676C-4451-BAE8-7B0BCD5DDEF6Q37366984-DAC9BC46-9864-4FAF-B441-8C44EFB24F21Q37533146-B9EB5663-A39E-4F13-9111-4B19B289E56AQ37654676-4012B53E-665F-458B-B04F-CABEEB4363FDQ37713217-5030F393-4680-441F-A579-5791DB6A94CDQ37924615-8B6044D0-D6D7-4B46-A1E0-7DBEFADED6E6Q37993739-9B64C372-FEA8-45E0-A0C9-7758218D156DQ38051033-5BEBB572-87DC-4077-9E89-7782EF0649A1Q38170555-6AB3A572-0560-47AB-AF5C-B5DD6C7E77B2Q38266457-A7CDBA11-72AF-4FBE-92BF-6D4CE4C5F04EQ38445061-89BAFE57-DCDF-4C2F-B97F-5DD1CC3F210F
P2860
Dendritic cells and hepatocytes use distinct pathways to process protective antigen from plasmodium in vivo
description
2011 nî lūn-bûn
@nan
2011 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի մարտին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Dendritic cells and hepatocyte ...... ntigen from plasmodium in vivo
@ast
Dendritic cells and hepatocyte ...... ntigen from plasmodium in vivo
@en
Dendritic cells and hepatocyte ...... ntigen from plasmodium in vivo
@nl
type
label
Dendritic cells and hepatocyte ...... ntigen from plasmodium in vivo
@ast
Dendritic cells and hepatocyte ...... ntigen from plasmodium in vivo
@en
Dendritic cells and hepatocyte ...... ntigen from plasmodium in vivo
@nl
prefLabel
Dendritic cells and hepatocyte ...... ntigen from plasmodium in vivo
@ast
Dendritic cells and hepatocyte ...... ntigen from plasmodium in vivo
@en
Dendritic cells and hepatocyte ...... ntigen from plasmodium in vivo
@nl
P2093
P2860
P1433
P1476
Dendritic cells and hepatocyte ...... ntigen from plasmodium in vivo
@en
P2093
Andrea J Radtke
Fidel Zavala
Photini Sinnis
Prakash Srinivasan
Sze-Wah Tse
Yun-Chi Chen
P2860
P304
P356
10.1371/JOURNAL.PPAT.1001318
P50
P577
2011-03-17T00:00:00Z