Predominant infection of CD150+ lymphocytes and dendritic cells during measles virus infection of macaques
about
Adherens junction protein nectin-4 is the epithelial receptor for measles virusMeasles virus infects both polarized epithelial and immune cells by using distinctive receptor-binding sites on its hemagglutininMeasles Virus Host Invasion and PathogenesisEarly target cells of measles virus after aerosol infection of non-human primatesT-Cell tropism of simian varicella virus during primary infectionMeasles immune suppression: lessons from the macaque modelIllumination of parainfluenza virus infection and transmission in living animals reveals a tissue-specific dichotomyInterferon Gamma: Influence on Neural Stem Cell Function in Neurodegenerative and Neuroinflammatory DiseaseThe Host Cell Receptors for Measles Virus and Their Interaction with the Viral Hemagglutinin (H) ProteinStructural basis of efficient contagion: measles variations on a theme by parainfluenza viruses.A human coronavirus responsible for the common cold massively kills dendritic cells but not monocytesMeasles virus entry through the signaling lymphocyte activation molecule governs efficacy of mantle cell lymphoma radiovirotherapy.DC-SIGN and CD150 have distinct roles in transmission of measles virus from dendritic cells to T-lymphocytes.Induction of membrane ceramides: a novel strategy to interfere with T lymphocyte cytoskeletal reorganisation in viral immunosuppression.Measles virus infection of alveolar macrophages and dendritic cells precedes spread to lymphatic organs in transgenic mice expressing human signaling lymphocytic activation molecule (SLAM, CD150)Measles virus selectively blind to signaling lymphocytic activation molecule (SLAM; CD150) is attenuated and induces strong adaptive immune responses in rhesus monkeys.The tumor-associated marker, PVRL4 (nectin-4), is the epithelial receptor for morbillivirusesDC-SIGN mediated sphingomyelinase-activation and ceramide generation is essential for enhancement of viral uptake in dendritic cellsTumor cell marker PVRL4 (nectin 4) is an epithelial cell receptor for measles virusMeasles virus-induced suppression of immune responses.Measles virus suppresses RIG-I-like receptor activation in dendritic cells via DC-SIGN-mediated inhibition of PP1 phosphatasesCotton rat (Sigmodon hispidus) signaling lymphocyte activation molecule (CD150) is an entry receptor for measles virusImmature CD4+CD8+ thymocytes are preferentially infected by measles virus in human thymic organ culturesPathological consequences of systemic measles virus infection.A prominent role for DC-SIGN+ dendritic cells in initiation and dissemination of measles virus infection in non-human primates.Early events following experimental infection with Peste-Des-Petits ruminants virus suggest immune cell targetingNeutral sphingomyelinase in physiological and measles virus induced T cell suppression.Phocine distemper virus: current knowledge and future directions.Cetacean morbillivirus: current knowledge and future directions.Recombinant subgroup B human respiratory syncytial virus expressing enhanced green fluorescent protein efficiently replicates in primary human cells and is virulent in cotton rats.Live-attenuated measles virus vaccine targets dendritic cells and macrophages in muscle of nonhuman primates.Nipah virus uses leukocytes for efficient dissemination within a host.A GFP expressing influenza A virus to report in vivo tropism and protection by a matrix protein 2 ectodomain-specific monoclonal antibody.Limited in vivo production of type I or type III interferon after infection of macaques with vaccine or wild-type strains of measles virusMeasles immune suppression: functional impairment or numbers game?Streptococcus pneumoniae Enhances Human Respiratory Syncytial Virus Infection In Vitro and In Vivo.SLAM- and nectin-4-independent noncytolytic spread of canine distemper virus in astrocytesWild-Type Measles Virus is Intrinsically Dual-Tropic.Wild-type measles virus with the hemagglutinin protein of the edmonston vaccine strain retains wild-type tropism in macaquesMeasles virus, immune control, and persistence.
P2860
Q24295305-B88C7BD3-40B9-4D71-A3FA-BFA15E14FDC4Q24655592-EEF7CB7C-DB03-4E13-852B-933071AF2634Q26739968-ACA89982-4730-4F43-A711-A504D92D32CEQ27312346-DDDB5687-0488-4EBD-B025-ADB4B9EAEF5CQ27334810-499E7925-FF85-4072-8A3B-5E5B35EC8434Q27342799-F50472BC-0CB0-472B-9F1B-01FDB614EAB6Q27349385-82F4DB2E-1109-4F8C-B575-364CB399D2E3Q27928023-97E3A866-4A60-4B39-B1F5-5C5F4E0936CBQ28069519-EA06A6EE-D2D2-47A4-8599-23AFB17C4C48Q30358662-A90906DD-1388-49D0-B887-185C8A5B701CQ30524109-051F7F44-BF7C-44B0-AE00-D662ED634E32Q30557338-9FA20867-07CE-4571-958A-AB3961672980Q33329098-F47071F3-6F28-488F-A4CB-804F944FA407Q33510915-C5A01824-B5ED-4240-8DC3-96ED36D03EA1Q33676460-FB7A306A-80D5-41F6-A4D4-9962E317494AQ33725565-4E8CCD69-F0D1-4D42-A95E-C5EF99CF002AQ33820699-59D9FB39-D1F0-4C1E-8865-A6B6069EBBB7Q33838276-44F54955-3C57-40B3-9A5B-07E5D6BBA2DBQ34013640-1FC37585-2311-49D0-9D46-C6C8D4FEE4BCQ34015320-A0039E2B-1C22-4FDE-8E3B-90596929474EQ34158123-20A8E53B-6D21-4C50-A9F1-1CB866CB648CQ34308888-ABD59CBC-2417-40B6-8FCB-18A5600B6D32Q34430558-0F7114EB-8360-4A2A-98AD-F7B0BB5234EDQ34442341-1F793B8B-4133-4AE6-9952-1A87BE961DA4Q34506876-B24D2328-539D-49A4-ACE2-ADDE1A1AB460Q34589606-35CC9A92-22AE-40FC-8916-C76ED71F47FDQ34734221-9390D19D-5153-48B8-9C74-14679A555259Q34774818-F512FF6F-1C5F-4E61-AE80-C0C01F812E67Q34774830-BE8CADED-FA31-4587-B4EF-7703F04FF343Q35076761-167BAAA0-B42C-4559-9994-C20677F33263Q35115588-2D237227-8E82-4835-8114-EABF222178C8Q35140337-D065079E-758A-42C4-902D-68B008FEBF67Q35225083-DAF0DB18-9AA6-4308-9373-FB9C1F82DA8FQ35324006-92000F3F-211A-44BA-8F07-A618AC645AA7Q35529680-E6656709-CD8C-4B38-94B8-7E90CB4B592BQ35603103-8553AAEF-87B1-40DF-89B3-2A13E681AE84Q35641553-FD38AD8E-5D45-48A4-BDB0-4A7579DEDB91Q35747417-9B5977E5-D1C0-404C-B0B2-68571E9D4DD6Q35826252-E4AF57E3-DB2F-4E16-A4D0-D7A323947628Q35870777-EB568B82-0395-4FC6-B262-088B5459176D
P2860
Predominant infection of CD150+ lymphocytes and dendritic cells during measles virus infection of macaques
description
2007 nî lūn-bûn
@nan
2007 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年学术文章
@wuu
2007年学术文章
@zh-cn
2007年学术文章
@zh-hans
2007年学术文章
@zh-my
2007年学术文章
@zh-sg
2007年學術文章
@yue
name
Predominant infection of CD150 ...... es virus infection of macaques
@ast
Predominant infection of CD150 ...... es virus infection of macaques
@en
Predominant infection of CD150 ...... es virus infection of macaques
@nl
type
label
Predominant infection of CD150 ...... es virus infection of macaques
@ast
Predominant infection of CD150 ...... es virus infection of macaques
@en
Predominant infection of CD150 ...... es virus infection of macaques
@nl
prefLabel
Predominant infection of CD150 ...... es virus infection of macaques
@ast
Predominant infection of CD150 ...... es virus infection of macaques
@en
Predominant infection of CD150 ...... es virus infection of macaques
@nl
P2093
P2860
P50
P921
P3181
P1433
P1476
Predominant infection of CD150 ...... es virus infection of macaques
@en
P2093
Geert van Amerongen
Lot de Witte
Selma Yüksel
Stephen McQuaid
Teunis B H Geijtenbeek
P2860
P3181
P356
10.1371/JOURNAL.PPAT.0030178
P407
P577
2007-11-01T00:00:00Z