about
Ontogeny of stromal organizer cells during lymph node development.Helios is associated with CD4 T cells differentiating to T helper 2 and follicular helper T cells in vivo independently of Foxp3 expression.Extrafollicular antibody responses.Dendritic cells capture and efficiently present antigen encapsulated in liposomes to T cells in vivo.Epigenetic and transcriptional signatures of stable versus plastic differentiation of proinflammatory γδ T cell subsets.Molecular Mechanisms of Differentiation of Murine Pro-Inflammatory γδ T Cell Subsets.γδ T cells in cancer.Effector γδ T Cell Differentiation Relies on Master but Not Auxiliary Th Cell Transcription Factors.Developmental and Functional Assays to Study Murine and Human γδ T Cells.Class I-restricted presentation of exogenous antigen acquired by Fcgamma receptor-mediated endocytosis is regulated in dendritic cells.Soluble flagellin coimmunization attenuates Th1 priming to Salmonella and clearance by modulating dendritic cell activation and cytokine production.IL-4 directs both CD4 and CD8 T cells to produce Th2 cytokines in vitro, but only CD4 T cells produce these cytokines in response to alum-precipitated protein in vivo.Loss of CD154 impairs the Th2 extrafollicular plasma cell response but not early T cell proliferation and interleukin-4 induction.Pinpointing IL-4-independent acquisition and IL-4-influenced maintenance of Th2 activity by CD4 T cells.Early simultaneous production of intranodal CD4 Th2 effectors and recirculating rapidly responding central-memory-like CD4 T cells.Low-dose ionizing radiation induces therapeutic neovascularization in a pre-clinical model of hindlimb ischemia.Soluble flagellin, FliC, induces an Ag-specific Th2 response, yet promotes T-bet-regulated Th1 clearance of Salmonella typhimurium infection.Molecular differences between the divergent responses of ovalbumin-specific CD4 T cells to alum-precipitated ovalbumin compared to ovalbumin expressed by Salmonella.Salmonella induces a switched antibody response without germinal centers that impedes the extracellular spread of infection.Responses to the soluble flagellar protein FliC are Th2, while those to FliC on Salmonella are Th1.CD8 T cells induce T-bet-dependent migration toward CXCR3 ligands by differentiated B cells produced during responses to alum-protein vaccines.Dendritic cells and monocyte/macrophages that create the IL-6/APRIL-rich lymph node microenvironments where plasmablasts mature.Recirculating CD4 memory T cells mount rapid secondary responses without major contributions from follicular CD4 effectors and B cells.Primary Tumors Limit Metastasis Formation through Induction of IL15-Mediated Cross-Talk between Patrolling Monocytes and NK Cells.MicroRNA-146a controls functional plasticity in γδ T cells by targeting NOD1Selective effects of NF-κB1 deficiency in CD4+ T cells on Th2 and TFh induction by alum-precipitated protein vaccinesCellular immunobiology of lymph nodes and spleenCover Picture: Eur. J. Immunol. 6/09Response to the Comments on "Dendritic Cells and Monocyte/Macrophages That Create the IL-6/APRIL-Rich Lymph Node Microenvironment Where Plasmablasts Mature"CD4 T cell help is required for primary CD8 T cell responses to vesicular antigen delivered to dendritic cellsin vivoLiposomes Targeted to Fc Receptors for Antigen Presentation by Dendritic Cells In Vitro and In Vivo∗Speaker AbstractsVirosome-mediated delivery of protein antigens to dendritic cellsClass I-restricted presentation of exogenous antigen acquired by Fcγ receptor-mediated endocytosis is regulated in dendritic cellsEngagement of B cell receptor regulates the invariant chain-dependent MHC class II presentation pathwayEfficient presentation of multivalent antigens targeted to various cell surface molecules of dendritic cells and surface Ig of antigen-specific B cells
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Q33823116-D745B8A6-F619-437C-832C-0D3917B94DB2Q33934058-F152B4E1-183A-4A69-BC2F-CDBA85C6FB5CQ34212117-B48686C7-E914-48F3-A634-5F4873EF4043Q35119251-F0A6DB2D-1A99-43E2-A202-818064997A44Q36807846-3BC6789F-6B5A-4DDA-AB04-5AD5724430A7Q38173753-B08D125C-42FF-4E90-B0DC-35E10DEB550FQ38602555-4761199A-EE3F-428B-BDAE-F4FE0C689D99Q39905612-8433F5CB-2BEF-458D-A5A6-536AB4E08E42Q40481854-9BDAA98D-1598-4CA5-B55E-C571BFB3A3CFQ40890519-56FFC1DD-4986-4D3D-BC82-C5D7DA199D59Q41189305-480AA66F-ED12-465D-B24C-20FEA8E37A65Q41996237-7059CE19-8413-46FA-8962-F1460F7BBBF1Q45067678-91FF4AF1-EE0D-4147-8484-78BA86243698Q46907814-0D562A04-0522-48B3-8217-F39574716E07Q47745032-100B3C4E-0600-47F3-874E-40A59779E2ABQ47782120-C3BE6F37-EF69-4A30-9C76-3C2839D3BC6EQ50042606-6DFC1F20-5479-46E3-910D-3D90402E971EQ50061014-A61878CF-3761-499C-BB96-741175FA042DQ50072223-48722FF2-9B70-42D7-9C2F-9C6E5D5039F1Q50096687-249FAA1D-4B50-4D73-B03E-00B55126B5C5Q50932933-A3C70649-EC77-4061-94EE-6885FE79FFF7Q51833354-108788A7-43EC-4E93-AF40-62235E4842EEQ51975220-DE4CFF3F-248B-4E69-AD5E-6A147A116E86Q54069190-2F485760-91A6-4FBB-B249-20031A79F413Q57926807-49C5B933-F0D1-49F8-96AC-6135AAD6F8BFQ60171270-5225A3D1-21C3-4594-B36F-E7723BBE8EB2Q60171272-71A70EC3-C933-4AD1-8EAC-DF164B24AF73Q60171273-3C2CB4F4-D44A-4BF5-B644-B13EE2C6D442Q60171275-CF174C0A-9D78-4A3D-939E-DE67D7681D90Q60171276-D2E2A592-1D28-459C-916D-0A776BBF2122Q60171277-25B746DC-3D66-4B77-AA28-2820038617AEQ60171279-0F0CAE1A-AB89-4A90-8F9C-39FFE1562AFAQ60171281-18EC5338-B05F-4A8D-B519-F1556F27A985Q60171282-2513FC19-3A2D-4755-BE12-18036172FAE5Q60171283-86012B28-7D20-438E-81D7-B73ED9B0D6ADQ60171284-7BB0C3CA-E15D-4461-8F89-8CBAF07C40A0
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description
hulumtuese
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Karine Serre
@ast
Karine Serre
@en
Karine Serre
@es
Karine Serre
@sl
type
label
Karine Serre
@ast
Karine Serre
@en
Karine Serre
@es
Karine Serre
@sl
prefLabel
Karine Serre
@ast
Karine Serre
@en
Karine Serre
@es
Karine Serre
@sl
P106
P1153
6602493849
P21
P2798
P31
P496
0000-0001-9152-4739