Journal: The Journal of Immunology
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Abbreviation
J Immunol
Publisher
AAI
51 results
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Publications 1 - 10 of 51
- The Salmonella Pathogenicity Island (SPI)-2 and SPI-1 Type III Secretion Systems Allow Salmonella Serovar typhimurium to Trigger Colitis via MyD88-Dependent and MyD88-Independent MechanismsItem type: Journal Article
The Journal of ImmunologyHapfelmeier, Siegfried; Stecher, Bärbel; Barthel, Manja; et al. (2005) - A Novel Th Cell Epitope of Candida albicans Mediates Protection from Fungal InfectionItem type: Journal Article
The Journal of ImmunologyBär, Eva; Gladiator, André; Bastidas, Sonia; et al. (2012) - Caspase-4 Is Required for Activation of InflammasomesItem type: Journal Article
The Journal of ImmunologySollberger, Gabriel; Strittmatter, Gerhard E.; Kistowska, Magdalena; et al. (2012) - MyD88-Dependent IFN-γ Production by NK Cells Is Key for Control of Legionella pneumophila InfectionItem type: Journal Article
The Journal of ImmunologySpörri, Roman; Joller, Nicole; Albers, Urs; et al. (2006) - The MHC Class II Immunopeptidome of Lymph Nodes in Health and in Chemically Induced ColitisItem type: Journal Article
The Journal of ImmunologyFugmann, Tim; Sofron, Adriana; Ritz, Danilo; et al. (2016) - Response to Comment on “Nonhematopoietic Cells Are Key Players in Innate Control of Bacterial Airway Infection”Item type: Other Journal Item
The Journal of ImmunologyLeibundGut-Landmann, Salomé; Oxenius, Annette (2011) - CXCR3 Identifies Human Naive CD8+ T Cells with Enhanced Effector Differentiation PotentialItem type: Journal Article
The Journal of ImmunologyDe Simone, Gabriele; Mazza, Emilia M.C.; Cassotta, Antonino; et al. (2019)n mice, the ability of naive T (TN) cells to mount an effector response correlates with TCR sensitivity for self-derived Ags, which can be quantified indirectly by measuring surface expression levels of CD5. Equivalent findings have not been reported previously in humans. We identified two discrete subsets of human CD8+ TN cells, defined by the absence or presence of the chemokine receptor CXCR3. The more abundant CXCR3+ TN cell subset displayed an effector-like transcriptional profile and expressed TCRs with physicochemical characteristics indicative of enhanced interactions with peptide–HLA class I Ags. Moreover, CXCR3+ TN cells frequently produced IL-2 and TNF in response to nonspecific activation directly ex vivo and differentiated readily into Ag-specific effector cells in vitro. Comparative analyses further revealed that human CXCR3+ TN cells were transcriptionally equivalent to murine CXCR3+ TN cells, which expressed high levels of CD5. These findings provide support for the notion that effector differentiation is shaped by heterogeneity in the preimmune repertoire of human CD8+ T cells. - Mechanisms of neonatal mucosal antibody protectionItem type: Journal Article
The Journal of ImmunologyHarris, Nicola L.; Spoerri, Iris; Schopfer, Jacqueline F.; et al. (2006) - Learning the high-dimensional immunogenomic features that predict public and private antibody repertoiresItem type: Journal Article
The Journal of ImmunologyGreiff, Victor; Weber, Cédric R.; Palme, Johannes; et al. (2017) - Functional Properties and Lineage Relationship of CD8+ T Cell Subsets Identified by Expression of IL-7 Receptor α and CD62LItem type: Journal Article
The Journal of ImmunologyBachmann, Martin F.; Wolint, Petra; Schwarz, Katrin; et al. (2005)
Publications 1 - 10 of 51