Tfr cell–derived IL-10 is important for B cell differentiation and the GC response. Tfr cell–derived IL-10 is important for B cell differentiation and.

Slides:



Advertisements
Similar presentations
Dominant IL-21 expression in TFH cells correlate with B cell pathology in HIV-infected LNs. Dominant IL-21 expression in TFH cells correlate with B cell.
Advertisements

Fibroblast activation in WT and NFATc2-deficient mice.
Cytotoxicity of MSP samples to normal and cancer cell lines.
Specific depletion of TFH and LCMV-specific CD4 T cells.
TPAD controller schematic and testing for WPC.
TPAD controller performance for three force components.
Antitumor effect of local cancer immunotherapy treatment toward distant B16F10 tumors. Antitumor effect of local cancer immunotherapy treatment toward.
CXCR5+/+ TFH cells are dispensable for maintenance of the LCMV-specific antibody response. CXCR5+/+ TFH cells are dispensable for maintenance of the LCMV-specific.
Specific depletion of CD4-DTR–derived CD4 T cells.
Three different types of transfer functions with a codomain of [0,1].
TPAD training protocol.
Tfr cells’ transcriptomic profile distinguishes them from Treg and Tfh cells. Tfr cells’ transcriptomic profile distinguishes them from Treg and Tfh cells.
Regulatory CD4+ T cell–derived IL-10 is important for B cell differentiation and the GC response. Regulatory CD4+ T cell–derived IL-10 is important for.
Core 2 O-glycan synthesis is stimulated by IL-15 signaling.
Memory CD8+ T cells that become terminally differentiated by multiple antigen encounters lose core 2 O-glycan synthesis activity. Memory CD8+ T cells that.
Human PBMC-derived MERS-CoV–specific T cells are multifunctional.
Group data during free walking between sessions 1 and 16.
Virus-specific T cell responses are detected in all MERS survivors.
Deficiency in myeloid-resident NRP1 affects systemic metabolism.
Platelets are required for hFcγRIIA-induced anaphylaxis.
NRP1-expressing myeloid cells influence adipocyte hypertrophy, development of fatty liver, and CLSs. NRP1-expressing myeloid cells influence adipocyte.
Human cells produce type I and III IFNs upon Af stimulation.
Reduced FOXO1 expression in GC B cells from mice lacking regulatory CD4+ T cell–derived IL-10. Reduced FOXO1 expression in GC B cells from mice lacking.
Comparison of repertoire distributions to baseline.
NRP1-expressing myeloid cells contribute to adipose tissue vascularization. NRP1-expressing myeloid cells contribute to adipose tissue vascularization.
Transfer of NRP1-expressing bone marrow improves the metabolic phenotype of LysM-Cre-Nrp1fl/fl mice. Transfer of NRP1-expressing bone marrow improves the.
β-Glucans do not modulate epithelial IL-33 or AHR.
Tfr cells robustly secrete IL-10 after acute viral infection.
Macrophage-resident NRP1 mitigates cytokine release and proinflammatory polarization. Macrophage-resident NRP1 mitigates cytokine release and proinflammatory.
Persistent TCR–pMHC-I signaling drives the formation and maintenance of exhausted-like TRM cells. Persistent TCR–pMHC-I signaling drives the formation.
T-bethi MP cells produce IFN-γ in response to IL-12.
Blood Tfr cells are lymphoid tissue–derived Tfr precursors.
BAP1 deficiency results in thymic atrophy and loss of thymocyte populations. BAP1 deficiency results in thymic atrophy and loss of thymocyte populations.
Evidence for platelet activation during human drug-induced anaphylaxis
Blood Tfr cells are indicators of ongoing humoral activity.
Antitumor effect of local cancer immunotherapy treatment in various tumor models. Antitumor effect of local cancer immunotherapy treatment in various tumor.
CXCR5+/+ TFH cells are essential for the generation of LCMV-neutralizing antibodies and clearance of a persistent LCMV infection. CXCR5+/+ TFH cells are.
Cell viability tests. Cell viability tests. SEM images of (A) MC3T3-E1 cells and (B) MSCs on days 1, 3, and 5 of culture. (C) Survival rates of MC3T3-E1.
Tumor control by necroptotic cells requires BATF3+cDC1 and CD8+leukocytes. Tumor control by necroptotic cells requires BATF3+cDC1 and CD8+leukocytes. (A)
Variable number of CD4-CTL precursors across donors.
Microrobots with different cell-carrying capacities under different grid lengths (lg) and burr lengths (lb). Microrobots with different cell-carrying capacities.
Platelet-released serotonin contributes to hypothermia in mice undergoing HA-hIgG–dependent anaphylaxis. Platelet-released serotonin contributes to hypothermia.
BAP1 is required for homeostatic and antigen-driven expansion of peripheral T cells. BAP1 is required for homeostatic and antigen-driven expansion of peripheral.
Vaccine MN confer protective innate and adaptive immunity.
Slc7a5 deficiency stimulates osteoclastogenesis in vitro.
Dectin-1 regulates innate IL-13.
RORα deficiency in Tregs results in exaggerated skin inflammation in response to EC sensitization. RORα deficiency in Tregs results in exaggerated skin.
Ado loss drives TNF-dependent immune evasion.
CypD-deficient mice are susceptible to Mtb infection.
CD25 surface expression and TCR signal strength predict T helper differentiation and memory potential of early effector T cells in vivo. CD25 surface expression.
In vitro cell-release experiments on a glass substrate.
Tfr cells respond better to immunization with self-antigens than with foreign antigens. Tfr cells respond better to immunization with self-antigens than.
Results of a representative participant with multiple training sessions. Results of a representative participant with multiple training sessions. Average.
AEGIS autonomous targeting process.
Human Tfr cells do not express CD25.
Fig. 3 Local Maraba treatment of TNBC tumors provides long-term systemic protection. Local Maraba treatment of TNBC tumors provides long-term systemic.
CD4+ memory T cells derived from either CD25hi or CD25lo effector cells respond robustly to secondary challenge. CD4+ memory T cells derived from either.
CD25 expression predicts effector and memory differentiation.
Blood Tfr cells are immature but are not committed in the thymus.
miR-146a is highly expressed selectively on γδ27− T cells.
IL-33 is not critical for initiation of allergic airways disease phenotype. IL-33 is not critical for initiation of allergic airways disease phenotype.
Fibroblast activation in WT and NFATc2-deficient mice.
Acute circadian disruption alters ILC3 cytokine secretion.
Circadian gene expression in ILC3s is associated with rhythmic cytokine expression. Circadian gene expression in ILC3s is associated with rhythmic cytokine.
Meningeal γδ T cell homeostasis is independent of inflammatory signals
In response to allergen, T cells and ILCs are equally important sources of IL-13. In response to allergen, T cells and ILCs are equally important sources.
T cell–derived IL-13 is essential for the inception of AHR.
Neutralizing activity of mAbs isolated from plasmablasts during acute ZIKV infection in DENV-experienced donors. Neutralizing activity of mAbs isolated.
CCR6 is dispensable for expansion of innate TCRαβ+ cells in oral candidiasis. CCR6 is dispensable for expansion of innate TCRαβ+ cells in oral candidiasis.
Fig. 1 TH17 cell differentiation was severely impaired in Cxxc1-deficient mice. TH17 cell differentiation was severely impaired in Cxxc1-deficient mice.
Presentation transcript:

Tfr cell–derived IL-10 is important for B cell differentiation and the GC response. Tfr cell–derived IL-10 is important for B cell differentiation and the GC response. (A) Analysis of the B cell response at day 15 after acute LCMV Armstrong infection in 50:50 Il10f/f/Bcl6f/fFoxp3-Cre or Il10f/fFoxp3-Cre/Bcl6f/fFoxp3-Cre mBMCs. Left: Schematic for the experiment. Right: Data are pooled from two experiments with four to five mice per group carried out 15 days after LCMV Armstrong infection. (B) Analysis of the B cell response at day 15 after acute LCMV Armstrong infection in 50:50 Il10f/f/SAP−/− or Il10f/fFoxp3-Cre/SAP−/− mBMCs. Left: Schematic for the experiment. Right: Data are from one experiment representative of two experiments with four to nine mice per group carried out 15 days after LCMV Armstrong infection. Statistical analyses were performed using unpaired two-tailed Student’s t test (*P < 0.05; **P < 0.01; ***P < 0.001). Brian J. Laidlaw et al. Sci. Immunol. 2017;2:eaan4767 Copyright © 2017 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works