Blood Tfr cells are lymphoid tissue–derived Tfr precursors.

Slides:



Advertisements
Similar presentations
High-dimensional analysis of lymphoid CD4+ T cells identified distinct TFH cell subsets in HIV+ patients and HCs. High-dimensional analysis of lymphoid.
Advertisements

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.
GC TFH cells exhibit HIV antigen–driven clonal expansion and selection
Identification of combination treatment–responsive effector/memory tumor-infiltrating CD8+ T cell population. Identification of combination treatment–responsive.
Diminished suppressive potency of primary Treg clones from IPEXA384T patients. Diminished suppressive potency of primary Treg clones from IPEXA384T patients.
Treg and Teff cell subsets show increased TCR overlap during colitis.
CsEN components reveal precisely timed cellular programs that characterize the dynamic changes of the peripheral immune system over the course of pregnancy.
Fibroblast activation in WT and NFATc2-deficient mice.
MP cells are generated from naïve cells in the periphery.
Expansion of Bacteroides species during colitis does not enhance TCR-specific T cell responses. Expansion of Bacteroides species during colitis does not.
FIP200 loss links to poor autophagy and high apoptosis in naïve T cells in tumor. FIP200 loss links to poor autophagy and high apoptosis in naïve T cells.
LV DNA, genome, and capsid are not required for DC activation and CD8+ T cell priming in vivo. LV DNA, genome, and capsid are not required for DC activation.
FIP200 deficiency alters mitochondria activation and ROS production in T cells. FIP200 deficiency alters mitochondria activation and ROS production in.
Specific depletion of TFH and LCMV-specific CD4 T cells.
VLPs activate DCs and antigen-specific CD8+ T cells via the STING and cGAS pathway. VLPs activate DCs and antigen-specific CD8+ T cells via the STING and.
CD8α+ DC-deficient mice are highly susceptible to Lm infection in the absence of CD169+ macrophages. CD8α+ DC-deficient mice are highly susceptible to.
TPAD controller schematic and testing for WPC.
TPAD controller performance for three force components.
Specific depletion of CD4-DTR–derived CD4 T cells.
Splenic CD169+ macrophages express a unique gene profile.
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.
CD169+ macrophages mediate Lm translocation to the splenic T cell zones. CD169+ macrophages mediate Lm translocation to the splenic T cell zones. (A) Confocal.
LV activation of DCs and subsequent CD8+ T cell priming are dependent on STING and cGAS but not on MyD88, TRIF, or MAVS. LV activation of DCs and subsequent.
Examples of AEGIS autonomous target selection.
Crystal structure of HCMV Pentamer.
FIP200 loss links to poor autophagy and high apoptosis in naïve T cells in tumor. FIP200 loss links to poor autophagy and high apoptosis in naïve T cells.
Human PBMC-derived MERS-CoV–specific T cells are multifunctional.
Virus-specific T cell responses are detected in all MERS survivors.
Protection from autoimmunity is not due to the expansion of Treg subsets. Protection from autoimmunity is not due to the expansion of Treg subsets. (A.
VH usage of cross-reactive B cells induced by H5N1 or H7N9 vaccination
Human cells produce type I and III IFNs upon Af stimulation.
Comparison of repertoire distributions to baseline.
Summary of time-limited events in early life promoting tolerance to gut bacterial antigens. Summary of time-limited events in early life promoting tolerance.
Tfr cells robustly secrete IL-10 after acute viral infection.
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.
DC subset cooperation for activation of antiviral T cells.
Donor and recipient BAL T cells are phenotypically and functionally memory T cells. Donor and recipient BAL T cells are phenotypically and functionally.
Differential expression of TRM markers by donor- and recipient-derived T cells with time. Differential expression of TRM markers by donor- and recipient-derived.
Blood Tfr cells show expression of follicular and regulatory markers.
Blood Tfr cells are indicators of ongoing humoral activity.
PD-L1 selectively marks circulating NCMs.
MP cells are generated from naïve cells in the periphery.
Fig. 1 ZIKV RNA in blood and tissues.
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)
Fig. 7 Bacterial dependency networks in IgA deficiency and HDs.
Evaluation of multidonor class Ig sequences obtained from H5N1 and H7N9 vaccinated donors. Evaluation of multidonor class Ig sequences obtained from H5N1.
T-CTLs are CD8+ TEMRA cells that can be expanded by IL-15 and IL-2 through selective proliferation and can be induced by LCs. T-CTLs are CD8+ TEMRA cells.
Blood Tfr cells do not show specialized humoral regulatory capacity.
RORα deficiency in Tregs results in exaggerated skin inflammation in response to EC sensitization. RORα deficiency in Tregs results in exaggerated skin.
CD25 expression identifies two transcriptionally distinct subsets of very early effector cells. CD25 expression identifies two transcriptionally distinct.
CD25 surface expression and TCR signal strength predict T helper differentiation and memory potential of early effector T cells in vivo. CD25 surface expression.
BMS blocks functional responses in primary immune cells driven by IFNα
CsEN components reveal precisely timed cellular programs that characterize the dynamic changes of the peripheral immune system over the course of pregnancy.
Tfr cells respond better to immunization with self-antigens than with foreign antigens. Tfr cells respond better to immunization with self-antigens than.
Examples of AEGIS autonomous target selection.
Human Tfr cells do not express CD25.
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.
Colonic Treg TCRs react to MA Helicobacter species.
Fig. 5. Vascularization of human liver seed grafts.
CD4-CTL effectors share TCR clonotypes with CD4-CTL precursors.
Tregs preferentially regulate TH2 cytokines in skin.
Human basophils are unresponsive to contact-dependent or contact-independent inhibition by Tregs. Human basophils are unresponsive to contact-dependent.
Blood Tfr cells are immature but are not committed in the thymus.
Fibroblast activation in WT and NFATc2-deficient mice.
IL-9–expressing TH cells are highly enriched in CCR4+/CCR8+ effector memory TH cells. IL-9–expressing THcells are highly enriched in CCR4+/CCR8+effector.
REV-ERBα deficiency reduces frequency and number of NKp46+ ILC3s.
Presentation transcript:

Blood Tfr cells are lymphoid tissue–derived Tfr precursors. Blood Tfr cells are lymphoid tissue–derived Tfr precursors. (A) CD45RO+CCR7− effector memory, CD45RO+CCR7+ central memory, and CD45RO−CCR7+ naïve subsets of Tfr cells and CXCR5− Treg cells in children blood (top) and tissues (bottom). Representative plots (left) and pooled data (right) (n = 6; Student’s t test) are shown. Tfh cells are represented in blue, CXCR5− Treg cells in black, and Tfr cells in red. CXCR5+ subsets in tonsils were defined as CXCR5+ICOS+ cells (fig. S2B). (B) Blood Tfh and Tfr cells from X-linked agammaglobulinemia (BTK-deficient) patients compared with sex- and age-matched HDs. Representative plots (left) and pooled data (right) (n = 5; Student’s t test) are shown. (C) Model of CXCR5+ Tfh and Treg cell generation and recirculation in humans upon antigen stimulation. Tfh cells are shown in red, and Tfr cells in blue. DC, dendritic cell. (D) Frequency of peripheral blood Tfr cells on the day of influenza vaccination (d0) and 7 days later in healthy volunteers. Schematic representation and representative plots (left) and pooled data (right) (n = 32; Student’s t test) are shown. Bars represent SEM. Valter R. Fonseca et al. Sci. Immunol. 2017;2:eaan1487 Copyright © 2017 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works