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

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

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.
Identification of combination treatment–responsive dysfunctional tumor-infiltrating CD8+ T cell population. Identification of combination treatment–responsive.
Correlation between endogenous STAT5ab signaling and circulating plasma factors. Correlation between endogenous STAT5ab signaling and circulating plasma.
A prospectively validated csEN model accurately predicts dynamic changes of the maternal immune system over the course of pregnancy. A prospectively validated.
CsEN components reveal precisely timed cellular programs that characterize the dynamic changes of the peripheral immune system over the course of pregnancy.
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.
FIP200 deficiency alters mitochondria activation and ROS production in T cells. FIP200 deficiency alters mitochondria activation and ROS production in.
Self-folding triangular devices at two scales.
CD8α+ DC-deficient mice are highly susceptible to Lm infection in the absence of CD169+ macrophages. CD8α+ DC-deficient mice are highly susceptible to.
CD169+ macrophages play a critical role in mediating innate immune cell reorganization. CD169+ macrophages play a critical role in mediating innate immune.
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.
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.
Examples of AEGIS autonomous target selection.
Volume 11, Issue 11, Pages (June 2015)
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
CD4-TEMRA cells show marked clonal expansion.
Human cells produce type I and III IFNs upon Af stimulation.
Comparison of repertoire distributions to baseline.
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 lymphoid tissue–derived Tfr precursors.
Fig. 4. Peanut-specific TH2A cells are specifically targeted during immunotherapy. Peanut-specific TH2A cells are specifically targeted during immunotherapy.
Evidence for platelet activation during human drug-induced anaphylaxis
Blood Tfr cells are indicators of ongoing humoral activity.
PD-L1 selectively marks circulating NCMs.
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.
Variable number of CD4-CTL precursors across donors.
CD169+ macrophages mediate the transport of bacteria to T cell zones by trans-infecting CD8α+ DCs. CD169+ macrophages mediate the transport of bacteria.
CD4-CTL precursor cells in the TEMRA subset.
CD4-TEMRA cells are heterogeneous across donors.
CD4+CLA+CD103+ T cells constitute a unique cell population in human blood. CD4+CLA+CD103+ T cells constitute a unique cell population in human blood. (A)
Shared phenotype of CD4+CLA+CD103+ T cells from human blood and skin.
MR1Ts are recognized by hpMR1 tetramers loaded with a heterogeneous mixture of microbially derived ligands. MR1Ts are recognized by hpMR1 tetramers loaded.
Blood Tfr cells do not show specialized humoral regulatory capacity.
CD25 expression identifies two transcriptionally distinct subsets of very early effector cells. CD25 expression identifies two transcriptionally distinct.
Memory-biased TCRs induce weaker TCR signals than effector-biased TCRs in vitro. Memory-biased TCRs induce weaker TCR signals than effector-biased TCRs.
CD25 surface expression and TCR signal strength predict T helper differentiation and memory potential of early effector T cells in vivo. CD25 surface expression.
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.
AEGIS autonomous targeting process.
Examples of AEGIS autonomous target selection.
Human Tfr cells do not express CD25.
CD25 expression predicts effector and memory differentiation.
CD4-CTL effectors share TCR clonotypes with CD4-CTL precursors.
CAR expression promotes tonic activation of signaling networks.
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.
Lin28b promotes the positive selection of CD5+ ImmB cells in neonatal mice. Lin28b promotes the positive selection of CD5+ ImmB cells in neonatal 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.
Acute circadian disruption alters ILC3 cytokine secretion.
REV-ERBα deficiency reduces frequency and number of NKp46+ ILC3s.
Circadian gene expression in ILC3s is associated with rhythmic cytokine expression. Circadian gene expression in ILC3s is associated with rhythmic cytokine.
Meningeal γδ T cells are biased toward IL-17 production.
Single-cell characterization of macrophages in fibrotic and regenerative microenvironments. Single-cell characterization of macrophages in fibrotic and.
Fig. 3 Gene expression analysis in 48-plex drug treatment experiments.
Bb monocolonization enhances Treg population in the cLP.
Correlation of TAN phenotypes and TIL effector function.
Presentation transcript:

High-dimensional analysis of lymphoid CD4+ T cells identified distinct TFH cell subsets in HIV+ patients and HCs. High-dimensional analysis of lymphoid CD4+ T cells identified distinct TFH cell subsets in HIV+ patients and HCs. (A) Representative gates used to identify GC TFH cells for t-SNE analysis. (B) Contour plots were generated using FACS output files from Cytobank (GC TFH cells) or “cytofkit” package in R (CXCR5+CD45RO+CD4+ T cells). Data include cells from 25 HIV+ patients and seven HCs. (C) Phenotypic clusters identified from CXCR5+ memory CD4+ T cells using DensVM. (D) Heatmap shows the average staining signal of indicated markers within each of the clusters identified in (C). Memory and naïve cells are shown at the bottom of the heatmap for comparison. Red-blue scale indicates staining intensity. Green-brown scale represents the relative frequency of HIV+ cells to total numbers of cells in each cluster. (E) Frequency of CD38 expression in CXCR5+ TFH cells or GC TFH cells from HC (n = 7) or HIV+ (n = 25) patients. Data are mean ± SEM. **P < 0.005 and ***P < 0.0005 by two-tailed t test. (F) Frequency of CD57+PD1+ GC subset within CD38− or CD38+CXCR5+ TFH cells from HIV+ patients (n = 25). ***P < 0.0005 by paired two-tailed t test. (G) Relationship between IL-21 expression and CD38 frequency in CXCR5+ TFH cells. (H) Relationship between peripheral CD4+ T cell count and IL-21+ GC TFH cells frequency. For (G) and (H), data are from 25 HIV+ patients; association was determined by Pearson correlation. Ben S. Wendel et al. Sci. Immunol. 2018;3:eaan8884 Copyright © 2018 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works