CAR expression promotes tonic activation of signaling networks.

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.
Expansion of Bacteroides species during colitis does not enhance TCR-specific T cell responses. Expansion of Bacteroides species during colitis does not.
Impaired development of Treg cell function upon overexpression of FOXP3A384T in naïve CD4+CD25− T cells. Impaired development of Treg cell function upon.
Splenic CD169+ macrophages express a unique gene profile.
Role of IL-27 in expression of PD-L1, LAG-3, and CTLA-4 depends on strength of α-CD3/28 signaling. Role of IL-27 in expression of PD-L1, LAG-3, and CTLA-4.
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.
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.
Platelets are required for hFcγRIIA-induced anaphylaxis.
VH usage of cross-reactive B cells induced by H5N1 or H7N9 vaccination
Tukey boxplots overlaid on data points from objective and subjective measures, displaying results from study 1. Tukey boxplots overlaid on data points.
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.
Neutrophil recruitment to the colonic lamina propria depends on CD4+ T cells. Neutrophil recruitment to the colonic lamina propria depends on CD4+ T cells.
Persistent TCR–pMHC-I signaling drives the formation and maintenance of exhausted-like TRM cells. Persistent TCR–pMHC-I signaling drives the formation.
TCR signaling is required for exhausted-like TRM cell formation and maintenance. TCR signaling is required for exhausted-like TRM cell formation and maintenance.
BAP1 deficiency results in thymic atrophy and loss of thymocyte populations. BAP1 deficiency results in thymic atrophy and loss of thymocyte populations.
Fig. 4. Peanut-specific TH2A cells are specifically targeted during immunotherapy. Peanut-specific TH2A cells are specifically targeted during immunotherapy.
NCMs regulate T cell survival in TLOs via PD-L1.
PD-L1 selectively marks circulating NCMs.
PD-L1 expression is maintained on NCMs under inflammatory conditions and PD-L1+NCMs are found in TLOs. PD-L1 expression is maintained on NCMs under inflammatory.
GPR55 restrains IEL accumulation in the small intestine.
Fig. 4 Labeling of Msmeg with DMN-Tre is fast and specific and depends on Ag85A function. Labeling of Msmeg with DMN-Tre is fast and specific and depends.
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)
CD4-TEMRA cells are heterogeneous across donors.
Fig. 1 Examples of experimental stimuli and behavioral performance.
Fig. 6 Comparison of properties of water models.
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)
Optimization of a MYC degradation screen.
Shared phenotype of CD4+CLA+CD103+ T cells from human blood and skin.
MR1Ts recognized by the hpMR1+EC tetramer are more likely to be TRAV1-2−. MR1Ts recognized by the hpMR1+EC tetramer are more likely to be TRAV1-2−. PBMCs.
MYC degradation screen identifies a compound that stabilizes MYC protein. MYC degradation screen identifies a compound that stabilizes MYC protein. (A)
Memory-biased TCRs induce weaker TCR signals than effector-biased TCRs in vitro. Memory-biased TCRs induce weaker TCR signals than effector-biased TCRs.
Fig. 1. CAR4 and CAR8 cells demonstrate in vitro and in vivo antileukemic efficacy. CAR4 and CAR8 cells demonstrate in vitro and in vivo antileukemic efficacy.
CD25 surface expression and TCR signal strength predict T helper differentiation and memory potential of early effector T cells in vivo. CD25 surface expression.
Fig. 3 BMS blocks functional responses in primary immune cells driven by IL-23 and IL-12. BMS blocks functional responses in primary immune.
BMS blocks functional responses in primary immune cells driven by IFNα
Fig. 1 Bioinspired design of AAD for promoting wound contraction.
Fig. 6 SNP rs is a functional SNP in 22Rv1 cells.
HRI depletion elevates γ-globin in primary erythroid CD34+ cells
Fig. 4 HRI regulates BCL11A levels.
Fig. 2 HRI depletion elevates γ-globin in HUDEP2 cells.
Fig. 3 The rs risk enhancer is a hub for intrachromosomal and interchromosomal interactions. The rs risk enhancer is a hub for intrachromosomal.
Fig. 4 Reconstitution of MCs in KitW-sh/W-sh mice increases IL-10+ Breg cells and suppresses the CHS response. Reconstitution of MCs in KitW-sh/W-sh mice.
Fig. 6 Caspase-3– and -7–deficient cells maintain mitochondrial membrane polarity following intrinsic or extrinsic apoptotic stimuli. Caspase-3– and -7–deficient.
Fig. 5 Simultaneous absence of caspase-3 and -7 is required for significant decrease of caspase-8 and -9 activation in intrinsic apoptosis. Simultaneous.
Human Tfr cells do not express CD25.
Fig. 2 Regulation of CD73 and CD39 cell membrane expressions and extracellular adenosine levels by ERs in osteoprogenitor cells. Regulation of CD73 and.
Fig. 3 Abundance for all OR-expressing OSN subtypes across mammalian evolution. Abundance for all OR-expressing OSN subtypes across mammalian evolution.
Fig. 1 Deficient CD73 and CD39 expressions and extracellular adenosine concentration in BM of OVX animals. Deficient CD73 and CD39 expressions and extracellular.
Fig. 6 Global sensitivity analysis illustrates the key model parameters that determine the sickling of RBCs. Global sensitivity analysis illustrates the.
by Geoffrey A. Smith, Jack Taunton, and Arthur Weiss
Fig. 2 Viperin promotes methionine oxidation of KSHV helicase.
CD4-CTL effectors share TCR clonotypes with CD4-CTL precursors.
Fig. 5 In vivo gene delivery by the T4-AAV nanoparticles.
UNC drives MYC protein loss.
Human basophils are unresponsive to contact-dependent or contact-independent inhibition by Tregs. Human basophils are unresponsive to contact-dependent.
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.
Fig. 5 IL-5–mediated signaling is critical for the development of CD1dintCD5+ Breg precursor cells and IL-10+ Breg cells. IL-5–mediated signaling is critical.
Fig. 2 Spatial distribution of five city groups.
Fig. 1 Spatial and cartilage depth-related distributions of deamidated proteins in human adult cartilage. Spatial and cartilage depth-related distributions.
Fig. 8 Immune correlates of protection.
Fig. 3 Three small molecules inhibit the transport of CCR5 and do not affect transport of CCR1 or CXCR4. Three small molecules inhibit the transport of.
Fig. 5 Treatment with molecules 13, 14, and 15 decreases HIV-1 R5 infection in human macrophages. Treatment with molecules 13, 14, and 15 decreases HIV-1.
Bb monocolonization enhances Treg population in the cLP.
Fig. 2 Time series of secularization versus GDP per capita, from four illustrative countries, over the 20th century. Time series of secularization versus.
Presentation transcript:

CAR expression promotes tonic activation of signaling networks. CAR expression promotes tonic activation of signaling networks. (A) Mass cytometry analysis of baseline phosphoprotein abundance in expanded CD8+ T cells transduced to express the CD19-28ζ CAR as indicated. Histograms are representative of three independent donors. (B) Mass cytometry analysis of baseline phosphoprotein abundance in CD4+ (green), CD8+ (blue), and Vδ2+ (yellow) T cells transduced to express the CD19-28ζ CAR. Correlation of EMD score with transduction efficiency is from analysis of at least three independent donors. (C and D) Mass cytometry analysis of phosphoprotein abundance in expanded T cells transduced with CD19-28ζ stimulated with antibodies against CD3 (blue), CD28 (green), CD3+CD28 (red), or CAR (violet). Correlation of EMD scores in untransduced and CAR-transduced cells (C) and EMD scores for pSLP-76, pERK, and pMAPKAPK2 (D) are means ± SEM of at least three independent donors. (E) Flow cytometry analysis of TIM-3 and PD-1 abundance on T cells expressing a CD19-28ζ, GD2-28ζ (huk666), or GD2-28ζ (14G2A) CAR. Data are means ± SEM pooled from at least four biological replicates (see also fig. S11). Pearson correlation (B) and analysis of covariance (ANCOVA) (C) P values are displayed; (D) *P < 0.05, **P < 0.01 by paired t test. ns, not significant. Jonathan Fisher et al., Sci. Signal. 2019;12:eaax1872 Copyright © 2019 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works