Therapeutic effects of TIP60 allosteric modification in DSS-induced colitis. Therapeutic effects of TIP60 allosteric modification in DSS-induced colitis.

Slides:



Advertisements
Similar presentations
Diminished suppressive potency of primary Treg clones from IPEXA384T patients. Diminished suppressive potency of primary Treg clones from IPEXA384T patients.
Advertisements

MP cells, but not pathogen-elicited effector CD4+ T lymphocytes, rapidly produce IFN-γ during T. gondii infection independently of pathogen antigens. MP.
Treg and Teff cell subsets show increased TCR overlap during colitis.
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.
Helicobacter species induce pTreg cell differentiation during homeostasis. Helicobacter species induce pTreg cell differentiation during homeostasis. (A)
Pathogenic potential of naïve Helicobacter-reactive CT6 cells in lymphopenic mice. Pathogenic potential of naïve Helicobacter-reactive CT6 cells in lymphopenic.
Enhancement of Treg suppressive function by allosteric modification of TIP60. Enhancement of Treg suppressive function by allosteric modification of TIP60.
Impaired development of Treg cell function upon overexpression of FOXP3A384T in naïve CD4+CD25− T cells. Impaired development of Treg cell function upon.
Colonic Treg TCRs (CT2 and CT6) drive Teff cell development in inflammation. Colonic Treg TCRs (CT2 and CT6) drive Teff cell development in inflammation.
FIP200 deficiency alters mitochondria activation and ROS production in T cells. FIP200 deficiency alters mitochondria activation and ROS production in.
CD8α+ DC-deficient mice are highly susceptible to Lm infection in the absence of CD169+ macrophages. CD8α+ DC-deficient mice are highly susceptible to.
Antitumor effect of local cancer immunotherapy treatment toward distant B16F10 tumors. Antitumor effect of local cancer immunotherapy treatment toward.
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.
CD169+ macrophages mediate Lm translocation to the splenic T cell zones. CD169+ macrophages mediate Lm translocation to the splenic T cell zones. (A) Confocal.
Improvement in the transcriptional activity of FOXP3A384T by enhancement of TIP60-FOXP3 interaction. Improvement in the transcriptional activity of FOXP3A384T.
Workspace comparison of Delta robots.
Increased resistance of GPR55-deficient mice to indomethacin-induced intestinal permeability. Increased resistance of GPR55-deficient mice to indomethacin-induced.
Human PBMC-derived MERS-CoV–specific T cells are multifunctional.
Role of TLR signaling in hY4-induced changes and effects of TLR inhibition. Role of TLR signaling in hY4-induced changes and effects of TLR inhibition.
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.
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.
Genetic FIP200 deletion impairs autophagy induction and causes T cell apoptosis. Genetic FIP200 deletion impairs autophagy induction and causes T cell.
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.
T-bethi MP cells produce IFN-γ in response to IL-12.
BAP1 deficiency results in thymic atrophy and loss of thymocyte populations. BAP1 deficiency results in thymic atrophy and loss of thymocyte populations.
Helicobacter species induce pTreg cell differentiation during homeostasis. Helicobacter species induce pTreg cell differentiation during homeostasis. (A)
Inhibiting or altering the timing of microbial antigen encounter results in inflammatory T cell responses against gut bacteria. Inhibiting or altering.
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.
Antigen-specific immune responses are enhanced in hypertension.
Hypertensive mice are predisposed to autoimmune diseases.
Fig. 6. Nontaxane chemotherapies induce TMEM-dependent prometastatic changes in the breast cancer microenvironment. Nontaxane chemotherapies induce TMEM-dependent.
MP cells, but not pathogen-elicited effector CD4+ T lymphocytes, rapidly produce IFN-γ during T. gondii infection independently of pathogen antigens. MP.
Ado loss drives TNF-dependent immune evasion.
CypD-deficient mice are susceptible to Mtb infection.
Fig. 5 Impaired colitis induction by LRH-1–deficient CD4+T cells.
Fig. 5 Treatment with BMS (PO BID) protects from wasting and colitis in two SCID mouse models. Treatment with BMS (PO BID) protects from.
Enhancement of Treg suppressive function by allosteric modification of TIP60. Enhancement of Treg suppressive function by allosteric modification of TIP60.
Inhibiting or altering the timing of microbial antigen encounter results in inflammatory T cell responses against gut bacteria and worsened colitis upon.
Fig. 1 Bcl11b removal in Treg cells results in early death of mice and increased CD4+ and CD8+ T cell activation. Bcl11b removal in Treg cells results.
Partial alteration of the Treg gene signature by the p.A384T mutation.
Fig. 3 Local Maraba treatment of TNBC tumors provides long-term systemic protection. Local Maraba treatment of TNBC tumors provides long-term systemic.
Fig. 1. The HCN channel blocker ivabradine (IVA) is analgesic in a mouse model of type 1 diabetes. The HCN channel blocker ivabradine (IVA) is analgesic.
Colonic Treg TCRs react to MA Helicobacter species.
GPR55 regulates γδT cell egress from PP and homing of gut-tropic CD8 T cells to the small intestine. GPR55 regulates γδT cell egress from PP and homing.
Fig. 4 Dox-CBD-SA treatment shows reduced toxicity.
Fig. 4 Alternate-day ocular dosing with DECON curbs HSV-1 in a murine model of ocular infection. Alternate-day ocular dosing with DECON curbs HSV-1 in.
Tregs preferentially regulate TH2 cytokines in skin.
Chronic Treg reduction exacerbates bleomycin-induced skin fibrosis.
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.
Fig. 5 Topical vaginal application of DECON on alternate days is as effective as daily systemic ACV dosing. Topical vaginal application of DECON on alternate.
Fig. 5 Minimal administration of ETL is tolerable and safe in mice.
ARQ 531 improves survival in the Eμ-TCL1 engraftment model compared with ibrutinib. ARQ 531 improves survival in the Eμ-TCL1 engraftment model compared.
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.
Fig. 3. Effects of SFN in mice with diet-induced diabetes.
Fig. 2 Cxxc1 deficiency restricts T cell–mediated autoimmunity and increases sensitivity to C. rodentium infection. Cxxc1 deficiency restricts T cell–mediated.
Bb monocolonization enhances Treg population in the cLP.
CCR6 is dispensable for expansion of innate TCRαβ+ cells in oral candidiasis. CCR6 is dispensable for expansion of innate TCRαβ+ cells in oral candidiasis.
CSGG-induced iTreg cells are capable of suppressing intestinal inflammation. CSGG-induced iTreg cells are capable of suppressing intestinal inflammation.
Presentation transcript:

Therapeutic effects of TIP60 allosteric modification in DSS-induced colitis. Therapeutic effects of TIP60 allosteric modification in DSS-induced colitis. Colitis was induced by adding 4% DSS to pH-balanced tap water of study mice. Disease progression was assessed by daily monitoring of body weight, stool consistency, and fecal blood. B7A (4 mg kg−1 day−1, 7 days) or DMSO control was injected intraperitoneally 1 week after DSS administration. The effects of B7A treatment on (A) body weight, (B) colon length, and (C) gut histology (hematoxylin and eosin–stained paraffin sections) are shown. (D) Frequency of FOXP3+ Treg cells in the spleen and lymph nodes of B7A-treated compared with DMSO-treated mice. n = 10 to 12 mice per group. Khalid Bin Dhuban et al. Sci. Immunol. 2017;2:eaai9297 Copyright © 2017 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works.