Mice with a B cell–specific loss of Ets1 have reduced marginal zone B cells and increased ASCs. (A) Flow cytometry analysis of CD21 versus CD23 in gated.

Slides:



Advertisements
Similar presentations
Anti-CD40 and CpG induce activation of T cells in draining lymph nodes
Advertisements

Detection of CD38+IgG1+ memory B cells adjacent to contracted GCs
Type 17 immunity is increased in STAT1−/− mice.
Inflammasome responses.
Depletion of CD169+ cells leads to increased expression of CD25 on enterotoxin A–specific Vβ3+ T cells. Depletion of CD169+ cells leads to increased expression.
IRF4 is required for anabolic induction of CD4+ T cells.
Volume 11, Issue 12, Pages (June 2015)
IL-21 inhibits T cell IL-2 production and impairs Treg homeostasis
CD1dhiCD5+ B cells are expanded in pancreatic neoplasia and are functionally important for sustaining growth of KrasG12D-PDEC in vivo. CD1dhiCD5+ B cells.
Frequencies of immune cell types show much stronger variations between tumor types in the tumor infiltrate compared with the spleen and tumor-draining.
Depo-Provera altered the expression of cell surface markers associated with HIV susceptibility. Depo-Provera altered the expression of cell surface markers.
Loss of Runx2 in the T cell compartment leads to a defect in the number of CD8+ memory precursor T cells during LCMV–Armstrong infection. Loss of Runx2.
FIP200 deficiency alters mitochondria activation and ROS production in T cells. FIP200 deficiency alters mitochondria activation and ROS production in.
PD‐L1 silencing in antigen presenting DCs results in hyperactivated pro‐inflammatory TCRhigh CD8+ T cells. PD‐L1 silencing in antigen presenting DCs results.
Colonization with N. musculi results in Ab production.
Loss of pathogen-specific T cell memory is due to the absence of Runx2 in CD8+ T cells. Loss of pathogen-specific T cell memory is due to the absence of.
Altered cytokine production by Klrk1−/− NOD CTL
Conditional expression of MHC II on B cells does not regulation atherosclerotic plaque development in Ldlr−/− mice. Conditional expression of MHC II on.
Volume 21, Issue 13, Pages (December 2017)
(A) Phospho-H2AX levels are significantly increased in CD4+ T cells, CD8+ T cells and monocytes from SLE compared with those from healthy controls (p=2.16×10−4,
Immune cell populations, activation, and NKG2D and H60a expression in the spleen of untreated and antibiotic-treated Klrk1+/+ and Klrk1−/− NOD mice. Immune.
Loss of DGKζ and Cbl-b results in a greater percentage of splenic CD8+ T cells with an activated phenotype. Loss of DGKζ and Cbl-b results in a greater.
Elicited and steady-state transport of skin self-antigens in PYNOD-KO mice. Elicited and steady-state transport of skin self-antigens in PYNOD-KO mice.
Inflammatory APC show highest expression of TNF superfamily ligands in the lung after LCMV infection. Inflammatory APC show highest expression of TNF superfamily.
Fig. 2. IL-2/rapamycin–expanded T cells express homing receptors to traffic to lymphoma sites and are resistant to SN-38 toxicity. IL-2/rapamycin–expanded.
CXCR5 expression accelerates Eμ-Tcl1 leukemogenesis and is indispensable for tumor cell recruitment to lymphoid B-cell follicles. CXCR5 expression accelerates.
Volume 43, Issue 5, Pages (November 2015)
IL-2c treatment preferentially expands injurious Tbet+ Tregs and inflammatory macrophages (MΦ) in skeletal muscle during chronic T. gondii infection. IL-2c.
Etifoxine modulation of T‐cell activity during EAE
Macrophage-resident NRP1 mitigates cytokine release and proinflammatory polarization. Macrophage-resident NRP1 mitigates cytokine release and proinflammatory.
Volume 50, Issue 2, Pages e4 (February 2019)
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.
Loss of Setdb1 in early B cells leads to impaired B cell development.
TCR signaling is required for exhausted-like TRM cell formation and maintenance. TCR signaling is required for exhausted-like TRM cell formation and maintenance.
The mucosal environment regulates CD160 expression on IELs
The microbiota downregulate CD160 expression on IELs
PD-L1 selectively marks circulating NCMs.
CD27 expression on bovine γδ and CD4 T cells ex vivo and in response to mitogen. CD27 expression on bovine γδ and CD4 T cells ex vivo and in response to.
PD-1 blockade results in increased expression of the chemokine receptor CXCR3. PD-1 blockade results in increased expression of the chemokine receptor.
Comparison of conventional NSG and hIL-7 expressing NSG humanized mice
SYK activity is required for anti-IgM–induced CD86 expression.
B cell development in wild-type and Syk-AQL mice.
Phenotypic characterization of splenic and islet-infiltrating B-cells in 12-week-old NOD female mice. Phenotypic characterization of splenic and islet-infiltrating.
Members of IL-1 family of cytokines favor the generation of IL-3–secreting CD4+ T cells in vitro. Members of IL-1 family of cytokines favor the generation.
Dynamic regulation of cell metabolism and mTORC1 activity and the requirement of RAPTOR in thymocyte development. Dynamic regulation of cell metabolism.
Lack of OcaB impairs age-associated B-lymphocyte accumulation in WAT
Spontaneous and strong Tfh cell but not Tfr cell development in IL-2 KO mice. Spontaneous and strong Tfh cell but not Tfr cell development in IL-2 KO mice.
Loss of Tfh and GC B cells in 2KO-Bcl6TC mice.
Overexpression of IL-27 upregulates expression of multiple IR by T cells in vivo. Overexpression of IL-27 upregulates expression of multiple IR by T cells.
Volume 21, Issue 13, Pages (December 2017)
Effects of Smo and Math5 double mutations on RGC and cone cell production. Effects of Smo and Math5 double mutations on RGC and cone cell production. A–P,
Volume 23, Issue 8, Pages (May 2018)
Vaginal CD11c+ DCs from IL-17A−/− mice are impaired in potentiating Th17 responses because of diminished IL-1β production. Vaginal CD11c+ DCs from IL-17A−/−
Fig. 2 Phenotypic analyses of Bcl11b-deficient Treg cells.
Nanoimmunotherapy production scale-up and evaluation in Apoe−/− mice
Deletion of Tgfbr2 in myeloid cells elevated IFN-γ production in CD8+ T cells, and systemic IFN-γ neutralization diminished metastasis inhibition in Tgfbr2MyeKO.
Tumor-resident CD8+ T cells rapidly expand after IL-15/IL-15Rα complex treatment. Tumor-resident CD8+ T cells rapidly expand after IL-15/IL-15Rα complex.
Hypoxic Ag-specific CD8+ T cells are less functional and less proliferative. Hypoxic Ag-specific CD8+ T cells are less functional and less proliferative.
Local proliferation of infiltrating circulating memory T cells.
Mice with a B cell–specific deletion of Ets1 have increased memory phenotype B cells but no increase in switching to IgG1. Mice with a B cell–specific.
Loss of polarity gene Dlg1 leads to an expansion of C'-1 stage cells during pre-B cell differentiation. Loss of polarity gene Dlg1 leads to an expansion.
IL35 regulation of tumor growth is accompanied by suppression of CD4+ effector T-cell activity and expansion of Tregs. IL35 regulation of tumor growth.
Lin28b promotes the positive selection of CD5+ ImmB cells in neonatal mice. Lin28b promotes the positive selection of CD5+ ImmB cells in neonatal mice.
Mice with a B cell–specific deletion of Ets1 do not have increased CD4+ T cell activation. Mice with a B cell–specific deletion of Ets1 do not have increased.
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.
IL2Cx alone or in combination with anti–CTLA-4 increases the CD8/Treg ratio in the tumor. IL2Cx alone or in combination with anti–CTLA-4 increases the.
E2 induces IL-17–producing γδ+ T cells in the FGT
Bb monocolonization enhances Treg population in the cLP.
Surface expression of chemokine receptors on M
Presentation transcript:

Mice with a B cell–specific loss of Ets1 have reduced marginal zone B cells and increased ASCs. (A) Flow cytometry analysis of CD21 versus CD23 in gated live, B220+ B cells showing that Ets1−/− and CD19-Cre Ets1fl/fl mice lack CD21hiCD23lo marginal zone B cells. Mice with a B cell–specific loss of Ets1 have reduced marginal zone B cells and increased ASCs. (A) Flow cytometry analysis of CD21 versus CD23 in gated live, B220+ B cells showing that Ets1−/− and CD19-Cre Ets1fl/fl mice lack CD21hiCD23lo marginal zone B cells. Gate positions were adjusted to enclose the major cell populations. (B) Quantification of the percent of marginal zone B cells and the mean fluorescence intensity (MFI) of CD23 on follicular B cells (n = 8 Ets1+/+, 6 Ets1−/−, 11 CD19-Cre Ets1+/+, and 8 CD19-Cre Ets1fl/fl mice). (C) Flow cytometry analysis of B220 versus CD138 in gated live cells showing that Ets1−/− and CD19-Cre Ets1fl/fl mice have increased percentages of B220loCD138+ Ab-secreting plasma cells. (D) Quantification of the percent of ASCs in the spleen and lymph nodes of the various strains of mice (n = 7 Ets1+/+, 6 Ets1−/−, 9 CD19-Cre Ets1+/+, and 11 CD19-Cre Ets1fl/fl mice). *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001. ns, not significant. Alex Sunshine et al. ImmunoHorizons 2019;3:331-340 Copyright © 2019 The Authors