Innate alloresponse is determined by a single Mendelian locus in the donor not linked to the Mhc. Innate alloresponse is determined by a single Mendelian.

Slides:



Advertisements
Similar presentations
Donor SIRPα binding to recipient CD47 is required for triggering the innate alloresponse. Donor SIRPα binding to recipient CD47 is required for triggering.
Advertisements

Fibroblast activation in WT and NFATc2-deficient mice.
MP cells are generated from naïve cells in the periphery.
The adjMFC end point is independent of baseline titers.
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.
Specific depletion of CD4-DTR–derived CD4 T cells.
Three different types of transfer functions with a codomain of [0,1].
The TGF-β pathway is activated in the skin after C
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.
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.
Workspace comparison of Delta robots.
Cytosolic entry of Lm required for CD8α+ DC recruitment.
Deficiency in myeloid-resident NRP1 affects systemic metabolism.
Comparison of repertoire distributions to baseline.
β-Glucans do not modulate epithelial IL-33 or AHR.
Tukey boxplots overlaid on data points from objective and subjective measures, displaying results from study 1. Tukey boxplots overlaid on data points.
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.
Differential expression of TRM markers by donor- and recipient-derived T cells with time. Differential expression of TRM markers by donor- and recipient-derived.
Fig. 7 Correlation of NHP and human ISGs.
TCRs bind to CD1b-PG complexes formed in cells.
T-bethi MP cells produce IFN-γ in response to IL-12.
Blood Tfr cells are lymphoid tissue–derived Tfr precursors.
Low accessibility to Ag for CTLs leads to low proliferation of effectors. Low accessibility to Ag for CTLs leads to low proliferation of effectors. Intravital.
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.
MP cells are generated from naïve cells in the periphery.
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.
Fig. 2 Global production, use, and fate of polymer resins, synthetic fibers, and additives (1950 to 2015; in million metric tons). Global production, use,
Fig. 1. MSCs undergo in vivo apoptosis after infusion without affecting immunosuppression. MSCs undergo in vivo apoptosis after infusion without affecting.
The adjMFC end point is independent of baseline titers.
BAP1 is required for homeostatic and antigen-driven expansion of peripheral T cells. BAP1 is required for homeostatic and antigen-driven expansion of peripheral.
Fig. 1 Examples of experimental stimuli and behavioral performance.
Fig. 2 Reference-fixing experiment, results.
RAPTOR deficiency impairs the DN-to-DP transition in αβ T cell development. RAPTOR deficiency impairs the DN-to-DP transition in αβ T cell development.
Dectin-1 regulates innate IL-13.
Fig. 1 Product lifetime distributions for the eight industrial use sectors plotted as log-normal probability distribution functions (PDF). Product lifetime.
CypD-deficient mice are susceptible to Mtb infection.
Fig. 3. Increased expression of exhaustion markers and apoptosis markers on CAR8 cells in the presence of TCR antigen. Increased expression of exhaustion.
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.
Fig. 5 Impaired colitis induction by LRH-1–deficient CD4+T cells.
Crystal structure of DS-A. 02:01 ESO 9V and WT-A
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 Distribution of total and fake news shares.
RAD sampler design. RAD sampler design. (A) One arm of the RAD sampler with revolute joints shown as dotted lines. A fold is initiated by rotating the.
MR1Ts respond to microbially derived ligands loaded on hpMR1 tetramers
AEGIS autonomous targeting process.
Fig. 3 Local Maraba treatment of TNBC tumors provides long-term systemic protection. Local Maraba treatment of TNBC tumors provides long-term systemic.
Fig. 3 Production of protein and Fe(II) at the end of growth correlated with increasing concentrations of ferrihydrite in the media that contained 0.2.
Fig. 5. Vascularization of human liver seed grafts.
Fig. 2 Top 10 countries, ecoregions, conservation hotspots, and KBAs with the largest area of restoration hotspots. Top 10 countries, ecoregions, conservation.
Fig. 5 Comparison of the liquid products generated from photocatalytic CO2 reduction reactions (CO2RR) and CO reduction reactions (CORR) on two catalysts.
In vivo prophylactic and therapeutic efficacy of C12G6 in mice
Fig. 1 Location of the Jirzankal Cemetery.
Fig. 4 CO2 emission changes triggered by the JJJ clean air policy.
Proprioception. Proprioception. (A) Computer-aided design (CAD) model of each component of the cylinder and the completed device with three different stiffness.
Fig. 5. High burdens of AA signature mutations and predicted immunogenicity in Taiwan HCCs. High burdens of AA signature mutations and predicted immunogenicity.
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. 2. Mechanism of PD-L1 down-regulation in NOD HSPCs.
Breakdown of incorrect participant responses.
Fig. 3 Performance of the generative model G, with and without stack-augmented memory. Performance of the generative model G, with and without stack-augmented.
Circadian gene expression in ILC3s is associated with rhythmic cytokine expression. Circadian gene expression in ILC3s is associated with rhythmic cytokine.
Fig. 4 Gallium increases P. aeruginosa sensitivity to peroxides.
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.
Magnitude of the host innate alloresponse is influenced by the genetic background of the donor. Magnitude of the host innate alloresponse is influenced.
CCR6 is dispensable for expansion of innate TCRαβ+ cells in oral candidiasis. CCR6 is dispensable for expansion of innate TCRαβ+ cells in oral candidiasis.
Presentation transcript:

Innate alloresponse is determined by a single Mendelian locus in the donor not linked to the Mhc. Innate alloresponse is determined by a single Mendelian locus in the donor not linked to the Mhc. Bone marrow plugs were transplanted individually under the kidney capsules of separate mice. All recipients were BRG except in (D) where they were CRG. Donor strains are shown on the x axis. Recipient mono-DCs in grafts were measured as in Fig. 1. (A) Responses of BRG recipients to grafts from parental NRG and BRG strains or to grafts from (BRG × NRG)F1 and F2 generations. All donors and recipients were on the Rag2−/−γc−/− background. (B) Effect of donor-recipient non-MHC mismatch (BALB.B grafts) or MHC mismatch (B6.C grafts) on the innate alloresponse of BRG recipients. (C) Effects of donor MHC I deficiency (NOD.scid.b2m−/− grafts) on the innate alloresponse of BRG recipients. (D) Effect of MHC II deficiency (B6.MHCII−/− grafts) on the innate alloresponse of CRG recipients. n = 5 to 6 mice per group per experiment, except in F2 experiment (n = 30 mice transplanted in two separate batches). Experiments were performed once or twice. Each dot represents an individual biological replicate. Bars are means. *P < 0.05, **P < 0.01, ***P < 0.001, ****P < 0.0001 (unpaired two-tailed t test). Hehua Dai et al. Sci. Immunol. 2017;2:eaam6202 Copyright © 2017 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works.