Donor TRM persistence is associated with reduced clinical complications. Donor TRM persistence is associated with reduced clinical complications. Patient.

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.
Identification of combination treatment–responsive dysfunctional tumor-infiltrating CD8+ T cell population. Identification of combination treatment–responsive.
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.
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.
Altered distribution of γδT IELs in GPR55-deficient mice.
Human PBMC-derived MERS-CoV–specific T cells are multifunctional.
Visual explanation of the interaction terms.
Virus-specific T cell responses are detected in all MERS survivors.
Visual explanation of the interaction terms.
Platelets are required for hFcγRIIA-induced anaphylaxis.
VH usage of cross-reactive B cells induced by H5N1 or H7N9 vaccination
CD4-TEMRA cells show marked clonal expansion.
Target cell lysis by ZnT8186–194-reactive CD8+ T cell clones.
Tukey boxplots overlaid on data points from objective and subjective measures, displaying results from study 1. Tukey boxplots overlaid on data points.
DC subset cooperation for activation of antiviral T cells.
Direct visualization by RNA FISH of TLR7 escape from X inactivation in B cells from women. Direct visualization by RNA FISH of TLR7 escape from X inactivation.
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.
EGFR activation in GCs inhibits GAP formation and luminal antigen delivery throughout life. EGFR activation in GCs inhibits GAP formation and luminal antigen.
Blood Tfr cells show expression of follicular and regulatory markers.
Evidence for platelet activation during human drug-induced anaphylaxis
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.
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)
Fig. 7 Bacterial dependency networks in IgA deficiency and HDs.
CD169+ macrophages mediate the transport of bacteria to T cell zones by trans-infecting CD8α+ DCs. CD169+ macrophages mediate the transport of bacteria.
CD4-TEMRA cells are heterogeneous across donors.
Microrobots with different cell-carrying capacities under different grid lengths (lg) and burr lengths (lb). Microrobots with different cell-carrying capacities.
Fig. 4 Rotation of nuclei in oocytes in the primordial follicles.
CD4+CLA+CD103+ T cells in skin and blood are clonally related.
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)
Fig. 2 Reference-fixing experiment, results.
CD4+CLA+CD103+T cells from human blood and skin share a functional profile. CD4+CLA+CD103+T cells from human blood and skin share a functional profile.
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.
Fig. 3 Rotation experiment, setup.
CD25 expression identifies two transcriptionally distinct subsets of very early effector cells. CD25 expression identifies two transcriptionally distinct.
Fig. 1 Reference-fixing experiment, setup.
Fig. 1 Bioinspired design of AAD for promoting wound contraction.
Tfr cells respond better to immunization with self-antigens than with foreign antigens. Tfr cells respond better to immunization with self-antigens than.
S-Affs colocalize with SUMO in mammalian cells.
AEGIS autonomous targeting process.
CD25 expression predicts effector and memory differentiation.
Fig. 2 Results of the learning and testing phases.
Fig. 2 IRF8 is expressed in CD68+ macrophages after SCI.
GSDMD localizes to the plasma membrane and is processed during NET formation. GSDMD localizes to the plasma membrane and is processed during NET formation.
Fig. 1 Deficient CD73 and CD39 expressions and extracellular adenosine concentration in BM of OVX animals. Deficient CD73 and CD39 expressions and extracellular.
Fig. 5. Vascularization of human liver seed grafts.
CD4-CTL effectors share TCR clonotypes with CD4-CTL precursors.
Fig. 4 Relationships between light and economic parameters.
IFN treatment of human midgestation villous explants induces syncytial knot formation. IFN treatment of human midgestation villous explants induces syncytial.
Human basophils are unresponsive to contact-dependent or contact-independent inhibition by Tregs. Human basophils are unresponsive to contact-dependent.
Fig. 6 Pig 5 tissue development.
Blood Tfr cells are immature but are not committed in the thymus.
Fig. 5 Proportions of EpCAM+ systemic tumor cells correlate with the clinical outcome of patients with MBC. Proportions of EpCAM+ systemic tumor cells.
Fig. 2 RVFV causes pathology within the liver, uterus, and placenta of pregnant dams. RVFV causes pathology within the liver, uterus, and placenta of pregnant.
Fig. 7 BEL immune response.
Fig. 5 Reconstitution of the dormant state using fetal ovaries.
Fig. 2 Spatial distribution of five city groups.
Cartoon model for the increased p-HLA display engendered by peptide splicing. Cartoon model for the increased p-HLA display engendered by peptide splicing.
In vivo function of MeTro sealants using rat incision model of lungs
Bb monocolonization enhances Treg population in the cLP.
Intratumoral spatial distribution of granulocytes and T cells.
Correlation of TAN phenotypes and TIL effector function.
Presentation transcript:

Donor TRM persistence is associated with reduced clinical complications. Donor TRM persistence is associated with reduced clinical complications. Patient records were examined for clinical complications including PGD and episodes of ACR at all time points of BAL acquisition (see Materials and Methods). (A) Graphs show percentage (mean ± SEM) of donor CD4+ (left) or CD8+ (right) T cells in the BAL over indicated times after transplantation in patients (n = 20) stratified on the basis of those who experienced PGD (red) or did not (blue). **P = 0.003 (left) and **P = 0.002 (right). Cumulative data across all time points showed increased proportion of donor CD8+ (P = 0.008) and trends in increased donor CD4+ (P = 0.06) T cells in those participants without PGD. (B) Donor CD4+ (left) and CD8+ (right) T cell frequencies over indicated times after transplantation in patients (n = 20 total patients; n = 7 patients with 10 discrete episodes of ACR at any time) based on the presence (solid squares) or absence (open circles) of ACR. ***P < 0.01. (C to E) Serial sections of a TBBx from one patient (P29) who experienced ACR at 1 month after lung transplant (grade 1); donor is HLA-A2+, and recipient is HLA-A2−. Immunofluorescence imaging stained for E-cadherin (purple), CD4 (green), HLA-A2 (red), and DAPI (blue). Yellow arrows indicate donor cells, and green arrows indicate recipient cells. “*” identifies a blood vessel (E) H&E stain, and “*” identifies blood vessel (*BV). (F) Frequency of donor origin CD4 (left) and CD8 (right) T cells in the BAL stratified on the basis of the presence or absence of a positive bacterial culture. *P < 0.05. Mark E. Snyder et al. Sci. Immunol. 2019;4:eaav5581 Copyright © 2019 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works