GC TFH cells exhibit HIV antigen–driven clonal expansion and selection

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.
Expansion of Bacteroides species during colitis does not enhance TCR-specific T cell responses. Expansion of Bacteroides species during colitis does not.
Longitudinal analysis of cross-group HA stem–binding lineages.
Colonic Treg TCRs (CT2 and CT6) drive Teff cell development in inflammation. Colonic Treg TCRs (CT2 and CT6) drive Teff cell development in inflammation.
Specific depletion of TFH and LCMV-specific CD4 T cells.
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.
Splenic CD169+ macrophages express a unique gene profile.
CCR2+ monocytes are a relevant source of type I IFN in response to Af.
Tfr cells’ transcriptomic profile distinguishes them from Treg and Tfh cells. Tfr cells’ transcriptomic profile distinguishes them from Treg and Tfh cells.
Longitudinal analysis of ZIKV E–specific memory B cell responses in the DENV-experienced donors. Longitudinal analysis of ZIKV E–specific memory B cell.
FIP200 controls Bak expression via maintaining microRNA1198-5p expression. FIP200 controls Bak expression via maintaining microRNA1198-5p expression. (A)
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.
CD169+ macrophages mediate Lm translocation to the splenic T cell zones. CD169+ macrophages mediate Lm translocation to the splenic T cell zones. (A) Confocal.
Examples of AEGIS autonomous target selection.
Assessment of repertoire elasticity and compartment replenishment after depletion. Assessment of repertoire elasticity and compartment replenishment after.
Protein sequence alignment of the NS3 helicase–encoding region of 63 flaviviruses demonstrates conservation of a KIR2DS2-binding peptide. Protein sequence.
Ex vivo testing of the soft robotic devices.
Human PBMC-derived MERS-CoV–specific T cells are multifunctional.
Virus-specific T cell responses are detected in all MERS survivors.
Docking footprint of PG90 TCR on CD1b-PG.
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.
Human cells produce type I and III IFNs upon Af stimulation.
Reduced FOXO1 expression in GC B cells from mice lacking regulatory CD4+ T cell–derived IL-10. Reduced FOXO1 expression in GC B cells from mice lacking.
Target cell lysis by ZnT8186–194-reactive CD8+ T cell clones.
Comparison of repertoire distributions to baseline.
Molecular and functional characterization of antibodies from PfCSP-reactive memory B cells and plasmablasts. Molecular and functional characterization.
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.
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.
Blood Tfr cells show expression of follicular and regulatory markers.
Analysis of plasmablast responses in one naïve and three DENV-experienced donors. Analysis of plasmablast responses in one naïve and three DENV-experienced.
Blood Tfr cells are lymphoid tissue–derived Tfr precursors.
Protein sequence alignment of the NS3 helicase–encoding region of 63 flaviviruses demonstrates conservation of a KIR2DS2-binding peptide. Protein sequence.
Evidence for platelet activation during human drug-induced anaphylaxis
FIP200 maintains microRNA1198-5p expression via Ago2 in naïve T cells.
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.
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.
Evaluation of multidonor class Ig sequences obtained from H5N1 and H7N9 vaccinated donors. Evaluation of multidonor class Ig sequences obtained from H5N1.
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.
CD4+CLA+CD103+ T cells in skin and blood are clonally related.
Fig. 1 Examples of experimental stimuli and behavioral performance.
BnmAbs 3D3 and 2D10 bind RSV G bnmAbs 3D3 and 2D10 bind RSV G (A) Schematic of the RSV G glycoprotein from RSV strain A2, including the.
Shared phenotype of CD4+CLA+CD103+ T cells from human blood and skin.
Blood Tfr cells do not show specialized humoral regulatory capacity.
Detection of neoantigen-specific T cell recognition in cancer.
CD25 expression identifies two transcriptionally distinct subsets of very early effector cells. CD25 expression identifies two transcriptionally distinct.
Memory-biased TCRs induce weaker TCR signals than effector-biased TCRs in vitro. Memory-biased TCRs induce weaker TCR signals than effector-biased TCRs.
CD25 surface expression and TCR signal strength predict T helper differentiation and memory potential of early effector T cells in vivo. CD25 surface expression.
Tfr cells respond better to immunization with self-antigens than with foreign antigens. Tfr cells respond better to immunization with self-antigens than.
MR1Ts respond to microbially derived ligands loaded on hpMR1 tetramers
AEGIS autonomous targeting process.
Examples of AEGIS autonomous target selection.
Human Tfr cells do not express CD25.
Fig. 2 Direct ex vivo cross-recognition analysis of disease-relevant islet-specific T cells. Direct ex vivo cross-recognition analysis of disease-relevant.
CD4+ memory T cells derived from either CD25hi or CD25lo effector cells respond robustly to secondary challenge. CD4+ memory T cells derived from either.
CD25 expression predicts effector and memory differentiation.
CD4-CTL effectors share TCR clonotypes with CD4-CTL precursors.
Blood Tfr cells are immature but are not committed in the thymus.
Fig. 2 Comparison of the observed DRs and the estimates by the VR model and FL. Comparison of the observed DRs and the estimates by the VR model and FL.
Evaluating the performance of the robotic system through comparison with human trackers. Evaluating the performance of the robotic system through comparison.
Presentation transcript:

GC TFH cells exhibit HIV antigen–driven clonal expansion and selection. GC TFH cells exhibit HIV antigen–driven clonal expansion and selection. (A) Gag-specific TCR clones overlap with HIV+ LN CD4+ T cell populations. Each thin slice of the arc represents a unique TCR sequence, ordered by the clone size (darker green for larger clones, inner circle). Gray curves indicate Gag-specific TCR nucleotide sequences found in naïve (gray, outer circle), memory (blue, outer circle), and GC TFH (orange, outer circle) populations. No Gag-overlapping clones were detected for one individual, H8 (not shown). (B) Number of Gag-specific TCR clones observed in naïve, memory, and GC TFH populations. Gray lines link the same patient. Bars indicate means (P values by two-tailed paired t test). (C) Mean clone size of Gag-specific T cells, HA-specific T cells, and bulk clones of unknown specificity from the GC TFH population. (D) Number of distinct nucleotide (nt) sequences per CDR3 amino acid (aa) sequence for Gag-specific T cells, HA-specific T cells, or bulk GC TFH cells. Data from all four individuals were aggregated for (C) and (D). Error bars indicate SEM. N.S., not significant. ***P < 0.001 by two-tailed t test. Ben S. Wendel et al. Sci. Immunol. 2018;3:eaan8884 Copyright © 2018 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works