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Image Search Results
Journal: bioRxiv
Article Title: Pathogenic IgE-fated B cell memory retains functional plasticity
doi: 10.1101/2023.11.28.567094
Figure Lengend Snippet: (A) Expression level of Ighc genes downstream of Ighg1 from scRNA-seq analysis of B cells isolated from spleens and inguinal LNs of CT-immunized mice and A4RA/IC-treated epicutaneously sensitized mice. Gene expression is plotted for cells within the MBC cluster . (B) VDJ analysis of MBC cluster. Plot depicts the assigned Ighc gene in MBCs with ≥3 nucleotide mutations compared to the germline sequence. (C) Representative contour plots of IgG1 + and IgG2c + populations from inguinal LNs of IC/A4RA-treated epicutaneously sensitized mice four weeks post-boost and antibody treatment. (D) IC/A4RA-treated mice were rested up to 15 weeks after re-exposures. IgG1 + (left) and IgG2c + (right) MBC frequency are plotted at four and 15 weeks post-boost. Pre-gated as OVA + B cells > CD38 + GL7 - > IgM - IgD - . (E) Epicutaneously sensitized mice were treated with A4RA, AIFNG, or both at the time of subcutaneous re-exposure. IgG1 + (left) and IgG2c + (right) MBC frequency are plotted at four weeks post-boost. Pre-gated as OVA + B cells > CD38 + GL7 - > IgM - IgD - . (F) OVA-specific serum immunoglobulin profiles of IC/A4RA-treated mice at zero to 15 weeks post-boost. (G) IC/A4RA-treated mice were rested for nine weeks to allow for clearance of OVA-specific IgG2c and clearance of IC/A4RA blocking antibodies. Subsequently, mice received tertiary OVA exposures and serum was collected at week 12. OVA-specific serum immunoglobulin profiles are depicted before and after tertiary exposures. (C-G) Data represents 2 experiments with at least 4 mice per group. Data are presented as mean ± SEM (F, G) or median ± min/max (D, E). * p < 0.05, ** p < 0.01, *** p < 0.001. Seq, sequences; swIg, class-switched; AIFNG, anti-IFN-ψR1; OD, optical density.
Article Snippet: The following anti-mouse fluorochrome-conjugated antibodies were used: B220-AF700 (RA3-6B2), CD138-PE/Dazzle 594 (281– ), CD3-BV711 (17A2), CD3-BV510 (17A2), F4/80-BV711 (BM8), F4/80-BV510 (BM8), CD38-PE/Cy7 (90), GL7-PerCP.Cy5.5 (GL7), GL7-BV421 (GL7; BD, Franklin Lakes, NJ), IgD-Pacific Blue (11-26c.2a), IgD-BV605 (11-26c.2a), IgM-BV786 (II/41; BD), IgM-FITC (II/41), IgG1-BV650 (RMG1-1), IgG2b-PECy7 (RMG2b-1),
Techniques: Expressing, Isolation, Gene Expression, Sequencing, Blocking Assay
Journal: bioRxiv
Article Title: Pathogenic IgE-fated B cell memory retains functional plasticity
doi: 10.1101/2023.11.28.567094
Figure Lengend Snippet: (A) Adoptive transfer schematic. (B) WT mice were immunized with OVA + Alum, CT, or CpG. Representative contour plots class-switched OVA + MBCs. Pre-gated as OVA + B cells > CD38 + GL7 - > IgM - IgD - . Numbers indicate the proportion of IgG1 + , IgG2b + , and IgG2c + cells from the parent class-switched MBC population. (C) OVA-enriched B cells were adoptively transferred from WT OVA-Alum donor mice to naïve muMT mice and recipient were boosted with either OVA + CT or OVA + CpG. Summary plots show OVA + IgG1 + and OVA + IgG2c + B cell frequency in recipient mice one week post-transfer and boost. (D) OVA-specific serum immunoglobulin profiles in recipient mice one week post-transfer and boost. Data represents 2 experiments, each with 2-4 mice per group. Data are presented as median ± min/max (B) or mean ± SEM (D). * p < 0.05.
Article Snippet: The following anti-mouse fluorochrome-conjugated antibodies were used: B220-AF700 (RA3-6B2), CD138-PE/Dazzle 594 (281– ), CD3-BV711 (17A2), CD3-BV510 (17A2), F4/80-BV711 (BM8), F4/80-BV510 (BM8), CD38-PE/Cy7 (90), GL7-PerCP.Cy5.5 (GL7), GL7-BV421 (GL7; BD, Franklin Lakes, NJ), IgD-Pacific Blue (11-26c.2a), IgD-BV605 (11-26c.2a), IgM-BV786 (II/41; BD), IgM-FITC (II/41), IgG1-BV650 (RMG1-1), IgG2b-PECy7 (RMG2b-1),
Techniques: Adoptive Transfer Assay