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Journal: Frontiers in Immunology
Article Title: Transplanted gene-modified placental cells boost FVIII activity in pediatric sheep without eliciting immunity, toxicity, or adverse events
doi: 10.3389/fimmu.2025.1716950
Figure Lengend Snippet: PLC-mcoET3 can be detected in tissues of pediatric sheep after IP and IV administration at 7–18 months post-administration by dPCR and by RT-qPCR. dPCR using human Alu-specific primers was performed in triplicate on DNA extracted from liver, lung, spleen, and thymus. All the tissues analyzed contained human DNA; the same tissue samples from control non-treated animals showed no target amplification. RT-qPCR was performed in triplicate using primers specific for mcoET3 and sheep GAPDH. Percentage of engraftment was determined by comparing ΔCt values to a standard curve consisting of increasing percentages of mcoET3-PLC (0, 0.01, 0.1, 1, 5, and 10%) in sheep stromal cells. (AH) Percentages of human cells present in liver (A, E) , lung (B, F) , spleen (C, G) , and thymus (D, H) as determined dPCR (A–D) and RT-qPCR (E–H) using human Alu- and mcoET3-specific primers, respectively; (I) H&E staining was also performed on sections from each tissue to determine whether engraftment of PLC-mcoET3 in each of the different tissues caused any untoward effects. Slides of the tissue sections were sent to a certified animal pathologist. Results showed no evidence of any lentivector-related toxicity in any of the tissues examined. Moreover, there were no changes in tissue architecture, ectopic tissue formation, gross tumor development, or areas of atypical cells or foci of hyperplasia or neoplasia. All images were acquired with a Leica DM4000 B microscope using a 10x objective. *p ≤ 0.05, **p ≤ 0.01, ***p ≤ 0.001, ns, not significant.
Article Snippet: Each reaction contained 200nM of Alu and RPL13A primers and 250nM of their respective probes in a final concentration of
Techniques: Quantitative RT-PCR, Control, Amplification, Staining, Microscopy
Journal: Frontiers in Immunology
Article Title: Transplanted gene-modified placental cells boost FVIII activity in pediatric sheep without eliciting immunity, toxicity, or adverse events
doi: 10.3389/fimmu.2025.1716950
Figure Lengend Snippet: Treatment of animals with pre-existing inhibitors with PLC-mcoET3 results in an increase in FVIII activity in two of three animals at most of the time points analyzed despite the rise in titers of inhibitory antibodies. Human PLC-mcoET3, producing 3.6 IU/10 6 cells/24hr of FVIII/ET3, were administered to 3 animals on 3 consecutive weeks (20IU/kg/24h) to reach a total dose of 60IU/kg/24h at 14–23 months after the administration of ET3 and/or FVIII protein. (A) Animals were chosen because they continued to harbor FVIII and ET3 inhibitors at the time of PLC-mcoET3 infusion; (B) PLC-mcoET3 infusion triggered an increase in inhibitors against ET3 (p<0.05) and FVIII (p<0.05) at W3, when compared to W0 in all 3 animals; (C) FVIII activity increased in two out of three animals at most of the time points analyzed, despite the rise in titers of inhibitory antibodies; (D) dPCR and (E) RT-qPCR were performed as described above, and PLC-mcoET3 were found to be present in all tissues analyzed. *p<0.05, **p<0.01, ***p<0.001. ns, not significant.
Article Snippet: Each reaction contained 200nM of Alu and RPL13A primers and 250nM of their respective probes in a final concentration of
Techniques: Activity Assay, Quantitative RT-PCR