1. Induction and role of regulatory CD4+CD25+ T cells in tolerance to the transgene product following hepatic in vivo gene transfer
by Ou Cao, Eric Dobrzynski, Lixin Wang, Sushrusha Nayak, Bethany Mingle, Cox Terhorst, and Roland W. Herzog
Blood
Volume 110(4):
August 15, 2007
©2007 by American Society of Hematology

2. Percent CD25+ T cells of CD4+ DO11. 10 TCR+ cells in DO11
Percent CD25+ T cells of CD4+ DO11.10 TCR+ cells in DO11.10-tg RAG-2−/− BALB/c mice as determined by flow cytometry.
Percent CD25+ T cells of CD4+ DO11.10 TCR+ cells in DO11.10-tg RAG-2−/− BALB/c mice as determined by flow cytometry. (A) Scatter graphs show staining of CD25 and DO11.10 TCR for gated CD4+ cells. This example represents inguinal lymph node cells from control mice and animals that received hepatic gene transfer with 1 × 1012 vg AAV-EF1α-ova vector. Mice were killed 8 weeks after gene transfer. Antibody stainings were FITC-conjugated KJ1-26 (for DO11.10 TCR) and PE-conjugated CD25. (B) Summary of results for different lymphoid organs including fold difference between groups. Mice had received no gene transfer or AAV-EF1α-GFP or AAV-EF1α-ova. Results from spleens and thymus were average (± SD), while lymph nodes cells were pooled prior to flow cytometry (n = 5/cohort). *P < .01 compared with control groups.
Ou Cao et al. Blood 2007;110:
©2007 by American Society of Hematology

3. Characterization of regulatory CD4+CD25+ cells isolated from AAV-EF1α-ova–transduced DO11.10-tg RAG-2−/− mice.
Characterization of regulatory CD4+CD25+ cells isolated from AAV-EF1α-ova–transduced DO11.10-tg RAG-2−/− mice. Expression of FoxP3 in a subpopulation of CD4+ splenocytes derived from DO11.10-tg BALB/c (RAG+) or DO11.10-tg RAG-2−/− (RAG−) mice. (A) Splenocytes were sorted into CD4+ cells and further separated into CD25+ or CD25− cells. cDNA from each population was subjected to PCR using FoxP3- or HPRT (hypoxanthine–guanine phosphoribosyl–transferase)–specific primers. (B) Quantification of relative FoxP3 mRNA levels in indicated CD4+ T-cell subsets. cDNA samples were subjected to real-time quantitative PCR analyses using primers and an internal fluorescent probe specific for FoxP3 or HPRT. The relative quantity of FoxP3 in each sample was normalized to the relative quantity of HPRT. Shown are average results for 3 independent experiments (± SD). (C) Flow cytometry for FoxP3 expression. Shown are examples for percent CD25+FoxP3+ of CD4+ splenocytes in individual mice (8 weeks after gene transfer with AAV-ova or naive control). (D) Cell dose–dependent suppression of IL-2 expression in DO11.10-tg CD4+CD25− cells by CD4+CD25+ isolated from AAV-EF1α-ova–transduced DO11.10-tg RAG-2−/− mice upon in vitro coculture (in the presence of APCs) and stimulation with ova. Data represent average (± SD) from n = 4 cultures based on cells pooled from several mice.
Ou Cao et al. Blood 2007;110:
©2007 by American Society of Hematology

4. Analyses of cell populations from lymphoid organs of DO11
Analyses of cell populations from lymphoid organs of DO11.10-tg RAG-2−/− mice by flow cytometry 60 days after AAV-EF1α-ova gene transfer.
Analyses of cell populations from lymphoid organs of DO11.10-tg RAG-2−/− mice by flow cytometry 60 days after AAV-EF1α-ova gene transfer. (A) Quantitation of CD25+ of TCR+CD4+, CD25+GITR+ and CD25+CTLA4+ of CD4+ cells from spleen in naive or vector-treated mice. Percentages of dual-positive cells (top-right quadrant) are indicated. Note that AAV-EF1α-ova–transduced mice showed substantial increase in CD25+, CD25+GITR+, and CD25+CTLA4+ of total CD4+ cells compared with control animals. Antibody stain was FITC-conjugated KJ1-26 or CD4, PE-conjugated GITR or CTLA4, and APC-conjugated CD25. Representative examples of FACS density plots are shown for individual samples of splenocytes from DO11.10-tg RAG-2−/− mice. Also graphed are percent GITR+ (B) and CTLA4+ (C) of CD4+CD25+ cells derived from spleen, thymus, portal nodes, and inguinal nodes 60 days after AAV-EF1α-ova gene delivery (B,C).
Ou Cao et al. Blood 2007;110:
©2007 by American Society of Hematology

5. Analyses of lymphocyte populations in DO11
Analyses of lymphocyte populations in DO11.10-tg RAG-2−/− mice as a function of time after administration of AAV-EF1α-ova.
Analyses of lymphocyte populations in DO11.10-tg RAG-2−/− mice as a function of time after administration of AAV-EF1α-ova. Examined tissues were spleens and thymus. Shown is the summary of percent CD25+ (A,D), CD25+GITR+ (B,E), and CD25+CTLA4+ (C,F) of total CD4+ cells derived from spleen or thymus. Note that more than 99% of CD4+ cells in these mice express ova-specific TCR DO11.10 and are therefore KJ Antibody staining was carried out using FITC-conjugated KJ1-26 or CD4, PE-conjugated GITR or CTLA4, APC-conjugated CD25. Results are average ± SD for n = 3 mice. Also shown is a summary of percent GITR+ (G,H), and CTLA4+ (I,J) of CD4+CD25+ cells from spleen (G,I) or thymus (H,J) as a function of time after vector administration.
Ou Cao et al. Blood 2007;110:
©2007 by American Society of Hematology

6. Plasma levels of IgG1 anti-hFIX 3 weeks after immunologic challenge by subcutaneous administration of 5 μg hFIX formulated in CFA in C57BL/6 mice that had received adoptive transfer of splenocytes from naive (white bars, controls) or vector-treated (hatched...
Plasma levels of IgG1 anti-hFIX 3 weeks after immunologic challenge by subcutaneous administration of 5 μg hFIX formulated in CFA in C57BL/6 mice that had received adoptive transfer of splenocytes from naive (white bars, controls) or vector-treated (hatched bars, AAV-FIX) C57BL/6 mice. Adoptive transfer was by tail vein injection 24 hours before challenge. Vector-treated mice had received hepatic gene transfer with 1011 vg/animal AAV-ApoE/hAAT-hFIX vector 6 weeks before the experiment. (A) Total splenocytes (5 × 107, bars 1-2), CD4+ T-cell–depleted splenocytes (5 × 107, bar 3), CD25+-depleted CD4+ T cells (9 × 106, bars 6, 8), MACS-purified CD4+ T cells (107, bars 4-5), or CD4+CD25+ cells (1 × 106, bars 7, 9) were transferred. Each bar is average antibody titer for 6 animals (± SD). *P < .05 compared with control splenocytes. **P < .01 compared with control CD4+ cells. ***P < .01 compared with CD4+CD25− cells or to control CD4+ cells. (B) CD4+GITR+ (bars 12-13) or CD4+GITR− splenocytes (bars 10-11) were transferred. Each bar is average antibody titer for 4 animals (± SD). *P < .05 compared with CD4+GITR− cells or to control CD4+GITR+ cells.
Ou Cao et al. Blood 2007;110:
©2007 by American Society of Hematology

7. Quantification of relative FoxP3 mRNA levels in CD4+ or CD4− T cells derived from naive control or AAV-ApoE/hAAT-hFIX gene-transferred C57BL/6 mice 60 days before the experiment.
Quantification of relative FoxP3 mRNA levels in CD4+ or CD4− T cells derived from naive control or AAV-ApoE/hAAT-hFIX gene-transferred C57BL/6 mice 60 days before the experiment. Some of control or gene-transduced animals were challenged by subcutaneous administration of 5 μg hFIX formulated in CFA 5 days prior to PCR analysis. cDNA samples were subjected to real-time quantitative PCR analyses using primers and an internal fluorescent probe specific for FoxP3 or HPRT. The relative quantity of FoxP3 in each sample was normalized to the relative quantity of HPRT. FoxP3 transcript levels in naive CD4+ cells are reported as 100%. Results were shown as average ± SD (n = 3 per group). *P < .05 compared with other experimental groups.
Ou Cao et al. Blood 2007;110:
©2007 by American Society of Hematology

8. Depletion of CD4+CD25+ cells in C57BL/6 mice after gene transfer with AAV-ApoE/hAAT-hFIX vector.
Depletion of CD4+CD25+ cells in C57BL/6 mice after gene transfer with AAV-ApoE/hAAT-hFIX vector. Shown are plasma levels of IgG anti-hFIX as a function of time after vector administration. Animals were injected intraperitoneally with either rat IgG1 (A, isotype control) or rat antimouse CD25 monoclonal antibody PC61 (B) every 2 weeks (up to week 6) starting on the day of liver-directed gene transfer (asterisk). Mice were challenged with 5 μg hFIX formulated in CFA at week 6. (C) Analyses of peripheral blood lymphocytes by flow cytometry showed depletion of CD4+CD25+ cells after repetitive anti-CD25 injection in C57BL/6 mice. Antibody staining was carried out using FITC-conjugated anti-CD4 and anti–PE-conjugated CD25.
Ou Cao et al. Blood 2007;110:
©2007 by American Society of Hematology