Mild preconditioning and low-level engraftment confer methotrexate resistance in mice transplanted with marrow expressing drug-resistant dihydrofolate.

Slides:



Advertisements
Similar presentations
Erik Ames, Salif Harouna, Colin Meyer, Lisbeth A. Welniak, William J
Advertisements

Respiration 2012;83:74–80 - DOI: /
A conditional knockout mouse model reveals endothelial cells as the principal and possibly exclusive source of plasma factor VIII by Scot A. Fahs, Matthew.
Lentiviral gene transfer and ex vivo expansion of human primitive stem cells capable of primary, secondary, and tertiary multilineage repopulation in NOD/SCID.
Combination therapy for adult T-cell leukemia–xenografted mice: flavopiridol and anti-CD25 monoclonal antibody by Meili Zhang, Zhuo Zhang, Carolyn K. Goldman,
Host-Derived CD8+ Dendritic Cells Protect Against Acute Graft-versus-Host Disease after Experimental Allogeneic Bone Marrow Transplantation  Michael Weber,
Volume 4, Issue 6, Pages (June 2009)
Expression of Chemokines in GVHD Target Organs Is Influenced by Conditioning and Genetic Factors and Amplified by GVHR  Markus Y. Mapara, Corinna Leng,
by David Traver, Alissa Winzeler, Howard M. Stern, Elizabeth A
IL-2–Targeted Therapy Ameliorates the Severity of Graft-versus-Host Disease: Ex Vivo Selective Depletion of Host-Reactive T Cells and In Vivo Therapy 
Identification of Stem Cell Transcriptional Programs Normally Expressed in Embryonic and Neural Stem Cells in Alloreactive CD8+ T Cells Mediating Graft-versus-Host.
A New Strategy for Treatment of Autoimmune Diseases in Chimeric Resistant MRL/lpr Mice by Kenji Takeuchi, Muneo Inaba, Shigeo Miyashima, Ryokei Ogawa,
Homing efficiency, cell cycle kinetics, and survival of quiescent and cycling human CD34+ cells transplanted into conditioned NOD/SCID recipients by Anna.
by Neil P. Rodrigues, Viktor Janzen, Randolf Forkert, David M
Apoptotic Donor Leukocytes Limit Mixed-Chimerism Induced by CD40-CD154 Blockade in Allogeneic Bone Marrow Transplantation  Jian-ming Li, John Gorechlad,
Revealing lymphoma growth and the efficacy of immune cell therapies using in vivo bioluminescence imaging by Matthias Edinger, Yu-An Cao, Michael R. Verneris,
Induction of heme oxygenase-1 before conditioning results in improved survival and reduced graft-versus-host disease after experimental allogeneic bone.
Novel function for interleukin-7 in dendritic cell development
Globin Gene Expression Is Reprogrammed in Chimeras Generated by Injecting Adult Hematopoietic Stem Cells into Mouse Blastocysts  Hartmut Geiger, Stefanie.
LBH589 Enhances T Cell Activation In Vivo and Accelerates Graft-versus-Host Disease in Mice  Dapeng Wang, Cristina Iclozan, Chen Liu, Changqing Xia, Claudio.
Jacob Andrade, Shundi Ge, Goar Symbatyan, Michael S. Rosol, Arthur J
Simple conditioning with monospecific CD4+CD25+ regulatory T cells for bone marrow engraftment and tolerance to multiple gene products by David-Alexandre.
by Hyung-Gyoon Kim, Kyoko Kojima, C. Scott Swindle, Claudiu V
The role of apoptosis in the development of AGM hematopoietic stem cells revealed by Bcl-2 overexpression by Claudia Orelio, Kirsty N. Harvey, Colin Miles,
Definitive Hematopoiesis Is Autonomously Initiated by the AGM Region
Lack of the adhesion molecules P-selectin and intercellular adhesion molecule-1 accelerate the development of BCR/ABL-induced chronic myeloid leukemia-like.
Low c-Kit Expression Level Induced by Stem Cell Factor Does Not Compromise Transplantation of Hematopoietic Stem Cells  Chia-Ling Chen, Katerina Faltusova,
IL-17 Gene Ablation Does Not Impact Treg-Mediated Suppression of Graft-Versus-Host Disease after Bone Marrow Transplantation  Lucrezia Colonna, Mareike.
by Oleg I. Krijanovski, Geoffrey R. Hill, Kenneth R
Graft-Versus-Leukemia Effect and Graft-Versus-Host Disease Can Be Differentiated by Cytotoxic Mechanisms in a Murine Model of Allogeneic Bone Marrow Transplantation.
Volume 10, Issue 3, Pages (September 2004)
Expression of connexin 43 (Cx43) is critical for normal hematopoiesis
Vaccination regimens incorporating CpG-containing oligodeoxynucleotides and IL-2 generate antigen-specific antitumor immunity from T-cell populations undergoing.
In vivo responses of AMLMLL to ATRi.
Pharmacologic Expansion of Donor-Derived, Naturally Occurring CD4+Foxp3+ Regulatory T Cells Reduces Acute Graft-versus-Host Disease Lethality Without.
Distinct classes of c-Kit–activating mutations differ in their ability to promote RUNX1-ETO–associated acute myeloid leukemia by Heidi J. Nick, Hyung-Gyoon.
Jacob Andrade, Shundi Ge, Goar Symbatyan, Michael S. Rosol, Arthur J
Treatment of SFTSV-infected IFNAR−/− mice with T-705 or ribavirin.
FTY720 Markedly Increases Alloengraftment but Does Not Eliminate Host Anti-Donor T Cells that Cause Graft Rejection on Its Withdrawal  Patricia A. Taylor,
Fig. 8. In vivo suppression of MM by CMLD
Quiz Page July 2009 American Journal of Kidney Diseases
Lentiviral-mediated RNAi inhibition of Sbds in murine hematopoietic progenitors impairs their hematopoietic potential by Amy S. Rawls, Alyssa D. Gregory,
Double Haploidentical Hematopoietic Stem Cell Transplantation Results in Successful Engraftment of Bone Marrow from Both Donors without Graft-versus-Host.
Survival and Function of MiHA Epitope-Specific Host CD8 TM Cells Following Ablative Conditioning and HCT  Alwi M. Shatry, Derry C. Roopenian, Robert B.
Essential Role of Interleukin-12/23p40 in the Development of Graft-versus-Host Disease in Mice  Yongxia Wu, David Bastian, Steven Schutt, Hung Nguyen,
T Cell and B Cell Immunity can be Reconstituted with Mismatched Hematopoietic Stem Cell Transplantation Without Alkylator Therapy in Artemis-Deficient.
PRO 140 Monoclonal Antibody to CCR5 Prevents Acute Xenogeneic Graft-versus-Host Disease in NOD-scid IL-2Rynull Mice  Denis R. Burger, Yvonne Parker, Kathryn.
Effector Cells Derived from Host CD8 Memory T Cells Mediate Rapid Resistance against Minor Histocompatibility Antigen-Mismatched Allogeneic Marrow Grafts.
A Radio-Resistant Perforin-Expressing Lymphoid Population Controls Allogeneic T Cell Engraftment, Activation, and Onset of Graft-versus-Host Disease in.
Dynamic Change and Impact of Myeloid-Derived Suppressor Cells in Allogeneic Bone Marrow Transplantation in Mice  Dapeng Wang, Yu Yu, Kelley Haarberg,
FGF-2 signaling mediates expansion of HSPCs
A CD4 Domain 1 CC′ Loop Peptide Analogue Enhances Engraftment in a Murine Model of Bone Marrow Transplantation with Sublethal Conditioning  Gabor Varadi,
VAY-736 combines effectively with ibrutinib in vivo.
In Situ Activation and Expansion of Host Tregs: A New Approach to Enhance Donor Chimerism and Stable Engraftment in Major Histocompatibility Complex-Matched.
Volume 9, Issue 1, Pages (July 2011)
Volume 6, Issue 1, Pages (July 2002)
Volume 3, Issue 1, Pages (January 2001)
Brile Chung, Eric Dudl, Akira Toyama, Lora Barsky, Kenneth I. Weinberg 
Early Vaccination with Tumor Lysate-Pulsed Dendritic Cells after Allogeneic Bone Marrow Transplantation Has Antitumor Effects  Jeffrey S. Moyer, Gabriel.
Lack of correlation between an assay used to determine early marrow allograft rejection and long-term chimerism after murine allogeneic bone marrow transplantation:
Hematopoietic Dysfunction in a Mouse Model for Fanconi Anemia Group D1
CAR T‐cell generation in human PBMC‐transplanted mice
The fatal anemia is induced by an Apc-haploinsufficient BM microenvironment (A) Kaplan-Meier survival curve of Apcfl/+ (WT) or Apcdel/+ recipients transplanted.
Pharmacological Immunosuppression Reduces But Does Not Eliminate the Need for Total-Body Irradiation in Nonmyeloablative Conditioning Regimens for Hematopoietic.
Repifermin (keratinocyte growth factor-2) reduces the severity of graft-versus-host disease while preserving a graft-versus-leukemia effect  Shawn G Clouthier,
Volume 2, Issue 3, Pages (March 2008)
All Hematopoietic Stem Cells Engraft in Submyeloablatively Irradiated Mice  Katarina Forgacova, Filipp Savvulidi, Ludek Sefc, Jana Linhartova, Emanuel.
Selective elimination of alloreactive donor T cells attenuates graft-versus-host disease and enhances T-cell reconstitution  Maria Gendelman, Maryam Yassai,
TH-302 has antileukemia activity in an in vivo primary AML xenograft murine model. TH-302 has antileukemia activity in an in vivo primary AML xenograft.
Optimal Donor Selection: Beyond HLA
Presentation transcript:

Mild preconditioning and low-level engraftment confer methotrexate resistance in mice transplanted with marrow expressing drug-resistant dihydrofolate reductase activity by Rohaizah I. James, Christopher A. Warlick, Miechaleen D. Diers, Roland Gunther, and R. Scott McIvor Blood Volume 96(4):1334-1341 August 15, 2000 ©2000 by American Society of Hematology

Methotrexate resistance of sublethally irradiated mice transplanted with DHFR transgenic marrow.Normal male mice were given 1, 2, or 4 Gy TBI one day before they underwent transplantation with 1 × 107 marrow cells from female line 04 (Tg04) DHFR transgenic ... Methotrexate resistance of sublethally irradiated mice transplanted with DHFR transgenic marrow.Normal male mice were given 1, 2, or 4 Gy TBI one day before they underwent transplantation with 1 × 107 marrow cells from female line 04 (Tg04) DHFR transgenic donors. They were then administered either PBS or MTX (up to 4 mg/kg) daily for 60 days (n = 10 for each group). (A) Kaplan–Meier plot showing the fraction of surviving mice per time in the MTX- administered groups. (B) Mean weekly hematocrit of surviving mice in the MTX-administered groups at each time point. Rohaizah I. James et al. Blood 2000;96:1334-1341 ©2000 by American Society of Hematology

TBI dose-dependent engraftment of transgenic marrow cells in sublethally irradiated BMT recipients.Survivors from Figure 1 were killed 120 days after transplantation. TBI dose-dependent engraftment of transgenic marrow cells in sublethally irradiated BMT recipients.Survivors from Figure 1 were killed 120 days after transplantation. Genomic DNA was isolated from bone marrow and spleen and subjected to quantitative Southern analysis as described in “Materials and Methods” (see Figure 4A for an example of the Southern hybridization signals used to quantitate DHFR transgenic cell engraftment levels). Values are presented as mean ± SD of between 5 and 9 samples. Results of statistical analyses between PBS- and MTX-administered animals are given as P values, displayed above each pair of groups. Rohaizah I. James et al. Blood 2000;96:1334-1341 ©2000 by American Society of Hematology

Methotrexate resistance of mice preconditioned with 1 Gy TBI and transplanted with line 04 DHFR transgenic marrow.Male mice were given 1 Gy TBI one day before transplantation with no marrow, 1 × 107 female normal (APP) marrow cells, or 1 × 107 female transg... Methotrexate resistance of mice preconditioned with 1 Gy TBI and transplanted with line 04 DHFR transgenic marrow.Male mice were given 1 Gy TBI one day before transplantation with no marrow, 1 × 107 female normal (APP) marrow cells, or 1 × 107 female transgenic DHFR (Tg04) marrow cells. The animals were then administered either PBS or MTX (final dose of 4 mg/kg) intraperitoneally daily for 60 days (n = 10 for each group). (A) Kaplan–Meier plot showing the fraction of surviving mice per time in the MTX-administered groups. (B) Mean weekly hematocrit of surviving mice in the MTX-administered groups at each time point. Rohaizah I. James et al. Blood 2000;96:1334-1341 ©2000 by American Society of Hematology

Engraftment of donor-derived cells in bone marrow and spleen of primary BMT recipients preconditioned with 1 Gy TBI.Surviving animals (depicted in Figure 3) were killed 120 days after transplantation. Engraftment of donor-derived cells in bone marrow and spleen of primary BMT recipients preconditioned with 1 Gy TBI.Surviving animals (depicted in Figure 3) were killed 120 days after transplantation. Genomic DNA samples isolated from bone marrow and spleen were subjected to quantitative Southern analysis as described in “Materials and methods.” (A) Representative Southern image of selected spleen samples. A DHFR probe was used to quantitate total DNA (En DHFR) and donor-derived DHFR transgenic DNA (Tg04 DHFR). An APP probe was used to quantitate donor-derived normal cells (APP), and a Y probe was used to quantitate the percentage of host cells (Y). (B) Levels of engrafted donor-derived cells. Signals from the Southern image were quantified using a PhosphorImager. Ratios of APP/En DHFR and Tg DHFR/En DHFR were used to calculate the percentage of donor-derived normal and Tg04 cells, respectively, from a standard curve. Values are presented as mean ± SD of 5 to 9 samples. Rohaizah I. James et al. Blood 2000;96:1334-1341 ©2000 by American Society of Hematology

Methotrexate resistance of mice transplanted with varying amounts of line 04 DHFR transgenic marrow cells.Normal male mice were given 1 Gy TBI the day before transplantation with 1 × 106, 5 × 106, or 1 × 107 marrow cells from female line 04 donors (as indic... Methotrexate resistance of mice transplanted with varying amounts of line 04 DHFR transgenic marrow cells.Normal male mice were given 1 Gy TBI the day before transplantation with 1 × 106, 5 × 106, or 1 × 107 marrow cells from female line 04 donors (as indicated). MTX was then administered at increasing doses (culminating at 4 mg/kg) daily for 60 days (n = 10 for each group). (A) Kaplan-Meier plot showing fraction of surviving mice. (B) Mean weekly hematocrit of surviving mice at each time point. Rohaizah I. James et al. Blood 2000;96:1334-1341 ©2000 by American Society of Hematology

Dose-dependent engraftment of transgenic marrow cells in sublethally irradiated BMT recipients.Survivors from the experiment described in Figure 5 were killed 120 days after transplantation. Dose-dependent engraftment of transgenic marrow cells in sublethally irradiated BMT recipients.Survivors from the experiment described in Figure 5 were killed 120 days after transplantation. Genomic DNA was isolated from bone marrow and spleen, subjecting samples to quantitative Southern analysis as described in Figure 4. Values are presented as mean ± SD of 6 to 8 samples. Rohaizah I. James et al. Blood 2000;96:1334-1341 ©2000 by American Society of Hematology