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Journal Articles

Mobilized Mouse and Human Peripheral Blood Containing Elevated Numbers of Donor Treg Cells Ameliorates Pre-Clinical GvHD and GVL Is Maintained in an MHC-Matched Allogeneic Murine Model

Henry Barreras, Jr., Sabrina N. Copsel, Ying Ding, Charles J. Cash, Cameron S. Bader, Cara L. Benjamin, Krishna V. Komanduri, Thomas R. Malek, Robert B. Levy

Blood (2021) 138 (Supplement 1): 2767.

https://doi.org/10.1182/blood-2021-153092

Published: 2021

Journal Articles

Heat shock protein vaccination and directed IL-2 therapy amplify tumor immunity rapidly following bone marrow transplantation in mice

Robert G. Newman, Michael J. Dee, Thomas R. Malek, Eckhard R. Podack, Robert B. Levy

Blood (2014) 123 (19): 3045–3055.

https://doi.org/10.1182/blood-2013-08-520775

Published: 2014

Includes: Supplemental data

Journal Articles

Allogeneic T regulatory cell–mediated transplantation tolerance in adoptive therapy depends on dominant peripheral suppression and central tolerance

Dennis Adeegbe, Robert B. Levy, Thomas R. Malek

Blood (2010) 115 (10): 1932–1940.

https://doi.org/10.1182/blood-2009-08-238584

Published: 2010

Journal Articles

Host CD4 + CD25 + T cells can expand and comprise a major component of the Treg compartment after experimental HCT

Allison L. Bayer, Monica Jones, Jackeline Chirinos, Lesley de Armas, Taylor H. Schreiber, Thomas R. Malek, Robert B. Levy

Blood (2009) 113 (3): 733–743.

https://doi.org/10.1182/blood-2008-08-173179

Published: 2009

Includes: Supplemental data

Journal Articles

Cytolytically Defective Tregs Can Prevent Spontaneous Autoimmune Disease and Gvhd, but Fail to Suppress Autochthonous Lymphoproliferation

Jackeline Gabriela Chirinos, Dennis Adeegbe, PhD, Monica Jones, Maite Urbieta, Thomas R. Malek, PhD, Robert B. Levy, PhD

Blood (2008) 112 (11): 3518.

https://doi.org/10.1182/blood.V112.11.3518.3518

Published: 2008

Journal Articles

Surviving Host CD4 + CD25 + Foxp3 + Cells Following Ablative Conditioning Expand and Comprise the Major Component of the Treg Compartment during the Lymphoid Reconstitution Period Following HCT.

Allison L. Bayer, PhD, Monica Jones, Maite Urbieta, BS, Jackeline Chirinos, Taylor Schreiber, BS, Leslie De Armas, BS, Thomas R. Malek, PhD, Robert B. Levy, PhD

Blood (2007) 110 (11): 65.

https://doi.org/10.1182/blood.V110.11.65.65

Published: 2007

Journal Articles

IL-7: a limited resource during thymopoiesis

Thomas R. Malek

Blood (2004) 104 (13): 3842.

https://doi.org/10.1182/blood-2004-09-3656

Published: 2004

NARROW

Mobilized Mouse and Human Peripheral Blood Containing Elevated Numbers of Donor Treg Cells Ameliorates Pre-Clinical GvHD and GVL Is Maintained in an MHC-Matched Allogeneic Murine Model

Heat shock protein vaccination and directed IL-2 therapy amplify tumor immunity rapidly following bone marrow transplantation in mice

Allogeneic T regulatory cell–mediated transplantation tolerance in adoptive therapy depends on dominant peripheral suppression and central tolerance

Host CD4 + CD25 + T cells can expand and comprise a major component of the Treg compartment after experimental HCT

Cytolytically Defective Tregs Can Prevent Spontaneous Autoimmune Disease and Gvhd, but Fail to Suppress Autochthonous Lymphoproliferation

Surviving Host CD4 + CD25 + Foxp3 + Cells Following Ablative Conditioning Expand and Comprise the Major Component of the Treg Compartment during the Lymphoid Reconstitution Period Following HCT.

IL-7: a limited resource during thymopoiesis

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ASH Publications

American Society of Hematology

Mobilized Mouse and Human Peripheral Blood Containing Elevated Numbers of Donor Treg Cells Ameliorates Pre-Clinical GvHD and GVL Is Maintained in an MHC-Matched Allogeneic Murine Model

Heat shock protein vaccination and directed IL-2 therapy amplify tumor immunity rapidly following bone marrow transplantation in mice

Allogeneic T regulatory cell–mediated transplantation tolerance in adoptive therapy depends on dominant peripheral suppression and central tolerance

Host CD4 + CD25 + T cells can expand and comprise a major component of the Treg compartment after experimental HCT

Cytolytically Defective Tregs Can Prevent Spontaneous Autoimmune Disease and Gvhd, but Fail to Suppress Autochthonous Lymphoproliferation

Surviving Host CD4 + CD25 + Foxp3 + Cells Following Ablative Conditioning Expand and Comprise the Major Component of the Treg Compartment during the Lymphoid Reconstitution Period Following HCT.

IL-7: a limited resource during thymopoiesis

Email alerts

ASH Publications

American Society of Hematology

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