E
Elizabeth J. Read
Researcher at National Institutes of Health
Publications - 92
Citations - 8364
Elizabeth J. Read is an academic researcher from National Institutes of Health. The author has contributed to research in topics: Transplantation & Lymphocyte. The author has an hindex of 41, co-authored 92 publications receiving 8153 citations. Previous affiliations of Elizabeth J. Read include University of Basel & University of Texas Southwestern Medical Center.
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Journal ArticleDOI
Regression of metastatic renal-cell carcinoma after nonmyeloablative allogeneic peripheral-blood stem-cell transplantation.
Richard W. Childs,Chernoff A,N. Contentin,E. Bahceci,Schrump D,Susan F. Leitman,Elizabeth J. Read,John F. Tisdale,Cynthia E. Dunbar,Linehan Wm,Neal S. Young,Austin John Barrett +11 more
TL;DR: Nonmyeloablative allogeneic stem-cell transplantation can induce sustained regression of metastatic renal-cell carcinoma in patients who have had no response to conventional immunotherapy, consistent with a graft-versus-tumor effect.
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Engraftment kinetics after nonmyeloablative allogeneic peripheral blood stem cell transplantation: full donor T-cell chimerism precedes alloimmune responses.
Richard W. Childs,Emmanuel Clave,N. Contentin,D. Jayasekera,Nancy F. Hensel,Susan F. Leitman,Elizabeth J. Read,Corey A. Carter,E. Bahceci,Neal S. Young,Austin John Barrett +10 more
TL;DR: The results emphasize the importance of lineage-specific chimerism analysis to successfully manipulate engraftment after nonmyeloablative allogeneic PBSC transplantation.
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Efficient magnetic cell labeling with protamine sulfate complexed to ferumoxides for cellular MRI.
Ali S. Arbab,Gene T. Yocum,Heather Kalish,Elaine K. Jordan,Stasia A. Anderson,Aarif Y. Khakoo,Elizabeth J. Read,Joseph A. Frank +7 more
TL;DR: In this article, the authors evaluated the efficiency and toxicity of labeling mammalian cells using two commercially available Food and Drug Administration (FDA)-approved agents, ferumoxides, a suspension of dextran-coated SPIO used as an MRI contrast agent, and protamine sulfate, conventionally used to reverse heparin anticoagulation but also used ex vivo as a cationic transfection agent.
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Lymphopenia and interleukin-2 therapy alter homeostasis of CD4+CD25+ regulatory T cells
Hua Zhang,Kevin S. Chua,Martin Guimond,Veena Kapoor,Margaret V. Brown,Thomas A. Fleisher,Lauren M. Long,Donna Bernstein,Brenna J. Hill,Daniel C. Douek,Jay A. Berzofsky,Charles S. Carter,Elizabeth J. Read,Lee J. Helman,Crystal L. Mackall +14 more
TL;DR: It is suggested that IL-2 and lymphopenia are primary modulators of CD4+CD25+ Treg cell homeostasis, and Treg cells generated byIL-2 therapy expressed similar levels of FOXP3 and had similar potency for suppression compared to T Reg cells present in normal hosts.
Journal ArticleDOI
Prolonged production of NADPH oxidase-corrected granulocytes after gene therapy of chronic granulomatous disease
Harry L. Malech,Phillip B. Maples,Narda L. Whiting-Theobald,Gilda F. Linton,Sudhir Sekhsaria,Sarah J. Vowells,Fei Li,Judi A. Miller,Ellen S. DeCarlo,Steven M. Holland,Susan F. Leitman,Charles S. Carter,Robert E. Butz,Elizabeth J. Read,Thomas A. Fleisher,Richard Schneiderman,Dennis E. Van Epps,S. Kaye Spratt,Christopher A. Maack,Joseph Rokovich,Lawrence K. Cohen,John I. Gallin +21 more
TL;DR: This trial piloted the use of animal protein-free medium and a blood-bank-compatible closed system of gas-permeable plastic containers for culture and transduction of the PBSCs and found that these features enhance the safety of PBSCs directed gene therapy.