Radioimmunotherapy of human colon carcinoma xenografts using a 213Bi-labeled domain-deleted humanized monoclonal antibody.
暂无分享,去创建一个
L. Chappell | M. Brechbiel | P. Albert | J. Schlom | E. Dadachova | D. Milenic | K. Garmestani | D. Hill
[1] J. Schlom,et al. A novel monoclonal antibody design for radioimmunotherapy. , 2003, Cancer biotherapy & radiopharmaceuticals.
[2] S. Adelstein,et al. Bystander effect produced by radiolabeled tumor cells in vivo , 2002, Proceedings of the National Academy of Sciences of the United States of America.
[3] J. Humm,et al. Targeted α particle immunotherapy for myeloid leukemia , 2002 .
[4] T. Waldmann,et al. Pretargeting radioimmunotherapy of a murine model of adult T-cell leukemia with the alpha-emitting radionuclide, bismuth 213. , 2002, Blood.
[5] T. Waldmann,et al. Vascular-Targeted Radioimmunotherapy with the Alpha-Particle Emitter 211At , 2002, Radiation research.
[6] L. Chappell,et al. In vivo comparison of macrocyclic and acyclic ligands for radiolabeling of monoclonal antibodies with 177Lu for radioimmunotherapeutic applications. , 2002, Nuclear medicine and biology.
[7] D. Goldenberg. The role of radiolabeled antibodies in the treatment of non-Hodgkin's lymphoma: the coming of age of radioimmunotherapy. , 2001, Critical reviews in oncology/hematology.
[8] M. Brechbiel,et al. The development of the alpha-particle emitting radionuclides 212Bi and 213Bi, and their decay chain related radionuclides, for therapeutic applications. , 2001, Chemical reviews.
[9] E. Kremmer,et al. Highly specific tumor binding of a 213Bi-labeled monoclonal antibody against mutant E-cadherin suggests its usefulness for locoregional alpha-radioimmunotherapy of diffuse-type gastric cancer. , 2001, Cancer research.
[10] S. Mirzadeh,et al. In vivo evaluation of bismuth-labeled monoclonal antibody comparing DTPA-derived bifunctional chelates. , 2001, Cancer biotherapy & radiopharmaceuticals.
[11] C. Cordon-Cardo,et al. An α-Particle Emitting Antibody ([213Bi]J591) for Radioimmunotherapy of Prostate Cancer , 2000 .
[12] L. Chappell,et al. Delivery of the alpha-emitting radioisotope bismuth-213 to solid tumors via single-chain Fv and diabody molecules. , 2000, Nuclear medicine and biology.
[13] D. Milenic. Radioimmunotherapy: designer molecules to potentiate effective therapy. , 2000, Seminars in radiation oncology.
[14] R. Meredith,et al. Clinical radioimmunotherapy. , 2000, Seminars in radiation oncology.
[15] T. Back,et al. Radioimmunotherapy of nude mice with intraperitoneally growing ovarian cancer xenograft utilizing 211At-labelled monoclonal antibody MOv18. , 2000, Anticancer research.
[16] Y. Erdi,et al. Pharmacokinetics and dosimetry of an alpha-particle emitter labeled antibody: 213Bi-HuM195 (anti-CD33) in patients with leukemia. , 1999, Journal of nuclear medicine : official publication, Society of Nuclear Medicine.
[17] D. Scheinberg,et al. Alpha-emitting bismuth cyclohexylbenzyl DTPA constructs of recombinant humanized anti-CD33 antibodies: pharmacokinetics, bioactivity, toxicity and chemistry. , 1999, Journal of nuclear medicine : official publication, Society of Nuclear Medicine.
[18] I. Pastan,et al. Aminosyn II effectively blocks renal uptake of 18F-labeled anti-tac disulfide-stabilized Fv. , 1998, Cancer research.
[19] S. Kennel,et al. Vascular targeted radioimmunotherapy with 213Bi-An α-particle emitter , 1998 .
[20] P. Hand,et al. A CDR-grafted (humanized) domain-deleted antitumor antibody. , 1997, Cancer biotherapy & radiopharmaceuticals.
[21] M. Brechbiel,et al. An Improved Generator for the Production of 213Bi from 225Ac , 1997 .
[22] R. Levy,et al. Yttrium-90-labeled anti-CD20 monoclonal antibody therapy of recurrent B-cell lymphoma. , 1996, Clinical cancer research : an official journal of the American Association for Cancer Research.
[23] D. Bigner,et al. Radioimmunotherapy with α-Particle Emitting Radioimmunoconjugates , 1996 .
[24] N. Kotite,et al. Lysine reduces renal accumulation of radioactivity associated with injection of the [177Lu]alpha-[2-(4-aminophenyl) ethyl]-1,4,7,10-tetraaza-cyclodecane-1,4,7,10-tetraacetic acid-CC49 Fab radioimmunoconjugate. , 1995, Cancer research.
[25] Wendy S. Becker,et al. Reduction of the renal uptake of radiolabeled monoclonal antibody fragments by cationic amino acids and their derivatives. , 1995, Cancer research.
[26] T. Waldmann,et al. Radioimmunotherapy of Nude Mice Bearing a Human Interleukin 2 Receptor α-expressing Lymphoma Utilizing the α-emitting Radionuclide-conjugated Monoclonal Antibody 212Bi-anti-Tac , 1994 .
[27] T. Yokota,et al. Microautoradiographic analysis of the normal organ distribution of radioiodinated single-chain Fv and other immunoglobulin forms. , 1993, Cancer research.
[28] P. Thorpe,et al. Targeting the vasculature of solid tumors , 1993 .
[29] T. Yokota,et al. Differential metabolic patterns of iodinated versus radiometal chelated anticarcinoma single-chain Fv molecules. , 1992, Cancer research.
[30] M. Brechbiel,et al. Effective α-Particle-mediated Radioimmunotherapy of Murine Leukemia , 1992 .
[31] M. Brechbiel,et al. Spectrophotometric method for the determination of a bifunctional DTPA ligand in DTPA-monoclonal antibody conjugates. , 1992, Bioconjugate chemistry.
[32] T. Yokota,et al. Rapid tumor penetration of a single-chain Fv and comparison with other immunoglobulin forms. , 1992, Cancer research.
[33] M. Brechbiel,et al. Synthesis of C-functionalized trans-cyclohexyldiethylenetriaminepenta-acetic acids for labelling of monoclonal antibodies with the bismuth-212 α-particle emitter , 1992 .
[34] T. Yokota,et al. Construction, binding properties, metabolism, and tumor targeting of a single-chain Fv derived from the pancarcinoma monoclonal antibody CC49. , 1991, Cancer research.
[35] S. Larson. Choosing the right radionuclide and antibody for intraperitoneal radioimmunotherapy. , 1991, Journal of the National Cancer Institute.
[36] K. Johnson,et al. Combined immunohistochemical and autoradiographic analyses of antigen/antibody interactions in tumor xenograft models. , 1991, Laboratory investigation; a journal of technical methods and pathology.
[37] J. Schlom,et al. Monoclonal antibody-based therapy of a human tumor xenograft with a 177lutetium-labeled immunoconjugate. , 1991, Cancer research.
[38] S. Mirzadeh,et al. Improved in vivo stability and tumor targeting of bismuth-labeled antibody. , 1990, Cancer research.
[39] M. Brechbiel,et al. 212Bismuth linked to an antipancreatic carcinoma antibody: model for alpha-particle-emitter radioimmunotherapy. , 1988, Journal of the National Cancer Institute.
[40] J L Humm,et al. Dosimetric aspects of radiolabeled antibodies for tumor therapy. , 1986, Journal of nuclear medicine : official publication, Society of Nuclear Medicine.
[41] M A Markwell,et al. A new solid-state reagent to iodinate proteins. I. Conditions for the efficient labeling of antiserum. , 1982, Analytical biochemistry.
[42] P. Fraker,et al. Protein and cell membrane iodinations with a sparingly soluble chloroamide, 1,3,4,6-tetrachloro-3a,6a-diphrenylglycoluril. , 1978, Biochemical and biophysical research communications.