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1.
Nat Med ; 8(8): 801-7, 2002 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-12101408

RESUMEN

The Human Combinatorial Antibody Library (HuCAL) was screened for antibodies specific to human leukocyte antigen-DR (HLA-DR) that induce programmed death of lymphoma/leukemia cells expressing the target antigen. The active Fab fragments were affinity-matured, and engineered to IgG(4) antibodies of sub-nanomolar affinity. The antibodies exhibited potent in vitro tumoricidal activity on several lymphoma and leukemia cell lines and on chronic lymphocytic leukemia patient samples. They were also active in vivo in xenograft models of non-Hodgkin lymphoma. Cell death occurred rapidly, without the need for exogenous immunological effector mechanisms, and was selective to activated/tumor-transformed cells. Although the expression of HLA-DR on normal hematopoietic cells is a potential safety concern, the antibodies caused no long-lasting hematological toxicity in primates, in vivo. Such monoclonal antibodies offer the potential for a novel therapeutic approach to lymphoid malignancies.


Asunto(s)
Anticuerpos Monoclonales/inmunología , Antineoplásicos/inmunología , Apoptosis , Antígenos HLA-DR/inmunología , Linfoma/patología , Animales , Anticuerpos Monoclonales/genética , Anticuerpos Monoclonales/uso terapéutico , Afinidad de Anticuerpos , Antineoplásicos/metabolismo , Antígenos HLA-DR/metabolismo , Humanos , Fragmentos Fab de Inmunoglobulinas/genética , Fragmentos Fab de Inmunoglobulinas/inmunología , Fragmentos Fab de Inmunoglobulinas/metabolismo , Inmunoglobulina G/genética , Inmunoglobulina G/inmunología , Inmunoglobulina G/metabolismo , Inmunoterapia , Linfocitos/inmunología , Linfocitos/metabolismo , Linfoma/fisiopatología , Macaca fascicularis , Ratones , Unión Proteica , Proteínas Recombinantes de Fusión/inmunología , Proteínas Recombinantes de Fusión/metabolismo , Células Tumorales Cultivadas
2.
J Biol Chem ; 278(40): 38194-205, 2003 Oct 03.
Artículo en Inglés | MEDLINE | ID: mdl-12842902

RESUMEN

The human combinatorial antibody library Fab 1 (HuCAL-Fab 1) was generated by transferring the heavy and light chain variable regions from the previously constructed single-chain Fv library (Knappik, A., Ge, L., Honegger, A., Pack, P., Fischer, M., Wellnhofer, G., Hoess, A., Wölle, J., Plückthun, A., and Virnekäs, B. (2000) J. Mol. Biol. 296, 57-86), diversified in both complementarity-determining regions 3 into a novel Fab display vector, yielding 2.1 x 10(10) different antibody fragments. The modularity has been retained in the Fab display and screening plasmids, ensuring rapid conversion into various antibody formats as well as antibody optimization using prebuilt maturation cassettes. HuCAL-Fab 1 was challenged against the human fibroblast growth factor receptor 3, a potential therapeutic antibody target, against which, to the best of our knowledge, no functional antibodies could be generated so far. A unique screening mode was designed utilizing recombinant functional proteins and cell lines differentially expressing fibroblast growth factor receptor isoforms diversified in expression and receptor dependence. Specific Fab fragments with subnanomolar affinities were isolated by selection without any maturation steps as determined by fluorescence flow cytometry. Some of the selected Fab fragments completely inhibit target-mediated cell proliferation, rendering them the first monoclonal antibodies against fibroblast growth factor receptors having significant function blocking activity. This study validates HuCAL-Fab 1 as a valuable source for the generation of target-specific antibodies for therapeutic applications.


Asunto(s)
Fragmentos Fab de Inmunoglobulinas/química , Fragmentos de Inmunoglobulinas/química , Biblioteca de Péptidos , Proteínas Tirosina Quinasas , Receptores de Factores de Crecimiento de Fibroblastos/química , Animales , Anticuerpos , Anticuerpos Monoclonales/química , Unión Competitiva , División Celular , Línea Celular , Separación Celular , Clonación Molecular , Disulfuros , Relación Dosis-Respuesta a Droga , Ensayo de Inmunoadsorción Enzimática , Epítopos , Escherichia coli/metabolismo , Citometría de Flujo , Biblioteca de Genes , Vectores Genéticos , Humanos , Cadenas Pesadas de Inmunoglobulina/química , Cadenas Ligeras de Inmunoglobulina/química , Región Variable de Inmunoglobulina/química , Concentración 50 Inhibidora , Cinética , Ligandos , Ratones , Plásmidos/metabolismo , Unión Proteica , Isoformas de Proteínas , Receptor Tipo 3 de Factor de Crecimiento de Fibroblastos , Proteínas Recombinantes de Fusión/metabolismo , Proteínas Recombinantes/química , Proteínas Recombinantes/metabolismo , Resonancia por Plasmón de Superficie , Temperatura , Factores de Tiempo
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