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J Med Primatol ; 23(5): 285-97, 1994 Jul.
Article in English | MEDLINE | ID: mdl-7869357

ABSTRACT

The feasibility to raise nonhuman primate antibodies against selected components of the human immune system was tested. The immunogens were whole cells (human T lymphocytes) or purified, recombinant human proteins (cytokines: TNF alpha or GM-CSF; soluble forms of cell surface antigens: sCD4 or sCD25). Significant immunizations, yielding functionally relevant antibodies, were readily achieved in rhesus monkeys, but, not surprisingly, may be less frequent in chimpanzees. The results suggest a general strategy for production of therapeutically useful MAB.


Subject(s)
Antibodies, Monoclonal/biosynthesis , Antibody Formation , Antigens, CD/immunology , Cytokines/immunology , Hominidae/immunology , Primates/immunology , T-Lymphocytes/immunology , Animals , CD4 Antigens/immunology , Enzyme-Linked Immunosorbent Assay , Flow Cytometry , Granulocyte-Macrophage Colony-Stimulating Factor/immunology , Humans , Immunization Schedule , Immunoglobulin G/biosynthesis , Macaca mulatta/immunology , Pan troglodytes/immunology , Papio/immunology , Receptors, Interleukin-2/immunology , Recombinant Proteins/immunology , Tumor Necrosis Factor-alpha/immunology
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