Development of rat anti-mouse interleukin 3 monoclonal antibodies which neutralize bioactivity in vitro

• Published in: The Journal of immunology (1950) Vol. 140; no. 1; pp. 131 - 137
• Main Authors: Abrams, JS, Pearce, MK
• Format: Journal Article
• Language: English
• Published: Bethesda, MD Am Assoc Immnol 01-01-1988; American Association of Immunologists
• Subjects: Analysis of the immune response. Humoral and cellular immunity; Animals; Antibodies, Monoclonal - immunology; Antigen-Antibody Reactions; Biological and medical sciences; Biological Assay; Epitopes; Fundamental and applied biological sciences. Psychology; Fundamental immunology; Immunobiology; Interleukin-3 - antagonists & inhibitors; Interleukin-3 - immunology; Lymphokines, interleukins ( function, expression); Rats; Regulatory factors and their cellular receptors; Rat; Rodentia; Hematopoietic cell; Hybridoma; Immune regulation; Lymphokine; Blocking antibody; Monoclonal antibody; Cell differentiation; Immunochemistry; Enzyme immunoassay; Biological activity; Colony forming cell; Active immunization; Characterization; Vertebrata; Mammalia; Mouse; Interleukin 3; Production; Inhibition; ELISA assay
• ISSN: 0022-1767; 1550-6606
• DOI: 10.4049/jimmunol.140.1.131

Several rat anti-mouse interleukin 3 (IL-3) monoclonal antibodies have been developed which inhibit the biologic activity of mouse IL-3. These antibodies were produced in rats immunized with preparations of purified, recombinant mouse IL-3, obtained from transiently transfected COS7 cell supernatant. Hybridomas secreting anti-IL-3 were selected initially either on the basis of their giving a positive signal in an indirect enzyme-linked immunosorbent assay, or for their ability to inhibit the proliferation of the IL-3-dependent mouse mast cell line, MC/9. Neutralizing rat monoclonal IgG1, IgG2a, and IgG2b antibodies have been identified; these also block IL-3-induced proliferation of the NFS-60 and IC2 cell lines. These antibodies also blocked the IL-3-induced proliferation of mouse bone marrow-derived colony-forming units-culture suggesting that the same epitopes on IL-3 influence receptor recognition for both the proliferation of factor-dependent cell lines as well as normal bone marrow cells. Fab fragments produced from certain of the IgG2a-neutralizing antibodies blocked as well as the parent IgG. Antibody cross-blocking studies identified one neutralizing antibody apparently recognizing an epitope that was spatially distinct from those recognized by the other blocking antibodies tested. The development of these neutralizing rat monoclonal antibodies to mouse IL-3 should facilitate further investigation on the role of this factor in hemopoietic regulation.