Cytotoxicity Acquired by Conjugation of an Anti‐Thy1.1 Monoclonal Antibody and the Ribosome‐Inactivating Protein, Gelonin
Open Access
- 1 June 1981
- journal article
- research article
- Published by Wiley in European Journal of Biochemistry
- Vol. 116 (3) , 447-454
- https://doi.org/10.1111/j.1432-1033.1981.tb05356.x
Abstract
Gelonin, a plant protein which can powerfully reduce the protein-synthetic capacity of ribosome preparations, was covalently coupled to anti-Thy1.1 antibody. The conjugate was prepared using N-succinimidyl-3-(2-pyridyldithio)propionate which generates a disulphide linkage between the component molecules. Two conjugate fractions were obtained with Mr of 180000 and > 200000. After its linkage to the antibody, gelonin suppressed those Thy1.1-bearing T lymphocytes from AKR mice which will respond to phytohaemagglutinin and concanavalin A in tissue culture. The [3H]leucine incorporation with the T-cell mitogens was inhibited by 50% with the 180000-Mr fraction at a concentration of 0.4 nM and with the > 200000-Mr fraction of pM. Unconjugated gelonin induced comparable reductions in T-cell responsiveness but at concentrations of 30 nM. The conjugates exerted little or no effect upon B lymphocytes or T lymphocytes from CBA mice (Thy1.2+ve). Two Thy1.1-expressing AKR lymphoma cell lines, AKR-A and BW5147, were found to be sensitive to the conjugates, albeit much less so than the normal T lymphocytes. The conjugates injected in vivo significantly prolonged the life of CBA mice bearing an AKR-A lymphoma allograft. It is concluded that gelonin can, by its linkage to an antibody, be rendered cytotoxic with a potency to match or exceed those of the toxins abrin and ricin.This publication has 44 references indexed in Scilit:
- High specific cytotoxicity of antibody-toxin hybrid molecules (immunotoxins) for target cellsImmunology Letters, 1980
- Increased Toxicity of Diphtheria Toxin for Human Lymphoblastoid Cells following Covalent Linkage to Anti-(human lymphocyte) Globulin or Its F(ab')2 FragmentEuropean Journal of Biochemistry, 1980
- Synthesis of a cytotoxic insulin cross-linked to diphtheria toxin fragment a capable of recognizing insulin receptorsBiochemical and Biophysical Research Communications, 1979
- Preparation of a hybrid of fragment Fab' of antibody and fragment a of diphtheria toxin and its cytotoxicityBiochemical and Biophysical Research Communications, 1979
- Purification and properties of a translation inhibitor from wheat germBiochemistry, 1979
- Isolation of pure IgG1, IgG2a and IgG2b immunoglobulins from mouse serum using protein A-SepharoseImmunochemistry, 1978
- Toxicity of diphtheria toxin for lymphoblastoid cells is increased by conjugation to antilymphocytic globulinNature, 1978
- Structure and toxicity of pure ricinus agglutininBiochimica et Biophysica Acta (BBA) - General Subjects, 1976
- Selective Destruction of Target Cells by Diphtheria Toxin Conjugated to Antibody Directed against Antigens on the CellsScience, 1970
- THE MITOTIC RESPONSE OF THYMUS-DERIVED CELLS TO ANTIGENIC STIMULUSTransplantation, 1966