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Immunotoxins: hybrid molecules of monoclonal antibodies and a toxin subunit specifically kill tumour cells
Several attempts to attack tumours in experimental systems have been made using conjugates of chemotherapeutic agents or potent toxins with antibodies (immunotoxins) 1–8 . In vitro studies have been highly successful, showing target specificity of a high order in some cases 6–8 . However, so far, su...
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Published in: | Nature (London) 1981-03, Vol.290 (5802), p.145-146 |
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container_title | Nature (London) |
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creator | Blythman, Hildur E Casellas, Pierre Gros, Olivier Gros, Pierre Jansen, Franz K Paolucci, Francis Pau, Bernard Vidal, Hubert |
description | Several attempts to attack tumours in experimental systems have been made using conjugates of chemotherapeutic agents or potent toxins with antibodies (immunotoxins)
1–8
.
In vitro
studies have been highly successful, showing target specificity of a high order in some cases
6–8
. However, so far, such conjugates have been inadequate
in vivo
, probably for two main reasons. First, conventional heteroclonal antibodies are perhaps inappropriate, because purification by biochemical methods leaves a large amount of non-antibody γ-globulins. The use of monoclonal antibodies may overcome this problem. Second, when whole toxins have been conjugated to antibodies there has been a strong residual nonspecific cytotoxicity due to the binding capacity of a subunit, the B-piece of the toxin. (Diphtheria toxin or ricin consist of two polypeptide subunits. The A-piece is responsible for inhibition of protein synthesis on ribosomes, and the B-piece binds to galactose residues on the cell membrane and facilitates the transmembrane passage of the A-piece.) In the present work the problem of nonspecific binding by the B-piece has been circumvented by using the A-piece only as the toxin component of immunotoxins; these immunotoxins are active both
in vitro
and
in vivo
. |
doi_str_mv | 10.1038/290145a0 |
format | article |
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1–8
.
In vitro
studies have been highly successful, showing target specificity of a high order in some cases
6–8
. However, so far, such conjugates have been inadequate
in vivo
, probably for two main reasons. First, conventional heteroclonal antibodies are perhaps inappropriate, because purification by biochemical methods leaves a large amount of non-antibody γ-globulins. The use of monoclonal antibodies may overcome this problem. Second, when whole toxins have been conjugated to antibodies there has been a strong residual nonspecific cytotoxicity due to the binding capacity of a subunit, the B-piece of the toxin. (Diphtheria toxin or ricin consist of two polypeptide subunits. The A-piece is responsible for inhibition of protein synthesis on ribosomes, and the B-piece binds to galactose residues on the cell membrane and facilitates the transmembrane passage of the A-piece.) In the present work the problem of nonspecific binding by the B-piece has been circumvented by using the A-piece only as the toxin component of immunotoxins; these immunotoxins are active both
in vitro
and
in vivo
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1–8
.
In vitro
studies have been highly successful, showing target specificity of a high order in some cases
6–8
. However, so far, such conjugates have been inadequate
in vivo
, probably for two main reasons. First, conventional heteroclonal antibodies are perhaps inappropriate, because purification by biochemical methods leaves a large amount of non-antibody γ-globulins. The use of monoclonal antibodies may overcome this problem. Second, when whole toxins have been conjugated to antibodies there has been a strong residual nonspecific cytotoxicity due to the binding capacity of a subunit, the B-piece of the toxin. (Diphtheria toxin or ricin consist of two polypeptide subunits. The A-piece is responsible for inhibition of protein synthesis on ribosomes, and the B-piece binds to galactose residues on the cell membrane and facilitates the transmembrane passage of the A-piece.) In the present work the problem of nonspecific binding by the B-piece has been circumvented by using the A-piece only as the toxin component of immunotoxins; these immunotoxins are active both
in vitro
and
in vivo
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1–8
.
In vitro
studies have been highly successful, showing target specificity of a high order in some cases
6–8
. However, so far, such conjugates have been inadequate
in vivo
, probably for two main reasons. First, conventional heteroclonal antibodies are perhaps inappropriate, because purification by biochemical methods leaves a large amount of non-antibody γ-globulins. The use of monoclonal antibodies may overcome this problem. Second, when whole toxins have been conjugated to antibodies there has been a strong residual nonspecific cytotoxicity due to the binding capacity of a subunit, the B-piece of the toxin. (Diphtheria toxin or ricin consist of two polypeptide subunits. The A-piece is responsible for inhibition of protein synthesis on ribosomes, and the B-piece binds to galactose residues on the cell membrane and facilitates the transmembrane passage of the A-piece.) In the present work the problem of nonspecific binding by the B-piece has been circumvented by using the A-piece only as the toxin component of immunotoxins; these immunotoxins are active both
in vitro
and
in vivo
.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>7207595</pmid><doi>10.1038/290145a0</doi><tpages>2</tpages></addata></record> |
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subjects | Animals Antibodies, Neoplasm - administration & dosage Antibody Specificity Antineoplastic Agents - administration & dosage Cells, Cultured Clone Cells Humanities and Social Sciences Immunoglobulin M - administration & dosage letter Leukemia, Experimental - drug therapy Mice Mice, Inbred BALB C multidisciplinary Neoplasm Transplantation Ricin - administration & dosage Science Science (multidisciplinary) Toxins, Biological - metabolism |
title | Immunotoxins: hybrid molecules of monoclonal antibodies and a toxin subunit specifically kill tumour cells |
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