Immunotoxins for targeted cancer therapy
Immunotoxins are proteins that contain a toxin along with an antibody or growth factor that binds specifically to target cells. Nearly all protein toxins work by enzymatically inhibiting protein synthesis. For the immunotoxin to work, it must bind to and be internalized by the target cells, and the...
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description | Immunotoxins are proteins that contain a toxin along with an antibody or growth factor that binds specifically to target cells. Nearly all protein toxins work by enzymatically inhibiting protein synthesis. For the immunotoxin to work, it must bind to and be internalized by the target cells, and the enzymatic fragment of the toxin must translocate to the cytosol. Once in the cytosol, 1 molecule is capable of killing a cell, making immunotoxins some of the most potent killing agents. Various plant and bacterial toxins have been genetically fused or chemically conjugated to ligands that bind to cancer cells. Among the most active clinically are those that bind to hematologic tumors. At present, only 1 agent, which contains human interleukin-2 and truncated diphtheria toxin, is approved for use in cutaneous T-cell lymphoma. Another, containing an anti-CD22 Fv and truncated Pseudomonas exotoxin, has induced complete remissions in a high proportion of cases of hairy-cell leukemia. Refinement of existing immunotoxins and development of new immunotoxins are underway to improve the treatment of cancer. |
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Nearly all protein toxins work by enzymatically inhibiting protein synthesis. For the immunotoxin to work, it must bind to and be internalized by the target cells, and the enzymatic fragment of the toxin must translocate to the cytosol. Once in the cytosol, 1 molecule is capable of killing a cell, making immunotoxins some of the most potent killing agents. Various plant and bacterial toxins have been genetically fused or chemically conjugated to ligands that bind to cancer cells. Among the most active clinically are those that bind to hematologic tumors. At present, only 1 agent, which contains human interleukin-2 and truncated diphtheria toxin, is approved for use in cutaneous T-cell lymphoma. Another, containing an anti-CD22 Fv and truncated Pseudomonas exotoxin, has induced complete remissions in a high proportion of cases of hairy-cell leukemia. 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Nearly all protein toxins work by enzymatically inhibiting protein synthesis. For the immunotoxin to work, it must bind to and be internalized by the target cells, and the enzymatic fragment of the toxin must translocate to the cytosol. Once in the cytosol, 1 molecule is capable of killing a cell, making immunotoxins some of the most potent killing agents. Various plant and bacterial toxins have been genetically fused or chemically conjugated to ligands that bind to cancer cells. Among the most active clinically are those that bind to hematologic tumors. At present, only 1 agent, which contains human interleukin-2 and truncated diphtheria toxin, is approved for use in cutaneous T-cell lymphoma. Another, containing an anti-CD22 Fv and truncated Pseudomonas exotoxin, has induced complete remissions in a high proportion of cases of hairy-cell leukemia. Refinement of existing immunotoxins and development of new immunotoxins are underway to improve the treatment of cancer.</description><subject>Antineoplastic Agents - administration & dosage</subject><subject>Antineoplastic Agents - therapeutic use</subject><subject>Bacterial Toxins - chemistry</subject><subject>Clinical Trials as Topic</subject><subject>Diphtheria Toxin - chemistry</subject><subject>Drug Delivery Systems</subject><subject>Humans</subject><subject>Immunoglobulin Fragments - metabolism</subject><subject>Immunotoxins - administration & dosage</subject><subject>Immunotoxins - therapeutic use</subject><subject>Interleukin-2 - chemistry</subject><subject>Leukemia, Hairy Cell - drug therapy</subject><subject>Recombinant Fusion Proteins - administration & dosage</subject><subject>Recombinant Fusion Proteins - therapeutic use</subject><subject>Sialic Acid Binding Ig-like Lectin 2 - chemistry</subject><issn>1550-7416</issn><issn>1550-7416</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkM1Lw0AQxRdRbK2evEtPIkh0ZnezSS6CFD8KBS96XiabbRtJsnE3EfvfG2nROpeZYX68eTzGzhFukEN6S9SGd0hBKHHAxhjHECUS1eHePGInYWBAcIF4zEaYAI95wsfsal7XfeM691U2Ybp0ftqRX9nOFlNDjbHDvrae2s0pO1pSFezZrk_Y2-PD6-w5Wrw8zWf3i8hIhC6y0iSoEiKeSI6pEcC5IoIMc4glIGBMNiOSkKicClkAN8BFmmeFkpBmYsLutrptn9e2MLbpPFW69WVNfqMdlfr_pSnXeuU-NU8UgsJB4HIn4N1Hb0On6zIYW1XUWNcHzXHwN9QAXm9B410I3i5_nyDon2T1XrIDfbHv64_dRSm-AUKXdAY</recordid><startdate>20060818</startdate><enddate>20060818</enddate><creator>Kreitman, Robert J</creator><general>Springer-Verlag</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7T5</scope><scope>C1K</scope><scope>H94</scope><scope>5PM</scope></search><sort><creationdate>20060818</creationdate><title>Immunotoxins for targeted cancer therapy</title><author>Kreitman, Robert J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c410t-e4c7167aa274218c30226aa091b05401015ae9aa4076bad4d02c0238b9d640893</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Antineoplastic Agents - administration & dosage</topic><topic>Antineoplastic Agents - therapeutic use</topic><topic>Bacterial Toxins - chemistry</topic><topic>Clinical Trials as Topic</topic><topic>Diphtheria Toxin - chemistry</topic><topic>Drug Delivery Systems</topic><topic>Humans</topic><topic>Immunoglobulin Fragments - metabolism</topic><topic>Immunotoxins - administration & dosage</topic><topic>Immunotoxins - therapeutic use</topic><topic>Interleukin-2 - chemistry</topic><topic>Leukemia, Hairy Cell - drug therapy</topic><topic>Recombinant Fusion Proteins - administration & dosage</topic><topic>Recombinant Fusion Proteins - therapeutic use</topic><topic>Sialic Acid Binding Ig-like Lectin 2 - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kreitman, Robert J</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Immunology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The AAPS journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kreitman, Robert J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Immunotoxins for targeted cancer therapy</atitle><jtitle>The AAPS journal</jtitle><addtitle>AAPS J</addtitle><date>2006-08-18</date><risdate>2006</risdate><volume>8</volume><issue>3</issue><spage>E532</spage><epage>E551</epage><pages>E532-E551</pages><issn>1550-7416</issn><eissn>1550-7416</eissn><abstract>Immunotoxins are proteins that contain a toxin along with an antibody or growth factor that binds specifically to target cells. Nearly all protein toxins work by enzymatically inhibiting protein synthesis. For the immunotoxin to work, it must bind to and be internalized by the target cells, and the enzymatic fragment of the toxin must translocate to the cytosol. Once in the cytosol, 1 molecule is capable of killing a cell, making immunotoxins some of the most potent killing agents. Various plant and bacterial toxins have been genetically fused or chemically conjugated to ligands that bind to cancer cells. Among the most active clinically are those that bind to hematologic tumors. At present, only 1 agent, which contains human interleukin-2 and truncated diphtheria toxin, is approved for use in cutaneous T-cell lymphoma. Another, containing an anti-CD22 Fv and truncated Pseudomonas exotoxin, has induced complete remissions in a high proportion of cases of hairy-cell leukemia. 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subjects | Antineoplastic Agents - administration & dosage Antineoplastic Agents - therapeutic use Bacterial Toxins - chemistry Clinical Trials as Topic Diphtheria Toxin - chemistry Drug Delivery Systems Humans Immunoglobulin Fragments - metabolism Immunotoxins - administration & dosage Immunotoxins - therapeutic use Interleukin-2 - chemistry Leukemia, Hairy Cell - drug therapy Recombinant Fusion Proteins - administration & dosage Recombinant Fusion Proteins - therapeutic use Sialic Acid Binding Ig-like Lectin 2 - chemistry |
title | Immunotoxins for targeted cancer therapy |
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