Recombinant Polymeric IgG: An Approach to Engineering More Potent Antibodies
IgM and IgG are the only classes of immunoglobulin capable of initiating the classical complement cascade. IgM, however, fixes complement much more effectively than IgG making it a more attractive Fc for some immunotherapeutic strategies. IgG, on the other hand, triggers additional effector function...
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Veröffentlicht in: | Bio/Technology 1994-07, Vol.12 (7), p.683-688 |
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creator | Smith, Richard I. F. Morrison, Sherie L. |
description | IgM and IgG are the only classes of immunoglobulin capable of initiating the classical complement cascade. IgM, however, fixes complement much more effectively than IgG making it a more attractive Fc for some immunotherapeutic strategies. IgG, on the other hand, triggers additional effector functions mediated through γ specific Fc receptors. Using a generalizable technique we have produced IgM-like polymers of IgG that possess both the Fcγ receptor binding properties of IgG and the more potent complement activity of IgM. |
doi_str_mv | 10.1038/nbt0794-683 |
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Pharmaceutical industry ; Hemolysis ; Humans ; Immunoglobulin G - biosynthesis ; Immunoglobulin G - blood ; Immunoglobulin G - metabolism ; Immunoglobulin M - metabolism ; Industrial applications and implications. 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F.</creatorcontrib><creatorcontrib>Morrison, Sherie L.</creatorcontrib><title>Recombinant Polymeric IgG: An Approach to Engineering More Potent Antibodies</title><title>Bio/Technology</title><addtitle>Nat Biotechnol</addtitle><addtitle>Biotechnology (N Y)</addtitle><description>IgM and IgG are the only classes of immunoglobulin capable of initiating the classical complement cascade. IgM, however, fixes complement much more effectively than IgG making it a more attractive Fc for some immunotherapeutic strategies. IgG, on the other hand, triggers additional effector functions mediated through γ specific Fc receptors. Using a generalizable technique we have produced IgM-like polymers of IgG that possess both the Fcγ receptor binding properties of IgG and the more potent complement activity of IgM.</description><subject>Agriculture</subject><subject>Animals</subject><subject>Bioinformatics</subject><subject>Biological and medical sciences</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedical Engineering/Biotechnology</subject><subject>Biomedicine</subject><subject>Biotechnology</subject><subject>Complement C1 - metabolism</subject><subject>Complement C1q - metabolism</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genetic Engineering</subject><subject>Half-Life</subject><subject>Health. Pharmaceutical industry</subject><subject>Hemolysis</subject><subject>Humans</subject><subject>Immunoglobulin G - biosynthesis</subject><subject>Immunoglobulin G - blood</subject><subject>Immunoglobulin G - metabolism</subject><subject>Immunoglobulin M - metabolism</subject><subject>Industrial applications and implications. Economical aspects</subject><subject>Life Sciences</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Monoclonal antibodies</subject><subject>Mutation</subject><subject>Production of active biomolecules</subject><subject>Receptors, Fc - metabolism</subject><subject>Recombinant Proteins - biosynthesis</subject><subject>Recombinant Proteins - metabolism</subject><issn>0733-222X</issn><issn>1087-0156</issn><issn>1546-1696</issn><issn>2331-3684</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkEtLxDAURoMoOj5WroUuxI1W82rauBsGXzCiiIK7kqQ3Y6VNxqSz8N-bYYorwdVdfOd-93IQOib4kmBWXTk94FLyXFRsC01IwUVOhBTbaIJLxnJK6fse2o_xE2NeCsp30W5ZCi4JnaD5Cxjf69YpN2TPvvvuIbQme1jcXWdTl02Xy-CV-cgGn924ResgxW6RPfoACR8gbU3d0GrftBAP0Y5VXYSjcR6gt9ub19l9Pn-6e5hN57lhXA45t9xSySxulDAWFyBEpXnZSKVkBVobU2mqMWWGYCEsB1VYLaBooBJEFg07QGeb3vTc1wriUPdtNNB1yoFfxboURSEEJ_-CSROlmMsEnm9AE3yMAWy9DG2vwndNcL2WXI-S6yQ50Sdj7Ur30Pyyo9WUn465ikZ1Nihn2viLcSIpK9ffXWywuFxLhVB_-lVwydyfV38Ad5WS6w</recordid><startdate>19940701</startdate><enddate>19940701</enddate><creator>Smith, Richard I. 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F. ; Morrison, Sherie L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c349t-4f4f293f0da6cf05e668b47d9aa98ebbcc8b2b023c1066f4ea5fb6e5de86195d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>Agriculture</topic><topic>Animals</topic><topic>Bioinformatics</topic><topic>Biological and medical sciences</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedical Engineering/Biotechnology</topic><topic>Biomedicine</topic><topic>Biotechnology</topic><topic>Complement C1 - metabolism</topic><topic>Complement C1q - metabolism</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Genetic Engineering</topic><topic>Half-Life</topic><topic>Health. Pharmaceutical industry</topic><topic>Hemolysis</topic><topic>Humans</topic><topic>Immunoglobulin G - biosynthesis</topic><topic>Immunoglobulin G - blood</topic><topic>Immunoglobulin G - metabolism</topic><topic>Immunoglobulin M - metabolism</topic><topic>Industrial applications and implications. Economical aspects</topic><topic>Life Sciences</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Monoclonal antibodies</topic><topic>Mutation</topic><topic>Production of active biomolecules</topic><topic>Receptors, Fc - metabolism</topic><topic>Recombinant Proteins - biosynthesis</topic><topic>Recombinant Proteins - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Smith, Richard I. F.</creatorcontrib><creatorcontrib>Morrison, Sherie L.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Bio/Technology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Smith, Richard I. F.</au><au>Morrison, Sherie L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Recombinant Polymeric IgG: An Approach to Engineering More Potent Antibodies</atitle><jtitle>Bio/Technology</jtitle><stitle>Nat Biotechnol</stitle><addtitle>Biotechnology (N Y)</addtitle><date>1994-07-01</date><risdate>1994</risdate><volume>12</volume><issue>7</issue><spage>683</spage><epage>688</epage><pages>683-688</pages><issn>0733-222X</issn><issn>1087-0156</issn><eissn>1546-1696</eissn><eissn>2331-3684</eissn><abstract>IgM and IgG are the only classes of immunoglobulin capable of initiating the classical complement cascade. IgM, however, fixes complement much more effectively than IgG making it a more attractive Fc for some immunotherapeutic strategies. IgG, on the other hand, triggers additional effector functions mediated through γ specific Fc receptors. Using a generalizable technique we have produced IgM-like polymers of IgG that possess both the Fcγ receptor binding properties of IgG and the more potent complement activity of IgM.</abstract><cop>New York</cop><pub>Nature Publishing Group US</pub><pmid>7764912</pmid><doi>10.1038/nbt0794-683</doi><tpages>6</tpages></addata></record> |
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subjects | Agriculture Animals Bioinformatics Biological and medical sciences Biomedical and Life Sciences Biomedical Engineering/Biotechnology Biomedicine Biotechnology Complement C1 - metabolism Complement C1q - metabolism Fundamental and applied biological sciences. Psychology Genetic Engineering Half-Life Health. Pharmaceutical industry Hemolysis Humans Immunoglobulin G - biosynthesis Immunoglobulin G - blood Immunoglobulin G - metabolism Immunoglobulin M - metabolism Industrial applications and implications. Economical aspects Life Sciences Mice Mice, Inbred BALB C Monoclonal antibodies Mutation Production of active biomolecules Receptors, Fc - metabolism Recombinant Proteins - biosynthesis Recombinant Proteins - metabolism |
title | Recombinant Polymeric IgG: An Approach to Engineering More Potent Antibodies |
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