Polymer-conjugated inhibitors of tumor necrosis factor-α for local control of inflammation
Burns, chronic wounds, osteoarthritis, and uveitis are examples of conditions characterized by local, intense inflammatory responses that can impede healing or even further tissue degradation. The most powerful anti-inflammatory drugs available are often administered systemically, but these carry si...
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description | Burns, chronic wounds, osteoarthritis, and uveitis are examples of conditions characterized by local, intense inflammatory responses that can impede healing or even further tissue degradation. The most powerful anti-inflammatory drugs available are often administered systemically, but these carry significant side effects and are not compatible for patients that have underlying complications associated with their condition. Conjugation of monoclonal antibodies that neutralize pro-inflammatory cytokines to high molecular weight hydrophilic polymers has been shown to be an effective strategy for local control of inflammation. Lead formulations are based on antibody inhibitors of tumor necrosis factor-α conjugated to hyaluronic acid having molecular weight greater than 1 MDa. This review will discuss fundamental aspects of medical conditions that could be treated with these conjugates and design principles for preparing these cytokine-neutralizing polymer conjugates. Results demonstrating that infliximab, an approved inhibitor of tumor necrosis factor-α, can be incorporated into the conjugates using a broad range of water-soluble polymers are also presented, along with a prospectus for clinical translation. |
doi_str_mv | 10.4161/biom.25597 |
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The most powerful anti-inflammatory drugs available are often administered systemically, but these carry significant side effects and are not compatible for patients that have underlying complications associated with their condition. Conjugation of monoclonal antibodies that neutralize pro-inflammatory cytokines to high molecular weight hydrophilic polymers has been shown to be an effective strategy for local control of inflammation. Lead formulations are based on antibody inhibitors of tumor necrosis factor-α conjugated to hyaluronic acid having molecular weight greater than 1 MDa. This review will discuss fundamental aspects of medical conditions that could be treated with these conjugates and design principles for preparing these cytokine-neutralizing polymer conjugates. 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The most powerful anti-inflammatory drugs available are often administered systemically, but these carry significant side effects and are not compatible for patients that have underlying complications associated with their condition. Conjugation of monoclonal antibodies that neutralize pro-inflammatory cytokines to high molecular weight hydrophilic polymers has been shown to be an effective strategy for local control of inflammation. Lead formulations are based on antibody inhibitors of tumor necrosis factor-α conjugated to hyaluronic acid having molecular weight greater than 1 MDa. This review will discuss fundamental aspects of medical conditions that could be treated with these conjugates and design principles for preparing these cytokine-neutralizing polymer conjugates. Results demonstrating that infliximab, an approved inhibitor of tumor necrosis factor-α, can be incorporated into the conjugates using a broad range of water-soluble polymers are also presented, along with a prospectus for clinical translation.</description><subject>Adjuvants, Immunologic - therapeutic use</subject><subject>Animals</subject><subject>Anti-Inflammatory Agents, Non-Steroidal - chemistry</subject><subject>Anti-Inflammatory Agents, Non-Steroidal - therapeutic use</subject><subject>Antibodies, Monoclonal - chemistry</subject><subject>Antibodies, Monoclonal - therapeutic use</subject><subject>drug delivery</subject><subject>Drug Delivery Systems</subject><subject>Humans</subject><subject>hyaluronic acid</subject><subject>Hyaluronic Acid - therapeutic use</subject><subject>Inflammation - drug therapy</subject><subject>Infliximab</subject><subject>polymer</subject><subject>Polymers</subject><subject>Special Focus Review</subject><subject>therapeutic antibody</subject><subject>tumor necrosis factor-alpha</subject><subject>Tumor Necrosis Factor-alpha - antagonists & inhibitors</subject><subject>Tumor Necrosis Factor-alpha - metabolism</subject><subject>wound healing</subject><issn>2159-2535</issn><issn>2159-2527</issn><issn>2159-2535</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>0YH</sourceid><sourceid>EIF</sourceid><recordid>eNptkc1KxTAQhYMoKurGB5AuRaim-WmbjSDiHwi60JWLkKaJRpKOJq1yH8sX8ZnM9aoomM2EzDcnwzkIbVd4n1V1ddA5CPuEc9EsoXVScVESTvnyr_sa2krpEefDWUsIX0VrhApMW0HX0d01-FkwsdQwPE73ajR94YYH17kRYirAFuMUIBaD0RGSS4VVOnfK97fC5mcPWvkiz44R_Jx2g_UqBDU6GDbRilU-ma2vuoFuT09ujs_Ly6uzi-Ojy1JTKpqSNz022FCmu5pYgrlubNdzUbeq551pW0q4Vra3Na5wbeqOKdp3rGVaNJQyTDfQ4UL3aeqC6bXJ2ygvn6ILKs4kKCf_dgb3IO_hRdKGCdKyLLD7JRDheTJplMElbbxXg4EpyYqTuqEVxiKjewt0bkeKxv58U2E5D0TOA5GfgWR45_diP-i3_RngCyDbBjGoV4i-l6OaeYg2qkG7JOk_wh_4PZxU</recordid><startdate>20130701</startdate><enddate>20130701</enddate><creator>Washburn, Newell R.</creator><creator>Prata, Joseph E.</creator><creator>Friedrich, Emily E.</creator><creator>Ramadan, Mohamed H.</creator><creator>Elder, Allison N.</creator><creator>Sun, Liang Tso</creator><general>Taylor & Francis</general><general>Landes Bioscience</general><scope>0YH</scope><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>7X8</scope><scope>5PM</scope></search><sort><creationdate>20130701</creationdate><title>Polymer-conjugated inhibitors of tumor necrosis factor-α for local control of inflammation</title><author>Washburn, Newell R. ; Prata, Joseph E. ; Friedrich, Emily E. ; Ramadan, Mohamed H. ; Elder, Allison N. ; Sun, Liang Tso</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3397-57d0e0e34cb62f205c7fbd5968ad5be88325cafdf60106e6b4a3db484c9733403</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Adjuvants, Immunologic - therapeutic use</topic><topic>Animals</topic><topic>Anti-Inflammatory Agents, Non-Steroidal - chemistry</topic><topic>Anti-Inflammatory Agents, Non-Steroidal - therapeutic use</topic><topic>Antibodies, Monoclonal - chemistry</topic><topic>Antibodies, Monoclonal - therapeutic use</topic><topic>drug delivery</topic><topic>Drug Delivery Systems</topic><topic>Humans</topic><topic>hyaluronic acid</topic><topic>Hyaluronic Acid - therapeutic use</topic><topic>Inflammation - drug therapy</topic><topic>Infliximab</topic><topic>polymer</topic><topic>Polymers</topic><topic>Special Focus Review</topic><topic>therapeutic antibody</topic><topic>tumor necrosis factor-alpha</topic><topic>Tumor Necrosis Factor-alpha - antagonists & inhibitors</topic><topic>Tumor Necrosis Factor-alpha - metabolism</topic><topic>wound healing</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Washburn, Newell R.</creatorcontrib><creatorcontrib>Prata, Joseph E.</creatorcontrib><creatorcontrib>Friedrich, Emily E.</creatorcontrib><creatorcontrib>Ramadan, Mohamed H.</creatorcontrib><creatorcontrib>Elder, Allison N.</creatorcontrib><creatorcontrib>Sun, Liang Tso</creatorcontrib><collection>Taylor & Francis Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Biomatter (Austin, TX)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Washburn, Newell R.</au><au>Prata, Joseph E.</au><au>Friedrich, Emily E.</au><au>Ramadan, Mohamed H.</au><au>Elder, Allison N.</au><au>Sun, Liang Tso</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Polymer-conjugated inhibitors of tumor necrosis factor-α for local control of inflammation</atitle><jtitle>Biomatter (Austin, TX)</jtitle><addtitle>Biomatter</addtitle><date>2013-07-01</date><risdate>2013</risdate><volume>3</volume><issue>3</issue><issn>2159-2535</issn><issn>2159-2527</issn><eissn>2159-2535</eissn><abstract>Burns, chronic wounds, osteoarthritis, and uveitis are examples of conditions characterized by local, intense inflammatory responses that can impede healing or even further tissue degradation. The most powerful anti-inflammatory drugs available are often administered systemically, but these carry significant side effects and are not compatible for patients that have underlying complications associated with their condition. Conjugation of monoclonal antibodies that neutralize pro-inflammatory cytokines to high molecular weight hydrophilic polymers has been shown to be an effective strategy for local control of inflammation. Lead formulations are based on antibody inhibitors of tumor necrosis factor-α conjugated to hyaluronic acid having molecular weight greater than 1 MDa. This review will discuss fundamental aspects of medical conditions that could be treated with these conjugates and design principles for preparing these cytokine-neutralizing polymer conjugates. 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subjects | Adjuvants, Immunologic - therapeutic use Animals Anti-Inflammatory Agents, Non-Steroidal - chemistry Anti-Inflammatory Agents, Non-Steroidal - therapeutic use Antibodies, Monoclonal - chemistry Antibodies, Monoclonal - therapeutic use drug delivery Drug Delivery Systems Humans hyaluronic acid Hyaluronic Acid - therapeutic use Inflammation - drug therapy Infliximab polymer Polymers Special Focus Review therapeutic antibody tumor necrosis factor-alpha Tumor Necrosis Factor-alpha - antagonists & inhibitors Tumor Necrosis Factor-alpha - metabolism wound healing |
title | Polymer-conjugated inhibitors of tumor necrosis factor-α for local control of inflammation |
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