Immunofilaments Are Well Tolerated after Local or Systemic Administration in Mice
The invention of nanosized biomaterials has paved the way for novel therapeutics that can manipulate cells on a nanoscale. Nanosized immunofilaments (IFs) are synthetic filamentous polymers consisting out of polyisocyanopeptides, which have been recently established as a powerful platform to activat...
Gespeichert in:
Veröffentlicht in: | ACS PHARMACOLOGY & TRANSLATIONAL SCIENCE 2024-05, Vol.7 (6), p.1874-1883 |
---|---|
Hauptverfasser: | , , , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 1883 |
---|---|
container_issue | 6 |
container_start_page | 1874 |
container_title | ACS PHARMACOLOGY & TRANSLATIONAL SCIENCE |
container_volume | 7 |
creator | Weiss, Lea Classens, Rene Schluck, Marjolein Grad, Emilia Dolen, Yusuf van der Woude, Lieke van Midden, Dominique Maassen, Lisa Verrijp, Kiek van Riessen, Koen van Dinther, Eric Hagemann, Philipp M Figdor, Carl G Hammink, Roel |
description | The invention of nanosized biomaterials has paved the way for novel therapeutics that can manipulate cells on a nanoscale. Nanosized immunofilaments (IFs) are synthetic filamentous polymers consisting out of polyisocyanopeptides, which have been recently established as a powerful platform to activate specific immune cells in vivo such that they raise an antitumor immune response. However, toxicological effects or immunogenicity toward the IFs have not yet been investigated. In this study, we evaluated potential toxic or immunogenic effects in C57BL/6 mice upon intravenous or subcutaneous injection of nonfunctionalized IFs or immunostimulatory IFs over 30 days. We here present a detailed analysis of the gross pathology, hematological parameters, blood biochemistry, histology, and antibody-response against the IF backbone. Our results demonstrate that IFs do not induce severe acute or chronic toxicity in mice. After 30 days, we only found elevated IgG-titers in intravenously injected but not subcutaneously injected mice. In summary, we demonstrate that IFs can be administered into a living organism without adverse side effects, thereby establishing the safety of IFs as a therapeutic intervention. |
format | Article |
fullrecord | <record><control><sourceid>kuleuven</sourceid><recordid>TN_cdi_kuleuven_dspace_20_500_12942_744742</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>20_500_12942_744742</sourcerecordid><originalsourceid>FETCH-kuleuven_dspace_20_500_12942_7447423</originalsourceid><addsrcrecordid>eNqVyr0KwjAUQOEgCor6DncWKrdpS-1YRFHQQRQcQ2hvIZofaVLRt9fBwVGnc4avx0Y8y7OoiHHR__ohm3p_QUSOmMQFjthha0xnXaO0NGSDh7IlOJPWcHKaWhmoBtkEamHnKqnBtXB8-kBGVVDWRlnlw1spZ0FZ2KuKJmzQSO1p-umYzdar03ITXTtN3Z2sqP1NViQ4igxRxLxIucjTNE958iee_4xFeITkBfsmUkM</addsrcrecordid><sourcetype>Institutional Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Immunofilaments Are Well Tolerated after Local or Systemic Administration in Mice</title><source>ACS Publications</source><source>Lirias (KU Leuven Association)</source><creator>Weiss, Lea ; Classens, Rene ; Schluck, Marjolein ; Grad, Emilia ; Dolen, Yusuf ; van der Woude, Lieke ; van Midden, Dominique ; Maassen, Lisa ; Verrijp, Kiek ; van Riessen, Koen ; van Dinther, Eric ; Hagemann, Philipp M ; Figdor, Carl G ; Hammink, Roel</creator><creatorcontrib>Weiss, Lea ; Classens, Rene ; Schluck, Marjolein ; Grad, Emilia ; Dolen, Yusuf ; van der Woude, Lieke ; van Midden, Dominique ; Maassen, Lisa ; Verrijp, Kiek ; van Riessen, Koen ; van Dinther, Eric ; Hagemann, Philipp M ; Figdor, Carl G ; Hammink, Roel</creatorcontrib><description>The invention of nanosized biomaterials has paved the way for novel therapeutics that can manipulate cells on a nanoscale. Nanosized immunofilaments (IFs) are synthetic filamentous polymers consisting out of polyisocyanopeptides, which have been recently established as a powerful platform to activate specific immune cells in vivo such that they raise an antitumor immune response. However, toxicological effects or immunogenicity toward the IFs have not yet been investigated. In this study, we evaluated potential toxic or immunogenic effects in C57BL/6 mice upon intravenous or subcutaneous injection of nonfunctionalized IFs or immunostimulatory IFs over 30 days. We here present a detailed analysis of the gross pathology, hematological parameters, blood biochemistry, histology, and antibody-response against the IF backbone. Our results demonstrate that IFs do not induce severe acute or chronic toxicity in mice. After 30 days, we only found elevated IgG-titers in intravenously injected but not subcutaneously injected mice. In summary, we demonstrate that IFs can be administered into a living organism without adverse side effects, thereby establishing the safety of IFs as a therapeutic intervention.</description><identifier>ISSN: 2575-9108</identifier><identifier>EISSN: 2575-9108</identifier><language>eng</language><publisher>AMER CHEMICAL SOC</publisher><ispartof>ACS PHARMACOLOGY & TRANSLATIONAL SCIENCE, 2024-05, Vol.7 (6), p.1874-1883</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,315,776,780,27837</link.rule.ids></links><search><creatorcontrib>Weiss, Lea</creatorcontrib><creatorcontrib>Classens, Rene</creatorcontrib><creatorcontrib>Schluck, Marjolein</creatorcontrib><creatorcontrib>Grad, Emilia</creatorcontrib><creatorcontrib>Dolen, Yusuf</creatorcontrib><creatorcontrib>van der Woude, Lieke</creatorcontrib><creatorcontrib>van Midden, Dominique</creatorcontrib><creatorcontrib>Maassen, Lisa</creatorcontrib><creatorcontrib>Verrijp, Kiek</creatorcontrib><creatorcontrib>van Riessen, Koen</creatorcontrib><creatorcontrib>van Dinther, Eric</creatorcontrib><creatorcontrib>Hagemann, Philipp M</creatorcontrib><creatorcontrib>Figdor, Carl G</creatorcontrib><creatorcontrib>Hammink, Roel</creatorcontrib><title>Immunofilaments Are Well Tolerated after Local or Systemic Administration in Mice</title><title>ACS PHARMACOLOGY & TRANSLATIONAL SCIENCE</title><description>The invention of nanosized biomaterials has paved the way for novel therapeutics that can manipulate cells on a nanoscale. Nanosized immunofilaments (IFs) are synthetic filamentous polymers consisting out of polyisocyanopeptides, which have been recently established as a powerful platform to activate specific immune cells in vivo such that they raise an antitumor immune response. However, toxicological effects or immunogenicity toward the IFs have not yet been investigated. In this study, we evaluated potential toxic or immunogenic effects in C57BL/6 mice upon intravenous or subcutaneous injection of nonfunctionalized IFs or immunostimulatory IFs over 30 days. We here present a detailed analysis of the gross pathology, hematological parameters, blood biochemistry, histology, and antibody-response against the IF backbone. Our results demonstrate that IFs do not induce severe acute or chronic toxicity in mice. After 30 days, we only found elevated IgG-titers in intravenously injected but not subcutaneously injected mice. In summary, we demonstrate that IFs can be administered into a living organism without adverse side effects, thereby establishing the safety of IFs as a therapeutic intervention.</description><issn>2575-9108</issn><issn>2575-9108</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>FZOIL</sourceid><recordid>eNqVyr0KwjAUQOEgCor6DncWKrdpS-1YRFHQQRQcQ2hvIZofaVLRt9fBwVGnc4avx0Y8y7OoiHHR__ohm3p_QUSOmMQFjthha0xnXaO0NGSDh7IlOJPWcHKaWhmoBtkEamHnKqnBtXB8-kBGVVDWRlnlw1spZ0FZ2KuKJmzQSO1p-umYzdar03ITXTtN3Z2sqP1NViQ4igxRxLxIucjTNE958iee_4xFeITkBfsmUkM</recordid><startdate>20240503</startdate><enddate>20240503</enddate><creator>Weiss, Lea</creator><creator>Classens, Rene</creator><creator>Schluck, Marjolein</creator><creator>Grad, Emilia</creator><creator>Dolen, Yusuf</creator><creator>van der Woude, Lieke</creator><creator>van Midden, Dominique</creator><creator>Maassen, Lisa</creator><creator>Verrijp, Kiek</creator><creator>van Riessen, Koen</creator><creator>van Dinther, Eric</creator><creator>Hagemann, Philipp M</creator><creator>Figdor, Carl G</creator><creator>Hammink, Roel</creator><general>AMER CHEMICAL SOC</general><scope>FZOIL</scope></search><sort><creationdate>20240503</creationdate><title>Immunofilaments Are Well Tolerated after Local or Systemic Administration in Mice</title><author>Weiss, Lea ; Classens, Rene ; Schluck, Marjolein ; Grad, Emilia ; Dolen, Yusuf ; van der Woude, Lieke ; van Midden, Dominique ; Maassen, Lisa ; Verrijp, Kiek ; van Riessen, Koen ; van Dinther, Eric ; Hagemann, Philipp M ; Figdor, Carl G ; Hammink, Roel</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-kuleuven_dspace_20_500_12942_7447423</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Weiss, Lea</creatorcontrib><creatorcontrib>Classens, Rene</creatorcontrib><creatorcontrib>Schluck, Marjolein</creatorcontrib><creatorcontrib>Grad, Emilia</creatorcontrib><creatorcontrib>Dolen, Yusuf</creatorcontrib><creatorcontrib>van der Woude, Lieke</creatorcontrib><creatorcontrib>van Midden, Dominique</creatorcontrib><creatorcontrib>Maassen, Lisa</creatorcontrib><creatorcontrib>Verrijp, Kiek</creatorcontrib><creatorcontrib>van Riessen, Koen</creatorcontrib><creatorcontrib>van Dinther, Eric</creatorcontrib><creatorcontrib>Hagemann, Philipp M</creatorcontrib><creatorcontrib>Figdor, Carl G</creatorcontrib><creatorcontrib>Hammink, Roel</creatorcontrib><collection>Lirias (KU Leuven Association)</collection><jtitle>ACS PHARMACOLOGY & TRANSLATIONAL SCIENCE</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Weiss, Lea</au><au>Classens, Rene</au><au>Schluck, Marjolein</au><au>Grad, Emilia</au><au>Dolen, Yusuf</au><au>van der Woude, Lieke</au><au>van Midden, Dominique</au><au>Maassen, Lisa</au><au>Verrijp, Kiek</au><au>van Riessen, Koen</au><au>van Dinther, Eric</au><au>Hagemann, Philipp M</au><au>Figdor, Carl G</au><au>Hammink, Roel</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Immunofilaments Are Well Tolerated after Local or Systemic Administration in Mice</atitle><jtitle>ACS PHARMACOLOGY & TRANSLATIONAL SCIENCE</jtitle><date>2024-05-03</date><risdate>2024</risdate><volume>7</volume><issue>6</issue><spage>1874</spage><epage>1883</epage><pages>1874-1883</pages><issn>2575-9108</issn><eissn>2575-9108</eissn><abstract>The invention of nanosized biomaterials has paved the way for novel therapeutics that can manipulate cells on a nanoscale. Nanosized immunofilaments (IFs) are synthetic filamentous polymers consisting out of polyisocyanopeptides, which have been recently established as a powerful platform to activate specific immune cells in vivo such that they raise an antitumor immune response. However, toxicological effects or immunogenicity toward the IFs have not yet been investigated. In this study, we evaluated potential toxic or immunogenic effects in C57BL/6 mice upon intravenous or subcutaneous injection of nonfunctionalized IFs or immunostimulatory IFs over 30 days. We here present a detailed analysis of the gross pathology, hematological parameters, blood biochemistry, histology, and antibody-response against the IF backbone. Our results demonstrate that IFs do not induce severe acute or chronic toxicity in mice. After 30 days, we only found elevated IgG-titers in intravenously injected but not subcutaneously injected mice. In summary, we demonstrate that IFs can be administered into a living organism without adverse side effects, thereby establishing the safety of IFs as a therapeutic intervention.</abstract><pub>AMER CHEMICAL SOC</pub><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2575-9108 |
ispartof | ACS PHARMACOLOGY & TRANSLATIONAL SCIENCE, 2024-05, Vol.7 (6), p.1874-1883 |
issn | 2575-9108 2575-9108 |
language | eng |
recordid | cdi_kuleuven_dspace_20_500_12942_744742 |
source | ACS Publications; Lirias (KU Leuven Association) |
title | Immunofilaments Are Well Tolerated after Local or Systemic Administration in Mice |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-16T02%3A22%3A29IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-kuleuven&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Immunofilaments%20Are%20Well%20Tolerated%20after%20Local%20or%20Systemic%20Administration%20in%20Mice&rft.jtitle=ACS%20PHARMACOLOGY%20&%20TRANSLATIONAL%20SCIENCE&rft.au=Weiss,%20Lea&rft.date=2024-05-03&rft.volume=7&rft.issue=6&rft.spage=1874&rft.epage=1883&rft.pages=1874-1883&rft.issn=2575-9108&rft.eissn=2575-9108&rft_id=info:doi/&rft_dat=%3Ckuleuven%3E20_500_12942_744742%3C/kuleuven%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |