{"id":3332,"date":"2025-01-07T21:57:42","date_gmt":"2025-01-07T20:57:42","guid":{"rendered":"https:\/\/rvh-synergie.org\/actualites\/la-therapie-genique-pourrait-traiter-lhypereosinophilie-chronique\/"},"modified":"2025-01-07T21:57:50","modified_gmt":"2025-01-07T20:57:50","slug":"la-therapie-genique-pourrait-traiter-lhypereosinophilie-chronique","status":"publish","type":"post","link":"https:\/\/rvh-synergie.org\/actualites\/la-therapie-genique-pourrait-traiter-lhypereosinophilie-chronique\/","title":{"rendered":"La th\u00e9rapie g\u00e9nique pourrait traiter l&rsquo;hyper\u00e9osinophilie chronique"},"content":{"rendered":"<div>\n<div class=\"article-gallery lightGallery\">\n<div data-thumb=\"https:\/\/scx1.b-cdn.net\/csz\/news\/tmb\/2025\/gene-therapy-to-treat.jpg\" data-src=\"https:\/\/scx2.b-cdn.net\/gfx\/news\/hires\/2025\/gene-therapy-to-treat.jpg\" data-sub-html=\"Specificity and selectivity of anti-Siglec8 hybridoma supernatants assessed by Siglec8 enzyme-linked immunosorbent assay (ELISA). &lt;b&gt;(A)&lt;\/b&gt; ELISA detection of Siglec8 antibody binding to recombinant His-tagged human Siglec8 protein. 2E2 anti-Siglec8 antibody (2 \u00b5g\/mL, GenScript, Piscataway, NJ) was used as a positive control for Siglec8 binding. Selective ELISA of Siglec8-specific antibodies showed no cross-reactivity toward closest Siglec family members (recombinant human Siglec-5 protein and recombinant human Siglec-7 protein) as assessed by ELISA. &lt;b&gt;(B\u2013E)&lt;\/b&gt; Half-maximal effective concentration (EC&lt;sub&gt;50&lt;\/sub&gt;) determination for each of the purified Siglec8 antibody candidates (&lt;i&gt;n&lt;\/i&gt; = 19). The anti-Siglec8-2E2 antibody (GenScript, Piscataway, NJ) was used as a positive control. The numbers in panel are the means of the antibodies; the numbers in panels &lt;b&gt;B&lt;\/b&gt;\u2013&lt;b&gt;E&lt;\/b&gt; are the lot numbers. Antibody 08C07 is lot 010. Credit: &lt;i&gt;Human Gene Therapy&lt;\/i&gt; (2024). DOI: 10.1089\/hum.2024.165\">\n<figure class=\"article-img\">\n<\/figure><\/div>\n<\/div>\n<p>Une \u00e9tude publi\u00e9e dans <i>Th\u00e9rapie g\u00e9nique humaine<\/i> a impliqu\u00e9 la g\u00e9n\u00e9ration d\u2019un anticorps monoclonal humain (mAb) dirig\u00e9 contre les \u00e9osinophiles humains. Les cha\u00eenes lourdes et l\u00e9g\u00e8res de ce mAb anti-\u00e9osinophile humain enti\u00e8rement humain ont \u00e9t\u00e9 administr\u00e9es via une th\u00e9rapie g\u00e9nique bas\u00e9e sur le virus ad\u00e9no-associ\u00e9 (AAV) \u00e0 des souris immunod\u00e9ficientes, o\u00f9 elles ont supprim\u00e9 les niveaux d&rsquo;\u00e9osinophiles humains in vivo.<\/p>\n<p>L&rsquo;hyper\u00e9osinophilie chronique est d\u00e9finie comme une \u00e9l\u00e9vation persistante des taux sanguins d&rsquo;\u00e9osinophiles. Elle est associ\u00e9e \u00e0 l&rsquo;infiltration des \u00e9osinophiles dans les tissus et aux l\u00e9sions organiques qui en r\u00e9sultent par la lib\u00e9ration par les \u00e9osinophiles de m\u00e9diateurs toxiques.<\/p>\n<p>\u00ab\u00a0En tant que nouvelle approche pour traiter l&rsquo;hyper\u00e9osinophilie chronique, nous avons \u00e9mis l&rsquo;hypoth\u00e8se que l&rsquo;administration par l&rsquo;AAV d&rsquo;un anticorps anti-\u00e9osinophile humain fournirait un traitement unique qui m\u00e9dierait la suppression persistante des taux d&rsquo;\u00e9osinophiles dans le sang\u00a0\u00bb, a d\u00e9clar\u00e9 Ronald Crystal, du Weill Cornell Medical College. , et co-auteurs de l\u2019\u00e9tude.<\/p>\n<p>Les chercheurs ont montr\u00e9 que la th\u00e9rapie g\u00e9nique in vivo chez la souris entra\u00eenait la destruction des \u00e9osinophiles humains et l&rsquo;activit\u00e9 de cytotoxicit\u00e9 cellulaire d\u00e9pendante des anticorps contre les \u00e9osinophiles humains. Ils ont conclu que le mAb anti-\u00e9osinophile humain \u00ab a le potentiel d\u2019offrir un b\u00e9n\u00e9fice th\u00e9rapeutique aux patients atteints d\u2019hyper\u00e9osinophilie chronique \u00bb.<\/p>\n<p>\u00ab\u00a0Cette \u00e9tude met en \u00e9vidence le potentiel du domaine de la th\u00e9rapie g\u00e9nique \u00e0 fournir des th\u00e9rapies efficaces \u00e0 long terme pour les maladies chroniques, qui n\u00e9cessitent actuellement des traitements fr\u00e9quents avec des effets secondaires douloureux et\/ou d\u00e9bilitants\u00a0\u00bb, d\u00e9clare le r\u00e9dacteur en chef de <i>Th\u00e9rapie g\u00e9nique humaine<\/i> Thomas Gallagher, Ph.D., de la facult\u00e9 de m\u00e9decine Chan de l&rsquo;Universit\u00e9 du Massachusetts.<\/p>\n<p>                                        <!-- print only --><\/p><\/div>\n","protected":false},"excerpt":{"rendered":"<p>Une \u00e9tude publi\u00e9e dans Th\u00e9rapie g\u00e9nique humaine a impliqu\u00e9 la g\u00e9n\u00e9ration d\u2019un anticorps monoclonal humain<\/p>\n","protected":false},"author":1,"featured_media":3333,"comment_status":"closed","ping_status":"","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[86],"tags":[250,1064,3392,203,1063,1165],"class_list":["post-3332","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-les-maladies","tag-chronique","tag-genique","tag-lhypereosinophilie","tag-pourrait","tag-therapie","tag-traiter","generate-columns","tablet-grid-50","mobile-grid-100","grid-parent","grid-50","resize-featured-image"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v23.4 - 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