Transient depletion of specific immune cell populations to improve adenovirus‐mediated transgene expression in the liver. (10th May 2014)

• Record Type: Journal Article
• Authors: Alzuguren, Pilar; Hervas‐Stubbs, Sandra; Gonzalez‐Aseguinolaza, Gloria; Poutou, Joanna; Fortes, Puri; Mancheno, Uxua; Bunuales, Maria; Olagüe, Cristina; Razquin, Nerea; Van Rooijen, Nico; Enguita, Monica; Hernandez‐Alcoceba, Ruben
• Is Part Of: Liver international. Volume 35:Number 4(2015:Apr.)
• Page Start: 1274
• Page End: 1289
• Publication Date: 2014-05-10
• Subjects: Liver -- Periodicals; Liver -- Diseases -- Periodicals; 616.362
• DOI: 10.1111/liv.12571
• Languages: English
• ISSNs: 1478-3223

Abstract

<abstract abstract-type="main" id="liv12571-abs-0001"> <title>Abstract</title> <sec id="liv12571-sec-0001" sec-type="section"> <title>Background & Aims</title> <p>Adenoviral (Ad) vectors are currently one of the most efficient tools for <italic>in vivo</italic> gene transfer to the liver. However, anti‐Ad immune responses limit the safety and efficacy of these vectors. The initial inflammatory reaction is a concern in terms of toxicity, and it favours the development of cellular and humoral responses leading to short transgene persistence and inefficient vector re‐administrations. Therefore, safe and simple ways to interfere with these processes are needed. Study ways to deplete specific immune cell populations and their impact on liver‐directed gene transfer.</p> </sec> <sec id="liv12571-sec-0002" sec-type="section"> <title>Methods</title> <p>First‐generation Ad vectors encoding reporter genes (luciferase or β‐galactosidase) were injected intravenously into Balb/c mice. Kupffer cells and splenic macrophages were depleted by intravenous administration of clodronate liposomes. B lymphocytes, CD4<sup>+</sup>, CD8<sup>+</sup> T lymphocytes or NK cells were depleted by intraperitoneal injection of anti‐M plus anti‐D, anti‐CD4, anti‐CD8 or anti‐asialo‐GM1 antibodies respectively. Long‐term evolution of luciferase expression in the liver was monitored by bioluminescence imaging.</p> </sec> <sec id="liv12571-sec-0003" sec-type="section"> <title>Results</title> <p>The anti‐CD4 monoclonal antibody impaired cellular and humoral immune responses, leading to efficient vector re‐administration. Clodronate liposomes had no impact on humoral responses but caused a 100–1000 fold increase in liver transduction, stabilized transgene expression, reduced the concentration of inflammatory cytokines, and inhibited lymphocyte activation.</p> </sec> <sec id="liv12571-sec-0004" sec-type="section"> <title>Conclusions</title> <p>Transient CD4<sup>+</sup> T‐cell depletion using antibodies is a clinically feasible procedure that allows efficient Ad redosing. Systemic administration of clodronate liposomes may further increase the safety and efficacy of vectors.</p> </sec> </abstract>