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Targeting delivery of anti-TNFα oligonucleotide into activated colonic macrophages protects against experimental colitis
  1. Longsheng Zuo,
  2. Zhen Huang,
  3. Lei Dong,
  4. Lingqing Xu,
  5. Yi'an Zhu,
  6. Ke Zeng,
  7. Chenyu Zhang,
  8. Jiangning Chen,
  9. Junfeng Zhang
  1. State Key Laboratory of Pharmaceutical Biotechnology, School of Life Sciences, Nanjing University, Nanjing, PR China
  1. Correspondence to Professor J Zhang, State Key Laboratory of Pharmaceutical Biotechnology, School of Life Sciences, Nanjing University, Nanjing 210093, China; jfzhang{at}nju.edu.cn

Abstract

Background and aims Tumour necrosis factor α (TNFα) is a focal point of the inflammatory cascade in Crohn's disease (CD). As an emerging approach to block cytokines, antisense oligonucleotide (ASO) has developed quickly, but is thwarted by a key obstacle—safe and effective delivery to specified cells. Here a novel nano-complex, based on galactosylated low molecular weight chitosan (gal-LMWC) and an ASO against TNFα, is presented which may be effective for CD treatment. The aim of this study was to investigate the targeting delivery ability of the gal-LMWC/ASO complex into activated macrophages and its potential therapeutic action in experimental colitis.

Methods Gal-LMWC was associated with ASO to form a stable nano-complex and the complex was injected into mice by intracolonic administration. Cellular localisation of the gal-LMWC/ASO complex in the colon was determined. The therapeutic effects were further studied in 2,4,6-trinitrobenzene sulfonic acid (TNBS)-induced colitis and CD4+CD45RBhi T cell transfer colitis.

Results Intracolonic administration of the gal-LMWC/ASO complex resulted in the successful delivery of ASO into activated colonic macrophages and a significant reduction of colonic TNFα in mice with colitis. A single injection in TNBS colitis or repeated treatment in CD45RBhi transfer colitis both significantly ameliorated the clinical and histopathological severity of the wasting disease, reduced tissue levels of inflammatory cytokines and abrogated body weight loss, diarrhoea and intestinal protein loss.

Conclusions It is the first time a non-viral gene vector has been combined with an ASO targeted to activated macrophages in the treatment of CD. The inhibition of TNFα by this strategy represents a promising therapeutic approach for the treatment of CD.

  • Antisense oligonucleotide
  • Crohn's disease
  • experimental colitis
  • galactosylated chitosan
  • gene therapy
  • targeting delivery
  • TNFα

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Footnotes

  • Funding This work was supported by the National Natural Science Foundation of China (50673041, 30771036 and BK2007144), the National Basic Research Foundation of China (973 Program 2006CB503909), the Key Program for Science and Technology Research from the Chinese Ministry of Education (01005) and the Chinese National Pharmaceutical Programs (2009ZX09503-028).

  • Competing interests None.

  • Provenance and peer review Not commissioned; externally peer reviewed.

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