Cutting-edge regenerative therapy for Hirschsprung disease and its allied disorders
- PMID: 37668735
- DOI: 10.1007/s00595-023-02741-6
Cutting-edge regenerative therapy for Hirschsprung disease and its allied disorders
Abstract
Hirschsprung disease (HSCR) and its associated disorders (AD-HSCR) often result in severe hypoperistalsis caused by enteric neuropathy, mesenchymopathy, and myopathy. Notably, HSCR involving the small intestine, isolated hypoganglionosis, chronic idiopathic intestinal pseudo-obstruction, and megacystis-microcolon-intestinal hypoperistalsis syndrome carry a poor prognosis. Ultimately, small-bowel transplantation (SBTx) is necessary for refractory cases, but it is highly invasive and outcomes are less than optimal, despite advances in surgical techniques and management. Thus, regenerative therapy has come to light as a potential form of treatment involving regeneration of the enteric nervous system, mesenchyme, and smooth muscle in affected areas. We review the cutting-edge regenerative therapeutic approaches for managing HSCR and AD-HSCR, including the use of enteric nervous system progenitor cells, embryonic stem cells, induced pluripotent stem cells, and mesenchymal stem cells as cell sources, the recipient intestine's microenvironment, and transplantation methods. Perspectives on the future of these treatments are also discussed.
Keywords: Allied disorders of Hirschsprung disease; Chronic idiopathic intestinal pseudo-obstruction; Hirschsprung disease; Hypoganglionosis; Regenerative therapy; Stem cell therapy.
© 2023. The Author(s) under exclusive licence to Springer Nature Singapore Pte Ltd.
Similar articles
-
The incidence and outcome of allied disorders of Hirschsprung's disease in Japan: Results from a nationwide survey.Asian J Surg. 2017 Jan;40(1):29-34. doi: 10.1016/j.asjsur.2015.04.004. Epub 2015 Jul 26. Asian J Surg. 2017. PMID: 26216257
-
Japanese clinical practice guidelines for allied disorders of Hirschsprung's disease, 2017.Pediatr Int. 2018 May;60(5):400-410. doi: 10.1111/ped.13559. Pediatr Int. 2018. PMID: 29878629
-
Classification and diagnostic criteria of variants of Hirschsprung's disease.Pediatr Surg Int. 2013 Sep;29(9):855-72. doi: 10.1007/s00383-013-3351-3. Pediatr Surg Int. 2013. PMID: 23943250 Review.
-
Recent advances in regenerative medicine to treat enteric neuropathies: use of human cells.Neurogastroenterol Motil. 2017 Jan;29(1). doi: 10.1111/nmo.12993. Neurogastroenterol Motil. 2017. PMID: 28028898 Review.
-
Human enteric nervous system progenitor transplantation improves functional responses in Hirschsprung disease patient-derived tissue.Gut. 2024 Aug 8;73(9):1441-1453. doi: 10.1136/gutjnl-2023-331532. Gut. 2024. PMID: 38816188 Free PMC article.
Cited by
-
Robotic intersphincteric resection for low rectal cancer: a cumulative sum analysis for the learning curve.Surg Today. 2024 Nov;54(11):1329-1336. doi: 10.1007/s00595-024-02841-x. Epub 2024 May 8. Surg Today. 2024. PMID: 38717597
-
Label-free diagnostic procedure for hirschsprung's disease to detect intestinal mucosal characteristics of aganglionosis by Raman spectroscopy with optimized decision algorithms.Lasers Med Sci. 2025 Aug 29;40(1):346. doi: 10.1007/s10103-025-04579-5. Lasers Med Sci. 2025. PMID: 40879800 Free PMC article.
-
Conditions that mimic Hirschsprung's disease, but that are not Hirschsprung's disease.World J Pediatr Surg. 2025 Mar 12;8(1):e000918. doi: 10.1136/wjps-2024-000918. eCollection 2025. World J Pediatr Surg. 2025. PMID: 40094120 Free PMC article. Review.
-
Surgical pathology of Hirschsprung disease (HSCR).World J Pediatr Surg. 2025 Jul 31;8(3):e000882. doi: 10.1136/wjps-2024-000882. eCollection 2025. World J Pediatr Surg. 2025. PMID: 40756452 Free PMC article. Review.
-
A Case Report of a Child with Constipation Diagnosed with Acquired Myenteric Hypoganglionosis.Reports (MDPI). 2025 Jul 15;8(3):108. doi: 10.3390/reports8030108. Reports (MDPI). 2025. PMID: 40700241 Free PMC article.
References
Publication types
MeSH terms
Supplementary concepts
LinkOut - more resources
Full Text Sources