Gene Therapy in Combination with Nitrogen Scavenger Pretreatment Corrects Biochemical and Behavioral Abnormalities of Infant Citrullinemia Type 1 Mice.
citrullinemia
gene therapy
hyperammonemia
rAAV
urea cycle
Journal
International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791
Informations de publication
Date de publication:
29 Nov 2022
29 Nov 2022
Historique:
received:
04
11
2022
revised:
22
11
2022
accepted:
23
11
2022
entrez:
11
12
2022
pubmed:
12
12
2022
medline:
15
12
2022
Statut:
epublish
Résumé
Citrullinemia type I (CTLN1) is a rare autosomal recessive disorder caused by mutations in the gene encoding argininosuccinate synthetase 1 (ASS1) that catalyzes the third step of the urea cycle. CTLN1 patients suffer from impaired elimination of nitrogen, which leads to neurotoxic levels of circulating ammonia and urea cycle byproducts that may cause severe metabolic encephalopathy, death or irreversible brain damage. Standard of care (SOC) of CTLN1 consists of daily nitrogen-scavenger administration, but patients remain at risk of life-threatening decompensations. We evaluated the therapeutic efficacy of a recombinant adeno-associated viral vector carrying the ASS1 gene under the control of a liver-specific promoter (VTX-804). When administered to three-week-old CTLN1 mice, all the animals receiving VTX-804 in combination with SOC gained body weight normally, presented with a normalization of ammonia and reduction of citrulline levels in circulation, and 100% survived for 7 months. Similar to what has been observed in CTLN1 patients, CTLN1 mice showed several behavioral abnormalities such as anxiety, reduced welfare and impairment of innate behavior. Importantly, all clinical alterations were notably improved after treatment with VTX-804. This study demonstrates the potential of VTX-804 gene therapy for future clinical translation to CTLN1 patients.
Identifiants
pubmed: 36499263
pii: ijms232314940
doi: 10.3390/ijms232314940
pmc: PMC9736988
pii:
doi:
Substances chimiques
Ammonia
7664-41-7
Nitrogen
N762921K75
Argininosuccinate Synthase
EC 6.3.4.5
Urea
8W8T17847W
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : Vivet Therapeutics
ID : Not apply
Références
Ann Neurol. 2019 Jul;86(1):116-128
pubmed: 31018246
Mol Ther Methods Clin Dev. 2020 Nov 17;20:169-180
pubmed: 33473356
Mol Ther. 2020 Jul 8;28(7):1717-1730
pubmed: 32359471
Mol Ther. 2009 Aug;17(8):1340-6
pubmed: 19384294
Mol Ther Nucleic Acids. 2021 Aug 19;25:585-602
pubmed: 34589280
J Mother Child. 2020 Oct 02;24(2):32-38
pubmed: 33179600
Pediatr Clin North Am. 2018 Apr;65(2):231-246
pubmed: 29502911
Lancet. 2017 Aug 26;390(10097):849-860
pubmed: 28712537
Ann Clin Transl Neurol. 2019 Sep;6(9):1858-1871
pubmed: 31469252
Gene Ther. 2013 Aug;20(8):785-96
pubmed: 23388701
J Clin Exp Hepatol. 2018 Sep;8(3):262-271
pubmed: 30302043
Nat Med. 2013 Dec;19(12):1643-8
pubmed: 24240184
Gene Ther. 2015 Feb;22(2):111-5
pubmed: 25474440
Clin Chim Acta. 2017 Jan;464:236-243
pubmed: 27923571
Mol Genet Metab. 2020 Dec;131(4):390-397
pubmed: 33288448
Mol Ther. 2018 Mar 7;26(3):801-813
pubmed: 29433939
Metab Brain Dis. 2013 Jun;28(2):269-75
pubmed: 23149878
Blood. 2003 Oct 1;102(7):2412-9
pubmed: 12791653
J Inherit Metab Dis. 2016 Jul;39(4):573-84
pubmed: 27215558
Nat Commun. 2018 Aug 29;9(1):3505
pubmed: 30158522
Hum Mutat. 2017 May;38(5):471-484
pubmed: 28111830
J Clin Transl Hepatol. 2019 Dec 28;7(4):352-361
pubmed: 31915605
Hum Mol Genet. 2016 Aug 15;25(16):3555-3563
pubmed: 27378686
J Hum Genet. 2019 Sep;64(9):833-847
pubmed: 31110235
Am J Pathol. 2010 Oct;177(4):1958-68
pubmed: 20724589
Mol Ther. 2012 Oct;20(10):1844-51
pubmed: 22760543
J Inherit Metab Dis. 2019 Nov;42(6):1147-1161
pubmed: 30723942
Clin Transl Immunology. 2022 Feb 24;11(2):e1375
pubmed: 35228870
Am J Med Genet A. 2004 Aug 15;129A(1):77-82
pubmed: 15266621
Adv Clin Chem. 2014;67:73-150
pubmed: 25735860
Sci Rep. 2021 Feb 11;11(1):3580
pubmed: 33574402
J Inherit Metab Dis. 2019 Nov;42(6):1176-1191
pubmed: 31268178
Mol Genet Metab. 2018 Nov;125(3):241-250
pubmed: 30253962
Neurochem Int. 2002 Aug-Sep;41(2-3):155-60
pubmed: 12020615
Mol Ther. 2003 Mar;7(3):375-85
pubmed: 12668133
Pediatr Transplant. 2017 Sep;21(6):
pubmed: 28608518
Am J Physiol. 1984 Sep;247(3 Pt 1):G290-5
pubmed: 6476119
Mol Ther. 2013 Oct;21(10):1823-31
pubmed: 23817206
J Inherit Metab Dis. 2018 Jul;41(4):657-667
pubmed: 29423830
N Engl J Med. 2014 Nov 20;371(21):1994-2004
pubmed: 25409372
Somat Cell Mol Genet. 1994 Jan;20(1):55-60
pubmed: 8197477
Proc Natl Acad Sci U S A. 2019 Oct 15;116(42):21150-21159
pubmed: 31501335
Hum Gene Ther. 2019 Oct;30(10):1190-1203
pubmed: 31347416
J Inherit Metab Dis. 2016 Mar;39(2):231-41
pubmed: 26310964
Mol Genet Metab. 2013 Sep-Oct;110(1-2):179-80
pubmed: 23972786
J Inherit Metab Dis. 2019 Nov;42(6):1192-1230
pubmed: 30982989
Mol Ther Methods Clin Dev. 2019 Sep 26;15:221-231
pubmed: 31709273
J Nutr. 2004 Oct;134(10 Suppl):2791S-2795S; discussion 2796S-2797S
pubmed: 15465786
Cell Rep. 2015 Aug 11;12(6):1056-68
pubmed: 26235624
Mol Genet Metab. 2012 Feb;105(2):203-11
pubmed: 22133298
Gene Ther. 2013 Dec;20(12):1188-91
pubmed: 24131980
Clin Liver Dis. 2000 Nov;4(4):815-30, vi
pubmed: 11232359