Literature DB >> 35838821

SLGT2 Inhibitor Rescues Myelopoiesis in G6PC3 Deficiency.

Prashant Hiwarkar1, Umair Bargir2, Ambreen Pandrowala3, Minnie Bodhanwala4, Naresh Thakker5, Prasad Taur6, Manisha Madkaikar2, Mukesh Desai6.   

Abstract

The energy metabolism of myeloid cells depends primarily on glycolysis. 1,5-Anhydroglucitol (1,5AG), a natural monosaccharide, is erroneously phosphorylated by glucose-phosphorylating enzymes to produce 1,5-anhydroglucitol-6-phosphate (1,5AG6P), a powerful inhibitor of hexokinases. The endoplasmic reticulum transporter (SLC37A4/G6PT) and the phosphatase G6PC3 cooperate to dephosphorylate 1,5AG6P. Failure to eliminate 1,5AG6P is the mechanism of neutrophil dysfunction and death in G6PC3-deficient mice. Sodium glucose cotransporter 2 (SLGT2) inhibitor reduces 1,5AG level in the blood and restores the neutrophil count in G6PC3-deficient mice. In the investigator-initiated study, a 30-year-old G6PC3-deficient woman with recurrent infections, distressing gastrointestinal symptoms, and multi-lineage cytopenia was treated with an SLGT2-inhibitor. A significant increase in all the hematopoietic cell lineages and substantial improvement in the quality of life was observed.
© 2022. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

Entities:  

Keywords:  Congenital neutropenia; Empagliflozin; G6PC3 deficiency; SLGT2 inhibitor

Year:  2022        PMID: 35838821     DOI: 10.1007/s10875-022-01323-4

Source DB:  PubMed          Journal:  J Clin Immunol        ISSN: 0271-9142            Impact factor:   8.542


  1 in total

1.  Dipyridamole and intravenous deoxycytidine therapy in a patient with adenosine deaminase deficiency.

Authors:  A J Ammann; M J Cowan; D W Martin; D W Wara
Journal:  Birth Defects Orig Artic Ser       Date:  1983
  1 in total

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