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PGM3 insufficiency: a glycosylation disorder causing a notable T cell defect.
- Source :
-
Frontiers in immunology [Front Immunol] 2024 Dec 24; Vol. 15, pp. 1500381. Date of Electronic Publication: 2024 Dec 24 (Print Publication: 2024). - Publication Year :
- 2024
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Abstract
- Background: Hypomorphic mutations in the phosphoacetylglucosamine mutase 3 ( PGM3 ) gene cause a glycosylation disorder that leads to immunodeficiency. It is often associated with recurrent infections and atopy. The exact etiology of this condition remains unclear.<br />Objective: This study aimed to characterize the phenotypes and immunological features associated with PGM3 insufficiency and investigate potential disease mechanisms.<br />Methods: A systematic review of 44 published cases of PGM3 variants was performed, followed by T-cell phenotyping of two patients with PGM3 variants. A genotype-phenotypic severity study was conducted by comparing the residual PGM3 expression of the 12 reconstituted variants in human B cells. A PGM3 inhibitor was used to assess its effect on CD4+ T cell proliferation and differentiation.<br />Results: Patients with PGM3 variants frequently presented with recurrent infections and atopy, accompanied by reduced naïve CD4+ T cell counts. A genotype-phenotype study showed that low levels of residual PGM3 expression are correlated with disease severity. Notably, inhibition of PGM3 activity impaired TCR-mediated CD4+ T cell proliferation and the synthesis of UDP-GlcNAc, complex N-glycans, O-GlcNAc, glycolytic stress, and mitochondrial respiration during proliferation in a dose-dependent manner. Partial loss of PGM3 activity was observed to preferentially enhance Th1 and Th2 differentiation, while attenuating Th17 and Treg differentiation, consistent with clinical observations.<br />Conclusion: PGM3 is a critical regulator of CD4+ T-cell proliferation and differentiation. These findings provide new insights into the diverse clinical manifestations and therapeutic development of PGM3 deficiency.<br />Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.<br /> (Copyright © 2024 Yang, Zerbato, Pessina, Brambilla, Andreani, Frey-Jakobs, Fliegauf, Barbouche, Zhang, Chiaradonna, Proietti, Du and Grimbacher.)
- Subjects :
- Humans
Cell Differentiation genetics
Cell Differentiation immunology
Cell Proliferation genetics
Glycosylation
Mutation
Phenotype
Lymphocyte Activation genetics
Lymphocyte Activation immunology
Phosphoglucomutase deficiency
Phosphoglucomutase genetics
Congenital Disorders of Glycosylation genetics
Congenital Disorders of Glycosylation immunology
Subjects
Details
- Language :
- English
- ISSN :
- 1664-3224
- Volume :
- 15
- Database :
- MEDLINE
- Journal :
- Frontiers in immunology
- Publication Type :
- Academic Journal
- Accession number :
- 39776909
- Full Text :
- https://doi.org/10.3389/fimmu.2024.1500381