# The research progress on the role of glucose-6-phosphate dehydrogenase in immune regulation

**Authors:** Dingmei Zhang, Yizhong Wang

PMC · DOI: 10.7717/peerj.20971 · PeerJ · 2026-03-19

## TL;DR

Glucose-6-phosphate dehydrogenase (G6PD) regulates immune cell function and is linked to autoimmune diseases, infections, and cancer, offering new therapeutic possibilities.

## Contribution

This paper reviews G6PD's dual role in immune regulation and its potential as a target for treating immune-related diseases.

## Key findings

- G6PD regulates immune cell metabolism and redox balance, affecting adaptive and innate immunity.
- G6PD deficiency or overexpression is linked to autoimmune diseases, infections, and tumor progression.
- Targeting G6PD with inhibitors or gene therapy shows promise for treating immune-related conditions.

## Abstract

Glucose-6-phosphate dehydrogenase (G6PD), the rate-limiting enzyme of the pentose phosphate pathway (PPP), plays a pivotal role in immune regulation by regulating metabolic reprogramming and redox homeostasis of immune cells. It mediates the production of nicotinamide adenine dinucleotide phosphate (NADPH) and ribose-5-phosphate (R5P), which are essential for the activation, proliferation, and effector function of T lymphocytes, B lymphocytes, macrophages, and neutrophils—specifically promoting T/B cell-mediated adaptive immunity and macrophage/neutrophil-mediated innate immune responses. Abnormal G6PD activity (deficiency or overexpression) is closely associated with the pathogenesis of immune-related diseases: G6PD deficiency increases susceptibility to autoimmune diseases (e.g., rheumatoid arthritis, systemic lupus erythematosus) and infectious diseases (e.g., hepatitis, malaria, COVID-19) by inducing oxidative stress and immune cell dysfunction; in tumor immunity, G6PD dualistically promotes tumor cell proliferation while regulating anti-tumor immunity via modulating cytoxic D8+ T cell exhaustion and macrophage polarization. Additionally, G6PD-targeted immunotherapies, including small-molecule inhibitors and gene therapy, have shown promising preclinical potential for treating immune-related diseases. These findings highlight G6PD as a key metabolic-immune hub, providing critical theoretical basis for understanding immune regulation mechanisms and developing novel diagnostic and therapeutic strategies for autoimmune diseases, infectious diseases, and tumors.

## Linked entities

- **Genes:** G6PD (glucose-6-phosphate dehydrogenase) [NCBI Gene 2539]
- **Chemicals:** nicotinamide adenine dinucleotide phosphate (PubChem CID 5885), ribose-5-phosphate (PubChem CID 77982)
- **Diseases:** rheumatoid arthritis (MONDO:0008383), systemic lupus erythematosus (MONDO:0007915), hepatitis (MONDO:0002251), malaria (MONDO:0005136), COVID-19 (MONDO:0100096)

## Full-text entities

- **Genes:** G6PD (glucose-6-phosphate dehydrogenase) [NCBI Gene 2539] {aka CNSHA1, G6PD1}
- **Diseases:** hepatitis, malaria (MESH:D008288), rheumatoid arthritis (MESH:D001172), immune-related diseases (MESH:D007154), tumor (MESH:D009369), systemic lupus erythematosus (MESH:D008180), autoimmune diseases (MESH:D001327), G6PD deficiency (MESH:D005955), COVID-19 (MESH:D000086382), infectious diseases (MESH:D003141)
- **Chemicals:** pentose phosphate (MESH:D010428), NADPH (MESH:D009249), R5P (MESH:C031626)

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13006011/full.md

## References

81 references — full list in the complete paper: https://tomesphere.com/paper/PMC13006011/full.md

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Source: https://tomesphere.com/paper/PMC13006011