# The Effects of Moxibustion on PD-1/PD-L1-Related Molecular Expression and Inflammatory Cytokine Levels in RA Rats

**Authors:** Yumei Zhong, Deli Lai, Linlin Zhang, Wenting Lu, Yanan Shang, Haiyan Zhou

PMC · DOI: 10.1155/2021/6658946 · Evidence-based Complementary and Alternative Medicine : eCAM · 2021-12-11

## TL;DR

This study shows that moxibustion reduces inflammation in rheumatoid arthritis by affecting the PD-1/PD-L1 pathway.

## Contribution

The study is the first to demonstrate that moxibustion's anti-inflammatory effects in RA are mediated through the PD-1/PD-L1 pathway.

## Key findings

- Moxibustion decreased IFN-γ and increased IL-4 and IL-10 levels in RA rats.
- Blocking PD-1 reduced the anti-inflammatory effects of moxibustion.
- Moxibustion alleviated synovial tissue proliferation in RA rats.

## Abstract

Rheumatoid arthritis (RA) is an autoimmune disease that starts with inflammation of the synovium. The pain and joint dysfunction caused by RA urgently need an effective treatment to alleviate the inflammatory reaction and delay the progression of the disease. The pathological damage of RA is proposed to associate with the dysfunction of the programmed cell death 1/programmed cell death ligand 1 (PD-1/PD-L1) pathway. Moxibustion, as a main complementary therapy of traditional Chinese medicine (TCM), has been proved effective to reduce chronic inflammatory reaction on RA, but whether the anti-inflammatory effects are mediated by PD-1/PD-L1 pathway is still unclear. Therefore, moxibustion was conducted in the rats with RA to investigate its effect on PD-1/PD-L1.

The rats' right hind paws were injected with Freundʼs complete adjuvant (FCA) to establish the model of RA. Seven days after the injection of FCA, moxibustion therapy was performed on the acupoints of Shenshu (BL23) and Zusanli (ST36) once a day for three weeks. Then, ELISA and immunohistochemical methods were used to analyze the influence of moxibustion on the expression of PD-1/PD-L1. If the moxibustion had an effect on the expression of PD-1/PD-L1-related molecules, we would knock down PD-1 with adenovirus vector. After moxibustion therapy, ELISA and histological analysis were performed to observe the anti-inflammatory effect of moxibustion.

The results demonstrated that moxibustion had an effect on the expression of PD-1-related molecules. The results of ELISA manifested that moxibustion decreased the level of IFN-γ and increased the level of IL-4 and IL-10. HE staining revealed that moxibustion alleviated the proliferation of synovial tissue. However, the anti-inflammatory effect and pathological improvement were weakened when PD-1 was blocked.

The results indicate that moxibustion affected the expression of PD-1/PD-L1-related molecules and can effectively treat RA damage. The anti-inflammatory effect of moxibustion was weakened when PD-1 was knocked down.

## Linked entities

- **Genes:** PDCD1 (programmed cell death 1) [NCBI Gene 5133], CD274 (CD274 molecule) [NCBI Gene 29126]
- **Chemicals:** IL-4 (PubChem CID 171905173), IL-10 (PubChem CID 146070)
- **Diseases:** rheumatoid arthritis (MONDO:0008383)
- **Species:** Rattus norvegicus (taxon 10116)

## Full-text entities

- **Genes:** PDCD1 (programmed cell death 1) [NCBI Gene 5133] {aka ADMIO4, AIMTBS, CD279, PD-1, PD1, SLEB2}, CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}, IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}, IL4 (interleukin 4) [NCBI Gene 3565] {aka BCGF-1, BCGF1, BSF-1, BSF1, IL-4}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}
- **Diseases:** autoimmune disease (MESH:D001327), pain (MESH:D010146), Inflammatory (MESH:D007249), RA (MESH:D001172), joint dysfunction (MESH:D007592)
- **Chemicals:** Chinese medicine (-), HE (MESH:D006371)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11407876/full.md

## References

46 references — full list in the complete paper: https://tomesphere.com/paper/PMC11407876/full.md

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Source: https://tomesphere.com/paper/PMC11407876