# Phosphodiesterase 4 inhibitor combined with secukinumab relieves clinical symptoms in patients with psoriasis via regulating p38MAPK activation and the immune response inflammation

**Authors:** Qian Zhang, Zihan Zhou, Li Zhang, Xingxing Wang, Huani Zhao, Changzheng Wei, Min Zhao

PMC · DOI: 10.4314/ahs.v25i1.35 · African Health Sciences · 2025-03-01

## TL;DR

Combining a PDE-4 inhibitor with secukinumab improves psoriasis symptoms by reducing inflammation and immune response.

## Contribution

The study demonstrates that combining PDE-4 inhibitors with secukinumab enhances treatment efficacy in psoriasis.

## Key findings

- The study group showed significantly lower PASI and symptom scores compared to the control group.
- The combination therapy reduced IL-6, IL-17, and p38MAPK expression more effectively than monotherapy.
- The total effective rate was higher in the combination therapy group (83.33%) than in the control group (60.00%).

## Abstract

The purpose of the present study was to explore the effect of phosphodiesterase 4 (PDE-4) inhibitor combined with secukinumab monoclonal antibody on the activation level of p38 mitogen-activated protein kinases (p38MAPK) in psoriatic leukocytes.

The clinical data of 60 patients with psoriasis were retrospectively analyzed, and they were divided into a control group (secukinumab monotherapy, 30 cases) and a study group (PDE-4 inhibitory therapy). Agent combined with secukinumab treatment(30 cases), all were treated for 3 months. The Psoriasis Area and Severity Index (PASI), clinical symptom score, serum inflammatory factors, p38MAPK gene expression in lesion tissue, and clinical outcome were compared between the two groups.

After treatment, the PSAI score (t=5.051) and symptom score (t=14.102) of the study group were lower than those of the control group, and the relative expression of interleukin-6 (IL-6) (t=7.514) and p38MAPK (t=4.219), the relative expression of interleukin-17 (IL-17) (t=2.579) was lower than that of the control group. The total effective rate in the study group (83.33% vs. 60.00%) was higher than that in the control group.

Secukinumab along with phosphodiesterase 4 inhibitors reduces p38MAPK activation, and improves immune response, inflammation, and clinical symptoms in patients with psoriasis.

## Linked entities

- **Genes:** P38mapk (p38 map kinase) [NCBI Gene 692545], IL6 (interleukin 6) [NCBI Gene 3569], IL17A (interleukin 17A) [NCBI Gene 3605]
- **Proteins:** PDE4A (phosphodiesterase 4A)
- **Diseases:** psoriasis (MONDO:0005083)

## Full-text entities

- **Genes:** IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, PDE4A (phosphodiesterase 4A) [NCBI Gene 5141] {aka DPDE2, PDE4, PDE46}, IL17A (interleukin 17A) [NCBI Gene 3605] {aka CTLA-8, CTLA8, IL-17, IL-17A, IL17, ILA17}
- **Diseases:** inflammation (MESH:D007249), psoriatic (MESH:D015535), Psoriasis (MESH:D011565)
- **Chemicals:** Secukinumab (MESH:C555450)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12865051/full.md

## References

17 references — full list in the complete paper: https://tomesphere.com/paper/PMC12865051/full.md

---
Source: https://tomesphere.com/paper/PMC12865051