# Efficacy of spleen aminopeptide combined with budesonide nebulization in the treatment of pediatric bronchial asthma and its impact on immune function and inflammatory cytokines

**Authors:** Su He, Ning Ran, Xu Yang, Bing Zhu, Dan Zhou

PMC · DOI: 10.12669/pjms.42.1.12488 · Pakistan Journal of Medical Sciences · 2026-01-01

## TL;DR

This study shows that combining spleen aminopeptide with budesonide improves asthma treatment in children by boosting immunity and reducing inflammation.

## Contribution

The novel contribution is demonstrating the added benefit of spleen aminopeptide in pediatric asthma treatment when combined with budesonide.

## Key findings

- The combination therapy improved clinical response rates significantly compared to budesonide alone.
- The treatment enhanced immune markers like CD3+ and CD4+ and reduced inflammatory cytokines such as TNF-α and IL-6.
- The combination therapy did not increase adverse drug reactions compared to standard treatment.

## Abstract

To evaluate the clinical efficacy of spleen aminopeptide(SAP) combined with budesonide nebulization(BN) in the treatment of pediatric bronchial asthma, and its impact on the immune function and inflammatory cytokines of the affected population.

This was a retrospective study. A total of 120 children with bronchial asthma admitted to Baoding Hospital, Beijing Children’s Hospital Affiliated to Capital Medical University from December 2022 to October 2024 were enrolled and randomly divided into the control group(received symptomatic treatment along with BN) and study group(received additional oral SAP based on the control group regimen), with 60 cases in each group. After treatment, the clinical efficacy, adverse drug reaction(ADR) rate, changes in immune markers, and inflammatory cytokines were compared between the two groups.

The overall response rate was 93% in the study group and 78% in the control group, with a statistically significant difference(p= 0.02). The ADR was 15% in the study group and 12% in the control group, with no significant difference between the groups(p= 0.60). After treatment, levels of CD3+, CD4+, and CD4+/CD8+ ratio were significantly higher in the study group compared to the control group(p= 0.00, respectively). Additionally, post-treatment levels of TNF-α, CRP, and IL-6 were significantly lower in the study group than in the control group(p = 0.00, respectively).

The combination therapy using SAP and BN demonstrates significant clinical efficacy in treating pediatric bronchial asthma. SAP plus BN can effectively enhance immune function and reduce levels of inflammatory cytokines without significantly increasing adverse reactions.

## Linked entities

- **Chemicals:** budesonide (PubChem CID 5281004), IL-6 (PubChem CID 165368475)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Genes:** IGHE (immunoglobulin heavy constant epsilon) [NCBI Gene 3497] {aka IgE}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, SH2D1A (SH2 domain containing 1A) [NCBI Gene 4068] {aka DSHP, EBVS, IMD5, LYP, MTCP1, SAP}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, IL2 (interleukin 2) [NCBI Gene 3558] {aka IL-2, TCGF, lymphokine}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}
- **Diseases:** asthmatic (MESH:D013224), respiratory diseases (MESH:D012140), nosocomial infections (MESH:D003428), Inflammatory (MESH:D007249), cough (MESH:D003371), cytotoxicity (MESH:D064420), airway edema (MESH:D004487), Bronchial asthma (MESH:D001249), ulcers (MESH:D014456), dyspnea (MESH:D004417), infections (MESH:D007239), hematologic, immune system disorders (MESH:D007154), malignancies (MESH:D009369), chest tightness (MESH:D002637), Type-I hypersensitivity (MESH:D006969), adrenal cortical dysfunction (MESH:D018246), allergy (MESH:D004342), oral or pharyngeal candidiasis (MESH:D002180), wheezing (MESH:D012135), throat discomfort (MESH:C538390), hoarseness (MESH:D006685), Cognitive impairments (MESH:D003072), infectious diseases (MESH:D003141), airway obstruction (MESH:D000402), pulmonary dysfunction (MESH:D011660), bronchial spasms (MESH:D001986), bronchial hypersensitivity (MESH:D001982), bronchial smooth muscle spasm (MESH:D018235)
- **Chemicals:** ADR (MESH:D004317), oxygen (MESH:D010100), Spleen aminopeptide (MESH:C000722215), BN (-), leukotrienes (MESH:D015289), BUD (MESH:D019819)
- **Species:** Homo sapiens (human, species) [taxon 9606], Bos taurus (bovine, species) [taxon 9913], Sus scrofa (pig, species) [taxon 9823]
- **Mutations:** rs510432

## Full text

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## References

20 references — full list in the complete paper: https://tomesphere.com/paper/PMC12927119/full.md

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Source: https://tomesphere.com/paper/PMC12927119