# Integrated Role of Microbial, Fungal, and Plant-Derived Interventions in the Management of Celiac Disease: A Narrative Review

**Authors:** Karolina Kubala, Tomasz Pietrucha, Mikolaj Goldyn, Magdalena Grabinska, Paulina Halik, Justyna Jusiak

PMC · DOI: 10.7759/cureus.102471 · Cureus · 2026-01-28

## TL;DR

This review explores additional biological strategies to manage celiac disease beyond a gluten-free diet, including enzymes, probiotics, and plant-based agents to improve gluten detoxification and intestinal health.

## Contribution

The paper provides a comprehensive overview of integrated biological interventions for celiac disease management, emphasizing novel enzymatic and microbiota-based approaches.

## Key findings

- Enzymatic approaches like latiglutenase can degrade harmful gluten peptides in the gut.
- Probiotics such as Lactobacillus and Bifidobacterium may reduce inflammation and support gliadin breakdown.
- Plant-derived cysteine proteases show promise for gluten detoxification and food processing safety.

## Abstract

Celiac disease (CeD) is a chronic autoimmune enteropathy triggered by gluten ingestion in genetically susceptible individuals carrying human leukocyte antigen (HLA)-DQ2 or HLA-DQ8 haplotypes. While a strict gluten-free diet (GFD) remains the primary treatment, many patients experience persistent symptoms and incomplete mucosal recovery, often due to accidental exposure. This narrative review evaluates complementary biological strategies that enhance gluten management beyond dietary avoidance. We discuss enzymatic approaches using bacterial and fungal prolyl endopeptidases (PEPs) and engineered enzyme combinations, such as latiglutenase, to degrade immunogenic peptides in the gastrointestinal tract. Furthermore, we examine the restoration of intestinal barrier integrity through zonulin antagonists such as larazotide acetate. The role of gut microbiota modulation with probiotics, such as Lactobacillus and Bifidobacterium strains, is analyzed for its potential to reduce inflammation and support gliadin degradation. Additionally, plant-derived cysteine proteases from sprouting cereals are presented as promising agents for gluten detoxification. Finally, the application of enzymatic degradation in food processing is considered to improve the safety and affordability of gluten-free products. Together, these strategies offer a multidimensional framework for enhancing clinical outcomes and quality of life for individuals with CeD.

## Linked entities

- **Proteins:** Hp (haptoglobin)
- **Diseases:** celiac disease (MONDO:0005130)
- **Species:** Lactobacillus (taxon 1578), Bifidobacterium (taxon 1678)

## Full-text entities

- **Genes:** TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040] {aka CAEND1, CED, DPD1, IBDIMDE, LAP, TGF-beta1}, KLRK1 (killer cell lectin like receptor K1) [NCBI Gene 22914] {aka CD314, D12S2489E, KLR, NKG2-D, NKG2D}, LAP3 (leucine aminopeptidase 3) [NCBI Gene 51056] {aka HEL-S-106, LAP, LAPEP, PEPS}, CD79A (CD79a molecule) [NCBI Gene 973] {aka IGA, IGAlpha, MB-1, MB1}, MICA (MHC class I polypeptide-related sequence A) [NCBI Gene 100507436] {aka MIC-A, PERB11.1}, IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}, ANPEP (alanyl aminopeptidase, membrane) [NCBI Gene 290] {aka AP-M, AP-N, APN, CD13, GP150, LAP1}, HP (haptoglobin) [NCBI Gene 3240] {aka HP2ALPHA2, HPA1S}, HLA-DQB1 (major histocompatibility complex, class II, DQ beta 1) [NCBI Gene 3119] {aka CELIAC1, HLA-DQB, IDDM1}, MYLK (myosin light chain kinase) [NCBI Gene 4638] {aka AAT7, KRP, MLCK, MLCK1, MLCK108, MLCK210}, IL15 (interleukin 15) [NCBI Gene 3600] {aka IL-15}
- **Diseases:** infertility (MESH:D007246), osteoporosis (MESH:D010024), dermatitis herpetiformis (MESH:D003874), symptoms (MESH:D012816), malabsorption (MESH:D008286), crypt hyperplasia (MESH:D006965), mucosal (MESH:D052016), villous atrophy (MESH:C564019), abdominal discomfort (MESH:D000007), dysbiosis (MESH:D064806), abdominal pain (MESH:D015746), anxiety (MESH:D001007), headache (MESH:D006261), inflammation (MESH:D007249), gastrointestinal symptoms (MESH:D012817), EATL (MESH:D058527), autoimmune enteropathy (MESH:C538273), neurological disorders (MESH:D009461), iron-deficiency anemia (MESH:D018798), CeD. (MESH:D002446), autoimmune (MESH:D001327), fatigue (MESH:D005221), chronic diarrhea (MESH:D003967), seropositive (MESH:D006679)
- **Chemicals:** IMGX003 (-), LA (MESH:C525167), glutamine (MESH:D005973), mannitol (MESH:D008353), proline (MESH:D011392), lactulose (MESH:D007792)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116], Myxococcus xanthus (species) [taxon 34], Homo sapiens (human, species) [taxon 9606], Bifidobacterium (genus) [taxon 1678], Novosphingobium capsulatum (species) [taxon 13688], Hordeum vulgare (barley, species) [taxon 4513], Elizabethkingia meningoseptica (species) [taxon 238], Streptomyces griseus (species) [taxon 1911], Lacticaseibacillus rhamnosus (species) [taxon 47715], Aspergillus niger (species) [taxon 5061], Lactobacillus (genus) [taxon 1578], Bifidobacterium longum (species) [taxon 216816], SC [taxon 544725], Mucor (genus) [taxon 4830]

## Full text

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## References

44 references — full list in the complete paper: https://tomesphere.com/paper/PMC12947713/full.md

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Source: https://tomesphere.com/paper/PMC12947713