Table 2.
Advantages and limitations for the non-pharmacological treatment of Helicobacter pylori.
Non-pharmacological | Advantages | Limitations | Reference |
---|---|---|---|
Probiotics therapy | Increased eradication rate, decreased side effects, less influence on gut microbiota | Low eradication rate of monotherapy | Losurdo et al. (2018), He et al. (2022), Viazis et al. (2022) |
Oxygen-enriched environment or hyperbaric oxygen therapy | Enhanced ability of immune cells to phagocytize, synergistic effect with antibiotics | Different genotypes of H. pylori respond differently to oxygen | Al-Waili and Butler (2006), Turhan et al. (2009), Park and Lee (2013) |
Antimicrobial photodynamic therapy | Targeting bacteria, killing the drug-resistant strains | Difficulty in vitro experiments | Luzzi and Tortora (2022), Yang et al. (2022) |
Nanomaterials | High efficacy and therapeutic index, excellent synergy with antibiotics, enhanced performance of drug delivery and release | Toxicity and difficulty in degradation | Mba and Nweze (2021), Patil-Sen (2021) |
Antimicrobial peptides | Significant selectivity to bacterial cells, broad-spectrum activity, cost-effective synthesis | Instability, poor bioavailability, short half-life and cytotoxicity | Li et al. (2022), Mba and Nweze (2022) |
Phage therapy | Easy to isolate, high specificity, no adverse immune responses and no impact on human microbiome | Susceptible to stomach acid and digestive enzymes | Nobrega et al. (2016), Vinner et al. (2019), Anyaegbunam et al. (2022) |
Modified lysins | Penetrating the outer membrane of bacteria | Producing neutralizing antibodies | Xu et al. (2020), Abdelrahman et al. (2021) |