Lacticaseibacillus paracasei GM-080 Ameliorates Allergic Airway Inflammation in Children with Allergic Rhinitis: From an Animal Model to a Double-Blind, Randomized, Placebo-Controlled Trial

Author:

Lin En-Kwang12,Chang Wen-Wei34ORCID,Jhong Jhih-Hua5ORCID,Tsai Wan-Hua6,Chou Chia-Hsuan6,Wang I-Jen78910ORCID

Affiliation:

1. Institute of Clinical Medicine, National Yang Ming Chiao Tung University, Taipei 112304, Taiwan

2. Division of Colorectal Surgery, Department of Surgery, Wanfang Hospital, Taipei Medical University, Taipei 110301, Taiwan

3. School of Biomedical Sciences, Chung Shan Medical University, Taichung 402306, Taiwan

4. Department of Medical Research, Chung Shan Medical University Hospital, Taichung 402306, Taiwan

5. Department of Medical Research, Hsinchu MacKay Memorial Hospital, Hsinchu 300044, Taiwan

6. Research and Development Department, GenMont Biotech Incorporation, Tainan 741014, Taiwan

7. Department of Pediatrics, Taipei Hospital, Ministry of Health and Welfare, New Taipei 242033, Taiwan

8. School of Medicine, National Yang Ming Chiao Tung University, Taipei 112304, Taiwan

9. College of Public Health, China Medical University, Taichung 406040, Taiwan

10. National Institute of Environmental Health Sciences, National Health Research Institutes, Miaoli 350401, Taiwan

Abstract

Background: Probiotics may facilitate the clinical management of allergic diseases. However, their effects on allergic rhinitis (AR) remain unclear. We examined the efficacy and safety of Lacticaseibacillus paracasei GM-080 in a mouse model of airway hyper-responsiveness (AHR) and in children with perennial AR (PAR) by using a double-blind, prospective, randomized, placebo-controlled design. Methods: The production of interferon (IFN)-γ and interleukin (IL)-12 was measured by using an enzyme-linked immunosorbent assay. GM-080 safety was evaluated via the whole-genome sequencing (WGS) of virulence genes. An ovalbumin (OVA)-induced AHR mouse model was constructed, and lung inflammation was evaluated by measuring the infiltrating leukocyte content of bronchoalveolar lavage fluid. A clinical trial was conducted with 122 children with PAR who were randomized to receive different doses of GM-080 or the placebo for 3 months, and their AHR symptom severity scores, total nasal symptom scores (TNSSs), and Investigator Global Assessment Scale scores were examined. Results: Among the tested L. paracasei strains, GM-080 induced the highest IFN-γ and IL-12 levels in mouse splenocytes. WGS analysis revealed the absence of virulence factors or antibiotic-resistance genes in GM-080. The oral administration of GM-080 at 1 × 107 colony forming units (CFU)/mouse/day for 8 weeks alleviated OVA-induced AHR and reduced airway inflammation in mice. In children with PAR, the oral consumption of GM-080 at 2 × 109 CFU/day for 3 months ameliorated sneezing and improved Investigator Global Assessment Scale scores significantly. GM-080 consumption led to a nonsignificant decrease in TNSS and also nonsignificantly reduced IgE but increased INF-γ levels. Conclusion: GM-080 may be used as a nutrient supplement to alleviate airway allergic inflammation.

Funder

Ministry of Science and Technology

GenMont Biotech

Publisher

MDPI AG

Subject

General Medicine

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