Biomol Ther.  2024 Sep;32(5):556-567. 10.4062/biomolther.2024.047.

Investigating the Immune-Stimulating Potential of β-Glucan from Aureobasidium pullulans in Cancer Immunotherapy

Affiliations
  • 1Department of Pharmacy, Kangwon National University, Chuncheon 24341, Republic of Korea
  • 2KNU Researcher training program for Innovative Drug Development Research Team for Intractable Diseases (BK21 plus), Kangwon National University, Chuncheon 24341, Republic of Korea
  • 3Global/Gangwon Innovative Biologics-Regional Leading Research Center (GIB-RLRC), Kangwon National University, Chuncheon 24341, Republic of Korea
  • 4Institute of Agricultural Science and Technology, Chonnam National University, Gwangju 61186, Republic of Korea
  • 5Department of Integrative Food, Bioscience and Biotechnology, Chonnam National University, Gwangju 61186, Republic of Korea
  • 6Nodcure, Inc., Gwangju 61186, Republic of Korea
  • 7Laboratory Animal Medicine, Animal Medical Institute, College of Veterinary Medicine, Chonnam National University, Gwangju 61186, Republic of Korea

Abstract

β-glucan, a polysaccharide found in various sources, exhibits unique physicochemical properties, yet its high polymerization limits clinical applications because of its solubility. Addressing this limitation, we introduce PPTEE-glycan, a highly purified soluble β-1,3/1,6-glucan derived from Aureobasidium pullulans. The refined PPTEE-glycan demonstrated robust immune stimulation in vitro, activated dendritic cells, and enhanced co-stimulatory markers, cytokines, and cross-presentation. Formulated as a PPTEE + microemulsion (ME), it elevated immune responses in vivo, promoting antigen-specific antibodies and CD8+ T cell proliferation. Intratumoral administration of PPTEE + ME in tumor-bearing mice induced notable tumor regression, which was linked to the activation of immunosuppressive cells. This study highlights the potential of high-purity Aureobasidium pullulans-derived β-glucan, particularly PPTEE, as promising immune adjuvants, offering novel avenues for advancing cancer immunotherapy.

Keyword

β-glucan; Vaccine; Antigen-presenting cell; Myeloid-derived suppressive cell; Formulation; Cancer
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