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Algal Glucan

Vaxjo ID 40
Vaccine Adjuvant Name Algal Glucan
Alternative Names β-glucan; glucan
Adjuvant VO ID VO_0001285
Description Algal Glucan, a nonantigenic carbohydrate adjuvant, enhances both humoral and cell-mediated immunity to oligopeptides in experimental animal models (Vogel and Powell, 1995).
Stage of Development Research
Components b-glucan; glucan; A linear b-D(1,3)-linked glucopyranose, polymer having a triple-helical conformation (Vogel and Powell, 1995).
Structure A linear β-D( 1,3)-linked glucopyranose, polymer having a triple-helical conformation.
Molecular Weight Highest measured
Appearance White, odorless crystalline material. Forms a suspension in aqueous solutions (Vogel and Powell, 1995).
Storage Stable to light. Store solid Algal Glucan at room temperature and aqueous suspensions at 4°C. No apparent degradation after storage of aqueous suspension for 24 months at 4°C. Optimal storage conditions are to be determined (Vogel and Powell, 1995).
Preparation Produced by an adapted strain of Euglena gracilis (SRI strain D86-G) grown heterotrophically in the dark. Obtained from the cytoplasm of the organism by methanol and chloroform extraction. Depyrogenized in hot I N HCI and washed sequentially in pyrogen-free water and pyrogen-free saline (Vogel and Powell, 1995).
Dosage In a study, mice were immunized by coadministration of herpes virus glycoprotein D (gD2) and 100 µg Algal Glucan, which produced anti-gD2 antibodies that were significantly higher in titer and persisted longer (p<0.01) than those in animals injected with gD2 alone (Vogel and Powell, 1995).
Function Administered with antigen for enhancement of both humoral and cell-mediated immunity. b-Glucans exert their immunostimulatory activities by binding to specific b-glucan receptors on macrophages. This ligand-receptor interaction results in macrophage activation and, in certain formulations, promotes antigen targeting (Vogel and Powell, 1995).
Safety In preclinical studies, Algal Glucan has been intravenously administered at doses up to 25 mg/kg body weight and was well tolerated. Human clinical trials of b-glucans isolated from either plants or microorganisms indicate the feasibility of administering these compounds to humans without toxicity. Glucan particles bioerode over time in a physiological environment (Vogel and Powell, 1995).
References
Vogel and Powell, 1995: Vogel FR, Powell MF. A compendium of vaccine adjuvants and excipients. Pharmaceutical biotechnology. 1995; 6; 141-228. [PubMed: 7551218].