PMID- 31809637 OWN - NLM STAT- MEDLINE DCOM- 20210621 LR - 20210621 IS - 2164-554X (Electronic) IS - 2164-5515 (Print) IS - 2164-5515 (Linking) VI - 16 IP - 7 DP - 2020 Jul 2 TI - Polysaccharide PCP-I isolated from Poria cocos enhances the immunogenicity and protection of an anthrax protective antigen-based vaccine. PG - 1699-1707 LID - 10.1080/21645515.2019.1675457 [doi] AB - Polysaccharides isolated from natural plants may represent a novel source of vaccine adjuvants. In this research, we focused on a natural plant polysaccharide, PCP-I, which is derived from Poria cocos, a Chinese traditional herbal medicine. We chose the anthrax protective antigen (PA) as a model to evaluate the adjuvant ability of PCP-I in enhancing the immunogenicity and protection of a PA-based anthrax vaccine. According to our results, PCP-I could significantly enhance anthrax specific anti-PA antibodies, toxin-neutralizing antibodies, anti-PA antibody affinity, as well as IgG1 and IgG2a levels. Besides, PCP-I increased the frequency of PA-specific memory B cells, increased the proliferation of PA-specific splenocytes, significantly stimulated the secretion of IL-4, and enhanced the activation of Dendritic cells (DCs) in vitro. The combination of PCP-I and CpG significantly enhanced the level of anti-PA antibodies and neutralizing antibodies, particularly PA-specific IgG2a, and shifted the Th2-bias to a Th1/Th2 balanced response. In addition, PCP-I with or without CpG could significantly improve the survival rate of immunized mice following challenge with the anthrax lethal toxin. These findings suggest that PCP-I may be a promising vaccine adjuvant that warrants further study. FAU - Liu, Kun AU - Liu K AD - Laboratory of Vaccine and Antibody Engineering, Beijing Institute of Biotechnology , Beijing, China. FAU - Yin, Ying AU - Yin Y AD - Laboratory of Vaccine and Antibody Engineering, Beijing Institute of Biotechnology , Beijing, China. FAU - Zhang, Jun AU - Zhang J AD - Laboratory of Vaccine and Antibody Engineering, Beijing Institute of Biotechnology , Beijing, China. FAU - Zai, Xiaodong AU - Zai X AD - Laboratory of Vaccine and Antibody Engineering, Beijing Institute of Biotechnology , Beijing, China. FAU - Li, Ruihua AU - Li R AD - Laboratory of Vaccine and Antibody Engineering, Beijing Institute of Biotechnology , Beijing, China. FAU - Ma, Hao AU - Ma H AD - Institute of Pharmacology and Toxicology , Academy of Military Medical Sciences, Beijing, China. FAU - Xu, Junjie AU - Xu J AD - Laboratory of Vaccine and Antibody Engineering, Beijing Institute of Biotechnology , Beijing, China. FAU - Shan, Junjie AU - Shan J AD - Institute of Pharmacology and Toxicology , Academy of Military Medical Sciences, Beijing, China. FAU - Chen, Wei AU - Chen W AD - Laboratory of Vaccine and Antibody Engineering, Beijing Institute of Biotechnology , Beijing, China. LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20191206 PL - United States TA - Hum Vaccin Immunother JT - Human vaccines & immunotherapeutics JID - 101572652 RN - 0 (Anthrax Vaccines) RN - 0 (Antibodies, Bacterial) RN - 0 (Antigens, Bacterial) RN - 0 (Bacterial Toxins) RN - 0 (Polysaccharides) RN - 0 (anthrax toxin) SB - IM MH - Animals MH - *Anthrax/prevention & control MH - *Anthrax Vaccines MH - Antibodies, Bacterial MH - Antigens, Bacterial MH - *Bacillus anthracis MH - Bacterial Toxins MH - Mice MH - Mice, Inbred BALB C MH - Polysaccharides MH - *Wolfiporia PMC - PMC7482710 OTO - NOTNLM OT - Poria cocos OT - Polysaccharide OT - anthrax OT - protective antigen OT - vaccine adjuvant EDAT- 2019/12/07 06:00 MHDA- 2021/06/22 06:00 PMCR- 2020/12/06 CRDT- 2019/12/07 06:00 PHST- 2019/12/07 06:00 [pubmed] PHST- 2021/06/22 06:00 [medline] PHST- 2019/12/07 06:00 [entrez] PHST- 2020/12/06 00:00 [pmc-release] AID - 1675457 [pii] AID - 10.1080/21645515.2019.1675457 [doi] PST - ppublish SO - Hum Vaccin Immunother. 2020 Jul 2;16(7):1699-1707. doi: 10.1080/21645515.2019.1675457. Epub 2019 Dec 6.