Hasegawa T, Kimura Y, Hiromatsu K, Kobayashi N, Yamada A, Makino M, Okuda M, Sano T, Nomoto K, Yoshikai Y
Research Laboratories, Chlorella industries Co., Ltd., Fukuoka, Japan.
Immunopharmacology. 1997 Jan;35(3):273-82. doi: 10.1016/s0162-3109(96)00150-6.
We have previously reported that oral administration of hot water extract of Chlorella vulgaris (CVE) enhances resistance to Listeria monocytogenes through augmentation of Listeria-specific cell-mediated immunity in normal mice and mice with murine acquired immunodeficiency syndrome (MAIDS) caused by murine leukemia virus (MuLV) LP-BM5. To elucidate the mechanisms whereby CVE augments the cell-mediated immunity, we examined the expression patterns of mRNA for cytokines in normal and MAIDS mice given CVE orally after L. monocytogenes infection. The expression levels of IL-1 alpha, IL-12, GM-CSF, MIP and TNF alpha genes were significantly augmented in the peritoneal adherent cells by oral administration of CVE for 2 weeks before Listeria infection. The expression levels of gamma IFN and IL-12 mRNA were significantly higher in the spleen after Listeria infection in CVE-treated mice than in normal mice, while the expression of IL-10 mRNA in the spleen was decreased by CVE administration. In MAIDS mice, oral administration of CVE also augmented the expression of gamma IFN and IL-12 mRNA in the spleen after Listeria infection, while it rather reduced the expression of IL-10 mRNA. These results suggest that CVE may preferentially augment THI responses against Listeria via activation of macrophages to produce IL-12 and enhance host defence against Listeria infection both in normal and MAIDS mice.
我们之前曾报道,口服普通小球藻热水提取物(CVE)可增强正常小鼠以及感染鼠白血病病毒(MuLV)LP - BM5所致的小鼠获得性免疫缺陷综合征(MAIDS)小鼠对单核细胞增生李斯特菌的抵抗力,这是通过增强针对李斯特菌的细胞介导免疫实现的。为阐明CVE增强细胞介导免疫的机制,我们检测了在单核细胞增生李斯特菌感染后口服CVE的正常小鼠和MAIDS小鼠中细胞因子mRNA的表达模式。在李斯特菌感染前连续2周口服CVE,可使腹膜黏附细胞中IL - 1α、IL - 12、GM - CSF、MIP和TNFα基因的表达水平显著升高。在CVE处理的小鼠中,李斯特菌感染后脾脏中γ干扰素和IL - 12 mRNA的表达水平显著高于正常小鼠,而CVE给药可使脾脏中IL - 10 mRNA的表达降低。在MAIDS小鼠中,口服CVE也可增强李斯特菌感染后脾脏中γ干扰素和IL - 12 mRNA的表达,同时降低IL - 10 mRNA的表达。这些结果表明,CVE可能通过激活巨噬细胞产生IL -