Levy J A, Ibrahim A B, Shirai T, Ohta K, Nagasawa R, Yoshida H, Estes J, Gardner M
Proc Natl Acad Sci U S A. 1982 Mar;79(6):1974-8. doi: 10.1073/pnas.79.6.1974.
Autoimmune-prone (NZB x NZW)F1 (B/W) mice fed three nearly isocaloric diets with varied fat content showed a marked difference in their spontaneous development of immune complex disease and their immune response. Those animals received the diets high in either unsaturated or saturated fats had more severe immune complex nephritis and died earlier than mice on the low-fat diet. Endogenous production of the mouse xenotropic virus was unaffected by dietary fats, but the serum lipoproteins associated with antiviral activity were increased to levels as high as 1:600,000 in the B/W mice on the high-fat diets. These lipoproteins may be partially responsible for the decreased mitogenic response of spleen cells from mice fed the two high-fat diets. The mice receiving a diet high in saturated fats produced substantially higher titers of natural thymocytotoxic autoantibody, an IgM class of antibody, than did the mice maintained either on the high-unsaturated-fat or low-fat diet. In contrast, the mice receiving the diet high in unsaturated fats made significantly greater levels of antibodies to double-stranded DNA, an IgG, than did the mice kept on the two other diets. These results suggest that the type of fat in the diet could affect the serum level of different immunoglobulin classes. The data provide further evidence that the amount of dietary lipids alone can influence cellular and humoral immune responses and the spontaneous development of immune complex disease.
喂食三种热量相近但脂肪含量不同的饮食的自身免疫易感(NZB×NZW)F1(B/W)小鼠,在免疫复合物疾病的自发发展及其免疫反应方面表现出显著差异。那些摄入富含不饱和脂肪或饱和脂肪饮食的动物,比摄入低脂饮食的小鼠患有更严重的免疫复合物肾炎,且死亡更早。小鼠嗜异性病毒的内源性产生不受饮食脂肪的影响,但在高脂饮食的B/W小鼠中,与抗病毒活性相关的血清脂蛋白增加到高达1:600,000的水平。这些脂蛋白可能部分导致了喂食两种高脂饮食的小鼠脾细胞促有丝分裂反应的降低。摄入富含饱和脂肪饮食的小鼠产生的天然胸腺细胞毒性自身抗体(一种IgM类抗体)滴度,比维持在高不饱和脂肪或低脂饮食的小鼠高得多。相比之下,摄入富含不饱和脂肪饮食的小鼠产生的抗双链DNA抗体(一种IgG)水平,比维持在其他两种饮食的小鼠显著更高。这些结果表明,饮食中的脂肪类型可能会影响不同免疫球蛋白类别的血清水平。这些数据进一步证明,仅饮食脂质的量就可以影响细胞和体液免疫反应以及免疫复合物疾病的自发发展。