Peter C P, Perkins E H, Peterson W J, Walburg H E, Makinodan T
Mech Ageing Dev. 1975 May-Aug;4(3-4):251-61. doi: 10.1016/0047-6374(75)90027-5.
The effect of various immunosuppressive treatments on mean life-span and disease incidence have been studied. Significant life shortening was seen only in mice which recieved X-irradiation early in life and can be ascribed primarily to an increased incidence of certain malignancies. Marginal life shortening was seen in cyclophosphamide-treated animals, however, survival patterns between those and control animals did not differ until 30 months of age and the magnitude of life-shortening never approached that seen in X-irradiated animals. Thymectomy, splenectomy or cortisone treatment did not alter survival. All immunosuppressive treatments enhanced mortality due to non-neoplastic diseases, however, only a small percentage of animals die with these disease entities. With the exception of cortisone all immunosuppressive treatments increased the incidence of neoplastic disease. However, their effects on various neoplastic processes were variable and unpredictable. Four primary patterns in terms of relative immune competence, disease incidence and life expectancy were seen. Thus, immunodepression may of may not correlate with increased disease incidence, which in turn may or may not have a life-shortening effect. These findings are discussed in terms of the marked reduction of both humoral and cell-mediated immunity normally seen in aged mice and the significance of postulated immune surveillance mechanisms to survival.
已经研究了各种免疫抑制治疗对平均寿命和疾病发病率的影响。仅在生命早期接受过X射线照射的小鼠中观察到明显的寿命缩短,这主要归因于某些恶性肿瘤发病率的增加。在环磷酰胺治疗的动物中观察到轻微的寿命缩短,然而,直到30个月大时,这些动物与对照动物的存活模式才出现差异,并且寿命缩短的幅度从未接近接受X射线照射的动物。胸腺切除术、脾切除术或皮质酮治疗均未改变存活率。所有免疫抑制治疗均增加了非肿瘤性疾病导致的死亡率,然而,只有一小部分动物死于这些疾病实体。除皮质酮外,所有免疫抑制治疗均增加了肿瘤性疾病的发病率。然而,它们对各种肿瘤过程的影响是可变的且不可预测的。根据相对免疫能力、疾病发病率和预期寿命观察到四种主要模式。因此,免疫抑制可能与疾病发病率增加相关,也可能不相关,而疾病发病率增加反过来可能对寿命有缩短作用,也可能没有。根据老年小鼠中通常观察到的体液免疫和细胞介导免疫的显著降低以及假定的免疫监视机制对生存的意义,对这些发现进行了讨论。