Ramiya V K, Lan M S, Wasserfall C H, Notkins A L, Maclaren N K
Department of Pathology and Laboratory Medicine, NIH, Bethesda, MD, USA.
J Autoimmun. 1997 Jun;10(3):287-92. doi: 10.1006/jaut.1997.0127.
Insulin-dependent diabetes (IDD), being an autoimmune disease, offers several opportunities for immunological interventions that may result either in the reduction of disease severity or in delaying diabetes onset. Among the various experimental preventative approaches, parenteral immunization with islet-specific autoantigens appears to be practically simpler and promising. We have previously shown that immunization with insulin, insulin B chain and B chain epitope (p9-23), but not insulin A chain, in incomplete Freund's adjuvant (IFA) and in alum (with B chain) delayed/prevented diabetes onset in NOD mice. Here we demonstrate the protective efficacy of affinity purified GAD65 in IFA. While both insulin B chain and GAD65 significantly delayed the onset of diabetes (P=0.001), a recently described tyrosine phosphatase (IA-2) antigen did not (P=0.38). Interestingly, B chain immunization reduced the incidence of cyclophosphamide (CY)-accelerated diabetes by about 50-55%. We also provide further evidence that B chain, upon increased adsorption to alum, could improve on its protective capacity in NOD mice.
胰岛素依赖型糖尿病(IDD)作为一种自身免疫性疾病,为免疫干预提供了多种机会,这些干预可能会减轻疾病严重程度或延缓糖尿病发病。在各种实验性预防方法中,用胰岛特异性自身抗原进行肠胃外免疫接种似乎实际上更简单且有前景。我们之前已经表明,在不完全弗氏佐剂(IFA)和明矾(与B链一起)中用胰岛素、胰岛素B链和B链表位(p9-23)而非胰岛素A链进行免疫接种,可延迟/预防非肥胖糖尿病(NOD)小鼠的糖尿病发病。在此我们证明了亲和纯化的谷氨酸脱羧酶65(GAD65)在IFA中的保护效力。虽然胰岛素B链和GAD65都显著延迟了糖尿病发病(P = 0.001),但最近描述的一种酪氨酸磷酸酶(IA-2)抗原却没有(P = 0.38)。有趣的是,B链免疫接种使环磷酰胺(CY)加速的糖尿病发病率降低了约50 - 55%。我们还提供了进一步的证据表明,B链在增加对明矾的吸附后,可提高其在NOD小鼠中的保护能力。