Tracy S, Drescher K M, Chapman N M, Kim K-S, Carson S D, Pirruccello S, Lane P H, Romero J R, Leser J S
Enterovirus Research Laboratory, University of Nebraska Medical Center, Omaha, Nebraska 68198, USA.
J Virol. 2002 Dec;76(23):12097-111. doi: 10.1128/jvi.76.23.12097-12111.2002.
Insulin-dependent (type 1) diabetes mellitus (T1D) onset is mediated by individual human genetics as well as undefined environmental influences such as viral infections. The group B coxsackieviruses (CVB) are commonly named as putative T1D-inducing agents. We studied CVB replication in nonobese diabetic (NOD) mice to assess how infection by diverse CVB strains affected T1D incidence in a model of human T1D. Inoculation of 4- or 8-week-old NOD mice with any of nine different CVB strains significantly reduced the incidence of T1D by 2- to 10-fold over a 10-month period relative to T1D incidences in mock-infected control mice. Greater protection was conferred by more-pathogenic CVB strains relative to less-virulent or avirulent strains. Two CVB3 strains were employed to further explore the relationship of CVB virulence phenotypes to T1D onset and incidence: a pathogenic strain (CVB3/M) and a nonvirulent strain (CVB3/GA). CVB3/M replicated to four- to fivefold-higher titers than CVB3/GA in the pancreas and induced widespread pancreatitis, whereas CVB3/GA induced no pancreatitis. Apoptotic nuclei were detected by TUNEL (terminal deoxynucleotidyltransferase-mediated dUTP-biotin nick end labeling) assay in CVB3/M-infected pancreata but not in CVB3/GA-infected pancreata. In situ hybridization detected CVB3 RNA in acinar tissue but not in pancreatic islets. Although islets demonstrated inflammatory infiltrates in CVB3-protected mice, insulin remained detectable by immunohistochemistry in these islets but not in those from diabetic mice. Enzyme-linked immunosorbent assay-based examination of murine sera for immunoglobulin G1 (IgG1) and IgG2a immunoreactivity against diabetic autoantigens insulin and HSP60 revealed no statistically significant relationship between CVB3-protected mice or diabetic mice and specific autoimmunity. However, when pooled sera from CVB3/M-protected mice were used to probe a Western blot of pancreatic proteins, numerous proteins were detected, whereas only one band was detected by sera from CVB3/GA-protected mice. No proteins were detected by sera from diabetic or normal mice. Cumulatively, these data do not support the hypothesis that CVB are causative agents of T1D. To the contrary, CVB infections provide significant protection from T1D onset in NOD mice. Possible mechanisms by which this virus-induced protection may occur are discussed.
胰岛素依赖型(1型)糖尿病(T1D)的发病由个体人类遗传学以及未明确的环境影响因素介导,如病毒感染。B组柯萨奇病毒(CVB)通常被认为是可能诱发T1D的病原体。我们研究了CVB在非肥胖糖尿病(NOD)小鼠中的复制情况,以评估不同CVB毒株感染如何影响人类T1D模型中的T1D发病率。相对于模拟感染的对照小鼠,用九种不同CVB毒株中的任何一种接种4周龄或8周龄的NOD小鼠,在10个月内T1D发病率显著降低了2至10倍。致病性更强的CVB毒株比毒性较弱或无毒的毒株提供了更大的保护作用。使用两种CVB3毒株进一步探究CVB毒力表型与T1D发病及发病率之间的关系:一种致病毒株(CVB3/M)和一种无毒毒株(CVB3/GA)。CVB3/M在胰腺中的复制滴度比CVB3/GA高4至5倍,并引发广泛的胰腺炎,而CVB3/GA未诱发胰腺炎。通过TUNEL(末端脱氧核苷酸转移酶介导的dUTP生物素缺口末端标记)检测发现,CVB3/M感染的胰腺中有凋亡细胞核,而CVB3/GA感染的胰腺中未检测到。原位杂交在腺泡组织中检测到CVB3 RNA,但在胰岛中未检测到。尽管在CVB3保护的小鼠胰岛中显示有炎性浸润,但通过免疫组织化学在这些胰岛中仍可检测到胰岛素,而糖尿病小鼠的胰岛中则检测不到。基于酶联免疫吸附测定法检测小鼠血清中针对糖尿病自身抗原胰岛素和HSP60的免疫球蛋白G1(IgG1)和IgG2a免疫反应性,结果显示CVB3保护的小鼠或糖尿病小鼠与特定自身免疫之间无统计学显著关系。然而,当用CVB3/M保护的小鼠的混合血清探测胰腺蛋白的蛋白质印迹时,检测到许多蛋白质,而CVB3/GA保护的小鼠的血清仅检测到一条带。糖尿病或正常小鼠的血清未检测到蛋白质。总体而言,这些数据不支持CVB是T1D病原体的假说。相反,CVB感染为NOD小鼠的T1D发病提供了显著的保护作用。文中讨论了这种病毒诱导保护作用可能发生的潜在机制。