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本文引用的文献

1
CARDIOVASCULAR DISEASES: NEW ETIOLOGICAL CONSIDERATIONS.心血管疾病:新的病因学考量
Am Heart J. 1964 Jan;67:139-41. doi: 10.1016/0002-8703(64)90412-0.
2
MULTIPLE SCLEROSIS AND POLIOMYELITIS.多发性硬化症与小儿麻痹症
Lancet. 1963 Nov 2;2(7314):917-21. doi: 10.1016/s0140-6736(63)90624-x.
3
Mutation, autoimmunity, and ageing.突变、自身免疫与衰老。
Lancet. 1963 Aug 10;2(7302):299-300. doi: 10.1016/s0140-6736(63)90200-9.
4
Disease alert.疾病警报。
JAMA. 1980 Mar 28;243(12):1231.
5
Increased pharyngeal bacterial colonization during viral illness.病毒感染期间咽部细菌定植增加。
Arch Intern Med. 1981 Nov;141(12):1599-603. doi: 10.1001/archinte.141.12.1599.
6
The normal microbial flora.正常微生物群
N Engl J Med. 1982 Jul 8;307(2):83-93. doi: 10.1056/NEJM198207083070203.
7
Multiple sclerosis and birth order.多发性硬化症与出生顺序
J Epidemiol Community Health. 1984 Mar;38(1):21-2. doi: 10.1136/jech.38.1.21.
8
Multiple sclerosis in Finland: evidence of increasing frequency and uneven geographic distribution.芬兰的多发性硬化症:发病率上升及地理分布不均的证据。
Neurology. 1984 Apr;34(4):457-61. doi: 10.1212/wnl.34.4.457.
9
Immunologic and genetic factors in autoimmune diseases.自身免疫性疾病中的免疫和遗传因素。
N Engl J Med. 1984 Oct 18;311(16):1019-29. doi: 10.1056/NEJM198410183111605.
10
Summary of clinical trials of inactivated influenza vaccine - 1978.1978年灭活流感疫苗临床试验总结
Rev Infect Dis. 1983 Jul-Aug;5(4):723-36. doi: 10.1093/clinids/5.4.723.

自身免疫:一种决策理论模型。

Autoimmunity: a decision theory model.

作者信息

Morris J A

出版信息

J Clin Pathol. 1987 Feb;40(2):210-5. doi: 10.1136/jcp.40.2.210.

DOI:10.1136/jcp.40.2.210
PMID:3818985
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1140870/
Abstract

Concepts from statistical decision theory were used to analyse the detection problem faced by the body's immune system in mounting immune responses to bacteria of the normal body flora. Given that these bacteria are potentially harmful, that there can be extensive cross reaction between bacterial antigens and host tissues, and that the decisions are made in uncertainty, there is a finite chance of error in immune response leading to autoimmune disease. A model of ageing in the immune system is proposed that is based on random decay in components of the decision process, leading to a steep age dependent increase in the probability of error. The age incidence of those autoimmune diseases which peak in early and middle life can be explained as the resultant of two processes: an exponentially falling curve of incidence of first contact with common bacteria, and a rapidly rising error function. Epidemiological data on the variation of incidence with social class, sibship order, climate and culture can be used to predict the likely site of carriage and mode of spread of the causative bacteria. Furthermore, those autoimmune diseases precipitated by common viral respiratory tract infections might represent reactions to nasopharyngeal bacterial overgrowth, and this theory can be tested using monoclonal antibodies to search the bacterial isolates for cross reacting antigens. If this model is correct then prevention of autoimmune disease by early exposure to low doses of bacteria might be possible.

摘要

统计决策理论中的概念被用于分析人体免疫系统在对正常身体菌群中的细菌产生免疫反应时所面临的检测问题。鉴于这些细菌具有潜在危害性,细菌抗原与宿主组织之间可能存在广泛的交叉反应,并且决策是在不确定的情况下做出的,因此免疫反应中存在导致自身免疫性疾病的有限错误几率。本文提出了一种免疫系统衰老模型,该模型基于决策过程中各组成部分的随机衰退,导致错误概率随年龄急剧增加。那些在中青年时期达到发病高峰的自身免疫性疾病的年龄发病率可解释为两个过程的结果:首次接触常见细菌的发病率呈指数下降曲线,以及错误函数迅速上升。关于发病率随社会阶层、出生顺序、气候和文化变化的流行病学数据可用于预测致病细菌的可能携带部位和传播方式。此外,由常见病毒性呼吸道感染引发的那些自身免疫性疾病可能代表对鼻咽部细菌过度生长的反应,这一理论可以通过使用单克隆抗体来搜索细菌分离株中的交叉反应抗原来进行验证。如果该模型正确,那么通过早期接触低剂量细菌来预防自身免疫性疾病可能是可行的。