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自身免疫的自组织临界性理论。

Self-organized criticality theory of autoimmunity.

机构信息

Department of Biophysics, Kobe University Graduate School of Health Science, Kobe, Japan.

出版信息

PLoS One. 2009 Dec 31;4(12):e8382. doi: 10.1371/journal.pone.0008382.

Abstract

BACKGROUND

The cause of autoimmunity, which is unknown, is investigated from a different angle, i.e., the defect in immune 'system', to explain the cause of autoimmunity.

METHODOLOGY/PRINCIPAL FINDINGS: Repeated immunization with antigen causes systemic autoimmunity in mice otherwise not prone to spontaneous autoimmune diseases. Overstimulation of CD4(+) T cells led to the development of autoantibody-inducing CD4(+) T (aiCD4(+) T) cell which had undergone T cell receptor (TCR) revision and was capable of inducing autoantibodies. The aiCD4(+) T cell was induced by de novo TCR revision but not by cross-reaction, and subsequently overstimulated CD8(+) T cells, driving them to become antigen-specific cytotoxic T lymphocytes (CTL). These CTLs could be further matured by antigen cross-presentation, after which they caused autoimmune tissue injury akin to systemic lupus erythematosus (SLE).

CONCLUSIONS/SIGNIFICANCE: Systemic autoimmunity appears to be the inevitable consequence of over-stimulating the host's immune 'system' by repeated immunization with antigen, to the levels that surpass system's self-organized criticality.

摘要

背景

自身免疫的病因不明,目前从免疫系统缺陷的角度对其进行了研究,以解释自身免疫的病因。

方法/主要发现:对不易自发产生自身免疫性疾病的小鼠进行抗原的重复免疫,会导致全身性自身免疫。过度刺激 CD4(+) T 细胞,会导致产生能够诱导自身抗体的诱导自身抗体产生的 CD4(+) T(aiCD4(+) T)细胞。aiCD4(+) T 细胞是由新的 TCR 修正引起的,而不是由交叉反应引起的,随后过度刺激 CD8(+) T 细胞,使其成为抗原特异性细胞毒性 T 淋巴细胞(CTL)。这些 CTL 可通过抗原交叉呈递进一步成熟,随后引起类似于系统性红斑狼疮(SLE)的自身免疫性组织损伤。

结论/意义:通过抗原的重复免疫过度刺激宿主的免疫系统,使其达到超越系统自组织临界性的水平,似乎是全身性自身免疫的必然结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3135/2795160/33994414f7fa/pone.0008382.g001.jpg

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