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本文引用的文献

1
Inflammaging: disturbed interplay between autophagy and inflammasomes.炎症衰老:自噬与炎性小体之间的相互作用紊乱
Aging (Albany NY). 2012 Mar;4(3):166-75. doi: 10.18632/aging.100444.
2
Effects of Aging on Inflammation and Hemostasis through the Continuum of Critical Illness.衰老对危重病连续体中炎症和止血的影响。
Aging Dis. 2011 Dec;2(6):501-11. Epub 2011 Dec 2.
3
Pathophysiology of age-related diseases.与年龄相关疾病的病理生理学。
Immun Ageing. 2009 Sep 8;6:12. doi: 10.1186/1742-4933-6-12.
4
Age-associated inflammation and toll-like receptor dysfunction prime the lungs for pneumococcal pneumonia.与年龄相关的炎症和Toll样受体功能障碍使肺部易患肺炎球菌肺炎。
J Infect Dis. 2009 Aug 15;200(4):546-54. doi: 10.1086/600870.
5
Associations between periodontal diseases and systemic diseases: a review of the inter-relationships and interactions with diabetes, respiratory diseases, cardiovascular diseases and osteoporosis.牙周疾病与全身疾病之间的关联:关于与糖尿病、呼吸系统疾病、心血管疾病和骨质疏松症的相互关系及相互作用的综述
Public Health. 2008 Apr;122(4):417-33. doi: 10.1016/j.puhe.2007.07.004. Epub 2007 Oct 29.
6
Blood-brain barrier: ageing and microvascular disease--systematic review and meta-analysis.血脑屏障:衰老与微血管疾病——系统评价与荟萃分析
Neurobiol Aging. 2009 Mar;30(3):337-52. doi: 10.1016/j.neurobiolaging.2007.07.015. Epub 2007 Sep 14.
7
Relationship between periodontal infections and systemic disease.牙周感染与全身性疾病之间的关系。
Clin Microbiol Infect. 2007 Oct;13 Suppl 4:3-10. doi: 10.1111/j.1469-0691.2007.01798.x.
8
Platelet-activating factor receptor and innate immunity: uptake of gram-positive bacterial cell wall into host cells and cell-specific pathophysiology.血小板活化因子受体与天然免疫:革兰氏阳性菌细胞壁被宿主细胞摄取及细胞特异性病理生理学
J Immunol. 2006 Nov 1;177(9):6182-91. doi: 10.4049/jimmunol.177.9.6182.
9
Immunosenescence and macrophage functional plasticity: dysregulation of macrophage function by age-associated microenvironmental changes.免疫衰老与巨噬细胞功能可塑性:年龄相关微环境变化导致巨噬细胞功能失调
Immunol Rev. 2005 Jun;205:60-71. doi: 10.1111/j.0105-2896.2005.00260.x.
10
Signal transduction and functional changes in neutrophils with aging.中性粒细胞随衰老的信号转导及功能变化
Aging Cell. 2004 Aug;3(4):217-26. doi: 10.1111/j.1474-9728.2004.00110.x.

免疫衰老是否是牙周疾病的一个促成因素?

Is immunesenescence a contributing factor for periodontal diseases?

作者信息

Rajendran Maheaswari, Priyadharshini V, Arora Gaurav

机构信息

Department of Periodontics, Tamil Nadu Government Dental College and Hospital, Chennai, Tamil Nadu, India.

出版信息

J Indian Soc Periodontol. 2013 Mar;17(2):169-74. doi: 10.4103/0972-124X.113064.

DOI:10.4103/0972-124X.113064
PMID:23869121
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3713746/
Abstract

Current concept in periodontal diseases (PDs) states that it is the host's response toward the periodontal pathogens which leads to tissue destruction and attachment loss. Hence the role of immune response in the progression and resolution of PD must be considered vital. Any alteration in the immune system disturbs the homeostasis of the periodontium. Decline in immune system is the hallmark of aging, leading to increased susceptibility of elderly individuals to bacterial infections. The periodontal apparatus which is being constantly exposed to plaque biofilm is more vulnerable to destruction in aged individuals. Ageing related alterations in immune system has been discussed elsewhere as a contributor to various chronic inflammatory diseases like atherosclerosis, preterm, and low birth weight, etc. This paper reviews on the possible role of aging in periodontal destruction through altered immunity. Aging has long been associated with altered systemic inflammation. It has been discussed whether (1) this systemic inflammation is a consequence of increased occurrence of chronic inflammatory diseases upon aging or (2) aging associated systemic inflammation leads to such diseases. The immune responses which are protective at the first stages of life might result detrimental in the elderly. Hence it might be very difficult to individuate genetic profiles that might allow to identify individuals with a major risk for one or more age related diseases. Taking this into consideration, the cause of PDs in elderly is addressed with a systemic approach in order to understand the complex interplay between the aging immunity and PDs.

摘要

当前牙周疾病(PDs)的概念表明,是宿主对牙周病原体的反应导致了组织破坏和附着丧失。因此,免疫反应在PD进展和消退中的作用必须被视为至关重要。免疫系统的任何改变都会扰乱牙周组织的稳态。免疫系统衰退是衰老的标志,导致老年人更容易受到细菌感染。不断暴露于菌斑生物膜的牙周组织在老年人中更容易受到破坏。免疫系统与衰老相关的改变在其他地方已被讨论为导致各种慢性炎症性疾病(如动脉粥样硬化、早产和低出生体重等)的一个因素。本文综述了衰老通过改变免疫在牙周破坏中可能发挥的作用。长期以来,衰老一直与全身性炎症的改变有关。人们一直在讨论:(1)这种全身性炎症是衰老后慢性炎症性疾病发生率增加的结果,还是(2)与衰老相关的全身性炎症导致了这些疾病。在生命早期具有保护作用的免疫反应在老年人中可能会产生有害影响。因此,可能很难确定能够识别出患一种或多种与年龄相关疾病风险较高个体的基因特征。考虑到这一点,本文采用系统方法探讨老年人PDs的病因,以了解衰老免疫与PDs之间复杂的相互作用。