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老年人细胞因子产生的改变。

Altered cytokine production in the elderly.

作者信息

Rink L, Cakman I, Kirchner H

机构信息

Institute of Immunology and Transfusion Medicine, University of Lübeck School of Medicine, Germany.

出版信息

Mech Ageing Dev. 1998 May 15;102(2-3):199-209. doi: 10.1016/s0047-6374(97)00153-x.

Abstract

Elderly persons are more susceptible to bacterial and virus infections and neoplasias than young adults. This is related to an impaired immune response. Lymphocytes of the elderly show a decreased proliferation after induction with mitogens. The decreased proliferation is correlated to a decreased release of interleukin (IL)-2 and soluble IL-2 receptor (sIL-2R). However, IL-2R expression on the cell surface is normal. Interferon (IFN)-gamma as the main T-helper-1 (TH1) cytokine is produced less by lymphocytes of the elderly, whereas the TH2 cytokines IL-4 and IL-10 are produced in higher amounts as compared to stimulated lymphocytes of young donors. The decreased production of IFN-gamma is correlated to a decreased number of CD45RO+/CD8+ T cells. Therefore in the elderly there seems to be a dysregulation in the TH1/TH2-system which is predominated by TH2-functions. Monocyte function seems to be increased in the elderly. Leukocytes of elderly persons produce higher amounts of IL-1, IL-6, IL-8 and tumor necrosis factor (TNF)-alpha after induction with lipopolysaccharide (LPS) than leukocytes from young donors. In contrast, in vitro induction of IFN-alpha by viruses is decreased in the elderly compared to the young. In conclusion, there are cellular defects and dysfunctions in the elderly resulting in an altered immune response.

摘要

与年轻人相比,老年人更容易受到细菌和病毒感染以及肿瘤的侵袭。这与免疫反应受损有关。老年人的淋巴细胞在有丝分裂原诱导后增殖减少。增殖减少与白细胞介素(IL)-2和可溶性IL-2受体(sIL-2R)释放减少相关。然而,细胞表面的IL-2R表达正常。作为主要的辅助性T细胞1(TH1)细胞因子的干扰素(IFN)-γ,老年人淋巴细胞产生较少,而与年轻供体受刺激的淋巴细胞相比,TH2细胞因子IL-4和IL-10产生量更高。IFN-γ产生减少与CD45RO+/CD8+ T细胞数量减少相关。因此,在老年人中,TH1/TH2系统似乎存在失调,以TH2功能为主导。老年人的单核细胞功能似乎增强。与年轻供体的白细胞相比,老年人的白细胞在用脂多糖(LPS)诱导后产生更高量的IL-1、IL-6、IL-8和肿瘤坏死因子(TNF)-α。相反,与年轻人相比,老年人中病毒对IFN-α的体外诱导减少。总之,老年人存在细胞缺陷和功能障碍,导致免疫反应改变。

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