Altered monocyte phenotypes but not impaired peripheral T cell immunity may explain susceptibility of the elderly to develop tuberculosis

被引:26
作者
Ault, Russell [1 ,2 ]
Dwivedi, Varun [1 ,2 ]
Koivisto, Elisha [1 ]
Nagy, Jenna [1 ]
Miller, Karin [3 ]
Nagendran, Kokila [4 ]
Chalana, Indu [4 ]
Pan, Xueliang [5 ]
Wang, Shu-Hua [1 ,4 ]
Turner, Joanne [1 ,2 ]
机构
[1] Ohio State Univ, Dept Microbial Infect & Immun, Columbus, OH 43210 USA
[2] Texas Biomed Res Inst, 8715 W Mil Dr, San Antonio, TX 78227 USA
[3] Johns Hopkins Univ, Sch Med, Dept Pathol, Baltimore, MD 21205 USA
[4] Ohio State Univ, Dept Internal Med, Div Infect Dis, Columbus, OH 43210 USA
[5] Ohio State Univ, Ctr Biostat, Columbus, OH 43210 USA
基金
美国国家卫生研究院;
关键词
Tuberculosis; Geriatrics; T cell; Monocyte; Inflammaging; Immunosenescence; MYCOBACTERIUM-TUBERCULOSIS; OLDER-ADULTS; ACTIVE TUBERCULOSIS; DISEASE; BLOOD; MICE; AGE; INTERLEUKIN-10; LYMPHOCYTES; MACROPHAGES;
D O I
10.1016/j.exger.2018.06.029
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Tuberculosis (TB) is the leading killer due to a single infectious disease worldwide. With the aging of the global population, the case rate and deaths due to TB are highest in the elderly population. While general immunosenescence associated with old age is thought to contribute to the susceptibility of the elderly to develop active TB disease, very few studies of immune function in elderly individuals with Mycobacterium tuberculosis (M.tb) infection or disease have been performed. In particular, impaired adaptive T cell immunity to M.tb is one proposed mechanism for the elderly's increased susceptibility primarily on the basis of the decreased delayed type hypersensitivity response to tuberculin-purified protein derivative in the skin of elderly individuals. To investigate immunological reasons why the elderly are susceptible to develop active TB disease, we performed a cross-sectional observational study over a five year period (2012-2016) enrolling participants from 2 age groups (adults: 25-44 years; elderly: 65 and older) and 3 M.tb infection statuses (active TB, latent TB infection, and healthy controls without history of M.tb infection). We hypothesized that impaired peripheral T cell immunity plays a role in the biological susceptibility of the elderly to TB. Contrary to our hypothesis, we observed no evidence of impaired M.tb specific T cell frequency or altered production of cytokines implicated in M.tb control (IFN-gamma, IL-10) in peripheral blood in the elderly. Instead, we observed alterations in monocyte proportion and phenotype with age and M.tb infection that suggest their potential role in the susceptibility of the elderly to develop active TB. Our results suggest a potential link between the known widespread low-grade systemic inflammation of old age, termed "inflammaging," with the elderly's specific susceptibility to developing active TB. Moreover, our results highlight the need for further research into the biological reasons why the elderly are more susceptible to disease and death from TB, so that public health systems can be better equipped to face the present and future problem of TB in an aging global population.
引用
收藏
页码:35 / 44
页数:10
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