Paradoxical changes in innate immunity in aging: recent progress and new directions

被引:100
作者
Montgomery, Ruth R. [1 ]
Shaw, Albert C. [2 ]
机构
[1] Yale Univ, Sch Med, Rheumatol Sect, Dept Internal Med, New Haven, CT 06520 USA
[2] Yale Univ, Sch Med, Infect Dis Sect, Dept Internal Med, New Haven, CT 06520 USA
基金
美国国家卫生研究院;
关键词
immunosenescence; Toll-like receptor; polymorphonuclear leukocyte; dendritic cell; systems immunology; PROINFLAMMATORY CYTOKINE PRODUCTION; INFLUENZA VACCINE RESPONSES; NLRP3; INFLAMMASOME; DNA METHYLATION; GENE-EXPRESSION; DENDRITIC CELLS; DEPENDENT ALTERATIONS; MASS CYTOMETRY; T-CELLS; AGE;
D O I
10.1189/jlb.5MR0315-104R
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Immunosenescence, describing alterations, including decline of immune responses with age, is comprised of inappropriate elevations, decreases, and dysregulated immune responses, leading to more severe consequences of bacterial and viral infections and reduced responses to vaccination. In adaptive immunity, these changes include increased proportions of antigen-experienced B and T cells at the cost of naive cell populations. Innate immune changes in aging are complex in spanning multiple cell types, activation states, and tissue context. Innate immune responses are dampened in aging, yet there is also a paradoxical increase in certain signaling pathways and cytokine levels. Here, we review recent progress and highlight novel directions for expected advances that can lead the aging field to a new era of discovery that will embrace the complexity of aging in human populations.
引用
收藏
页码:937 / 943
页数:7
相关论文
共 87 条
[31]  
Giesen C, 2014, NAT METHODS, V11, P417, DOI [10.1038/nmeth.2869, 10.1038/NMETH.2869]
[32]   Lipidomics in longevity and healthy aging [J].
Gonzalez-Covarrubias, Vanessa .
BIOGERONTOLOGY, 2013, 14 (06) :663-672
[33]   Understanding immunosenescence to improve responses to vaccines [J].
Goronzy, Joerg J. ;
Weyand, Cornelia M. .
NATURE IMMUNOLOGY, 2013, 14 (05) :428-436
[34]   Impaired neutrophil extracellular trap formation: a novel defect in the innate immune system of aged individuals [J].
Hazeldine, Jon ;
Harris, Phillipa ;
Chapple, Iain L. ;
Grant, Melissa ;
Greenwood, Hannah ;
Livesey, Amy ;
Sapey, Elizabeth ;
Lord, Janet M. .
AGING CELL, 2014, 13 (04) :690-698
[35]   Age-Associated Inflammation and Toll-Like Receptor Dysfunction Prime the Lungs for Pneumococcal Pneumonia [J].
Hinojosa, Ernesto ;
Boyd, Angela R. ;
Orihuela, Carlos J. .
JOURNAL OF INFECTIOUS DISEASES, 2009, 200 (04) :546-554
[36]   TLR7 Recognition Is Dispensable for Influenza Virus A Infection but Important for the Induction of Hemagglutinin-Specific Antibodies in Response to the 2009 Pandemic Split Vaccine in Mice [J].
Jeisy-Scott, Victoria ;
Kim, Jin Hyang ;
Davis, William G. ;
Cao, Weiping ;
Katz, Jacqueline M. ;
Sambhara, Suryaprakash .
JOURNAL OF VIROLOGY, 2012, 86 (20) :10988-10998
[37]   Next-generation sequencing of microRNAs uncovers expression signatures in polarized macrophages [J].
Jimenez, Viviana Cobos ;
Bradley, Edward J. ;
Willemsen, Antonius M. ;
van Kampen, Antoine H. C. ;
Baas, Frank ;
Kootstra, Neeltje A. .
PHYSIOLOGICAL GENOMICS, 2014, 46 (03) :91-103
[38]  
Jung HJ, 2012, CURR GENOMICS, V13, P548, DOI 10.2174/138920212803251436
[39]   Aging and DNA methylation [J].
Jung, Marc ;
Pfeifer, Gerd P. .
BMC BIOLOGY, 2015, 13
[40]   Identification of a prognostic signature for old-age mortality by integrating genome-wide transcriptomic data with the conventional predictors: the Vitality 90+Study [J].
Jylhava, Juulia ;
Raitanen, Jani ;
Marttila, Saara ;
Hervonen, Antti ;
Jylha, Marja ;
Hurme, Mikko .
BMC MEDICAL GENOMICS, 2014, 7