Nature Immunology, Journal Year: 2018, Volume and Issue: 19(3), P. 302 - 314
Published: Feb. 20, 2018
Language: Английский
Nature Immunology, Journal Year: 2018, Volume and Issue: 19(3), P. 302 - 314
Published: Feb. 20, 2018
Language: Английский
Cell Metabolism, Journal Year: 2017, Volume and Issue: 26(1), P. 94 - 109
Published: July 1, 2017
Language: Английский
Citations
472Nature reviews. Immunology, Journal Year: 2016, Volume and Issue: 16(5), P. 310 - 320
Published: April 28, 2016
Language: Английский
Citations
401Nature Medicine, Journal Year: 2019, Volume and Issue: 25(6), P. 947 - 953
Published: April 22, 2019
Language: Английский
Citations
383Signal Transduction and Targeted Therapy, Journal Year: 2023, Volume and Issue: 8(1)
Published: May 13, 2023
Abstract Infection susceptibility, poor vaccination efficacy, age-related disease onset, and neoplasms are linked to innate adaptive immune dysfunction that accompanies aging (known as immunosenescence). During aging, organisms tend develop a characteristic inflammatory state expresses high levels of pro-inflammatory markers, termed inflammaging. This chronic inflammation is typical phenomenon immunosenescence it considered the major risk factor for diseases. Thymic involution, naïve/memory cell ratio imbalance, dysregulated metabolism, epigenetic alterations striking features immunosenescence. Disturbed T-cell pools antigen stimulation mediate premature senescence cells, senescent cells proinflammatory senescence-associated secretory phenotype exacerbates Although underlying molecular mechanisms remain be addressed, well documented T inflammaging might driving forces in Potential counteractive measures will discussed, including intervention cellular metabolic-epigenetic axes mitigate In recent years, has attracted increasing attention its role tumor development. As result limited participation elderly patients, impact on cancer immunotherapy unclear. Despite some surprising results from clinical trials drugs, necessary investigate other
Language: Английский
Citations
337Trends in Immunology, Journal Year: 2014, Volume and Issue: 35(7), P. 299 - 310
Published: May 28, 2014
Language: Английский
Citations
335Journal of Clinical Investigation, Journal Year: 2020, Volume and Issue: 130(11), P. 5976 - 5988
Published: Oct. 4, 2020
BACKGROUND. Therapeutic vaccinations against cancer have mainly targeted differentiation antigens, cancer-testis and overexpressed antigens thus far resulted in little clinical benefit. Studies conducted by multiple groups demonstrated that T cells recognizing neoantigens are present most cancers offer a specific highly immunogenic target for personalized vaccination.
Language: Английский
Citations
325Immunity, Journal Year: 2018, Volume and Issue: 48(5), P. 872 - 895
Published: May 1, 2018
Language: Английский
Citations
316Nature reviews. Immunology, Journal Year: 2015, Volume and Issue: 16(2), P. 90 - 101
Published: Dec. 21, 2015
Language: Английский
Citations
310Annual Review of Immunology, Journal Year: 2016, Volume and Issue: 34(1), P. 317 - 334
Published: May 11, 2016
CD4 + T helper (Th) cells play a central role in the adaptive immune response by providing help to B and cytotoxic releasing different types of cytokines tissues mediate protection against wide range pathogenic microorganisms. These functions are performed Th endowed with distinct migratory capacities effector functions. Here we discuss how studies human cell microbes have advanced our understanding functional heterogeneity, particular discovery Th1 subset involved Mycobacteria characterization two Th17 specific for extracellular bacteria or fungi. We also review new approaches dissect at clonal level induced pathogens vaccines that revealed an unexpected degree intraclonal diversification propose progressive selective model differentiation.
Language: Английский
Citations
310The Journal of Experimental Medicine, Journal Year: 2018, Volume and Issue: 215(10), P. 2520 - 2535
Published: Aug. 28, 2018
CD8+ T cells infiltrating tumors are largely dysfunctional, but whether a subset maintains superior functionality remains ill defined. By high-dimensional single cell analysis of millions from 53 individuals with lung cancer, we defined those subsets that enriched in compared cancer-free tissues and blood. Besides exhausted activated cells, identified CXCR5+ TIM-3– partial phenotype, while retaining gene networks responsible for stem-like plasticity cytotoxicity, as revealed by sequencing the whole transcriptome. Ex vivo, displayed enhanced self-renewal multipotency more differentiated were polyfunctional. Analysis inhibitory costimulatory receptors PD-1, TIGIT, CD27 possible targets immunotherapy. We thus demonstrate hierarchy differentiation context exhaustion human cancer similar to chronically infected mice, which is further shown disappear disease progression.
Language: Английский
Citations
303