Nature Immunology, Journal Year: 2022, Volume and Issue: 23(10), P. 1412 - 1423
Published: Sept. 22, 2022
Language: Английский
Nature Immunology, Journal Year: 2022, Volume and Issue: 23(10), P. 1412 - 1423
Published: Sept. 22, 2022
Language: Английский
Nature, Journal Year: 2021, Volume and Issue: 596(7872), P. 410 - 416
Published: July 12, 2021
Language: Английский
Citations
456Nature Immunology, Journal Year: 2022, Volume and Issue: 23(4), P. 543 - 555
Published: March 14, 2022
Language: Английский
Citations
335Cell, Journal Year: 2022, Volume and Issue: 185(5), P. 916 - 938.e58
Published: Jan. 21, 2022
Treatment of severe COVID-19 is currently limited by clinical heterogeneity and incomplete description specific immune biomarkers. We present here a comprehensive multi-omic blood atlas for patients with varying severity in an integrated comparison influenza sepsis versus healthy volunteers. identify signatures correlates host response. Hallmarks disease involved cells, their inflammatory mediators networks, including progenitor cells myeloid lymphocyte subsets, features the repertoire, acute phase response, metabolism, coagulation. Persisting activation involving AP-1/p38MAPK was feature COVID-19. The plasma proteome enabled sub-phenotyping into patient clusters, predictive outcome. Systems-based integrative analyses tensor matrix decomposition all modalities revealed groupings linked specificity compared to sepsis. Our approach will support future drug development, trial design, personalized medicine approaches
Language: Английский
Citations
265Cell, Journal Year: 2023, Volume and Issue: 186(18), P. 3882 - 3902.e24
Published: Aug. 1, 2023
Language: Английский
Citations
134PLoS Pathogens, Journal Year: 2021, Volume and Issue: 17(10), P. e1009928 - e1009928
Published: Oct. 25, 2021
Non-specific protective effects of certain vaccines have been reported, and long-term boosting innate immunity, termed trained has proposed as one the mechanisms mediating these effects. Several epidemiological studies suggested cross-protection between influenza vaccination COVID-19. In a large academic Dutch hospital, we found that SARS-CoV-2 infection was less common among employees who had received previous vaccination: relative risk reductions 37% 49% were observed following during first second COVID-19 waves, respectively. The quadrivalent inactivated vaccine induced immunity program boosted immune responses against various viral stimuli fine-tuned anti-SARS-CoV-2 response, which may result in better protection Influenza led to transcriptional reprogramming monocytes reduced systemic inflammation. These immunological data argue for potential benefits COVID-19, future randomized trials are warranted test this possibility.
Language: Английский
Citations
130Physiological Reviews, Journal Year: 2022, Volume and Issue: 103(1), P. 313 - 346
Published: Aug. 18, 2022
The mechanisms underlying innate immune memory have been extensively explored in the last decades but are fact largely unknown. Although specificity of adaptive vertebrates is ensured through recombination immunoglobulin family genes and clonal expansion, basic cells’ nonspecific increased responsiveness rely on epigenetic, transcriptional, metabolic programs after transient stimulation. Changes these result enhanced to secondary challenges with a wide variety stimuli. This phenomenon termed “trained immunity” or “innate memory.” On one hand, trained immunity improves response infections vaccination, facilitating stronger responses protection against microbial Conversely, may contribute pathophysiology cardiovascular, autoinflammatory, neurodegenerative diseases. In this review, we gather current body knowledge field summarize foundations immunity, different cell types involved, its consequences for health disease, potential modulation as therapeutic tool.
Language: Английский
Citations
92Nature, Journal Year: 2023, Volume and Issue: 614(7949), P. 752 - 761
Published: Jan. 4, 2023
Language: Английский
Citations
59Aging Cell, Journal Year: 2023, Volume and Issue: 22(4)
Published: Feb. 24, 2023
Diverse mouse strains have different health and life spans, mimicking the diversity among humans. To capture conserved aging signatures, we studied long-lived C57BL/6J short-lived NZO/HILtJ by profiling transcriptomes epigenomes of immune cells from peripheral blood spleen young old mice. Transcriptional activation AP-1 transcription factor complex, particularly Fos, Junb, Jun genes, was most significant signature across tissues strains. ATAC-seq data analyses showed that chromatin around these genes more accessible with age there were significantly binding sites for TFs all tissues, targeting pro-inflammatory molecules including Il6. Age-related increases in JUN FOS factors also human data. Single-cell RNA-seq cell atlas Tabula Muris Senis expression increased B, T, NK cells, macrophages, macrophages mice expressing abundantly than other cells. Functional upon myeloid via poly(I:C), levels protein its activity compared to In addition, activation, produced IL6 sum, aging-related transcriptional Fos family members complex is long- short-living strains, possibly contributing inflammation age.
Language: Английский
Citations
50Nature reviews. Immunology, Journal Year: 2023, Volume and Issue: 24(1), P. 33 - 48
Published: July 3, 2023
Language: Английский
Citations
45Nature Immunology, Journal Year: 2023, Volume and Issue: 25(1), P. 41 - 53
Published: Nov. 30, 2023
Language: Английский
Citations
45