Abstract
The immune system consists of many specialized cell populations that communicate with each other to achieve systemic immune responses. Our analyses of various measured immune cell population frequencies in healthy humans and their responses to diverse stimuli show that human immune variation is continuous in nature, rather than characterized by discrete groups of similar individuals. We show that the same three key combinations of immune cell population frequencies can define an individual’s immunotype and predict a diverse set of functional responses to cytokine stimulation. We find that, even though interindividual variations in specific cell population frequencies can be large, unrelated individuals of younger age have more homogeneous immunotypes than older individuals. Across age groups, cytomegalovirus seropositive individuals displayed immunotypes characteristic of older individuals. The conceptual framework for defining immunotypes suggested by our results could guide the development of better therapies that appropriately modulate collective immunotypes, rather than individual immune components.
Original language | English |
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Pages (from-to) | E6097-E6106 |
Journal | Proceedings of the National Academy of Sciences of the United States of America |
Volume | 114 |
Issue number | 30 |
DOIs | |
State | Published - 25 Jul 2017 |
Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2017, National Academy of Sciences. All rights reserved.
Funding
We thank all members of the A.K.C. and P.B. laboratories for insightful comments on this study. A.K.C. and K.J.K. received financial support from NIH Grant R01 HL120724 and the Ragon Institute of Massachusetts General Hospital, Massachusetts Institute of Technology and Harvard University. K.J.K. was also a National Science Foundation predoctoral fellow. P.B. is supported by a starting grant from the European Research Council, the Swedish Research Council, the Swedish Society for Medical Research, the Swedish Cancer Foundation, and Karolinska Institutet.
Funders | Funder number |
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Ragon Institute of Massachusetts General Hospital | |
National Science Foundation | |
National Institutes of Health | R01 HL120724 |
National Institute of Allergy and Infectious Diseases | U19AI057229 |
Massachusetts Institute of Technology | |
Harvard University | |
Swedish Cancer Foundation | |
European Commission | |
Svenska Sällskapet för Medicinsk Forskning | |
Karolinska Institutet | |
Vetenskapsrådet |
Keywords
- Aging
- Human immune variation
- Immune cell composition
- Systems immunology