Towards multiscale modeling of the CD8+ T cell response to viral infections. (27th February 2019)
- Record Type:
- Journal Article
- Title:
- Towards multiscale modeling of the CD8+ T cell response to viral infections. (27th February 2019)
- Main Title:
- Towards multiscale modeling of the CD8+ T cell response to viral infections
- Authors:
- Baral, Subhasish
Raja, Rubesh
Sen, Pramita
Dixit, Narendra M. - Abstract:
- Abstract : The CD8 + T cell response is critical to the control of viral infections. Yet, defining the CD8 + T cell response to viral infections quantitatively has been a challenge. Following antigen recognition, which triggers an intracellular signaling cascade, CD8 + T cells can differentiate into effector cells, which proliferate rapidly and destroy infected cells. When the infection is cleared, they leave behind memory cells for quick recall following a second challenge. If the infection persists, the cells may become exhausted, retaining minimal control of the infection while preventing severe immunopathology. These activation, proliferation and differentiation processes as well as the mounting of the effector response are intrinsically multiscale and collective phenomena. Remarkable experimental advances in the recent years, especially at the single cell level, have enabled a quantitative characterization of several underlying processes. Simultaneously, sophisticated mathematical models have begun to be constructed that describe these multiscale phenomena, bringing us closer to a comprehensive description of the CD8 + T cell response to viral infections. Here, we review the advances made and summarize the challenges and opportunities ahead. This article is categorized under: Analytical and Computational Methods > Computational Methods Biological Mechanisms > Cell Fates Biological Mechanisms > Cell Signaling Models of Systems Properties and Processes > MechanisticAbstract : The CD8 + T cell response is critical to the control of viral infections. Yet, defining the CD8 + T cell response to viral infections quantitatively has been a challenge. Following antigen recognition, which triggers an intracellular signaling cascade, CD8 + T cells can differentiate into effector cells, which proliferate rapidly and destroy infected cells. When the infection is cleared, they leave behind memory cells for quick recall following a second challenge. If the infection persists, the cells may become exhausted, retaining minimal control of the infection while preventing severe immunopathology. These activation, proliferation and differentiation processes as well as the mounting of the effector response are intrinsically multiscale and collective phenomena. Remarkable experimental advances in the recent years, especially at the single cell level, have enabled a quantitative characterization of several underlying processes. Simultaneously, sophisticated mathematical models have begun to be constructed that describe these multiscale phenomena, bringing us closer to a comprehensive description of the CD8 + T cell response to viral infections. Here, we review the advances made and summarize the challenges and opportunities ahead. This article is categorized under: Analytical and Computational Methods > Computational Methods Biological Mechanisms > Cell Fates Biological Mechanisms > Cell Signaling Models of Systems Properties and Processes > Mechanistic Models Abstract : Multiscale modeling of CD8 + T cell signaling, differentiation, and effector responses facilitate a quantitative understanding of viral infections and treatments. … (more)
- Is Part Of:
- Wiley interdisciplinary reviews. Volume 11:Number 4(2019)
- Journal:
- Wiley interdisciplinary reviews
- Issue:
- Volume 11:Number 4(2019)
- Issue Display:
- Volume 11, Issue 4 (2019)
- Year:
- 2019
- Volume:
- 11
- Issue:
- 4
- Issue Sort Value:
- 2019-0011-0004-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2019-02-27
- Subjects:
- cell fate -- effector function -- exhaustion -- mathematical models
Systems biology -- Periodicals
Medicine -- Periodicals
610 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/%28ISSN%291939-005X ↗
http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1939-005X ↗
http://www3.interscience.wiley.com/journal/122288632/home ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/wsbm.1446 ↗
- Languages:
- English
- ISSNs:
- 1939-5094
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 23736.xml