Memory T cell: Difference between revisions
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[[Image:lymphocyte.jpg|thumb|right|A [[lymphocyte]] is a shown in the center of this picture]] |
[[Image:lymphocyte.jpg|thumb|right|A [[lymphocyte]] is a shown in the center of this picture]] |
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[[Image:T cell prolif.jpg|thumb|right| 1. After the [[naive T cell]] (N) encounters an [[antigen]] it becomes [[T cell activation|activated]] and begins to proliferate ([[Cell division|divide]]) into many clones or daughter cells.<BR>2. Some of the T cell clones will differentiate into [[effector T cell]]s (E) that will perform the function of that cell (e.g. produce [[cytokine]]s in the case of [[helper T cell]]s or invoke cell killing in the case of [[cytotoxic T cell]]s).<BR>3. Some of the cells will form memory T cells (M) that will survive in an inactive state in the host for a long period of time until they re-encounter the same antigen and reactivate.]] |
[[Image:T cell prolif.jpg|thumb|right| 1. After the [[naive T cell]] (N) encounters an [[antigen]] it becomes [[T cell activation|activated]] and begins to proliferate ([[Cell division|divide]]) into many clones or daughter cells.<BR>2. Some of the T cell clones will differentiate into [[effector T cell]]s (E) that will perform the function of that cell (e.g. produce [[cytokine]]s in the case of [[helper T cell]]s or invoke cell killing in the case of [[cytotoxic T cell]]s).<BR>3. Some of the cells will form memory T cells (M) that will survive in an inactive state in the host for a long period of time until they re-encounter the same antigen and reactivate.]] |
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'''Memory T cells''' are a specific type of [[infection]]-fighting [[T cell]] (also known as a [[T lymphocyte]]) that can recognize foreign invaders such as [[bacteria]] or [[virus]]es, that were encountered during a prior infection or [[vaccination]]. At a second encounter with the invader, memory T cells can reproduce to mount a faster and stronger [[immune response]] than the first time the immune system responded to the invader. This behaviour is utilized in T lymphocyte proliferation assays, which can reveal exposure to specific antigens. |
'''Memory T cells''' are a specific type of [[infection]]-fighting [[T cell]] (also known as a [[T lymphocyte]]) that can recognize foreign invaders such as [[bacteria]] or [[virus]]es, that were encountered during a prior infection or [[vaccination]]. At a second encounter with the invader, memory T cells can reproduce to mount a faster and stronger [[immune response]] than the first Pauls mum also produces these cells.... time the immune system responded to the invader. This behaviour is utilized in T lymphocyte proliferation assays, which can reveal exposure to specific antigens. |
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==Sub-populations== |
==Sub-populations== |
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* central memory (T<sub>CM</sub>). The T<sub>CM</sub> cells are thought to represent memory [[stem cells]]. T<sub>CM</sub> display a capacity for self-renewal due to high levels of [[phosphorylation]] of an important [[transcription factor]] known as [[STAT5]]. <ref>{{cite journal |author=Willinger T, Freeman T, Hasegawa H, McMichael A, Callan M |title=Molecular signatures distinguish human central memory from effector memory CD8 T cell subsets |journal=J Immunol |volume=175 |issue=9 |pages=5895-903 |year=2005 |pmid=16237082}}</ref> |
* central memory (T<sub>CM</sub>). The T<sub>CM</sub> cells are thought to represent memory [[stem cells]]. T<sub>CM</sub> display a capacity for self-renewal due to high levels of [[phosphorylation]] of an important [[transcription factor]] known as [[STAT5]]. <ref>{{cite journal |author=Willinger T, Freeman T, Hasegawa H, McMichael A, Callan M |title=Molecular signatures distinguish human central memory from effector memory CD8 T cell subsets |journal=J Immunol |volume=175 |issue=9 |pages=5895-903 |year=2005 |pmid=16237082}}</ref> |
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* two highly related effector memory sub-types, which strongly express genes for molecules essential to the [[cytotoxic]] function of CD8 T cells: |
* two highly related effector memory sub-types, which strongly express genes for molecules essential to the [[cytotoxic]] function of CD8 T cells: |
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** effector memory (T<sub>EM</sub>) |
** effector memory (T<sub>EM</sub>) |
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** effector memory RA (T<sub>EMRA</sub>) |
** effector memory RA (T<sub>EMRA</sub>) |
Revision as of 22:49, 17 February 2008
Memory T cells are a specific type of infection-fighting T cell (also known as a T lymphocyte) that can recognize foreign invaders such as bacteria or viruses, that were encountered during a prior infection or vaccination. At a second encounter with the invader, memory T cells can reproduce to mount a faster and stronger immune response than the first Pauls mum also produces these cells.... time the immune system responded to the invader. This behaviour is utilized in T lymphocyte proliferation assays, which can reveal exposure to specific antigens.
Sub-populations
Within the human cytotoxic T cell population, three distinct sub-populations have now been described:
- central memory (TCM). The TCM cells are thought to represent memory stem cells. TCM display a capacity for self-renewal due to high levels of phosphorylation of an important transcription factor known as STAT5. [1]
- two highly related effector memory sub-types, which strongly express genes for molecules essential to the cytotoxic function of CD8 T cells:
Pauls mum
- effector memory (TEM)
- effector memory RA (TEMRA)
Memory T cells can be recognized by the differential expression of certain molecules.
- Central memory TCM cells express L-selectin and the chemokine receptor CCR7, they secrete IL-2, but not IFNγ or IL-4.
- Effector memory TEM cells, however, do not express L-selectin or CCR7 but produce effector cytokines like IFNγ and IL-4.
Antigen-specific memory T cells against viruses or other microbial molecules can be found in both TCM and TEM subsets. Although most information is currently based on observations in the Cytotoxic T cells (CD8-positive) subset, similar populations appear to exist for both the Helper T cells (CD4-positive) and the cytotoxic T cells.
See also
References
- ^ Willinger T, Freeman T, Hasegawa H, McMichael A, Callan M (2005). "Molecular signatures distinguish human central memory from effector memory CD8 T cell subsets". J Immunol. 175 (9): 5895–903. PMID 16237082.
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Further reading
- Janeway CA, Jr.; et al. (2005). Immunobiology (6th ed. ed.). Garland Science. ISBN 978-0-443-07310-6.
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- Cellular and Molecular Immunology (5th Ed.) Abbas AK, and Lichtman, Editor: Saunders, Philadelphia, 2003.