Abstract
The mechanisms of CD4+ T-cell memory formation in the immune system are debated. With the well-established concept of memory formation in the central nervous system (CNS), we propose that formation of CD4+ T-cell memory depends on the interaction of two different cell systems handling two types of stored information. First, information about antigen (event) and challenge (context) is taken up by antigen-presenting cells, as initial storage. Second, event and context information is transferred to CD4+ T cells. During activation, two categories of CD4+ T cell develop: effector CD4+ T cells, carrying event and context information, enabling them to efficiently focus their response to tissues under attack; and persisting CD4+ T cells, providing context-independent antigen-specific memories and long-term storage. This novel hypothesis is supported by the observation that mammalian sleep can improve both CNS and CD4+ T-cell memory.
| Originalsprache | Englisch |
|---|---|
| Zeitschrift | Trends in Immunology |
| Jahrgang | 40 |
| Ausgabenummer | 8 |
| Seiten (von - bis) | 674-686 |
| Seitenumfang | 13 |
| ISSN | 1471-4906 |
| DOIs | |
| Publikationsstatus | Veröffentlicht - 08.2019 |
Fördermittel
We thank Marc Jenkins, Peter König, Tamas Laskay, Andrea Schampel, Werner Solbach, Johannes Textor, and the members of our laboratories for valuable comments. This work was supported by grants from the Deutsche Forschungsgemeinschaft ( TR-SFB 654 ‘Plasticity and Sleep’).
UN SDGs
Dieser Output leistet einen Beitrag zu folgendem(n) Ziel(en) für nachhaltige Entwicklung
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SDG 3 – Gesundheit und Wohlergehen
Strategische Forschungsbereiche und Zentren
- Forschungsschwerpunkt: Infektion und Entzündung - Zentrum für Infektions- und Entzündungsforschung Lübeck (ZIEL)
- Forschungsschwerpunkt: Gehirn, Hormone, Verhalten - Center for Brain, Behavior and Metabolism (CBBM)
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