The precursors of CD8 + tissue resident memory T cells: from lymphoid organs to infected tissues
CD8 tissue resident memory T cells (T cells) are essential for immune defence against pathogens and malignancies, and the molecular processes that lead to T cell formation are therefore of substantial biomedical interest. Prior work has demonstrated that signals present in the inflamed tissue micro-...
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| Published in: | Nature reviews. Immunology Vol. 22; no. 5; pp. 283 - 293 |
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| Main Authors: | , , |
| Format: | Journal Article |
| Language: | English |
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01.05.2022
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| ISSN: | 1474-1733, 1474-1741, 1474-1741 |
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| Abstract | CD8
tissue resident memory T cells (T
cells) are essential for immune defence against pathogens and malignancies, and the molecular processes that lead to T
cell formation are therefore of substantial biomedical interest. Prior work has demonstrated that signals present in the inflamed tissue micro-environment can promote the differentiation of memory precursor cells into mature T
cells, and it was therefore long assumed that T
cell formation adheres to a 'local divergence' model, in which T
cell lineage decisions are exclusively made within the tissue. However, a growing body of work provides evidence for a 'systemic divergence' model, in which circulating T cells already become preconditioned to preferentially give rise to the T
cell lineage, resulting in the generation of a pool of T
cell-poised T cells within the lymphoid compartment. Here, we review the emerging evidence that supports the existence of such a population of circulating T
cell progenitors, discuss current insights into their formation and highlight open questions in the field. |
|---|---|
| AbstractList | CD8+ tissue resident memory T cells (TRM cells) are essential for immune defence against pathogens and malignancies, and the molecular processes that lead to TRM cell formation are therefore of substantial biomedical interest. Prior work has demonstrated that signals present in the inflamed tissue micro-environment can promote the differentiation of memory precursor cells into mature TRM cells, and it was therefore long assumed that TRM cell formation adheres to a 'local divergence' model, in which TRM cell lineage decisions are exclusively made within the tissue. However, a growing body of work provides evidence for a 'systemic divergence' model, in which circulating T cells already become preconditioned to preferentially give rise to the TRM cell lineage, resulting in the generation of a pool of TRM cell-poised T cells within the lymphoid compartment. Here, we review the emerging evidence that supports the existence of such a population of circulating TRM cell progenitors, discuss current insights into their formation and highlight open questions in the field.CD8+ tissue resident memory T cells (TRM cells) are essential for immune defence against pathogens and malignancies, and the molecular processes that lead to TRM cell formation are therefore of substantial biomedical interest. Prior work has demonstrated that signals present in the inflamed tissue micro-environment can promote the differentiation of memory precursor cells into mature TRM cells, and it was therefore long assumed that TRM cell formation adheres to a 'local divergence' model, in which TRM cell lineage decisions are exclusively made within the tissue. However, a growing body of work provides evidence for a 'systemic divergence' model, in which circulating T cells already become preconditioned to preferentially give rise to the TRM cell lineage, resulting in the generation of a pool of TRM cell-poised T cells within the lymphoid compartment. Here, we review the emerging evidence that supports the existence of such a population of circulating TRM cell progenitors, discuss current insights into their formation and highlight open questions in the field. CD8+ tissue resident memory T cells (TRM cells) are essential for immune defence against pathogens and malignancies, and the molecular processes that lead to TRM cell formation are therefore of substantial biomedical interest. Prior work has demonstrated that signals present in the inflamed tissue micro-environment can promote the differentiation of memory precursor cells into mature TRM cells, and it was therefore long assumed that TRM cell formation adheres to a ‘local divergence’ model, in which TRM cell lineage decisions are exclusively made within the tissue. However, a growing body of work provides evidence for a ‘systemic divergence’ model, in which circulating T cells already become preconditioned to preferentially give rise to the TRM cell lineage, resulting in the generation of a pool of TRM cell-poised T cells within the lymphoid compartment. Here, we review the emerging evidence that supports the existence of such a population of circulating TRM cell progenitors, discuss current insights into their formation and highlight open questions in the field.CD8+ tissue resident memory T cells (TRM cells) are essential for defence against pathogens and malignancies. Prior work had indicated that these cells form within inflamed tissue, but there is emerging evidence that a pool of TRM cell precursors exists within the circulation. This Review examines the processes and signals within the lymphoid compartment that determine lineage decisions towards the formation of TRM cells. CD8 tissue resident memory T cells (T cells) are essential for immune defence against pathogens and malignancies, and the molecular processes that lead to T cell formation are therefore of substantial biomedical interest. Prior work has demonstrated that signals present in the inflamed tissue micro-environment can promote the differentiation of memory precursor cells into mature T cells, and it was therefore long assumed that T cell formation adheres to a 'local divergence' model, in which T cell lineage decisions are exclusively made within the tissue. However, a growing body of work provides evidence for a 'systemic divergence' model, in which circulating T cells already become preconditioned to preferentially give rise to the T cell lineage, resulting in the generation of a pool of T cell-poised T cells within the lymphoid compartment. Here, we review the emerging evidence that supports the existence of such a population of circulating T cell progenitors, discuss current insights into their formation and highlight open questions in the field. |
| Author | Schumacher, Ton N Masopust, David Kok, Lianne |
| Author_xml | – sequence: 1 givenname: Lianne orcidid: 0000-0002-0445-7548 surname: Kok fullname: Kok, Lianne organization: Division of Molecular Oncology & Immunology, Oncode Institute, The Netherlands Cancer Institute, Amsterdam, The Netherlands – sequence: 2 givenname: David orcidid: 0000-0002-9440-3884 surname: Masopust fullname: Masopust, David organization: Department of Microbiology and Immunology, Center for Immunology, University of Minnesota Medical School, Minneapolis, MN, USA – sequence: 3 givenname: Ton N orcidid: 0000-0003-0517-8804 surname: Schumacher fullname: Schumacher, Ton N email: t.schumacher@nki.nl organization: Division of Molecular Oncology & Immunology, Oncode Institute, The Netherlands Cancer Institute, Amsterdam, The Netherlands. t.schumacher@nki.nl |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/34480118$$D View this record in MEDLINE/PubMed |
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| Snippet | CD8
tissue resident memory T cells (T
cells) are essential for immune defence against pathogens and malignancies, and the molecular processes that lead to T... CD8+ tissue resident memory T cells (TRM cells) are essential for immune defence against pathogens and malignancies, and the molecular processes that lead to... |
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| SubjectTerms | CD8 antigen CD8-Positive T-Lymphocytes Cell Differentiation Cell Lineage Humans Immune system Immunologic Memory Immunological memory Inflammation Lymphocytes Lymphocytes T Memory cells Memory T Cells Pathogens Progenitor cells Tissues |
| Title | The precursors of CD8 + tissue resident memory T cells: from lymphoid organs to infected tissues |
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