Are CD8+CD122+ cells regulatory T cells or memory T cells? 2008

Haruhiko Suzuki, and Zhe Shi, and Yusuke Okuno, and Ken-ichi Isobe
Department of Immunology, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya 466-8550, Japan. harusuzu@med.nagoya-u.ac.jp

We identified CD8(+)CD122(+) regulatory T cells in the mouse. Some immunologists consider CD8(+)CD122(+) cells to be memory T cells despite our report of their regulatory function. Here, we propose a dual phenotype of these cells. Murine CD8(+)CD122(+) T cells demonstrate both memory and regulatory features in their functional profiles. Human CD8(+)CXCR3(+) T cells, which are thought to be the human counterpart of murine CD8(+)CD122(+) regulatory T cells, do not match human central memory T cells of the CD8(+)CD45RA(-)CCR7(+) phenotype. Thus, we must consider human CD8(+) regulatory T cells and murine CD8(+) regulatory T cells separately. Of human CD8(+) regulatory T cells, CD8(+)CXCR3(+) regulatory T cells can be divided into further subsets and we may be able to distinguish memory T cells and regulatory T cells. Of murine CD8(+)CD122(+) regulatory T cells, it seems to be impossible to divide CD8(+)CD122(+)CD44(+)CD62L(+) regulatory T cells into further subsets at present, indicating that this single population of cells has activities of both regulatory T cells and memory T cells.

UI MeSH Term Description Entries
D007156 Immunologic Memory The altered state of immunologic responsiveness resulting from initial contact with antigen, which enables the individual to produce antibodies more rapidly and in greater quantity in response to secondary antigenic stimulus. Immune Memory,Immunological Memory,Memory, Immunologic,Immune Memories,Immunologic Memories,Immunological Memories,Memory, Immune,Memory, Immunological
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000818 Animals Unicellular or multicellular, heterotrophic organisms, that have sensation and the power of voluntary movement. Under the older five kingdom paradigm, Animalia was one of the kingdoms. Under the modern three domain model, Animalia represents one of the many groups in the domain EUKARYOTA. Animal,Metazoa,Animalia
D015703 Antigens, CD Differentiation antigens residing on mammalian leukocytes. CD stands for cluster of differentiation, which refers to groups of monoclonal antibodies that show similar reactivity with certain subpopulations of antigens of a particular lineage or differentiation stage. The subpopulations of antigens are also known by the same CD designation. CD Antigen,Cluster of Differentiation Antigen,Cluster of Differentiation Marker,Differentiation Antigens, Leukocyte, Human,Leukocyte Differentiation Antigens, Human,Cluster of Differentiation Antigens,Cluster of Differentiation Markers,Antigen Cluster, Differentiation,Antigen, CD,CD Antigens,Differentiation Antigen Cluster,Differentiation Marker Cluster,Marker Cluster, Differentiation
D016176 T-Lymphocyte Subsets A classification of T-lymphocytes, especially into helper/inducer, suppressor/effector, and cytotoxic subsets, based on structurally or functionally different populations of cells. T-Cell Subset,T-Cell Subsets,T-Lymphocyte Subset,Subset, T-Cell,Subset, T-Lymphocyte,Subsets, T-Cell,Subsets, T-Lymphocyte,T Cell Subset,T Cell Subsets,T Lymphocyte Subset,T Lymphocyte Subsets
D051379 Mice The common name for the genus Mus. Mice, House,Mus,Mus musculus,Mice, Laboratory,Mouse,Mouse, House,Mouse, Laboratory,Mouse, Swiss,Mus domesticus,Mus musculus domesticus,Swiss Mice,House Mice,House Mouse,Laboratory Mice,Laboratory Mouse,Mice, Swiss,Swiss Mouse,domesticus, Mus musculus
D053646 Interleukin-2 Receptor beta Subunit A receptor subunit that is a shared component of the INTERLEUKIN 2 RECEPTOR and the INTERLEUKIN-15 RECEPTOR. High affinity receptor complexes are formed with each of these receptors when their respective alpha subunits are combined with this beta subunit and the INTERLEUKIN RECEPTOR COMMON GAMMA-CHAIN. Antigens, CD122,CD122 Antigens,Interleukin-15 Receptor beta Subunit,Interleukin-2, 15 Receptor beta Subunit,CD122 Antigen,IL-2-15 Receptor-beta,IL-2R BETA,IL-2Rbeta2,Interleukin 2-15 Receptors-beta,Interleukin-2 Receptor beta,Interleukin-2 Receptor beta Chain,Interleukin-2-15 Receptor-beta,Interleukin-Binding Peptide p75,IL 2 15 Receptor beta,IL 2R BETA,IL 2Rbeta2,Interleukin 15 Receptor beta Subunit,Interleukin 2 15 Receptor beta,Interleukin 2 15 Receptors beta,Interleukin 2 Receptor beta,Interleukin 2 Receptor beta Chain,Interleukin 2 Receptor beta Subunit,Interleukin 2, 15 Receptor beta Subunit,Interleukin Binding Peptide p75,Receptor-beta, IL-2-15
D054367 Receptors, CXCR3 CXCR receptors that are expressed on the surface of a number of cell types, including T-LYMPHOCYTES; NK CELLS; DENDRITIC CELLS; and a subset of B-LYMPHOCYTES. The receptors are activated by CHEMOKINE CXCL9; CHEMOKINE CXCL10; and CHEMOKINE CXCL11. Antigens, CD183,CD183 Antigens,CXC Chemokine Receptor 3,CXCR3 Receptors,CMKBR3 Chemokine Receptors,CXC Chemokine Receptors 3,CXCR3 Receptor,Chemokine (C-C Motif) Receptor 3,Chemokine Receptors, CMKBR3,Receptor, CXCR3,Receptors, CMKBR3 Chemokine
D054400 Receptors, CCR7 CCR receptors with specificity for CHEMOKINE CCL19 and CHEMOKINE CCL21. They are expressed at high levels in T-LYMPHOCYTES; B-LYMPHOCYTES; and DENDRITIC CELLS. Antigens, CD197,CC Chemokine Receptor 7,CCR7 Receptors,CD197 Antigens,CC Chemokine Receptor CCR7,CD197 Antigen,Antigen, CD197
D018414 CD8-Positive T-Lymphocytes A critical subpopulation of regulatory T-lymphocytes involved in MHC Class I-restricted interactions. They include both cytotoxic T-lymphocytes (T-LYMPHOCYTES, CYTOTOXIC) and CD8+ suppressor T-lymphocytes. Suppressor T-Lymphocytes, CD8-Positive,T8 Cells,T8 Lymphocytes,CD8-Positive Lymphocytes,Suppressor T-Cells, CD8-Positive,CD8 Positive Lymphocytes,CD8 Positive T Lymphocytes,CD8-Positive Lymphocyte,CD8-Positive Suppressor T-Cell,CD8-Positive Suppressor T-Cells,CD8-Positive Suppressor T-Lymphocyte,CD8-Positive Suppressor T-Lymphocytes,CD8-Positive T-Lymphocyte,Cell, T8,Cells, T8,Lymphocyte, CD8-Positive,Lymphocyte, T8,Lymphocytes, CD8-Positive,Lymphocytes, T8,Suppressor T Cells, CD8 Positive,Suppressor T Lymphocytes, CD8 Positive,Suppressor T-Cell, CD8-Positive,Suppressor T-Lymphocyte, CD8-Positive,T-Cell, CD8-Positive Suppressor,T-Cells, CD8-Positive Suppressor,T-Lymphocyte, CD8-Positive,T-Lymphocyte, CD8-Positive Suppressor,T-Lymphocytes, CD8-Positive,T-Lymphocytes, CD8-Positive Suppressor,T8 Cell,T8 Lymphocyte

Related Publications

Haruhiko Suzuki, and Zhe Shi, and Yusuke Okuno, and Ken-ichi Isobe
July 2010, Journal of immunology (Baltimore, Md. : 1950),
Haruhiko Suzuki, and Zhe Shi, and Yusuke Okuno, and Ken-ichi Isobe
October 2018, The Journal of clinical investigation,
Haruhiko Suzuki, and Zhe Shi, and Yusuke Okuno, and Ken-ichi Isobe
January 2014, American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons,
Haruhiko Suzuki, and Zhe Shi, and Yusuke Okuno, and Ken-ichi Isobe
November 2004, The Journal of experimental medicine,
Haruhiko Suzuki, and Zhe Shi, and Yusuke Okuno, and Ken-ichi Isobe
January 2015, Frontiers in immunology,
Haruhiko Suzuki, and Zhe Shi, and Yusuke Okuno, and Ken-ichi Isobe
July 2021, European journal of immunology,
Haruhiko Suzuki, and Zhe Shi, and Yusuke Okuno, and Ken-ichi Isobe
February 2013, Journal of immunology (Baltimore, Md. : 1950),
Haruhiko Suzuki, and Zhe Shi, and Yusuke Okuno, and Ken-ichi Isobe
January 2019, Journal of leukocyte biology,
Haruhiko Suzuki, and Zhe Shi, and Yusuke Okuno, and Ken-ichi Isobe
March 2016, Proceedings of the National Academy of Sciences of the United States of America,
Haruhiko Suzuki, and Zhe Shi, and Yusuke Okuno, and Ken-ichi Isobe
January 2017, American journal of translational research,
Copied contents to your clipboard!