Heterogeneity of the Memory CD4 T Cell Response: Persisting Effectors and Resting Memory T Cells
Defining the cellular composition of the memory T cell pool has been complicated by an inability to distinguish effector and memory T cells. We present here an activation profile assay, using anti-CD3 and antigenic stimuli, that clearly distinguishes effector and memory CD4 T cells and defines subse...
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Veröffentlicht in: | The Journal of immunology (1950) 2001-01, Vol.166 (2), p.926-935 |
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container_title | The Journal of immunology (1950) |
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creator | Ahmadzadeh, Mojgan Hussain, S. Farzana Farber, Donna L |
description | Defining the cellular composition of the memory T cell pool has been complicated by an inability to distinguish effector and memory T cells. We present here an activation profile assay, using anti-CD3 and antigenic stimuli, that clearly distinguishes effector and memory CD4 T cells and defines subsets of long-lived memory CD4 T cells based on CD62 ligand (CD62L) expression. The CD62L(low) memory subset functionally resembles effector cells, exhibiting hyper-responsiveness to antigenic and anti-CD3 mediated stimuli, high proliferative capacity, and rapid activation kinetics. The CD62L(high) memory subset functionally resembles resting memory cells, exhibiting hyporesponsiveness to anti-CD3 stimuli, lower proliferative capacity, and slower activation kinetics. Our results indicate that the memory CD4 T cell pool is heterogeneous, consisting of persisting effectors and resting memory T cells. |
doi_str_mv | 10.4049/jimmunol.166.2.926 |
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The CD62L(high) memory subset functionally resembles resting memory cells, exhibiting hyporesponsiveness to anti-CD3 stimuli, lower proliferative capacity, and slower activation kinetics. Our results indicate that the memory CD4 T cell pool is heterogeneous, consisting of persisting effectors and resting memory T cells.</description><subject>Adoptive Transfer</subject><subject>Animals</subject><subject>CD4-Positive T-Lymphocytes - cytology</subject><subject>CD4-Positive T-Lymphocytes - immunology</subject><subject>CD4-Positive T-Lymphocytes - metabolism</subject><subject>CD4-Positive T-Lymphocytes - transplantation</subject><subject>CD62L protein</subject><subject>Cell Separation</subject><subject>Cell Survival - immunology</subject><subject>Cytokines - biosynthesis</subject><subject>Epitopes, T-Lymphocyte - immunology</subject><subject>Flow Cytometry</subject><subject>Hemagglutinin Glycoproteins, Influenza Virus - immunology</subject><subject>Histocompatibility Antigens Class II</subject><subject>Immunologic Memory</subject><subject>Interphase - immunology</subject><subject>L-Selectin - biosynthesis</subject><subject>Lymphocyte Activation</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Mice, Knockout</subject><subject>Mice, Transgenic</subject><subject>Receptors, Antigen, T-Cell - genetics</subject><subject>Receptors, Antigen, T-Cell - physiology</subject><subject>T-Lymphocyte Subsets - cytology</subject><subject>T-Lymphocyte Subsets - immunology</subject><subject>T-Lymphocyte Subsets - metabolism</subject><subject>T-Lymphocyte Subsets - transplantation</subject><issn>0022-1767</issn><issn>1550-6606</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc1OwzAQhC0EoqXwAhyQT9xS1k5iN9xQ-SlSEQiVs3GSdZsqiYudqurbY2hRj5xWWn0zO9oh5JLBMIEku1lWTbNubT1kQgz5MOPiiPRZmkIkBIhj0gfgPGJSyB45834JAAJ4ckp6jLEkFSLrk88JdujsHFusui21hnYLpC_YWLel4_uEzugY65q-o1_Z1uMtfUPnK99V7Zw-GINFZ52nui1_kN_tXrwT-nNyYnTt8WI_B-Tj8WE2nkTT16fn8d00KmIOIpIjWRgpUzMqmZGMg2bMpFKXISkyyCBPIB4FEkTBRVrkSZLJWOtc5rnRZRwPyPXOd-Xs1zpEUU3li5BAt2jXXklIZQxM_guykIKnWRZAvgMLZ713aNTKVY12W8VA_RSg_gpQoQDFVSggiK727uu8wfIg2X_8cH5RzRebyqHyja7rgDO12WwOTt_1aY-p</recordid><startdate>20010115</startdate><enddate>20010115</enddate><creator>Ahmadzadeh, Mojgan</creator><creator>Hussain, S. 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The CD62L(low) memory subset functionally resembles effector cells, exhibiting hyper-responsiveness to antigenic and anti-CD3 mediated stimuli, high proliferative capacity, and rapid activation kinetics. The CD62L(high) memory subset functionally resembles resting memory cells, exhibiting hyporesponsiveness to anti-CD3 stimuli, lower proliferative capacity, and slower activation kinetics. Our results indicate that the memory CD4 T cell pool is heterogeneous, consisting of persisting effectors and resting memory T cells.</abstract><cop>United States</cop><pub>Am Assoc Immnol</pub><pmid>11145669</pmid><doi>10.4049/jimmunol.166.2.926</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adoptive Transfer Animals CD4-Positive T-Lymphocytes - cytology CD4-Positive T-Lymphocytes - immunology CD4-Positive T-Lymphocytes - metabolism CD4-Positive T-Lymphocytes - transplantation CD62L protein Cell Separation Cell Survival - immunology Cytokines - biosynthesis Epitopes, T-Lymphocyte - immunology Flow Cytometry Hemagglutinin Glycoproteins, Influenza Virus - immunology Histocompatibility Antigens Class II Immunologic Memory Interphase - immunology L-Selectin - biosynthesis Lymphocyte Activation Mice Mice, Inbred BALB C Mice, Knockout Mice, Transgenic Receptors, Antigen, T-Cell - genetics Receptors, Antigen, T-Cell - physiology T-Lymphocyte Subsets - cytology T-Lymphocyte Subsets - immunology T-Lymphocyte Subsets - metabolism T-Lymphocyte Subsets - transplantation |
title | Heterogeneity of the Memory CD4 T Cell Response: Persisting Effectors and Resting Memory T Cells |
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