Kinetics of Major Histocompatibility Class I Antigen Presentation in Acute Infection
Ag presentation within the regional lymph node is crucial for the initiation of CD8+ T cell responses following viral infection. The magnitude and quality of the CD8+ T cell response are regulated by the interplay between the size of the APC population and duration of Ag presentation. To understand...
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Veröffentlicht in: | The Journal of immunology (1950) 2009-01, Vol.182 (2), p.902-911 |
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description | Ag presentation within the regional lymph node is crucial for the initiation of CD8+ T cell responses following viral infection. The magnitude and quality of the CD8+ T cell response are regulated by the interplay between the size of the APC population and duration of Ag presentation. To understand how these parameters are finely regulated during an immune response, we have investigated the dynamics of Ag presentation in influenza A virus and HSV-1 infection. In both infections, APC production was calculated to occur over the first few days of infection, after which there was slow exponential decay over a period of up to 2 wk. This production rate is most likely determined by the Ag availability and recruitment and/or maturation rate of dendritic cells. APC production was found to closely parallel lymph node cell recruitment in both infections. This was greatest in the first 6 h of infection for HSV and over the second and third day for influenza. In HSV infection, the peak production also coincides with peak viral levels. By contrast, in influenza infection, APC production ceased between the third and fourth day despite the presence of high levels of virus until 5 days after infection. These analyses demonstrate that two quite different self-limiting infections generate the APC necessary to drive T cell responses early in infection at different rates. Understanding how such contrasting kinetics of Ag presentation impacts on the growth and size of developing protective T cell populations has important implications for the design of vaccines and immunotherapies. |
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H ; Zhang, Lei ; Ribeiro, Ruy M ; Mueller, Scott N ; Belz, Gabrielle T ; Davenport, Miles P</creator><creatorcontrib>Lay, Matthew D. H ; Zhang, Lei ; Ribeiro, Ruy M ; Mueller, Scott N ; Belz, Gabrielle T ; Davenport, Miles P</creatorcontrib><description>Ag presentation within the regional lymph node is crucial for the initiation of CD8+ T cell responses following viral infection. The magnitude and quality of the CD8+ T cell response are regulated by the interplay between the size of the APC population and duration of Ag presentation. To understand how these parameters are finely regulated during an immune response, we have investigated the dynamics of Ag presentation in influenza A virus and HSV-1 infection. In both infections, APC production was calculated to occur over the first few days of infection, after which there was slow exponential decay over a period of up to 2 wk. This production rate is most likely determined by the Ag availability and recruitment and/or maturation rate of dendritic cells. APC production was found to closely parallel lymph node cell recruitment in both infections. This was greatest in the first 6 h of infection for HSV and over the second and third day for influenza. In HSV infection, the peak production also coincides with peak viral levels. By contrast, in influenza infection, APC production ceased between the third and fourth day despite the presence of high levels of virus until 5 days after infection. These analyses demonstrate that two quite different self-limiting infections generate the APC necessary to drive T cell responses early in infection at different rates. Understanding how such contrasting kinetics of Ag presentation impacts on the growth and size of developing protective T cell populations has important implications for the design of vaccines and immunotherapies.</description><identifier>ISSN: 0022-1767</identifier><identifier>EISSN: 1550-6606</identifier><identifier>DOI: 10.4049/jimmunol.182.2.902</identifier><identifier>PMID: 19124733</identifier><language>eng</language><publisher>United States: Am Assoc Immnol</publisher><subject>Acute Disease ; Animals ; Antigen Presentation - immunology ; CD8-Positive T-Lymphocytes - immunology ; CD8-Positive T-Lymphocytes - metabolism ; CD8-Positive T-Lymphocytes - virology ; Cell Movement - immunology ; Dendritic Cells - immunology ; Dendritic Cells - metabolism ; Dendritic Cells - virology ; H-2 Antigens - immunology ; H-2 Antigens - metabolism ; Herpes Simplex - immunology ; Herpes Simplex - pathology ; Herpes Simplex - virology ; Herpesvirus 1, Human - immunology ; Histocompatibility Antigen H-2D ; Influenza A Virus, H3N2 Subtype - immunology ; Leukocyte Count - statistics & numerical data ; Linear Models ; Lymph Nodes - immunology ; Lymph Nodes - pathology ; Lymph Nodes - virology ; Mice ; Mice, Inbred C57BL ; Models, Immunological ; Orthomyxoviridae Infections - immunology ; Orthomyxoviridae Infections - pathology ; Orthomyxoviridae Infections - virology ; Peptide Fragments - immunology ; Peptide Fragments - metabolism ; Viral Core Proteins - immunology ; Viral Core Proteins - metabolism</subject><ispartof>The Journal of immunology (1950), 2009-01, Vol.182 (2), p.902-911</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c376t-fb3c4f91c906ff45b90ff7134c839b3e5e13d68d8cd315aaf8e69306e61c3e603</citedby><cites>FETCH-LOGICAL-c376t-fb3c4f91c906ff45b90ff7134c839b3e5e13d68d8cd315aaf8e69306e61c3e603</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19124733$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lay, Matthew D. H</creatorcontrib><creatorcontrib>Zhang, Lei</creatorcontrib><creatorcontrib>Ribeiro, Ruy M</creatorcontrib><creatorcontrib>Mueller, Scott N</creatorcontrib><creatorcontrib>Belz, Gabrielle T</creatorcontrib><creatorcontrib>Davenport, Miles P</creatorcontrib><title>Kinetics of Major Histocompatibility Class I Antigen Presentation in Acute Infection</title><title>The Journal of immunology (1950)</title><addtitle>J Immunol</addtitle><description>Ag presentation within the regional lymph node is crucial for the initiation of CD8+ T cell responses following viral infection. The magnitude and quality of the CD8+ T cell response are regulated by the interplay between the size of the APC population and duration of Ag presentation. To understand how these parameters are finely regulated during an immune response, we have investigated the dynamics of Ag presentation in influenza A virus and HSV-1 infection. In both infections, APC production was calculated to occur over the first few days of infection, after which there was slow exponential decay over a period of up to 2 wk. This production rate is most likely determined by the Ag availability and recruitment and/or maturation rate of dendritic cells. APC production was found to closely parallel lymph node cell recruitment in both infections. This was greatest in the first 6 h of infection for HSV and over the second and third day for influenza. In HSV infection, the peak production also coincides with peak viral levels. By contrast, in influenza infection, APC production ceased between the third and fourth day despite the presence of high levels of virus until 5 days after infection. These analyses demonstrate that two quite different self-limiting infections generate the APC necessary to drive T cell responses early in infection at different rates. Understanding how such contrasting kinetics of Ag presentation impacts on the growth and size of developing protective T cell populations has important implications for the design of vaccines and immunotherapies.</description><subject>Acute Disease</subject><subject>Animals</subject><subject>Antigen Presentation - immunology</subject><subject>CD8-Positive T-Lymphocytes - immunology</subject><subject>CD8-Positive T-Lymphocytes - metabolism</subject><subject>CD8-Positive T-Lymphocytes - virology</subject><subject>Cell Movement - immunology</subject><subject>Dendritic Cells - immunology</subject><subject>Dendritic Cells - metabolism</subject><subject>Dendritic Cells - virology</subject><subject>H-2 Antigens - immunology</subject><subject>H-2 Antigens - metabolism</subject><subject>Herpes Simplex - immunology</subject><subject>Herpes Simplex - pathology</subject><subject>Herpes Simplex - virology</subject><subject>Herpesvirus 1, Human - immunology</subject><subject>Histocompatibility Antigen H-2D</subject><subject>Influenza A Virus, H3N2 Subtype - immunology</subject><subject>Leukocyte Count - statistics & numerical data</subject><subject>Linear Models</subject><subject>Lymph Nodes - immunology</subject><subject>Lymph Nodes - pathology</subject><subject>Lymph Nodes - virology</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Models, Immunological</subject><subject>Orthomyxoviridae Infections - immunology</subject><subject>Orthomyxoviridae Infections - pathology</subject><subject>Orthomyxoviridae Infections - virology</subject><subject>Peptide Fragments - immunology</subject><subject>Peptide Fragments - metabolism</subject><subject>Viral Core Proteins - immunology</subject><subject>Viral Core Proteins - metabolism</subject><issn>0022-1767</issn><issn>1550-6606</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkEtLAzEUhYMotj7-gAvJyt3UPGYyk2UpaouKLuo6ZNIbmzKT1EmG0n_vSCtdXTh851z4ELqjZJKTXD5uXNv2PjQTWrEJm0jCztCYFgXJhCDiHI0JYSyjpShH6CrGDSFEEJZfohGVlOUl52O0fHUekjMRB4vf9SZ0eO5iCia0W51c7RqX9njW6BjxAk99ct_g8WcHEXwagOCx83hq-gR44S2Yv-gGXVjdRLg93mv09fy0nM2zt4-XxWz6lhleipTZmpvcSmokEdbmRS2JtSXluam4rDkUQPlKVKvKrDgttLYVCMmJAEENB0H4NXo47G678NNDTKp10UDTaA-hj0qIUuZlxQeQHUDThRg7sGrbuVZ3e0WJ-nOp_l2qwaVianA5lO6P633dwupUOco7vV-77_XOdaBiq5tmwKna7XanpV8uzIAM</recordid><startdate>20090115</startdate><enddate>20090115</enddate><creator>Lay, Matthew D. H</creator><creator>Zhang, Lei</creator><creator>Ribeiro, Ruy M</creator><creator>Mueller, Scott N</creator><creator>Belz, Gabrielle T</creator><creator>Davenport, Miles P</creator><general>Am Assoc Immnol</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20090115</creationdate><title>Kinetics of Major Histocompatibility Class I Antigen Presentation in Acute Infection</title><author>Lay, Matthew D. H ; Zhang, Lei ; Ribeiro, Ruy M ; Mueller, Scott N ; Belz, Gabrielle T ; Davenport, Miles P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c376t-fb3c4f91c906ff45b90ff7134c839b3e5e13d68d8cd315aaf8e69306e61c3e603</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Acute Disease</topic><topic>Animals</topic><topic>Antigen Presentation - immunology</topic><topic>CD8-Positive T-Lymphocytes - immunology</topic><topic>CD8-Positive T-Lymphocytes - metabolism</topic><topic>CD8-Positive T-Lymphocytes - virology</topic><topic>Cell Movement - immunology</topic><topic>Dendritic Cells - immunology</topic><topic>Dendritic Cells - metabolism</topic><topic>Dendritic Cells - virology</topic><topic>H-2 Antigens - immunology</topic><topic>H-2 Antigens - metabolism</topic><topic>Herpes Simplex - immunology</topic><topic>Herpes Simplex - pathology</topic><topic>Herpes Simplex - virology</topic><topic>Herpesvirus 1, Human - immunology</topic><topic>Histocompatibility Antigen H-2D</topic><topic>Influenza A Virus, H3N2 Subtype - immunology</topic><topic>Leukocyte Count - statistics & numerical data</topic><topic>Linear Models</topic><topic>Lymph Nodes - immunology</topic><topic>Lymph Nodes - pathology</topic><topic>Lymph Nodes - virology</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Models, Immunological</topic><topic>Orthomyxoviridae Infections - immunology</topic><topic>Orthomyxoviridae Infections - pathology</topic><topic>Orthomyxoviridae Infections - virology</topic><topic>Peptide Fragments - immunology</topic><topic>Peptide Fragments - metabolism</topic><topic>Viral Core Proteins - immunology</topic><topic>Viral Core Proteins - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lay, Matthew D. H</creatorcontrib><creatorcontrib>Zhang, Lei</creatorcontrib><creatorcontrib>Ribeiro, Ruy M</creatorcontrib><creatorcontrib>Mueller, Scott N</creatorcontrib><creatorcontrib>Belz, Gabrielle T</creatorcontrib><creatorcontrib>Davenport, Miles P</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of immunology (1950)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lay, Matthew D. H</au><au>Zhang, Lei</au><au>Ribeiro, Ruy M</au><au>Mueller, Scott N</au><au>Belz, Gabrielle T</au><au>Davenport, Miles P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Kinetics of Major Histocompatibility Class I Antigen Presentation in Acute Infection</atitle><jtitle>The Journal of immunology (1950)</jtitle><addtitle>J Immunol</addtitle><date>2009-01-15</date><risdate>2009</risdate><volume>182</volume><issue>2</issue><spage>902</spage><epage>911</epage><pages>902-911</pages><issn>0022-1767</issn><eissn>1550-6606</eissn><abstract>Ag presentation within the regional lymph node is crucial for the initiation of CD8+ T cell responses following viral infection. The magnitude and quality of the CD8+ T cell response are regulated by the interplay between the size of the APC population and duration of Ag presentation. To understand how these parameters are finely regulated during an immune response, we have investigated the dynamics of Ag presentation in influenza A virus and HSV-1 infection. In both infections, APC production was calculated to occur over the first few days of infection, after which there was slow exponential decay over a period of up to 2 wk. This production rate is most likely determined by the Ag availability and recruitment and/or maturation rate of dendritic cells. APC production was found to closely parallel lymph node cell recruitment in both infections. This was greatest in the first 6 h of infection for HSV and over the second and third day for influenza. In HSV infection, the peak production also coincides with peak viral levels. By contrast, in influenza infection, APC production ceased between the third and fourth day despite the presence of high levels of virus until 5 days after infection. 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subjects | Acute Disease Animals Antigen Presentation - immunology CD8-Positive T-Lymphocytes - immunology CD8-Positive T-Lymphocytes - metabolism CD8-Positive T-Lymphocytes - virology Cell Movement - immunology Dendritic Cells - immunology Dendritic Cells - metabolism Dendritic Cells - virology H-2 Antigens - immunology H-2 Antigens - metabolism Herpes Simplex - immunology Herpes Simplex - pathology Herpes Simplex - virology Herpesvirus 1, Human - immunology Histocompatibility Antigen H-2D Influenza A Virus, H3N2 Subtype - immunology Leukocyte Count - statistics & numerical data Linear Models Lymph Nodes - immunology Lymph Nodes - pathology Lymph Nodes - virology Mice Mice, Inbred C57BL Models, Immunological Orthomyxoviridae Infections - immunology Orthomyxoviridae Infections - pathology Orthomyxoviridae Infections - virology Peptide Fragments - immunology Peptide Fragments - metabolism Viral Core Proteins - immunology Viral Core Proteins - metabolism |
title | Kinetics of Major Histocompatibility Class I Antigen Presentation in Acute Infection |
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