A simple and efficient method for the monitoring of antigen-specific T cell responses using peptide pool arrays in a modified ELISpot assay
In this study, we describe a simple and efficient method for both the monitoring of antigen-specific CD4 and CD8 T cell responses as well as the identification of novel CD4 and CD8 T cell epitopes using a modified ELISpot assay and pools of 20mer peptides. We have demonstrated that pools containing...
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Veröffentlicht in: | Journal of immunological methods 2001-08, Vol.254 (1), p.59-66 |
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description | In this study, we describe a simple and efficient method for both the monitoring of antigen-specific CD4 and CD8 T cell responses as well as the identification of novel CD4 and CD8 T cell epitopes using a modified ELISpot assay and pools of 20mer peptides. We have demonstrated that pools containing as many as 64 20mer peptides may be used to screen for CD4 and CD8 T cell responses to HPV16 L1, E1, and E7 in mice. Using arrays of pools of overlapping 20mer peptides, we have identified novel CD4 and CD8 epitopes in both HPV16L1 and HPV16E1 which are presented in Balb/c mice. We have further shown that the use of 20mer peptides is equivalent to using minimal 9mer epitopes for the stimulation of CD8 T cell responses in our assay. While our experiments are conducted in mice, the use of peptide pool arrays allows for the identification of epitope-specific responses using far fewer cells than is required for testing a panel of overlapping peptides individually, making this strategy particularly useful in clinical settings where immune cells may be limiting. |
doi_str_mv | 10.1016/S0022-1759(01)00397-0 |
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We have demonstrated that pools containing as many as 64 20mer peptides may be used to screen for CD4 and CD8 T cell responses to HPV16 L1, E1, and E7 in mice. Using arrays of pools of overlapping 20mer peptides, we have identified novel CD4 and CD8 epitopes in both HPV16L1 and HPV16E1 which are presented in Balb/c mice. We have further shown that the use of 20mer peptides is equivalent to using minimal 9mer epitopes for the stimulation of CD8 T cell responses in our assay. While our experiments are conducted in mice, the use of peptide pool arrays allows for the identification of epitope-specific responses using far fewer cells than is required for testing a panel of overlapping peptides individually, making this strategy particularly useful in clinical settings where immune cells may be limiting.</description><identifier>ISSN: 0022-1759</identifier><identifier>EISSN: 1872-7905</identifier><identifier>DOI: 10.1016/S0022-1759(01)00397-0</identifier><identifier>PMID: 11406153</identifier><identifier>CODEN: JIMMBG</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>AE1 protein ; AE7 protein ; AL1 protein ; Animals ; Biological and medical sciences ; Capsid Proteins ; CD4 antigen ; CD4-Positive T-Lymphocytes - immunology ; CD8 antigen ; CD8-Positive T-Lymphocytes - immunology ; Diverse techniques ; E1 protein ; E7 protein ; ELISpot ; Enzyme-Linked Immunosorbent Assay - methods ; epitope ; Epitope Mapping ; Epitopes, T-Lymphocyte - genetics ; Epitopes, T-Lymphocyte - immunology ; Fundamental and applied biological sciences. Psychology ; Fundamental immunology ; Human papilloma virus type 16 ; human papillomavirus 16 ; Humans ; Immunologic Techniques ; Interferon-gamma - biosynthesis ; L1 protein ; Mice ; Mice, Inbred BALB C ; Microbiology ; Molecular and cellular biology ; Molecular immunology ; Oncogene Proteins - genetics ; Oncogene Proteins - immunology ; Oncogene Proteins, Viral - genetics ; Oncogene Proteins, Viral - immunology ; Papillomavirus E7 Proteins ; Peptides - immunology ; Techniques</subject><ispartof>Journal of immunological methods, 2001-08, Vol.254 (1), p.59-66</ispartof><rights>2001</rights><rights>2002 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c422t-ba139680c59ace054cab28c6c7c3f6488c06677a70fd36f3dcb8f69cc77c4e243</citedby><cites>FETCH-LOGICAL-c422t-ba139680c59ace054cab28c6c7c3f6488c06677a70fd36f3dcb8f69cc77c4e243</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0022175901003970$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=14163580$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11406153$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tobery, Timothy W</creatorcontrib><creatorcontrib>Wang, Su</creatorcontrib><creatorcontrib>Wang, Xin-Min</creatorcontrib><creatorcontrib>Neeper, Michael P</creatorcontrib><creatorcontrib>Jansen, Kathrin U</creatorcontrib><creatorcontrib>McClements, William L</creatorcontrib><creatorcontrib>Caulfield, Michael J</creatorcontrib><title>A simple and efficient method for the monitoring of antigen-specific T cell responses using peptide pool arrays in a modified ELISpot assay</title><title>Journal of immunological methods</title><addtitle>J Immunol Methods</addtitle><description>In this study, we describe a simple and efficient method for both the monitoring of antigen-specific CD4 and CD8 T cell responses as well as the identification of novel CD4 and CD8 T cell epitopes using a modified ELISpot assay and pools of 20mer peptides. We have demonstrated that pools containing as many as 64 20mer peptides may be used to screen for CD4 and CD8 T cell responses to HPV16 L1, E1, and E7 in mice. Using arrays of pools of overlapping 20mer peptides, we have identified novel CD4 and CD8 epitopes in both HPV16L1 and HPV16E1 which are presented in Balb/c mice. We have further shown that the use of 20mer peptides is equivalent to using minimal 9mer epitopes for the stimulation of CD8 T cell responses in our assay. While our experiments are conducted in mice, the use of peptide pool arrays allows for the identification of epitope-specific responses using far fewer cells than is required for testing a panel of overlapping peptides individually, making this strategy particularly useful in clinical settings where immune cells may be limiting.</description><subject>AE1 protein</subject><subject>AE7 protein</subject><subject>AL1 protein</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Capsid Proteins</subject><subject>CD4 antigen</subject><subject>CD4-Positive T-Lymphocytes - immunology</subject><subject>CD8 antigen</subject><subject>CD8-Positive T-Lymphocytes - immunology</subject><subject>Diverse techniques</subject><subject>E1 protein</subject><subject>E7 protein</subject><subject>ELISpot</subject><subject>Enzyme-Linked Immunosorbent Assay - methods</subject><subject>epitope</subject><subject>Epitope Mapping</subject><subject>Epitopes, T-Lymphocyte - genetics</subject><subject>Epitopes, T-Lymphocyte - immunology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fundamental immunology</subject><subject>Human papilloma virus type 16</subject><subject>human papillomavirus 16</subject><subject>Humans</subject><subject>Immunologic Techniques</subject><subject>Interferon-gamma - biosynthesis</subject><subject>L1 protein</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Microbiology</subject><subject>Molecular and cellular biology</subject><subject>Molecular immunology</subject><subject>Oncogene Proteins - genetics</subject><subject>Oncogene Proteins - immunology</subject><subject>Oncogene Proteins, Viral - genetics</subject><subject>Oncogene Proteins, Viral - immunology</subject><subject>Papillomavirus E7 Proteins</subject><subject>Peptides - immunology</subject><subject>Techniques</subject><issn>0022-1759</issn><issn>1872-7905</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1v1DAQhi0EoqXwE0C-gOAQGOfDTk5VVRWotBKHlrPlnYxboyQOHi_S_gb-NEl3RY89zeV5X8_4EeKtgs8KlP5yA1CWhTJN9xHUJ4CqMwU8E6eqNWVhOmiei9P_yIl4xfwLABRoeClOlKpBq6Y6FX8vJIdxHki6qZfkfcBAU5Yj5fvYSx-TzPckxziFHFOY7mT0C5rDHU0Fz4RhSchbiTQMMhHPcWJiueMVnWnOoSc5xzhIl5LbswyTdEtdv-Sol1eb65s5ZumY3f61eOHdwPTmOM_Ez69Xt5ffi82Pb9eXF5sC67LMxdapqtMtYNM5JGhqdNuyRY0GK6_rtkXQ2hhnwPeV9lWP29brDtEYrKmsqzPx4dA7p_h7R5ztGHg9wE0Ud2wNdKqplX4SVC2YrjblAjYHEFNkTuTtnMLo0t4qsKsu-6DLri4sKPugy8KSe3d8YLcdqX9MHf0swPsj4Bjd4JObMPAjt27ZtGvR-YGj5d_-BEqWV49IfUiE2fYxPLHKP7_9suM</recordid><startdate>20010801</startdate><enddate>20010801</enddate><creator>Tobery, Timothy W</creator><creator>Wang, Su</creator><creator>Wang, Xin-Min</creator><creator>Neeper, Michael P</creator><creator>Jansen, Kathrin U</creator><creator>McClements, William L</creator><creator>Caulfield, Michael J</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>IQODW</scope><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>7QO</scope><scope>7T5</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20010801</creationdate><title>A simple and efficient method for the monitoring of antigen-specific T cell responses using peptide pool arrays in a modified ELISpot assay</title><author>Tobery, Timothy W ; Wang, Su ; Wang, Xin-Min ; Neeper, Michael P ; Jansen, Kathrin U ; McClements, William L ; Caulfield, Michael J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c422t-ba139680c59ace054cab28c6c7c3f6488c06677a70fd36f3dcb8f69cc77c4e243</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>AE1 protein</topic><topic>AE7 protein</topic><topic>AL1 protein</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Capsid Proteins</topic><topic>CD4 antigen</topic><topic>CD4-Positive T-Lymphocytes - immunology</topic><topic>CD8 antigen</topic><topic>CD8-Positive T-Lymphocytes - immunology</topic><topic>Diverse techniques</topic><topic>E1 protein</topic><topic>E7 protein</topic><topic>ELISpot</topic><topic>Enzyme-Linked Immunosorbent Assay - methods</topic><topic>epitope</topic><topic>Epitope Mapping</topic><topic>Epitopes, T-Lymphocyte - genetics</topic><topic>Epitopes, T-Lymphocyte - immunology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Fundamental immunology</topic><topic>Human papilloma virus type 16</topic><topic>human papillomavirus 16</topic><topic>Humans</topic><topic>Immunologic Techniques</topic><topic>Interferon-gamma - biosynthesis</topic><topic>L1 protein</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Microbiology</topic><topic>Molecular and cellular biology</topic><topic>Molecular immunology</topic><topic>Oncogene Proteins - genetics</topic><topic>Oncogene Proteins - immunology</topic><topic>Oncogene Proteins, Viral - genetics</topic><topic>Oncogene Proteins, Viral - immunology</topic><topic>Papillomavirus E7 Proteins</topic><topic>Peptides - immunology</topic><topic>Techniques</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tobery, Timothy W</creatorcontrib><creatorcontrib>Wang, Su</creatorcontrib><creatorcontrib>Wang, Xin-Min</creatorcontrib><creatorcontrib>Neeper, Michael P</creatorcontrib><creatorcontrib>Jansen, Kathrin U</creatorcontrib><creatorcontrib>McClements, William L</creatorcontrib><creatorcontrib>Caulfield, Michael J</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Immunology Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of immunological methods</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tobery, Timothy W</au><au>Wang, Su</au><au>Wang, Xin-Min</au><au>Neeper, Michael P</au><au>Jansen, Kathrin U</au><au>McClements, William L</au><au>Caulfield, Michael J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A simple and efficient method for the monitoring of antigen-specific T cell responses using peptide pool arrays in a modified ELISpot assay</atitle><jtitle>Journal of immunological methods</jtitle><addtitle>J Immunol Methods</addtitle><date>2001-08-01</date><risdate>2001</risdate><volume>254</volume><issue>1</issue><spage>59</spage><epage>66</epage><pages>59-66</pages><issn>0022-1759</issn><eissn>1872-7905</eissn><coden>JIMMBG</coden><abstract>In this study, we describe a simple and efficient method for both the monitoring of antigen-specific CD4 and CD8 T cell responses as well as the identification of novel CD4 and CD8 T cell epitopes using a modified ELISpot assay and pools of 20mer peptides. We have demonstrated that pools containing as many as 64 20mer peptides may be used to screen for CD4 and CD8 T cell responses to HPV16 L1, E1, and E7 in mice. Using arrays of pools of overlapping 20mer peptides, we have identified novel CD4 and CD8 epitopes in both HPV16L1 and HPV16E1 which are presented in Balb/c mice. We have further shown that the use of 20mer peptides is equivalent to using minimal 9mer epitopes for the stimulation of CD8 T cell responses in our assay. While our experiments are conducted in mice, the use of peptide pool arrays allows for the identification of epitope-specific responses using far fewer cells than is required for testing a panel of overlapping peptides individually, making this strategy particularly useful in clinical settings where immune cells may be limiting.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>11406153</pmid><doi>10.1016/S0022-1759(01)00397-0</doi><tpages>8</tpages></addata></record> |
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subjects | AE1 protein AE7 protein AL1 protein Animals Biological and medical sciences Capsid Proteins CD4 antigen CD4-Positive T-Lymphocytes - immunology CD8 antigen CD8-Positive T-Lymphocytes - immunology Diverse techniques E1 protein E7 protein ELISpot Enzyme-Linked Immunosorbent Assay - methods epitope Epitope Mapping Epitopes, T-Lymphocyte - genetics Epitopes, T-Lymphocyte - immunology Fundamental and applied biological sciences. Psychology Fundamental immunology Human papilloma virus type 16 human papillomavirus 16 Humans Immunologic Techniques Interferon-gamma - biosynthesis L1 protein Mice Mice, Inbred BALB C Microbiology Molecular and cellular biology Molecular immunology Oncogene Proteins - genetics Oncogene Proteins - immunology Oncogene Proteins, Viral - genetics Oncogene Proteins, Viral - immunology Papillomavirus E7 Proteins Peptides - immunology Techniques |
title | A simple and efficient method for the monitoring of antigen-specific T cell responses using peptide pool arrays in a modified ELISpot assay |
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