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Generation of antigen specific CD8 + cytotoxic T cells following immunization with soluble protein formulated with novel glycoside adjuvants
Presentation of peptide on MHC class I molecules is essential to elicit cytolytic T cell (CTL) activity. Such peptides are a result of the cytosolic, or class I, antigen processing pathway. Due to the segregation of the class I and the exogenous processing pathway, soluble protein cannot enter the c...
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Published in: | Vaccine 1999-08, Vol.17 (23), p.2974-2982 |
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container_issue | 23 |
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container_title | Vaccine |
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creator | Sheikh, N.A Rajananthanan, P Attard, G.S Morrow, W.J.W |
description | Presentation of peptide on MHC class I molecules is essential to elicit cytolytic T cell (CTL) activity. Such peptides are a result of the cytosolic, or class I, antigen processing pathway. Due to the segregation of the class I and the exogenous processing pathway, soluble protein cannot enter the class I pathway and is thus incapable of inducing CTL. However careful formulation with adjuvants can overcome this obstacle. In this study we evaluated the capacity of two novel amphiphilic adjuvants, better termed delivery vehicles, to elicit CTL activity in a C57Bl/6 murine model with ovalbumin (OVA) as an antigen. Incomplete Freund's adjuvant and aluminium hydroxide (Alhydrogel) were used as reference adjuvants. In addition the oil-in-water emulsion Provax was used throughout as a positive control adjuvant. Both amphiphile preparations were capable of eliciting potent CTL activity after administration of one immunizing dose of ovalbumin. CTL were CD8
+ restricted as assessed by in vitro depletion of CD8
+ and CD4
+ T cells. CTL activity was also MHC-restricted as well as specific for the H-2K
b OVA motif SIINFEKL. |
doi_str_mv | 10.1016/S0264-410X(99)00173-5 |
format | article |
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Psychology</subject><subject>Glycolipids - immunology</subject><subject>Glycolipids - pharmacology</subject><subject>H-2 Antigens - immunology</subject><subject>Histocompatibility Antigens Class I - immunology</subject><subject>Immunization</subject><subject>Lipopolysaccharides - analysis</subject><subject>Lymphocyte Activation - immunology</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Microbiology</subject><subject>Ovalbumin - immunology</subject><subject>Ovalbumin - pharmacology</subject><subject>Peptide</subject><subject>Peptide Fragments</subject><subject>Soluble protein</subject><subject>T-Lymphocytes, Cytotoxic - immunology</subject><subject>Tomatine - pharmacology</subject><subject>Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies (general aspects)</subject><issn>0264-410X</issn><issn>1873-2518</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><recordid>eNqFkc9u1DAQxi0EotvCI4B8QKgILXiSOGufEFqgIFXiQJG4WY49WVw59jZ2tizPwEPjbVbAjZPHnt_88fcR8gTYK2DQvv7CqrZZNsC-nUv5gjFY1Ut-jyxAlKDiIO6TxR_khJymdM0Y4zXIh-QEWNNWVV0tyK8LDDjq7GKgsac6ZLfBQNMWjeudoet3gr6kZp9jjj_K_Yoa9D7RPnofb13YUDcMU3A_5xa3Ln-nKfqp80i3Y8zoQmHHYfI6o53zIe7Q043fm5icRart9bQrk9Mj8qDXPuHj43lGvn54f7X-uLz8fPFp_fZyaWrJ8pI3puNNbStrOyN6IxCF7oC1LdRND4avAKpGcysAhAboTXnoxEo3UiPvWH1Gns99y4Y3E6asBpcO_9IB45RUK6WohVwVkM-gGWNKI_ZqO7pBj3sFTB1sUHc2qIPGSkp1Z4Pipe7pccDUDWj_qZp1L8CzI6CT0b4fdTAu_eUkA9k2BXszY1jU2DkcVTIOg0HrRjRZ2ej-s8lv9UyniQ</recordid><startdate>19990806</startdate><enddate>19990806</enddate><creator>Sheikh, N.A</creator><creator>Rajananthanan, P</creator><creator>Attard, G.S</creator><creator>Morrow, W.J.W</creator><general>Elsevier Ltd</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>7X8</scope></search><sort><creationdate>19990806</creationdate><title>Generation of antigen specific CD8 + cytotoxic T cells following immunization with soluble protein formulated with novel glycoside adjuvants</title><author>Sheikh, N.A ; Rajananthanan, P ; Attard, G.S ; Morrow, W.J.W</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c390t-54cb543d2ddbc8fc8ee8ab1066134f1c571124a5d8118a11fc711b87a49ae5b03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Adjuvants, Immunologic - pharmacology</topic><topic>Aluminum Hydroxide - pharmacology</topic><topic>Animals</topic><topic>Antigen Presentation - immunology</topic><topic>Applied microbiology</topic><topic>Biological and medical sciences</topic><topic>CD8 Antigens - immunology</topic><topic>CTL</topic><topic>Cytotoxicity, Immunologic</topic><topic>Egg Proteins - immunology</topic><topic>Epitopes, T-Lymphocyte - immunology</topic><topic>Female</topic><topic>Freund's Adjuvant - pharmacology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Glycolipids - immunology</topic><topic>Glycolipids - pharmacology</topic><topic>H-2 Antigens - immunology</topic><topic>Histocompatibility Antigens Class I - immunology</topic><topic>Immunization</topic><topic>Lipopolysaccharides - analysis</topic><topic>Lymphocyte Activation - immunology</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Microbiology</topic><topic>Ovalbumin - immunology</topic><topic>Ovalbumin - pharmacology</topic><topic>Peptide</topic><topic>Peptide Fragments</topic><topic>Soluble protein</topic><topic>T-Lymphocytes, Cytotoxic - immunology</topic><topic>Tomatine - pharmacology</topic><topic>Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies (general aspects)</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sheikh, N.A</creatorcontrib><creatorcontrib>Rajananthanan, P</creatorcontrib><creatorcontrib>Attard, G.S</creatorcontrib><creatorcontrib>Morrow, W.J.W</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>MEDLINE - Academic</collection><jtitle>Vaccine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sheikh, N.A</au><au>Rajananthanan, P</au><au>Attard, G.S</au><au>Morrow, W.J.W</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Generation of antigen specific CD8 + cytotoxic T cells following immunization with soluble protein formulated with novel glycoside adjuvants</atitle><jtitle>Vaccine</jtitle><addtitle>Vaccine</addtitle><date>1999-08-06</date><risdate>1999</risdate><volume>17</volume><issue>23</issue><spage>2974</spage><epage>2982</epage><pages>2974-2982</pages><issn>0264-410X</issn><eissn>1873-2518</eissn><coden>VACCDE</coden><abstract>Presentation of peptide on MHC class I molecules is essential to elicit cytolytic T cell (CTL) activity. Such peptides are a result of the cytosolic, or class I, antigen processing pathway. Due to the segregation of the class I and the exogenous processing pathway, soluble protein cannot enter the class I pathway and is thus incapable of inducing CTL. However careful formulation with adjuvants can overcome this obstacle. In this study we evaluated the capacity of two novel amphiphilic adjuvants, better termed delivery vehicles, to elicit CTL activity in a C57Bl/6 murine model with ovalbumin (OVA) as an antigen. Incomplete Freund's adjuvant and aluminium hydroxide (Alhydrogel) were used as reference adjuvants. In addition the oil-in-water emulsion Provax was used throughout as a positive control adjuvant. Both amphiphile preparations were capable of eliciting potent CTL activity after administration of one immunizing dose of ovalbumin. CTL were CD8
+ restricted as assessed by in vitro depletion of CD8
+ and CD4
+ T cells. CTL activity was also MHC-restricted as well as specific for the H-2K
b OVA motif SIINFEKL.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><pmid>10462232</pmid><doi>10.1016/S0264-410X(99)00173-5</doi><tpages>9</tpages></addata></record> |
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subjects | Adjuvants, Immunologic - pharmacology Aluminum Hydroxide - pharmacology Animals Antigen Presentation - immunology Applied microbiology Biological and medical sciences CD8 Antigens - immunology CTL Cytotoxicity, Immunologic Egg Proteins - immunology Epitopes, T-Lymphocyte - immunology Female Freund's Adjuvant - pharmacology Fundamental and applied biological sciences. Psychology Glycolipids - immunology Glycolipids - pharmacology H-2 Antigens - immunology Histocompatibility Antigens Class I - immunology Immunization Lipopolysaccharides - analysis Lymphocyte Activation - immunology Mice Mice, Inbred C57BL Microbiology Ovalbumin - immunology Ovalbumin - pharmacology Peptide Peptide Fragments Soluble protein T-Lymphocytes, Cytotoxic - immunology Tomatine - pharmacology Vaccines, antisera, therapeutical immunoglobulins and monoclonal antibodies (general aspects) |
title | Generation of antigen specific CD8 + cytotoxic T cells following immunization with soluble protein formulated with novel glycoside adjuvants |
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