The involvement of antigen processing in determinant selection by class II MHC and its relationship to immunodominance
Identifieur interne : 004605 ( Main/Exploration ); précédent : 004604; suivant : 004606The involvement of antigen processing in determinant selection by class II MHC and its relationship to immunodominance
Auteurs : Hongkui Deng [États-Unis] ; Lisa Fosdick [États-Unis] ; Eli Sercarz [États-Unis]Source :
- APMIS [ 0903-4641 ] ; 1993-07.
English descriptors
- Teeft :
- Acad, Antigen, Antigen complexed, Antigen presentation, Antigen processing, Antigenic, Antigenic peptides, Autoimmune, Autoimmune disease, Cell biol, Cell biology, Cell determinants, Cell epitopes, Cell hybridomas, Cell recognition, Cell repertoire, Cell response, Chimeric peptide, Cryptic determinants, Deng, Determinant, Determinant expression, Determinant influences, Determinant selection, Different types, Dominant determinant, Dominant expression, Endogenous, Endogenous antigen presentation, Endogenous antigens, Exogenous, Histocompatibility, Immune, Immune response, Immunodominance, Immunogenic peptides, Immunol, Initial processing, Intact proteins, Intracellular transport, Intramolecular competition, Invariant chain, Large antigen fragments, Large fragments, Limited number, Long peptides, Macrophage, Major histocompatibility, Molecular context, Molecule, Natl, Negative selection, Peptide, Peptide binding, Personal communication, Possible determinants, Possible mechanisms, Proc, Protein antigen, Recent studies, Recent study, Same compartment, Same molecule, Selective process, Sercarz, Single determinant, Subcellular fractions, Subdominant, Subdominant determinants.
Abstract
The T cell response in vivo to many whole proteins is focused on a limited number of possible determinants which can be termed immunodominant. Antigen processing for class II antigen presentation appears to play a major role in this selective process. With experimental evidence accumulated in our laboratory as well as others, we review several possible mechanisms involved in antigen processing responsible for selective or differential determinant expression. In particular, we discuss the determinant capture model in which MHC class II molecules initially capture large antigen fragments, such that bound determinants are protected from proteolysis by the MHC molecules and eventually become dominant while the flanking determinants are trimmed away. Such flanking determinants therefore become subdominant or cryptic. This mechanism underlies the capturing role of MHC molecules in the physiological processing of antigens.
Url:
DOI: 10.1111/j.1699-0463.1993.tb00161.x
Affiliations:
Links toward previous steps (curation, corpus...)
- to stream Istex, to step Corpus: 001424
- to stream Istex, to step Curation: 001424
- to stream Istex, to step Checkpoint: 001C16
- to stream Main, to step Merge: 004671
- to stream Main, to step Curation: 004605
Le document en format XML
<record><TEI wicri:istexFullTextTei="biblStruct"><teiHeader><fileDesc><titleStmt><title xml:lang="en">The involvement of antigen processing in determinant selection by class II MHC and its relationship to immunodominance</title>
<author><name sortKey="Deng, Hongkui" sort="Deng, Hongkui" uniqKey="Deng H" first="Hongkui" last="Deng">Hongkui Deng</name>
</author>
<author><name sortKey="Fosdick, Lisa" sort="Fosdick, Lisa" uniqKey="Fosdick L" first="Lisa" last="Fosdick">Lisa Fosdick</name>
</author>
<author><name sortKey="Sercarz, Eli" sort="Sercarz, Eli" uniqKey="Sercarz E" first="Eli" last="Sercarz">Eli Sercarz</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">ISTEX</idno>
<idno type="RBID">ISTEX:FA62FF86BEC441C452FF0E5ACBF84FD54F97C4D8</idno>
<date when="1993" year="1993">1993</date>
<idno type="doi">10.1111/j.1699-0463.1993.tb00161.x</idno>
<idno type="url">https://api.istex.fr/ark:/67375/WNG-BCJRZK9H-8/fulltext.pdf</idno>
<idno type="wicri:Area/Istex/Corpus">001424</idno>
<idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Corpus" wicri:corpus="ISTEX">001424</idno>
<idno type="wicri:Area/Istex/Curation">001424</idno>
<idno type="wicri:Area/Istex/Checkpoint">001C16</idno>
<idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Checkpoint">001C16</idno>
<idno type="wicri:doubleKey">0903-4641:1993:Deng H:the:involvement:of</idno>
<idno type="wicri:Area/Main/Merge">004671</idno>
<idno type="wicri:Area/Main/Curation">004605</idno>
<idno type="wicri:Area/Main/Exploration">004605</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title level="a" type="main">The involvement of antigen processing in determinant selection by class II MHC and its relationship to immunodominance</title>
<author><name sortKey="Deng, Hongkui" sort="Deng, Hongkui" uniqKey="Deng H" first="Hongkui" last="Deng">Hongkui Deng</name>
<affiliation wicri:level="2"><country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Microbiology and Molecular Genetics University of California, Los Angeles, Los Angeles, California</wicri:regionArea>
<placeName><region type="state">Californie</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Fosdick, Lisa" sort="Fosdick, Lisa" uniqKey="Fosdick L" first="Lisa" last="Fosdick">Lisa Fosdick</name>
<affiliation wicri:level="2"><country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Microbiology and Molecular Genetics University of California, Los Angeles, Los Angeles, California</wicri:regionArea>
<placeName><region type="state">Californie</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Sercarz, Eli" sort="Sercarz, Eli" uniqKey="Sercarz E" first="Eli" last="Sercarz">Eli Sercarz</name>
<affiliation wicri:level="2"><country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Microbiology and Molecular Genetics University of California, Los Angeles, Los Angeles, California</wicri:regionArea>
<placeName><region type="state">Californie</region>
</placeName>
</affiliation>
<affiliation wicri:level="1"><country xml:lang="fr" wicri:curation="lc">États-Unis</country>
<wicri:regionArea>Correspondence address: Department of Microbiology and Molecular Genetics, University of California, Los Angeles, California 90024‐1489</wicri:regionArea>
<wicri:noRegion>California 90024‐1489</wicri:noRegion>
</affiliation>
</author>
</analytic>
<monogr></monogr>
<series><title level="j" type="main">APMIS</title>
<title level="j" type="alt">APMIS</title>
<idno type="ISSN">0903-4641</idno>
<idno type="eISSN">1600-0463</idno>
<imprint><biblScope unit="vol">101</biblScope>
<biblScope unit="issue">7‐12</biblScope>
<biblScope unit="page" from="655">655</biblScope>
<biblScope unit="page" to="662">662</biblScope>
<biblScope unit="page-count">8</biblScope>
<publisher>Blackwell Publishing Ltd</publisher>
<pubPlace>Oxford, UK</pubPlace>
<date type="published" when="1993-07">1993-07</date>
</imprint>
<idno type="ISSN">0903-4641</idno>
</series>
</biblStruct>
</sourceDesc>
<seriesStmt><idno type="ISSN">0903-4641</idno>
</seriesStmt>
</fileDesc>
<profileDesc><textClass><keywords scheme="Teeft" xml:lang="en"><term>Acad</term>
<term>Antigen</term>
<term>Antigen complexed</term>
<term>Antigen presentation</term>
<term>Antigen processing</term>
<term>Antigenic</term>
<term>Antigenic peptides</term>
<term>Autoimmune</term>
<term>Autoimmune disease</term>
<term>Cell biol</term>
<term>Cell biology</term>
<term>Cell determinants</term>
<term>Cell epitopes</term>
<term>Cell hybridomas</term>
<term>Cell recognition</term>
<term>Cell repertoire</term>
<term>Cell response</term>
<term>Chimeric peptide</term>
<term>Cryptic determinants</term>
<term>Deng</term>
<term>Determinant</term>
<term>Determinant expression</term>
<term>Determinant influences</term>
<term>Determinant selection</term>
<term>Different types</term>
<term>Dominant determinant</term>
<term>Dominant expression</term>
<term>Endogenous</term>
<term>Endogenous antigen presentation</term>
<term>Endogenous antigens</term>
<term>Exogenous</term>
<term>Histocompatibility</term>
<term>Immune</term>
<term>Immune response</term>
<term>Immunodominance</term>
<term>Immunogenic peptides</term>
<term>Immunol</term>
<term>Initial processing</term>
<term>Intact proteins</term>
<term>Intracellular transport</term>
<term>Intramolecular competition</term>
<term>Invariant chain</term>
<term>Large antigen fragments</term>
<term>Large fragments</term>
<term>Limited number</term>
<term>Long peptides</term>
<term>Macrophage</term>
<term>Major histocompatibility</term>
<term>Molecular context</term>
<term>Molecule</term>
<term>Natl</term>
<term>Negative selection</term>
<term>Peptide</term>
<term>Peptide binding</term>
<term>Personal communication</term>
<term>Possible determinants</term>
<term>Possible mechanisms</term>
<term>Proc</term>
<term>Protein antigen</term>
<term>Recent studies</term>
<term>Recent study</term>
<term>Same compartment</term>
<term>Same molecule</term>
<term>Selective process</term>
<term>Sercarz</term>
<term>Single determinant</term>
<term>Subcellular fractions</term>
<term>Subdominant</term>
<term>Subdominant determinants</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">The T cell response in vivo to many whole proteins is focused on a limited number of possible determinants which can be termed immunodominant. Antigen processing for class II antigen presentation appears to play a major role in this selective process. With experimental evidence accumulated in our laboratory as well as others, we review several possible mechanisms involved in antigen processing responsible for selective or differential determinant expression. In particular, we discuss the determinant capture model in which MHC class II molecules initially capture large antigen fragments, such that bound determinants are protected from proteolysis by the MHC molecules and eventually become dominant while the flanking determinants are trimmed away. Such flanking determinants therefore become subdominant or cryptic. This mechanism underlies the capturing role of MHC molecules in the physiological processing of antigens.</div>
</front>
</TEI>
<affiliations><list><country><li>États-Unis</li>
</country>
<region><li>Californie</li>
</region>
</list>
<tree><country name="États-Unis"><region name="Californie"><name sortKey="Deng, Hongkui" sort="Deng, Hongkui" uniqKey="Deng H" first="Hongkui" last="Deng">Hongkui Deng</name>
</region>
<name sortKey="Fosdick, Lisa" sort="Fosdick, Lisa" uniqKey="Fosdick L" first="Lisa" last="Fosdick">Lisa Fosdick</name>
<name sortKey="Sercarz, Eli" sort="Sercarz, Eli" uniqKey="Sercarz E" first="Eli" last="Sercarz">Eli Sercarz</name>
<name sortKey="Sercarz, Eli" sort="Sercarz, Eli" uniqKey="Sercarz E" first="Eli" last="Sercarz">Eli Sercarz</name>
</country>
</tree>
</affiliations>
</record>
Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Sante/explor/MersV1/Data/Main/Exploration
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 004605 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd -nk 004605 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien |wiki= Sante |area= MersV1 |flux= Main |étape= Exploration |type= RBID |clé= ISTEX:FA62FF86BEC441C452FF0E5ACBF84FD54F97C4D8 |texte= The involvement of antigen processing in determinant selection by class II MHC and its relationship to immunodominance }}
This area was generated with Dilib version V0.6.33. |