Serveur d'exploration MERS

Attention, ce site est en cours de développement !
Attention, site généré par des moyens informatiques à partir de corpus bruts.
Les informations ne sont donc pas validées.

Atheroprotective vaccination with MHC-II-restricted ApoB peptides induces peritoneal IL-10-producing CD4 T cells.

Identifieur interne : 000E84 ( Main/Exploration ); précédent : 000E83; suivant : 000E85

Atheroprotective vaccination with MHC-II-restricted ApoB peptides induces peritoneal IL-10-producing CD4 T cells.

Auteurs : Takayuki Kimura ; Kevin Tse ; Sara Mcardle ; Teresa Gerhardt ; Jacqueline Miller ; Zbigniew Mikulski ; John Sidney [États-Unis] ; Alessandro Sette [États-Unis] ; Dennis Wolf ; Klaus Ley

Source :

RBID : pubmed:28087520

Descripteurs français

English descriptors

Abstract

Although immunization with major histocompatibility complex (MHC) class II-restricted apolipoprotein B (ApoB) peptides has been shown to be atheroprotective, the mechanism is unclear. Here, we investigated CD4+ T cell populations in immunized atherosclerotic mice. Peptides (16-mers) from mouse ApoB, the core protein of low-density lipoprotein (LDL), were screened for binding to I-Ab by computer prediction and confirmed by radiolabeled peptide competition. Three new peptides, P101 (FGKQGFFPDSVNKALY, 5.5 nM IC50), P102 (TLYALSHAVNSYFDVD, 6.8 nM), and P103 (LYYKEDKTSLSASAAS, 95 nM), were tested in an atherosclerosis model (Apoe-/- mice on Western diet). Immunization with each of the three peptides (1 time in complete Freund's adjuvant subcuntaneously and 4 time in incomplete Freund's adjuvant intraperitoneally) but not with adjuvant alone showed significantly reduced atherosclerotic plaques in the aortic root by serial sections and in the whole aorta by en face staining. There were no differences in body weight, LDL cholesterol, or triglycerides. Peritoneal leukocytes from ApoB peptide-immunized mice, but not control mice, secreted significant amounts of IL-10 (150 pg/ml). Flow cytometry showed that peptide immunization induced IL-10 in 10% of peritoneal CD4+ T cells, some of which also expressed chemokine (C-C motif) receptor 5 (CCR5). Vaccination with ApoB peptides expanded peritoneal FoxP3+ regulatory CD4+ T cells and more than tripled the number of CCR5+FoxP3+ cells. Similar trends were also seen in the draining mediastinal lymph nodes but not in the nondraining inguinal lymph nodes. We conclude that vaccination with MHC class II-restricted autologous ApoB peptides induces regulatory T cells (Tregs) and IL-10, suggesting a plausible mechanism for atheroprotection.NEW & NOTEWORTHY Vaccination against apolipoprotein B (ApoB), the protein of LDL, attracts attention as a novel approach to prevent atherosclerosis. We discovered major histocompatibility complex class II-restricted ApoB peptides, which reduce atherosclerosis and induce IL-10-producing CD4+ T cells and chemokine (C-C motif) receptor 5 expression on regulatory T cells, suggesting that immunization with ApoB peptides inhibits atherosclerosis by inducing anti-inflammatory cytokines.

DOI: 10.1152/ajpheart.00798.2016
PubMed: 28087520


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

<record>
<TEI>
<teiHeader>
<fileDesc>
<titleStmt>
<title xml:lang="en">Atheroprotective vaccination with MHC-II-restricted ApoB peptides induces peritoneal IL-10-producing CD4 T cells.</title>
<author>
<name sortKey="Kimura, Takayuki" sort="Kimura, Takayuki" uniqKey="Kimura T" first="Takayuki" last="Kimura">Takayuki Kimura</name>
<affiliation>
<nlm:affiliation>Division of Inflammation Biology, La Jolla Institute for Allergy and Immunology, La Jolla, California; and.</nlm:affiliation>
<wicri:noCountry code="subField">California; and</wicri:noCountry>
</affiliation>
</author>
<author>
<name sortKey="Tse, Kevin" sort="Tse, Kevin" uniqKey="Tse K" first="Kevin" last="Tse">Kevin Tse</name>
<affiliation>
<nlm:affiliation>Division of Inflammation Biology, La Jolla Institute for Allergy and Immunology, La Jolla, California; and.</nlm:affiliation>
<wicri:noCountry code="subField">California; and</wicri:noCountry>
</affiliation>
</author>
<author>
<name sortKey="Mcardle, Sara" sort="Mcardle, Sara" uniqKey="Mcardle S" first="Sara" last="Mcardle">Sara Mcardle</name>
<affiliation>
<nlm:affiliation>Division of Inflammation Biology, La Jolla Institute for Allergy and Immunology, La Jolla, California; and.</nlm:affiliation>
<wicri:noCountry code="subField">California; and</wicri:noCountry>
</affiliation>
</author>
<author>
<name sortKey="Gerhardt, Teresa" sort="Gerhardt, Teresa" uniqKey="Gerhardt T" first="Teresa" last="Gerhardt">Teresa Gerhardt</name>
<affiliation>
<nlm:affiliation>Division of Inflammation Biology, La Jolla Institute for Allergy and Immunology, La Jolla, California; and.</nlm:affiliation>
<wicri:noCountry code="subField">California; and</wicri:noCountry>
</affiliation>
</author>
<author>
<name sortKey="Miller, Jacqueline" sort="Miller, Jacqueline" uniqKey="Miller J" first="Jacqueline" last="Miller">Jacqueline Miller</name>
<affiliation>
<nlm:affiliation>Division of Inflammation Biology, La Jolla Institute for Allergy and Immunology, La Jolla, California; and.</nlm:affiliation>
<wicri:noCountry code="subField">California; and</wicri:noCountry>
</affiliation>
</author>
<author>
<name sortKey="Mikulski, Zbigniew" sort="Mikulski, Zbigniew" uniqKey="Mikulski Z" first="Zbigniew" last="Mikulski">Zbigniew Mikulski</name>
<affiliation>
<nlm:affiliation>Division of Inflammation Biology, La Jolla Institute for Allergy and Immunology, La Jolla, California; and.</nlm:affiliation>
<wicri:noCountry code="subField">California; and</wicri:noCountry>
</affiliation>
</author>
<author>
<name sortKey="Sidney, John" sort="Sidney, John" uniqKey="Sidney J" first="John" last="Sidney">John Sidney</name>
<affiliation wicri:level="2">
<nlm:affiliation>Division of Vaccine Discovery, La Jolla Institute for Allergy and Immunology, La Jolla, California.</nlm:affiliation>
<country>États-Unis</country>
<placeName>
<region type="state">Californie</region>
</placeName>
<wicri:cityArea>Division of Vaccine Discovery, La Jolla Institute for Allergy and Immunology, La Jolla</wicri:cityArea>
</affiliation>
</author>
<author>
<name sortKey="Sette, Alessandro" sort="Sette, Alessandro" uniqKey="Sette A" first="Alessandro" last="Sette">Alessandro Sette</name>
<affiliation wicri:level="2">
<nlm:affiliation>Division of Vaccine Discovery, La Jolla Institute for Allergy and Immunology, La Jolla, California.</nlm:affiliation>
<country>États-Unis</country>
<placeName>
<region type="state">Californie</region>
</placeName>
<wicri:cityArea>Division of Vaccine Discovery, La Jolla Institute for Allergy and Immunology, La Jolla</wicri:cityArea>
</affiliation>
</author>
<author>
<name sortKey="Wolf, Dennis" sort="Wolf, Dennis" uniqKey="Wolf D" first="Dennis" last="Wolf">Dennis Wolf</name>
<affiliation>
<nlm:affiliation>Division of Inflammation Biology, La Jolla Institute for Allergy and Immunology, La Jolla, California; and.</nlm:affiliation>
<wicri:noCountry code="subField">California; and</wicri:noCountry>
</affiliation>
</author>
<author>
<name sortKey="Ley, Klaus" sort="Ley, Klaus" uniqKey="Ley K" first="Klaus" last="Ley">Klaus Ley</name>
<affiliation>
<nlm:affiliation>Division of Inflammation Biology, La Jolla Institute for Allergy and Immunology, La Jolla, California; and klaus@lji.org.</nlm:affiliation>
<wicri:noCountry code="subField">California; and klaus@lji.org.</wicri:noCountry>
</affiliation>
</author>
</titleStmt>
<publicationStmt>
<idno type="wicri:source">PubMed</idno>
<date when="2017">2017</date>
<idno type="RBID">pubmed:28087520</idno>
<idno type="pmid">28087520</idno>
<idno type="doi">10.1152/ajpheart.00798.2016</idno>
<idno type="wicri:Area/PubMed/Corpus">000E15</idno>
<idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Corpus" wicri:corpus="PubMed">000E15</idno>
<idno type="wicri:Area/PubMed/Curation">000E15</idno>
<idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Curation">000E15</idno>
<idno type="wicri:Area/PubMed/Checkpoint">000D84</idno>
<idno type="wicri:explorRef" wicri:stream="Checkpoint" wicri:step="PubMed">000D84</idno>
<idno type="wicri:Area/Ncbi/Merge">001915</idno>
<idno type="wicri:Area/Ncbi/Curation">001915</idno>
<idno type="wicri:Area/Ncbi/Checkpoint">001915</idno>
<idno type="wicri:Area/Main/Merge">000E87</idno>
<idno type="wicri:Area/Main/Curation">000E84</idno>
<idno type="wicri:Area/Main/Exploration">000E84</idno>
</publicationStmt>
<sourceDesc>
<biblStruct>
<analytic>
<title xml:lang="en">Atheroprotective vaccination with MHC-II-restricted ApoB peptides induces peritoneal IL-10-producing CD4 T cells.</title>
<author>
<name sortKey="Kimura, Takayuki" sort="Kimura, Takayuki" uniqKey="Kimura T" first="Takayuki" last="Kimura">Takayuki Kimura</name>
<affiliation>
<nlm:affiliation>Division of Inflammation Biology, La Jolla Institute for Allergy and Immunology, La Jolla, California; and.</nlm:affiliation>
<wicri:noCountry code="subField">California; and</wicri:noCountry>
</affiliation>
</author>
<author>
<name sortKey="Tse, Kevin" sort="Tse, Kevin" uniqKey="Tse K" first="Kevin" last="Tse">Kevin Tse</name>
<affiliation>
<nlm:affiliation>Division of Inflammation Biology, La Jolla Institute for Allergy and Immunology, La Jolla, California; and.</nlm:affiliation>
<wicri:noCountry code="subField">California; and</wicri:noCountry>
</affiliation>
</author>
<author>
<name sortKey="Mcardle, Sara" sort="Mcardle, Sara" uniqKey="Mcardle S" first="Sara" last="Mcardle">Sara Mcardle</name>
<affiliation>
<nlm:affiliation>Division of Inflammation Biology, La Jolla Institute for Allergy and Immunology, La Jolla, California; and.</nlm:affiliation>
<wicri:noCountry code="subField">California; and</wicri:noCountry>
</affiliation>
</author>
<author>
<name sortKey="Gerhardt, Teresa" sort="Gerhardt, Teresa" uniqKey="Gerhardt T" first="Teresa" last="Gerhardt">Teresa Gerhardt</name>
<affiliation>
<nlm:affiliation>Division of Inflammation Biology, La Jolla Institute for Allergy and Immunology, La Jolla, California; and.</nlm:affiliation>
<wicri:noCountry code="subField">California; and</wicri:noCountry>
</affiliation>
</author>
<author>
<name sortKey="Miller, Jacqueline" sort="Miller, Jacqueline" uniqKey="Miller J" first="Jacqueline" last="Miller">Jacqueline Miller</name>
<affiliation>
<nlm:affiliation>Division of Inflammation Biology, La Jolla Institute for Allergy and Immunology, La Jolla, California; and.</nlm:affiliation>
<wicri:noCountry code="subField">California; and</wicri:noCountry>
</affiliation>
</author>
<author>
<name sortKey="Mikulski, Zbigniew" sort="Mikulski, Zbigniew" uniqKey="Mikulski Z" first="Zbigniew" last="Mikulski">Zbigniew Mikulski</name>
<affiliation>
<nlm:affiliation>Division of Inflammation Biology, La Jolla Institute for Allergy and Immunology, La Jolla, California; and.</nlm:affiliation>
<wicri:noCountry code="subField">California; and</wicri:noCountry>
</affiliation>
</author>
<author>
<name sortKey="Sidney, John" sort="Sidney, John" uniqKey="Sidney J" first="John" last="Sidney">John Sidney</name>
<affiliation wicri:level="2">
<nlm:affiliation>Division of Vaccine Discovery, La Jolla Institute for Allergy and Immunology, La Jolla, California.</nlm:affiliation>
<country>États-Unis</country>
<placeName>
<region type="state">Californie</region>
</placeName>
<wicri:cityArea>Division of Vaccine Discovery, La Jolla Institute for Allergy and Immunology, La Jolla</wicri:cityArea>
</affiliation>
</author>
<author>
<name sortKey="Sette, Alessandro" sort="Sette, Alessandro" uniqKey="Sette A" first="Alessandro" last="Sette">Alessandro Sette</name>
<affiliation wicri:level="2">
<nlm:affiliation>Division of Vaccine Discovery, La Jolla Institute for Allergy and Immunology, La Jolla, California.</nlm:affiliation>
<country>États-Unis</country>
<placeName>
<region type="state">Californie</region>
</placeName>
<wicri:cityArea>Division of Vaccine Discovery, La Jolla Institute for Allergy and Immunology, La Jolla</wicri:cityArea>
</affiliation>
</author>
<author>
<name sortKey="Wolf, Dennis" sort="Wolf, Dennis" uniqKey="Wolf D" first="Dennis" last="Wolf">Dennis Wolf</name>
<affiliation>
<nlm:affiliation>Division of Inflammation Biology, La Jolla Institute for Allergy and Immunology, La Jolla, California; and.</nlm:affiliation>
<wicri:noCountry code="subField">California; and</wicri:noCountry>
</affiliation>
</author>
<author>
<name sortKey="Ley, Klaus" sort="Ley, Klaus" uniqKey="Ley K" first="Klaus" last="Ley">Klaus Ley</name>
<affiliation>
<nlm:affiliation>Division of Inflammation Biology, La Jolla Institute for Allergy and Immunology, La Jolla, California; and klaus@lji.org.</nlm:affiliation>
<wicri:noCountry code="subField">California; and klaus@lji.org.</wicri:noCountry>
</affiliation>
</author>
</analytic>
<series>
<title level="j">American journal of physiology. Heart and circulatory physiology</title>
<idno type="eISSN">1522-1539</idno>
<imprint>
<date when="2017" type="published">2017</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc>
<textClass>
<keywords scheme="KwdEn" xml:lang="en">
<term>Amino Acid Sequence</term>
<term>Animals</term>
<term>Apolipoproteins B (immunology)</term>
<term>Apolipoproteins E (genetics)</term>
<term>Apolipoproteins E (immunology)</term>
<term>Atherosclerosis (immunology)</term>
<term>Atherosclerosis (pathology)</term>
<term>Atherosclerosis (prevention & control)</term>
<term>CD4-Positive T-Lymphocytes (immunology)</term>
<term>CD4-Positive T-Lymphocytes (metabolism)</term>
<term>Female</term>
<term>Forkhead Transcription Factors (metabolism)</term>
<term>Genes, MHC Class II (immunology)</term>
<term>Immunoglobulin G (immunology)</term>
<term>Interleukin-10 (biosynthesis)</term>
<term>Lipoproteins, LDL (immunology)</term>
<term>Lymph Nodes (cytology)</term>
<term>Lymph Nodes (immunology)</term>
<term>Mice</term>
<term>Mice, Inbred C57BL</term>
<term>Mice, Knockout</term>
<term>Peptides (immunology)</term>
<term>Vaccination</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr">
<term>Animaux</term>
<term>Apolipoprotéines B (immunologie)</term>
<term>Apolipoprotéines E (génétique)</term>
<term>Apolipoprotéines E (immunologie)</term>
<term>Athérosclérose ()</term>
<term>Athérosclérose (anatomopathologie)</term>
<term>Athérosclérose (immunologie)</term>
<term>Facteurs de transcription Forkhead (métabolisme)</term>
<term>Femelle</term>
<term>Gènes MHC de classe II (immunologie)</term>
<term>Immunoglobuline G (immunologie)</term>
<term>Interleukine-10 (biosynthèse)</term>
<term>Lipoprotéines LDL (immunologie)</term>
<term>Lymphocytes T CD4+ (immunologie)</term>
<term>Lymphocytes T CD4+ (métabolisme)</term>
<term>Noeuds lymphatiques (cytologie)</term>
<term>Noeuds lymphatiques (immunologie)</term>
<term>Peptides (immunologie)</term>
<term>Souris</term>
<term>Souris de lignée C57BL</term>
<term>Souris knockout</term>
<term>Séquence d'acides aminés</term>
<term>Vaccination</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="biosynthesis" xml:lang="en">
<term>Interleukin-10</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en">
<term>Apolipoproteins E</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="immunology" xml:lang="en">
<term>Apolipoproteins B</term>
<term>Apolipoproteins E</term>
<term>Immunoglobulin G</term>
<term>Lipoproteins, LDL</term>
<term>Peptides</term>
</keywords>
<keywords scheme="MESH" qualifier="anatomopathologie" xml:lang="fr">
<term>Athérosclérose</term>
</keywords>
<keywords scheme="MESH" qualifier="biosynthèse" xml:lang="fr">
<term>Interleukine-10</term>
</keywords>
<keywords scheme="MESH" qualifier="cytologie" xml:lang="fr">
<term>Noeuds lymphatiques</term>
</keywords>
<keywords scheme="MESH" qualifier="cytology" xml:lang="en">
<term>Lymph Nodes</term>
</keywords>
<keywords scheme="MESH" qualifier="génétique" xml:lang="fr">
<term>Apolipoprotéines E</term>
</keywords>
<keywords scheme="MESH" qualifier="immunologie" xml:lang="fr">
<term>Apolipoprotéines B</term>
<term>Apolipoprotéines E</term>
<term>Athérosclérose</term>
<term>Gènes MHC de classe II</term>
<term>Immunoglobuline G</term>
<term>Lipoprotéines LDL</term>
<term>Lymphocytes T CD4+</term>
<term>Noeuds lymphatiques</term>
<term>Peptides</term>
</keywords>
<keywords scheme="MESH" qualifier="immunology" xml:lang="en">
<term>Atherosclerosis</term>
<term>CD4-Positive T-Lymphocytes</term>
<term>Genes, MHC Class II</term>
<term>Lymph Nodes</term>
</keywords>
<keywords scheme="MESH" qualifier="metabolism" xml:lang="en">
<term>CD4-Positive T-Lymphocytes</term>
<term>Forkhead Transcription Factors</term>
</keywords>
<keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr">
<term>Facteurs de transcription Forkhead</term>
<term>Lymphocytes T CD4+</term>
</keywords>
<keywords scheme="MESH" qualifier="pathology" xml:lang="en">
<term>Atherosclerosis</term>
</keywords>
<keywords scheme="MESH" qualifier="prevention & control" xml:lang="en">
<term>Atherosclerosis</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Amino Acid Sequence</term>
<term>Animals</term>
<term>Female</term>
<term>Mice</term>
<term>Mice, Inbred C57BL</term>
<term>Mice, Knockout</term>
<term>Vaccination</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr">
<term>Animaux</term>
<term>Athérosclérose</term>
<term>Femelle</term>
<term>Souris</term>
<term>Souris de lignée C57BL</term>
<term>Souris knockout</term>
<term>Séquence d'acides aminés</term>
<term>Vaccination</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">Although immunization with major histocompatibility complex (MHC) class II-restricted apolipoprotein B (ApoB) peptides has been shown to be atheroprotective, the mechanism is unclear. Here, we investigated CD4
<sup>+</sup>
T cell populations in immunized atherosclerotic mice. Peptides (16-mers) from mouse ApoB, the core protein of low-density lipoprotein (LDL), were screened for binding to I-A
<sup>b</sup>
by computer prediction and confirmed by radiolabeled peptide competition. Three new peptides, P101 (FGKQGFFPDSVNKALY, 5.5 nM IC
<sub>50</sub>
), P102 (TLYALSHAVNSYFDVD, 6.8 nM), and P103 (LYYKEDKTSLSASAAS, 95 nM), were tested in an atherosclerosis model (
<i>Apoe
<sup>-/-</sup>
</i>
mice on Western diet). Immunization with each of the three peptides (1 time in complete Freund's adjuvant subcuntaneously and 4 time in incomplete Freund's adjuvant intraperitoneally) but not with adjuvant alone showed significantly reduced atherosclerotic plaques in the aortic root by serial sections and in the whole aorta by en face staining. There were no differences in body weight, LDL cholesterol, or triglycerides. Peritoneal leukocytes from ApoB peptide-immunized mice, but not control mice, secreted significant amounts of IL-10 (150 pg/ml). Flow cytometry showed that peptide immunization induced IL-10 in 10% of peritoneal CD4
<sup>+</sup>
T cells, some of which also expressed chemokine (C-C motif) receptor 5 (CCR5). Vaccination with ApoB peptides expanded peritoneal FoxP3
<sup>+</sup>
regulatory CD4
<sup>+</sup>
T cells and more than tripled the number of CCR5
<sup>+</sup>
FoxP3
<sup>+</sup>
cells. Similar trends were also seen in the draining mediastinal lymph nodes but not in the nondraining inguinal lymph nodes. We conclude that vaccination with MHC class II-restricted autologous ApoB peptides induces regulatory T cells (Tregs) and IL-10, suggesting a plausible mechanism for atheroprotection.
<b>NEW & NOTEWORTHY</b>
Vaccination against apolipoprotein B (ApoB), the protein of LDL, attracts attention as a novel approach to prevent atherosclerosis. We discovered major histocompatibility complex class II-restricted ApoB peptides, which reduce atherosclerosis and induce IL-10-producing CD4
<sup>+</sup>
T cells and chemokine (C-C motif) receptor 5 expression on regulatory T cells, suggesting that immunization with ApoB peptides inhibits atherosclerosis by inducing anti-inflammatory cytokines.</div>
</front>
</TEI>
<affiliations>
<list>
<country>
<li>États-Unis</li>
</country>
<region>
<li>Californie</li>
</region>
</list>
<tree>
<noCountry>
<name sortKey="Gerhardt, Teresa" sort="Gerhardt, Teresa" uniqKey="Gerhardt T" first="Teresa" last="Gerhardt">Teresa Gerhardt</name>
<name sortKey="Kimura, Takayuki" sort="Kimura, Takayuki" uniqKey="Kimura T" first="Takayuki" last="Kimura">Takayuki Kimura</name>
<name sortKey="Ley, Klaus" sort="Ley, Klaus" uniqKey="Ley K" first="Klaus" last="Ley">Klaus Ley</name>
<name sortKey="Mcardle, Sara" sort="Mcardle, Sara" uniqKey="Mcardle S" first="Sara" last="Mcardle">Sara Mcardle</name>
<name sortKey="Mikulski, Zbigniew" sort="Mikulski, Zbigniew" uniqKey="Mikulski Z" first="Zbigniew" last="Mikulski">Zbigniew Mikulski</name>
<name sortKey="Miller, Jacqueline" sort="Miller, Jacqueline" uniqKey="Miller J" first="Jacqueline" last="Miller">Jacqueline Miller</name>
<name sortKey="Tse, Kevin" sort="Tse, Kevin" uniqKey="Tse K" first="Kevin" last="Tse">Kevin Tse</name>
<name sortKey="Wolf, Dennis" sort="Wolf, Dennis" uniqKey="Wolf D" first="Dennis" last="Wolf">Dennis Wolf</name>
</noCountry>
<country name="États-Unis">
<region name="Californie">
<name sortKey="Sidney, John" sort="Sidney, John" uniqKey="Sidney J" first="John" last="Sidney">John Sidney</name>
</region>
<name sortKey="Sette, Alessandro" sort="Sette, Alessandro" uniqKey="Sette A" first="Alessandro" last="Sette">Alessandro Sette</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 000E84 | SxmlIndent | more

Ou

HfdSelect -h $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd -nk 000E84 | 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=     pubmed:28087520
   |texte=   Atheroprotective vaccination with MHC-II-restricted ApoB peptides induces peritoneal IL-10-producing CD4 T cells.
}}

Pour générer des pages wiki

HfdIndexSelect -h $EXPLOR_AREA/Data/Main/Exploration/RBID.i   -Sk "pubmed:28087520" \
       | HfdSelect -Kh $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd   \
       | NlmPubMed2Wicri -a MersV1 

Wicri

This area was generated with Dilib version V0.6.33.
Data generation: Mon Apr 20 23:26:43 2020. Site generation: Sat Mar 27 09:06:09 2021