Characterization of cells infiltrating the lungs of x-irradiated and nude mice after influenza virus infection.
Identifieur interne : 000490 ( PubMed/Checkpoint ); précédent : 000489; suivant : 000491Characterization of cells infiltrating the lungs of x-irradiated and nude mice after influenza virus infection.
Auteurs : E. Shimomura ; F. Suzuki ; N. IshidaSource :
- Microbiology and immunology [ 0385-5600 ] ; 1982.
Descripteurs français
- KwdFr :
- Animaux, Cellules tueuses naturelles (physiologie), Cinétique, Infections à Orthomyxoviridae (anatomopathologie), Lymphocytes (cytologie), Lymphocytes (physiologie), Lymphocytes T (physiologie), Pneumopathie virale (anatomopathologie), Poumon (anatomopathologie), Souris, Souris de lignée BALB C, Souris de lignée C3H, Souris nude.
- MESH :
- anatomopathologie : Infections à Orthomyxoviridae, Pneumopathie virale, Poumon.
- cytologie : Lymphocytes.
- physiologie : Cellules tueuses naturelles, Lymphocytes, Lymphocytes T.
- Animaux, Cinétique, Souris, Souris de lignée BALB C, Souris de lignée C3H, Souris nude.
English descriptors
- KwdEn :
- MESH :
- cytology : Lymphocytes.
- pathology : Lung, Orthomyxoviridae Infections, Pneumonia, Viral.
- physiology : Killer Cells, Natural, Lymphocytes, T-Lymphocytes.
- Animals, Kinetics, Mice, Mice, Inbred BALB C, Mice, Inbred C3H, Mice, Nude.
Abstract
After X-irradiated and nonirradiated mice (C3H/He) as well as athymic nude mice and haired littermates (BALB/c) were infected with influenza A virus (Kumamoto strain, H2N2), they were examined for survival period, the development of consolidation in the lungs and the characteristics of the cells infiltrating the lung tissues. In two different T-cell deficient groups, there was a definite delay in the development of consolidation compared with their respective controls and this was reflected in prolonged survival periods: 5 days longer for irradiated mice and 6 days longer for nude mice. In both T-cell deficient and normal groups, about 70% of the cells obtained from consolidated lung tissues after virus infection were found to be small lymphoid cells and there were no morphological differences between the T-cell deficient and normal groups. None of these small lymphoid cells from the peripheral blood or the spleen of T-cell deficient mice responded to concanavalin A. In the lungs of both X-irradiated mice and nude mice, however, a definite increase in cells having natural killer activity was found at the late stages of the influenza infection, suggesting their participation in the development of consolidation.
DOI: 10.1111/j.1348-0421.1982.tb00162.x
PubMed: 6979669
Affiliations:
Links toward previous steps (curation, corpus...)
Links to Exploration step
pubmed:6979669Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Characterization of cells infiltrating the lungs of x-irradiated and nude mice after influenza virus infection.</title>
<author><name sortKey="Shimomura, E" sort="Shimomura, E" uniqKey="Shimomura E" first="E" last="Shimomura">E. Shimomura</name>
</author>
<author><name sortKey="Suzuki, F" sort="Suzuki, F" uniqKey="Suzuki F" first="F" last="Suzuki">F. Suzuki</name>
</author>
<author><name sortKey="Ishida, N" sort="Ishida, N" uniqKey="Ishida N" first="N" last="Ishida">N. Ishida</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">PubMed</idno>
<date when="1982">1982</date>
<idno type="RBID">pubmed:6979669</idno>
<idno type="pmid">6979669</idno>
<idno type="doi">10.1111/j.1348-0421.1982.tb00162.x</idno>
<idno type="wicri:Area/PubMed/Corpus">000567</idno>
<idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Corpus" wicri:corpus="PubMed">000567</idno>
<idno type="wicri:Area/PubMed/Curation">000567</idno>
<idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Curation">000567</idno>
<idno type="wicri:Area/PubMed/Checkpoint">000490</idno>
<idno type="wicri:explorRef" wicri:stream="Checkpoint" wicri:step="PubMed">000490</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title xml:lang="en">Characterization of cells infiltrating the lungs of x-irradiated and nude mice after influenza virus infection.</title>
<author><name sortKey="Shimomura, E" sort="Shimomura, E" uniqKey="Shimomura E" first="E" last="Shimomura">E. Shimomura</name>
</author>
<author><name sortKey="Suzuki, F" sort="Suzuki, F" uniqKey="Suzuki F" first="F" last="Suzuki">F. Suzuki</name>
</author>
<author><name sortKey="Ishida, N" sort="Ishida, N" uniqKey="Ishida N" first="N" last="Ishida">N. Ishida</name>
</author>
</analytic>
<series><title level="j">Microbiology and immunology</title>
<idno type="ISSN">0385-5600</idno>
<imprint><date when="1982" type="published">1982</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Animals</term>
<term>Killer Cells, Natural (physiology)</term>
<term>Kinetics</term>
<term>Lung (pathology)</term>
<term>Lymphocytes (cytology)</term>
<term>Lymphocytes (physiology)</term>
<term>Mice</term>
<term>Mice, Inbred BALB C</term>
<term>Mice, Inbred C3H</term>
<term>Mice, Nude</term>
<term>Orthomyxoviridae Infections (pathology)</term>
<term>Pneumonia, Viral (pathology)</term>
<term>T-Lymphocytes (physiology)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr"><term>Animaux</term>
<term>Cellules tueuses naturelles (physiologie)</term>
<term>Cinétique</term>
<term>Infections à Orthomyxoviridae (anatomopathologie)</term>
<term>Lymphocytes (cytologie)</term>
<term>Lymphocytes (physiologie)</term>
<term>Lymphocytes T (physiologie)</term>
<term>Pneumopathie virale (anatomopathologie)</term>
<term>Poumon (anatomopathologie)</term>
<term>Souris</term>
<term>Souris de lignée BALB C</term>
<term>Souris de lignée C3H</term>
<term>Souris nude</term>
</keywords>
<keywords scheme="MESH" qualifier="anatomopathologie" xml:lang="fr"><term>Infections à Orthomyxoviridae</term>
<term>Pneumopathie virale</term>
<term>Poumon</term>
</keywords>
<keywords scheme="MESH" qualifier="cytologie" xml:lang="fr"><term>Lymphocytes</term>
</keywords>
<keywords scheme="MESH" qualifier="cytology" xml:lang="en"><term>Lymphocytes</term>
</keywords>
<keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Lung</term>
<term>Orthomyxoviridae Infections</term>
<term>Pneumonia, Viral</term>
</keywords>
<keywords scheme="MESH" qualifier="physiologie" xml:lang="fr"><term>Cellules tueuses naturelles</term>
<term>Lymphocytes</term>
<term>Lymphocytes T</term>
</keywords>
<keywords scheme="MESH" qualifier="physiology" xml:lang="en"><term>Killer Cells, Natural</term>
<term>Lymphocytes</term>
<term>T-Lymphocytes</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Animals</term>
<term>Kinetics</term>
<term>Mice</term>
<term>Mice, Inbred BALB C</term>
<term>Mice, Inbred C3H</term>
<term>Mice, Nude</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr"><term>Animaux</term>
<term>Cinétique</term>
<term>Souris</term>
<term>Souris de lignée BALB C</term>
<term>Souris de lignée C3H</term>
<term>Souris nude</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">After X-irradiated and nonirradiated mice (C3H/He) as well as athymic nude mice and haired littermates (BALB/c) were infected with influenza A virus (Kumamoto strain, H2N2), they were examined for survival period, the development of consolidation in the lungs and the characteristics of the cells infiltrating the lung tissues. In two different T-cell deficient groups, there was a definite delay in the development of consolidation compared with their respective controls and this was reflected in prolonged survival periods: 5 days longer for irradiated mice and 6 days longer for nude mice. In both T-cell deficient and normal groups, about 70% of the cells obtained from consolidated lung tissues after virus infection were found to be small lymphoid cells and there were no morphological differences between the T-cell deficient and normal groups. None of these small lymphoid cells from the peripheral blood or the spleen of T-cell deficient mice responded to concanavalin A. In the lungs of both X-irradiated mice and nude mice, however, a definite increase in cells having natural killer activity was found at the late stages of the influenza infection, suggesting their participation in the development of consolidation.</div>
</front>
</TEI>
<pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">6979669</PMID>
<DateCompleted><Year>1982</Year>
<Month>08</Month>
<Day>14</Day>
</DateCompleted>
<DateRevised><Year>2019</Year>
<Month>08</Month>
<Day>21</Day>
</DateRevised>
<Article PubModel="Print"><Journal><ISSN IssnType="Print">0385-5600</ISSN>
<JournalIssue CitedMedium="Print"><Volume>26</Volume>
<Issue>2</Issue>
<PubDate><Year>1982</Year>
</PubDate>
</JournalIssue>
<Title>Microbiology and immunology</Title>
<ISOAbbreviation>Microbiol. Immunol.</ISOAbbreviation>
</Journal>
<ArticleTitle>Characterization of cells infiltrating the lungs of x-irradiated and nude mice after influenza virus infection.</ArticleTitle>
<Pagination><MedlinePgn>129-38</MedlinePgn>
</Pagination>
<Abstract><AbstractText>After X-irradiated and nonirradiated mice (C3H/He) as well as athymic nude mice and haired littermates (BALB/c) were infected with influenza A virus (Kumamoto strain, H2N2), they were examined for survival period, the development of consolidation in the lungs and the characteristics of the cells infiltrating the lung tissues. In two different T-cell deficient groups, there was a definite delay in the development of consolidation compared with their respective controls and this was reflected in prolonged survival periods: 5 days longer for irradiated mice and 6 days longer for nude mice. In both T-cell deficient and normal groups, about 70% of the cells obtained from consolidated lung tissues after virus infection were found to be small lymphoid cells and there were no morphological differences between the T-cell deficient and normal groups. None of these small lymphoid cells from the peripheral blood or the spleen of T-cell deficient mice responded to concanavalin A. In the lungs of both X-irradiated mice and nude mice, however, a definite increase in cells having natural killer activity was found at the late stages of the influenza infection, suggesting their participation in the development of consolidation.</AbstractText>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Shimomura</LastName>
<ForeName>E</ForeName>
<Initials>E</Initials>
</Author>
<Author ValidYN="Y"><LastName>Suzuki</LastName>
<ForeName>F</ForeName>
<Initials>F</Initials>
</Author>
<Author ValidYN="Y"><LastName>Ishida</LastName>
<ForeName>N</ForeName>
<Initials>N</Initials>
</Author>
</AuthorList>
<Language>eng</Language>
<PublicationTypeList><PublicationType UI="D003160">Comparative Study</PublicationType>
<PublicationType UI="D016428">Journal Article</PublicationType>
<PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType>
</PublicationTypeList>
</Article>
<MedlineJournalInfo><Country>Australia</Country>
<MedlineTA>Microbiol Immunol</MedlineTA>
<NlmUniqueID>7703966</NlmUniqueID>
<ISSNLinking>0385-5600</ISSNLinking>
</MedlineJournalInfo>
<CitationSubset>IM</CitationSubset>
<MeshHeadingList><MeshHeading><DescriptorName UI="D000818" MajorTopicYN="N">Animals</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D007694" MajorTopicYN="N">Killer Cells, Natural</DescriptorName>
<QualifierName UI="Q000502" MajorTopicYN="Y">physiology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D007700" MajorTopicYN="N">Kinetics</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008168" MajorTopicYN="N">Lung</DescriptorName>
<QualifierName UI="Q000473" MajorTopicYN="Y">pathology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008214" MajorTopicYN="N">Lymphocytes</DescriptorName>
<QualifierName UI="Q000166" MajorTopicYN="N">cytology</QualifierName>
<QualifierName UI="Q000502" MajorTopicYN="Y">physiology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D051379" MajorTopicYN="N">Mice</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008807" MajorTopicYN="N">Mice, Inbred BALB C</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008809" MajorTopicYN="N">Mice, Inbred C3H</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008819" MajorTopicYN="N">Mice, Nude</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D009976" MajorTopicYN="N">Orthomyxoviridae Infections</DescriptorName>
<QualifierName UI="Q000473" MajorTopicYN="Y">pathology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D011024" MajorTopicYN="N">Pneumonia, Viral</DescriptorName>
<QualifierName UI="Q000473" MajorTopicYN="Y">pathology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D013601" MajorTopicYN="N">T-Lymphocytes</DescriptorName>
<QualifierName UI="Q000502" MajorTopicYN="N">physiology</QualifierName>
</MeshHeading>
</MeshHeadingList>
</MedlineCitation>
<PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>1982</Year>
<Month>1</Month>
<Day>1</Day>
</PubMedPubDate>
<PubMedPubDate PubStatus="medline"><Year>1982</Year>
<Month>1</Month>
<Day>1</Day>
<Hour>0</Hour>
<Minute>1</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="entrez"><Year>1982</Year>
<Month>1</Month>
<Day>1</Day>
<Hour>0</Hour>
<Minute>0</Minute>
</PubMedPubDate>
</History>
<PublicationStatus>ppublish</PublicationStatus>
<ArticleIdList><ArticleId IdType="pubmed">6979669</ArticleId>
<ArticleId IdType="doi">10.1111/j.1348-0421.1982.tb00162.x</ArticleId>
</ArticleIdList>
</PubmedData>
</pubmed>
<affiliations><list></list>
<tree><noCountry><name sortKey="Ishida, N" sort="Ishida, N" uniqKey="Ishida N" first="N" last="Ishida">N. Ishida</name>
<name sortKey="Shimomura, E" sort="Shimomura, E" uniqKey="Shimomura E" first="E" last="Shimomura">E. Shimomura</name>
<name sortKey="Suzuki, F" sort="Suzuki, F" uniqKey="Suzuki F" first="F" last="Suzuki">F. Suzuki</name>
</noCountry>
</tree>
</affiliations>
</record>
Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Sante/explor/H2N2V1/Data/PubMed/Checkpoint
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 000490 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/PubMed/Checkpoint/biblio.hfd -nk 000490 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien |wiki= Sante |area= H2N2V1 |flux= PubMed |étape= Checkpoint |type= RBID |clé= pubmed:6979669 |texte= Characterization of cells infiltrating the lungs of x-irradiated and nude mice after influenza virus infection. }}
Pour générer des pages wiki
HfdIndexSelect -h $EXPLOR_AREA/Data/PubMed/Checkpoint/RBID.i -Sk "pubmed:6979669" \ | HfdSelect -Kh $EXPLOR_AREA/Data/PubMed/Checkpoint/biblio.hfd \ | NlmPubMed2Wicri -a H2N2V1
![]() | This area was generated with Dilib version V0.6.33. | ![]() |