Characterization of cells infiltrating the lungs of x-irradiated and nude mice after influenza virus infection.
Identifieur interne : 000567 ( PubMed/Corpus ); précédent : 000566; suivant : 000568Characterization 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.
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
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pubmed:6979669Le document en format XML
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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="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="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></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. 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