Cellular composition of lymph in experimental lymphedema.
Identifieur interne : 009501 ( Ncbi/Merge ); précédent : 009500; suivant : 009502Cellular composition of lymph in experimental lymphedema.
Auteurs : H. Galkowska ; W L OlszewskiSource :
- Lymphology [ 0024-7766 ] ; 1986.
Descripteurs français
- KwdFr :
- MESH :
- anatomopathologie : Lymphoedème.
- cytologie : Lymphe.
- immunologie : Lymphe, Lymphoedème.
- pharmacologie : Mitogènes.
- Activation des lymphocytes, Animaux, Chiens, Cytotoxicité immunologique, Numération cellulaire, Récepteur Fc, Récepteurs au C3b du complément, Récepteurs au complément.
English descriptors
- KwdEn :
- MESH :
- chemical , pharmacology : Mitogens.
- cytology : Lymph.
- immunology : Lymph, Lymphedema.
- pathology : Lymphedema.
- Animals, Cell Count, Cytotoxicity, Immunologic, Dogs, Lymphocyte Activation, Receptors, Complement, Receptors, Complement 3b, Receptors, Fc.
Abstract
Lymph cell populations were characterized immunologically in dogs with chronic post-surgical lymphedema. There was a 10- to 30-fold increase in lymph total cell count as compared with normal (control) dogs. Morphologically, these were predominantly small lymphocytes with approximately 4-6% monocytes and veiled cells. In contrast, lymph from normal dogs contained 33% granulocytes and 27% monocytes. The Fc-R+ and C3b-R+ mononuclear nonadherent cells were less represented in lymph in chronic stasis than in normals. A high autotransformation rate of lymph cells and marked responsiveness to PHA and Con A were also observed. In chronic lymphedema K-cell and NK-cell cytotoxicity were lower than in normal lymph. Interruption or retardation of the lymphocyte recirculation pathway with lymph stasis may alter regulation of immune responsiveness in lymphedematous tissue.
PubMed: 2951567
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pubmed:2951567Le document en format XML
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<author><name sortKey="Galkowska, H" sort="Galkowska, H" uniqKey="Galkowska H" first="H" last="Galkowska">H. Galkowska</name>
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<author><name sortKey="Olszewski, W L" sort="Olszewski, W L" uniqKey="Olszewski W" first="W L" last="Olszewski">W L Olszewski</name>
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<author><name sortKey="Olszewski, W L" sort="Olszewski, W L" uniqKey="Olszewski W" first="W L" last="Olszewski">W L Olszewski</name>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Animals</term>
<term>Cell Count</term>
<term>Cytotoxicity, Immunologic</term>
<term>Dogs</term>
<term>Lymph (cytology)</term>
<term>Lymph (immunology)</term>
<term>Lymphedema (immunology)</term>
<term>Lymphedema (pathology)</term>
<term>Lymphocyte Activation</term>
<term>Mitogens (pharmacology)</term>
<term>Receptors, Complement</term>
<term>Receptors, Complement 3b</term>
<term>Receptors, Fc</term>
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<keywords scheme="KwdFr" xml:lang="fr"><term>Activation des lymphocytes</term>
<term>Animaux</term>
<term>Chiens</term>
<term>Cytotoxicité immunologique</term>
<term>Lymphe (cytologie)</term>
<term>Lymphe (immunologie)</term>
<term>Lymphoedème (anatomopathologie)</term>
<term>Lymphoedème (immunologie)</term>
<term>Mitogènes (pharmacologie)</term>
<term>Numération cellulaire</term>
<term>Récepteur Fc</term>
<term>Récepteurs au C3b du complément</term>
<term>Récepteurs au complément</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="pharmacology" xml:lang="en"><term>Mitogens</term>
</keywords>
<keywords scheme="MESH" qualifier="anatomopathologie" xml:lang="fr"><term>Lymphoedème</term>
</keywords>
<keywords scheme="MESH" qualifier="cytologie" xml:lang="fr"><term>Lymphe</term>
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<keywords scheme="MESH" qualifier="cytology" xml:lang="en"><term>Lymph</term>
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<keywords scheme="MESH" qualifier="immunologie" xml:lang="fr"><term>Lymphe</term>
<term>Lymphoedème</term>
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<keywords scheme="MESH" qualifier="immunology" xml:lang="en"><term>Lymph</term>
<term>Lymphedema</term>
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<keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Lymphedema</term>
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<keywords scheme="MESH" qualifier="pharmacologie" xml:lang="fr"><term>Mitogènes</term>
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<keywords scheme="MESH" xml:lang="en"><term>Animals</term>
<term>Cell Count</term>
<term>Cytotoxicity, Immunologic</term>
<term>Dogs</term>
<term>Lymphocyte Activation</term>
<term>Receptors, Complement</term>
<term>Receptors, Complement 3b</term>
<term>Receptors, Fc</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr"><term>Activation des lymphocytes</term>
<term>Animaux</term>
<term>Chiens</term>
<term>Cytotoxicité immunologique</term>
<term>Numération cellulaire</term>
<term>Récepteur Fc</term>
<term>Récepteurs au C3b du complément</term>
<term>Récepteurs au complément</term>
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<front><div type="abstract" xml:lang="en">Lymph cell populations were characterized immunologically in dogs with chronic post-surgical lymphedema. There was a 10- to 30-fold increase in lymph total cell count as compared with normal (control) dogs. Morphologically, these were predominantly small lymphocytes with approximately 4-6% monocytes and veiled cells. In contrast, lymph from normal dogs contained 33% granulocytes and 27% monocytes. The Fc-R+ and C3b-R+ mononuclear nonadherent cells were less represented in lymph in chronic stasis than in normals. A high autotransformation rate of lymph cells and marked responsiveness to PHA and Con A were also observed. In chronic lymphedema K-cell and NK-cell cytotoxicity were lower than in normal lymph. Interruption or retardation of the lymphocyte recirculation pathway with lymph stasis may alter regulation of immune responsiveness in lymphedematous tissue.</div>
</front>
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<Title>Lymphology</Title>
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<ArticleTitle>Cellular composition of lymph in experimental lymphedema.</ArticleTitle>
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<Abstract><AbstractText>Lymph cell populations were characterized immunologically in dogs with chronic post-surgical lymphedema. There was a 10- to 30-fold increase in lymph total cell count as compared with normal (control) dogs. Morphologically, these were predominantly small lymphocytes with approximately 4-6% monocytes and veiled cells. In contrast, lymph from normal dogs contained 33% granulocytes and 27% monocytes. The Fc-R+ and C3b-R+ mononuclear nonadherent cells were less represented in lymph in chronic stasis than in normals. A high autotransformation rate of lymph cells and marked responsiveness to PHA and Con A were also observed. In chronic lymphedema K-cell and NK-cell cytotoxicity were lower than in normal lymph. Interruption or retardation of the lymphocyte recirculation pathway with lymph stasis may alter regulation of immune responsiveness in lymphedematous tissue.</AbstractText>
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