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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
1984-3-23
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pubmed:abstractText |
Previously, it was shown that macrophages isolated from liver granulomas of Schistosoma mansoni-infected mice constituted about 30% of the granuloma cell population, were highly activated, and more than 50% displayed H-2 I region-associated antigens. Moreover, the degree of macrophage maturation/activation correlated with the intensity of the granulomatous response. Thus, inflammatory macrophages from the vigorous granulomas of acutely infected mice (VigGrM phi) displayed greater phagocytic and tumoricidal activity than did M phi from the T suppressor cell-modulated granulomas (ModGrM phi) of chronically infected animals. No difference was seen, however, in the percentage of Ia-bearing M phi isolated from vigorous or modulated liver granulomas. Presently, accessory activity of GrM phi was assayed by reconstitution of the proliferative responses of M phi-depleted lymphocytes. Both VigGrM phi and ModGrM phi were able to reconstitute the Con-A induced proliferation of normal thymoctyes. Moreover, both types of GrM phi could reconstitute parasite egg antigen-specific proliferation of the mesenteric lymph node cells from acutely infected mice. Reconstitution was dependent on M phi that displayed I-A and I-E subregion-encoded determinants. In higher doses the activated VigGrM phi were more suppressive toward lymphocytic proliferation than were the less activated ModGrM phi. Apparently, the degree of M phi suppressor activity was in direct relationship to the state of M phi maturation/activation. These data indicate that the inflammatory M phi of the schistosome granuloma may be involved in the focal immune accessory/regulatory events that occur within these T cell-mediated lesions.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0022-1767
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
132
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1506-10
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:6319495-Animals,
pubmed-meshheading:6319495-Antigens,
pubmed-meshheading:6319495-Cell Separation,
pubmed-meshheading:6319495-Female,
pubmed-meshheading:6319495-Granuloma,
pubmed-meshheading:6319495-Histocompatibility Antigens Class II,
pubmed-meshheading:6319495-Liver Diseases, Parasitic,
pubmed-meshheading:6319495-Lymphocyte Activation,
pubmed-meshheading:6319495-Lymphocyte Cooperation,
pubmed-meshheading:6319495-Macrophages,
pubmed-meshheading:6319495-Mice,
pubmed-meshheading:6319495-Mice, Inbred CBA,
pubmed-meshheading:6319495-Ovum,
pubmed-meshheading:6319495-Receptors, Cell Surface,
pubmed-meshheading:6319495-Receptors, Fibronectin,
pubmed-meshheading:6319495-Schistosoma mansoni,
pubmed-meshheading:6319495-Schistosomiasis
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pubmed:year |
1984
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pubmed:articleTitle |
Schistosome egg antigen(s) presentation and regulatory activity by macrophages isolated from vigorous or immunomodulated liver granulomas of Schistosoma mansoni-infected mice.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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