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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
12
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pubmed:dateCreated |
1993-3-8
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pubmed:abstractText |
Despite numerous scientific efforts, the etiology of otosclerosis still remains unknown. Pathogenically, there are several signs of a chronic inflammatory process of the bony otic capsule. In this study, we tried to characterize the components of chronic inflammation by immunohistochemical techniques. Within otosclerotic lesions a mixed cellular infiltrate can be observed, consisting of lymphocytes, macrophages and plasma cells. Macrophages which are capable of presenting antigen in association with major histocompatibility antigens (MHC) class I and class II to CD8(+)-, and CD4(+)-T cells, respectively, were found in otosclerotic lesions based on their expression of the MAC387 antigen. Furthermore, HLA-DR positive cells and complement C3 have been found in resorption lacunae of otosclerotic lesions. Several osteoblasts and chondrocytes in active otosclerotic lesions reveal a strong surface expression of beta-2-microglobulin, indicating an increased MHC class I antigen expression in active otosclerotic lesions. In agreement with recently published data we found that a large fraction of the lymphoid cells are antigen-primed T-cells expressing an alpha/beta T-cell receptor in association with CD3 molecules on their surfaces. CD4+ lymphocytes which functionally represent lymphokine-secreting cells are activated through the specific recognition of antigen, presented in context with MHC class II molecules such as HLA-DR. Therefore, the presence of MHC class II positive cells are crucial for the initiation of a local immune response. Thus, our observation of HLA-DR positive cells in otosclerotic lesions is of particular interest.(ABSTRACT TRUNCATED AT 250 WORDS)
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pubmed:language |
ger
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD3,
http://linkedlifedata.com/resource/pubmed/chemical/Histocompatibility Antigens Class I,
http://linkedlifedata.com/resource/pubmed/chemical/Histocompatibility Antigens Class II,
http://linkedlifedata.com/resource/pubmed/chemical/beta 2-Microglobulin
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pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
0017-6192
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
40
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
476-9
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:1493967-Adult,
pubmed-meshheading:1493967-Aged,
pubmed-meshheading:1493967-Antigens, CD3,
pubmed-meshheading:1493967-Female,
pubmed-meshheading:1493967-Histocompatibility Antigens Class I,
pubmed-meshheading:1493967-Histocompatibility Antigens Class II,
pubmed-meshheading:1493967-Humans,
pubmed-meshheading:1493967-Immunity, Cellular,
pubmed-meshheading:1493967-Immunoenzyme Techniques,
pubmed-meshheading:1493967-Male,
pubmed-meshheading:1493967-Middle Aged,
pubmed-meshheading:1493967-Otosclerosis,
pubmed-meshheading:1493967-Stapes,
pubmed-meshheading:1493967-beta 2-Microglobulin
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pubmed:year |
1992
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pubmed:articleTitle |
[Immunohistochemical findings in otosclerotic lesions].
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pubmed:affiliation |
Pathologisches Institut, Universität Bern.
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pubmed:publicationType |
Journal Article,
English Abstract
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