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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
1986-6-18
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pubmed:abstractText |
Leu-M2 (Mac-120) is a mouse anti-human monoclonal antibody that reacts with an antigen on the surface of most peripheral blood monocytes. The presence of Leu-M2 positivity has been associated with the capacity of monocytes to present antigen to T cells. We found that anti-Leu-M2 does not react with an intrinsic monocyte antigen but instead binds to platelets present on the surface of monocytes. Leu-M2 staining is lost from monocytes after they are treated with calcium chelating agents which remove platelets bound to the monocyte surface. Staining for Leu-M2 can be reintroduced by incubating monocytes with autologous platelets. Human alveolar, peritoneal, and tissue macrophages and the U937 cell failed to stain for Leu-M2 antigen. Leu-M2 does not appear to represent either platelet glycoprotein IIb/IIIa or thrombospondin. Our study underscores the importance of carefully screening antimonocyte antibodies for their reactivity with platelets.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
0090-1229
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
39
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
442-51
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:3516471-Antibodies, Monoclonal,
pubmed-meshheading:3516471-Antigens, Surface,
pubmed-meshheading:3516471-Blood Platelets,
pubmed-meshheading:3516471-Cell Adhesion,
pubmed-meshheading:3516471-Cells, Cultured,
pubmed-meshheading:3516471-Flow Cytometry,
pubmed-meshheading:3516471-Fluorescent Antibody Technique,
pubmed-meshheading:3516471-Humans,
pubmed-meshheading:3516471-Immunoenzyme Techniques,
pubmed-meshheading:3516471-Macrophages,
pubmed-meshheading:3516471-Monocytes
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pubmed:year |
1986
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pubmed:articleTitle |
Leu-M2 (Mac-120) is a platelet antigen and is not constitutively expressed by macrophages.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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