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A monoclonal antibody raised against Alzheimer cortex that specifically recognizes a subpopulation of microglial cells.
Author(s) -
Patrick Cras,
J. Gheuens,
Ursula Lübke,
Jef Boons,
M. Vandermeeren,
Hugo Van Heuverswijn,
JeanJacques Martin
Publication year - 1990
Publication title -
journal of histochemistry and cytochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.971
H-Index - 124
eISSN - 1551-5044
pISSN - 0022-1554
DOI - 10.1177/38.8.2195115
Subject(s) - pathology , microglia , senile plaques , monoclonal antibody , antigen , epitope , biology , parenchyma , antibody , white matter , spleen , immunology , alzheimer's disease , medicine , inflammation , disease , radiology , magnetic resonance imaging
A monoclonal antibody (MAb), termed AMC30, was raised after in vitro immunization with sonicated neurofibrillary tangle (NFT)-enriched fractions prepared from Alzheimer's brain. The antigen to which AMC30 is directed was expressed by microglial cells in senile plaques of Alzheimer's disease (AD). Microglia in the parenchyma surrounding brain tumors or infarctions, multinuclear giant cells, perivascular and parenchymal macrophages throughout the brain of AIDS patients were also labeled. Different non-nervous system lesions in which macrophages participate were also stained. Microglial cells in normal areas of the cortex or white matter were not labeled with MAb AMC30. The antigen to which AMC30 is directed was not detected in normal bone marrow, lymph nodes, lung, or spleen monocytes or macrophages. The epitope recognized by MAb AMC30 was present after formalin fixation and paraffin embedding. Our findings suggest that this MAb is directed against an antigen that is specifically expressed in a subpopulation of microglial cells and macrophages reactive to various pathological conditions.

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