H. Li et al., CHARACTERIZATION AND DISTRIBUTION OF PHAGOCYTIC MACROPHAGES IN MULTIPLE-SCLEROSIS PLAQUES, Neuropathology and applied neurobiology, 19(3), 1993, pp. 214-223
Populations of phagocytic cells in multiple sclerosis (MS) plaques wer
e examined by quantitative immunocytochemical analysis of macrophage m
arkers and myelin degradation products in serial cryostat sections fro
m 10 cases of MS. Around lesions with ongoing demyelination expression
of the Class II antigen HLA-DQ appeared to be a marker of microglial
activation. Alpha 1-antichymotrypsin+ monocytes and myelin-laden macro
phages expressing the later differentiation markers Ber-MAC3 and RFD7
were predominantly perivascular in location. On the basis of the distr
ibution of oil red 0 (ORO)+ phagocytes and myelin loss, plaques were d
ivided into groups representing different stages in lesion development
. In early lesions (group 1), there was no apparent myelin loss around
ORO+ macrophages although these cells contained material stained with
antibodies against myelin basic protein (MBP) epitopes and neoepitope
s. However, patchy myelin loss was detectable around the phagocytic ma
crophages uniformly distributed throughout group 2 plaques. ORO+ macro
phages containing MBP peptides were confined to the hypercellular bord
er of group 4 lesions, in which the demyelinating process may be recur
rent.