EVALUATION OF POSSIBLE INTERFERENCE OF ANTIINFLAMMATORY DRUGS UPON SCINTIGRAPHIC IMAGING WITH MACROPHAGE TARGETING TC-99M-J001X - EFFECTS OF METHYLPREDNISOLONE, DEXAMETHASONE, INDOMETHACIN AND METHOTREXATE
F. Perin et al., EVALUATION OF POSSIBLE INTERFERENCE OF ANTIINFLAMMATORY DRUGS UPON SCINTIGRAPHIC IMAGING WITH MACROPHAGE TARGETING TC-99M-J001X - EFFECTS OF METHYLPREDNISOLONE, DEXAMETHASONE, INDOMETHACIN AND METHOTREXATE, Nuclear medicine and biology, 21(8), 1994, pp. 1093-1100
J001X, an acylated poly-(1,3)-galactoside isolated from Klebsiella pne
umoniae proteoglycan, has been developed to target cells from the mono
cyte-macrophage lineage. Recent experimental work and initial clinical
trials have proved the potential of this molecule labeled with Tc-99m
for the scintigraphy of inflammatory foci. In a model of radiation-in
duced inflammation in pigs, the scintigraphic contrast was observed to
be very sensitive to a single injection of methylprednisolone given 1
2 h before scintigraphy. The present study was undertaken to confirm t
his effect and to estimate the possible interference of various anti-i
nflammatory agents on the in vivo targeting of macrophages by J001X. M
ethylprednisolone, dexamethasone, indomethacin and methotrexate used a
t an immunosuppressive dose were tested to assess the possible risk of
false-negative examinations in patients thus treated. Analysis of the
results indicated that among the four drugs tested, only methylpredni
solone at 0.5-1 mg/kg could interfere with J001X scintigraphy.