Circulation, Vol 58, 1137-1142, Copyright © 1978 by American Heart Association
BA Khaw, HK Gold, RC Leinbach, JT Fallon, W Strauss, GM Pohost and E Haber
We examined the feasibility of early imaging of myocardial infarcts by
intracoronary injection of 131I-labelled cardiac myosin-specific antibody
(Fab')2. The left anterior descending coronary artery was occluded for 5
hours by a balloon catheter introduced through the carotid artery in 12
dogs. The catheter was withdrawn and 1 mCi 201Tl was injected intravenously
and 500 muCi of 131I antibody were injected into the main left coronary
artery. Six of these animals demonstrated evidence of myocardial infarction
by ECG and subsequent triphenyl- tetrazolium chloride staining, while the
others did not. In each of the infarcted animals, in vivo scintograms
one-half hour after injection of isotope showed uptake of 131I in the
anteroapical region of the heart corresponding to the region of absent
201Tl uptake. This relationship was confirmed in the excised hearts and in
heart slices. In slices, 131I uptake corresponded to regions that did not
stain with triphenyltetrazolium chloride. In the six animals that did not
show evidence for infarction after coronary occlusion, uptake of 131I was
not demonstrated, either in vivo or in excised specimens. In four
additional dogs subjected to the same procedure, 125I-labelled (Fab')2 from
nonimmune IgG was injected simultaneously into the left main coronary
artery with 131I-labelled canine myosin-specific antibody (Fab')2. The
ratio of uptake between infarct center and normal tissue was 34.3 +/- 1.5
(mean+/-SEM) for the specific antibody fragment as contrasted to 6.6+/-0.4
for the nonimmune IgG fragment, indicating that intracoronary injection
does not favor nonspecific sequestration of protein in regions of
infarction. Thus, the intracoronary administration of myosin-specific
antibody fragments leads to early and specific one-half hour imaging of
myocardial infarcts.
ARTICLES
Early imaging of experimental myocardial infarction by intracoronary administraion of 131I-labelled anticardiac myosin (Fab')2 fragments
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