7.15 INTERVERTEBRAL DISC INJURY CAN BE DETECTED USING
RADIOLABELED MONOCLONAL ANTIBODY KERATAN SULPHATE
K.J.A. Kairemo, A. Lappalainen,
E. Kääpä, 0. Laitinen, T. Hyytinen, S. Strömberg, T. Erselcan, S-L. Karonen, M.
Grönblad
Depts. of Clin. Chem and Phys. Medicine &
Rehab., Helsinki Univ.
Central Hospital, Univ. of Veterinary Medicine,
Helsinki, Finland.
Kalevi.Kairemo@huch.fi
We have developed an
intervertebral disc injury model for analyzing sulphated glycosaminoglycans in vivo.
Keratan sulphate (KS) is most abundant of these in the inner nucleus pulposus (NP) and
less abundant in the outer fibrosus (AF).
A radioiodinated (I-125)
monoclonal antibody (MAb) raised against KS was injected into rats (n=6) and following
biodistribution data was obtained at 72 hr: blood 0.18, heart 0.38, liver 0.48, spleen
0.45, kidney 0.65, bone 0. 16 and muscle 0. 17 X 10-2 % injected, activity/gram
tissue. In the disc injury model two tail discs in each animal with both acute (2 wk) and
subacute (7 wk) injuries were studied for in vivo antibody uptake. There was a significant
difference in the antibody uptake between injured discs (0.39 X 10-2 % ID/g,
n=12) and adjacent healthy discs (0.34 X 10-2 % ID/g, n=12) both after acute
and subacute injury.
In vivo gamma imaging using
I-125-MAb demonstrated increased take in other animals having lumbar disc injuries (2, 7
and 17 days Id). Cartilaginous tissue, such as trachea, was studied separately, and t
demonstrated extremely high antibody uptake. Rat trachea was also visualized on gamma
images.
Our data suggests that antibodies
against NP structures, such as proteoglycans, can be used for in vivo detection of
intervertebral disc injury. This is inspite of minimal circulation in the AF itself and
NP. |