TY - JOUR
T1 - Use of combination of monoclonal antibodies directed against three distinct epitopes of a tumor-associated antigen
T2 - Analysis of cell binding and internalization
AU - Casalini, P.
AU - Mezzanzanica, D.
AU - Canevari, S.
AU - Della Torre, G.
AU - Miotti, S.
AU - Colnaghi, M. I.
AU - Matzku, S.
PY - 1991
Y1 - 1991
N2 - Three monoclonal antibodies (MAbs), MOv17, MOv18 and MOv19 with tumor-restricted specificity for human ovarian carcinoma, were tested alone or in double combination with the aim of analyzing their binding and internalization behavior on different in vitro cell lines. Biochemical studies indicated that the 3 MAbs were directed against 3 epitopes of the same 38 kDa surface molecules. By immuno-electronmicroscopy they exhibited a different internalization behavior since MOv17 induced evident endocytosis through coated vesicles, whereas MOv18 gave rise to occasional uncoated vessicles and MOv19 was completely unable to promote internalization of the relevant molecule. When tested 2 by 2 there was a binding synergy in one of the 9 possible combinations (125I-labelled MOv18 and unlabelled MOv19), but no change in the internalization behavior. The binding synergy, which was highly reproducible, was temperature-dependent and was also evident on glutaraldehyde-fixed cells. A metabolism involvement is therefore unlikely. This could be attributed to an easier accessibility of the CaMOv18 due to a conformational change of the molecule after MOv19 MAb binding.
AB - Three monoclonal antibodies (MAbs), MOv17, MOv18 and MOv19 with tumor-restricted specificity for human ovarian carcinoma, were tested alone or in double combination with the aim of analyzing their binding and internalization behavior on different in vitro cell lines. Biochemical studies indicated that the 3 MAbs were directed against 3 epitopes of the same 38 kDa surface molecules. By immuno-electronmicroscopy they exhibited a different internalization behavior since MOv17 induced evident endocytosis through coated vesicles, whereas MOv18 gave rise to occasional uncoated vessicles and MOv19 was completely unable to promote internalization of the relevant molecule. When tested 2 by 2 there was a binding synergy in one of the 9 possible combinations (125I-labelled MOv18 and unlabelled MOv19), but no change in the internalization behavior. The binding synergy, which was highly reproducible, was temperature-dependent and was also evident on glutaraldehyde-fixed cells. A metabolism involvement is therefore unlikely. This could be attributed to an easier accessibility of the CaMOv18 due to a conformational change of the molecule after MOv19 MAb binding.
UR - http://www.scopus.com/inward/record.url?scp=0025782612&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0025782612&partnerID=8YFLogxK
M3 - Article
C2 - 1708366
AN - SCOPUS:0025782612
SN - 0020-7136
VL - 48
SP - 284
EP - 290
JO - International Journal of Cancer
JF - International Journal of Cancer
IS - 2
ER -