Extended lacto-series type 1 chain antigens lacking type 2 chain core have recently been shown to comprise a new type of tumor-associated carbohydrate antigen. Examples are Lea/Lea (IV3Galβ1→3[Fucα1→4] GlcNAcLc4Cer) and Leb/Lea (IV3Fucα1→2Galβ1→3[Fucα1→4]Glc-NAcLc4Cer) (M. R. Stroud, et al., J. Biol. Chem., 266: 8439–8446, 1991; Eur. J. Biochem., 203: 577–586, 1992). We have now established an IgG3 mouse monoclonal antibody (IMH2) after immunization of mice with Leb/Lea antigen; however, monoclonal antibody (MAb) IMH2 reacted not only with the immunogen used but also with Ley/Lex and to a lesser degree with short-chain Ley or Leb with hexasaccharide ceramide (i.e., IV2FucIII3FucnLc4Cer or IV2FucIII4FucLc4Cer). It showed a high incidence of staining and strong reactivity with carcinomas of colon, rectum, liver, pancreas, and endometrium, but no reactivity with normal colonic mucosa at various loci, and minimal reactivity with normal liver, pancreas, or uterine endometrium. On the other hand, it reacted with normal gastric mucosa, cecal mucosa, urothelium, adrenal glands, and thymus. Its expression in colorectal tumors and normal cecal tissue was independent of secretor status, whereas that in normal urothelium was dependent on secretor status. MAb IMH2 displayed strong lymphocyte-activated or complement-dependent killing of human colonic cancer Colo205 cells in vitro, and inhibition of Colo205 growth in vivo; this inhibition was comparable to that by MAb NCC-ST-421, which is directed to Lea/Lea epitope (M. Watanabe, et al., Cancer Res., 51: 2199, 1991). These results indicate that a new extended type 1 chain structure, Leb/Lea, is a useful tumor marker associated with carcinomas of colon, rectum, pancreas, liver, and endometrium and that MAb IMH2 has potential diagnostic or therapeutic applicability for these carcinomas.

1

This study was supported by National Cancer Institute Outstanding Investigator Grant CA42505 (to Si. H.) and funds from The Biomembrane Institute, in part under a research contract with Otsuka Pharmaceutical Co. T. F. Ø. and P. M. were supported by the Danish Cancer Society.

This content is only available via PDF.