PRODUCTION OF HUMAN MONOCLONAL-ANTIBODIES TO I-BLOOD-GROUP BY EBV-INDUCED TRANSFORMATION - POSSIBLE PRESENCE OF A NEW GLYCOLIPID IN CORD RED-CELL MEMBRANES AND HUMAN HEMATOPOIETIC-CELL LINES
Y. Nagatsuka et al., PRODUCTION OF HUMAN MONOCLONAL-ANTIBODIES TO I-BLOOD-GROUP BY EBV-INDUCED TRANSFORMATION - POSSIBLE PRESENCE OF A NEW GLYCOLIPID IN CORD RED-CELL MEMBRANES AND HUMAN HEMATOPOIETIC-CELL LINES, Immunology letters, 46(1-2), 1995, pp. 93-100
To study the differentiation-associated glycolipid two anti-i mAb prod
ucers, GL-1 and GL-2, were established from the combination of EBV-ind
uced transformation of normal PBL and immune lysis of fluorescent dye-
trapped liposome-containing bovine i-active glycolipid. The mAb GL-1 r
eacted with both sialosylparagloboside and pentahexosyl ceramide and t
he bovine i-active glycolipid whereas mAb GL-2 reacted only with the b
ovine i-active glycolipid in LILA. Both mAbs cold-agglutinate human co
rd red cells but not adult red cells. However, unexpectedly, the major
ity of the reactivity of these mAbs in human cord red cells on TLC was
not identical to the i-active glycolipid. The GL-1 antigenic substanc
e is considered to be a glycolipid distinct from the i-active glycolip
id because the immunoreactivity was canceled with endoglycoceramidase
which cleaves a linkage between the oligosaccharide and ceramide. Base
d on complement cytolysis with the mAb, 15 hematopoietic cell lines an
d normal peripheral lymphocytes were screened for susceptibility to th
e mAbs. A Burkitt lymphoma cell line, Ramos, was most sensitive among
those tested, and BJA-B, Daudi, Namalwa in the B cell lines, TALL-1, J
urkatt in the T-cell lines and HL-60 in the non-lymphoid cell lines we
re sensitive whereas normal lymphocytes or other 8 cell lines were not
. An immunoreactive spot with the same Rf with cord red cells was also
detected in sensitive cell lines. The possible presence of a new glyc
olipid antigen determined from the mAb and related to the differentiat
ion of hematopoietic cells was speculated.