PRE-IMMUNOTHERAPY SERUM CA27.29 (MUC-1) MUCIN LEVEL AND CD69(-TN-KLH CANCER VACCINE IN ACTIVE SPECIFIC IMMUNOTHERAPY() LYMPHOCYTES CORRELATE WITH EFFECTS OF THERATOPE(R) SIALYL)
Ma. Reddish et al., PRE-IMMUNOTHERAPY SERUM CA27.29 (MUC-1) MUCIN LEVEL AND CD69(-TN-KLH CANCER VACCINE IN ACTIVE SPECIFIC IMMUNOTHERAPY() LYMPHOCYTES CORRELATE WITH EFFECTS OF THERATOPE(R) SIALYL), Cancer immunology and immunotherapy, 42(5), 1996, pp. 303-309
Patients with metastatic breast, colorectal or ovarian cancers receive
d active specific immunotherapy (ASI) with Theratope(R) sialyl-Tn-KLH
(keyhole limpet hemocyanin) cancer vaccine emulsified in Detox(TM) adj
uvant. The median log(2) anti-STn IgG titer generated by ASI, estimate
d by enzyme-linked immunosorbent assay with solid-phase ovine submaxil
lary mucin, was 5.322 (range = 0-9.322). Following ASI, 51 patients wh
o generated titers higher than the median value for anti-STn(+) mucin
IgG survived longer than 46 patients who generated lower titers below
the median. 38 of the patients were phenotyped for CD69 prior to ASI.
The patients with lower numbers of CD69(+) peripheral blood lymphocyte
s prior to immunotherapy (pre-ASI) also had low serum CA27.29 cancer a
ntigen (MUC-1) levels, and had longer times to disease progression and
improved survival following ASI. Elevated pre-ASI serum CA27.29 tumor
antigen levels were associated with higher numbers of CD69(+) PBL, wi
th decreased anti-STn antibody production and decreased survival follo
wing ASI. The data are compatible with the hypothesis that elevated se
rum MUC-1 mucin is specifically immunosuppressive.