D. Dericqles et al., BREAST-CANCER AND T-CELL-MEDIATED IMMUNITY TO PROTEINS OF THE MOUSE MAMMARY-TUMOR VIRUS (MMTV), European cytokine network, 4(2), 1993, pp. 153-160
We have previously reported that breast cancer patients and some healt
hy subjects show positive T-cell-mediated immune responses to a semi-p
urified mouse mammary tumour viral pool (MMTV). We have now used Weste
rn blotting to analyse the specificity of the response and to determin
e the target polypeptides. Two types of T-cell response to the viral a
ntigens were examined, proliferation and MIF release, the latter impli
es a DTH status in vivo where primed lymphocytes are involved. Two vir
al fractions were used, one containing a glycoprotein, the 52 kD major
virus envelope , and the other containing the 28 kD main virus core p
rotein. We analysed both patients and healthy subjects whose T-cells p
roliferated to the MMTV total extract (viral pool). The T-cell respons
e in the patients was shown to be viral specific since both the T-cell
proliferation (21/25) and MIF release (17/19) were directed against v
iral components of the pool (gp 52 and/or p 28). The T-cell response i
n the healthy control subjects was shown to be mostly directed against
a species-specific albumin component of the extract. In addition, the
monocyte integrity required for the MIF response was altered in the b
reast cancer patients. The monocytes from one patient out of three rai
led to respond to MIF, even though the lymphokine was released normall
y by the patients' activated T-cells.