H. Terao et al., TH1 TYPE CD4(-CELLS MAY BE A POTENT EFFECTOR AGAINST POORLY IMMUNOGENIC SYNGENEIC TUMORS - ANTITUMOR-ACTIVITY OF TH1 TYPE CD4(+) T-CELLS() T), Biotherapy, 8(2), 1995, pp. 143-151
We examined the possibility that Th1 type CD4(+) T cells may be an eff
ector against three kinds of syngeneic tumors such as highly immunogen
ic B16 melanoma (B16) and two poorly immunogenic lines of MCA fibrosar
coma (MCA) and 3LL carcinoma (3LL). In a proliferation assay, the Th1
type CD4(+) T cell clone (MH2) recognized the purified protein derivat
ives (PPD) derived from Mycobacterium tuberculosis. In a tumor-neutral
izing assay, MH2 showed anti-tumor activity against both B16 and MCA.
In a model of pulmonary metastasis, MH2 also showed anti-tumor activit
y against both B16 and 3LL. In an assay of cytolysis, MH2 showed a mod
erate level of tumor necrosis factor-dependent cytolytic activity only
against MCA. In a cytostasis assay, MH2 showed a high level of interf
eron gamma-dependent cytostatic activity against the three tumors in t
he presence of macrophages. The anti-tumor activity of MH2 against B16
and 3LL was suggested to be, at least in part, attributable to the au
gmented natural killer activity. Taken together, these findings sugges
t that we may potentially be able to utilize Th1 type CD4(+) T cells a
s an effector for immunotherapy against poorly immunogenic tumors.