M. Meta et al., DETECTION OF OLIGOCLONAL T-LYMPHOCYTES IN LYMPH-NODES DRAINING FROM ADVANCED NON-SMALL-CELL LUNG-CANCER, Cancer immunology and immunotherapy, 40(4), 1995, pp. 235-240
Despite the combined use of surgery and chemoradiotherapy, the poor pr
ognosis of advanced non-small-cell lung cancer (NSCLC) requires the de
finition of new therapeutic approaches. The presence of T lymphocytes,
with peculiar phenotypic, functional and molecular characteristics wi
thin the tumour, suggested the possible use of these cells, expanded i
n vitro, in protocols of adoptive immunotherapy. We have described how
a population of oligoclonal T lymphocytes, derived from advanced NSCL
C, can be expanded in vitro and has the capability of lysing autologou
s cancer cells. What is more important, we observed that patients with
advanced NSCLC, treated with Tn expanded in vitro and recombinant int
erleukin-2, seemed to have a disease-free period longer than that of p
atients treated with conventional chemoradiotherapy. In an attempt to
find new sources of specific lymphocytes for immunotherapy, we describ
e the analysis of the phenotypic, functional and molecular characteris
tics of T lymphocytes, derived from lymph nodes draining advanced NSCL
C. In this paper we show that these cells, have restriction patterns o
f T cell receptor beta chain similar to those detectable in the popula
tion of infiltrating T lymphocytes. This finding suggests that T cells
derived from draining lymph nodes of advanced NSCLC have peculiar cha
racteristics and can be a suitable source of effector cells for protoc
ols of adoptive immunotherapy in lung cancer treatment.