The immune response is impaired in patients with malignancy, and radia
tion therapy (RT) can exacerbate the cancer induced-attenuation of imm
une response. In order to search for the fine mechanisms behind the RT
-induced attenuation of cell-mediated immune response, we measured the
number of lymphocytes in peripheral blood, its subsets, and lymphobla
st transformation induced by phytohemagglutinin (PHA), purified protei
n derivatives (PPD), mitogenic monoclonal antibody anti-CD3, and mitog
enic combination of anti-CD2 antibodies 9-1 and 9.6 before and after R
T in 19 patients with squamous cell lung cancer. Radiation therapy sig
nificantly decreased the total numbers of lymphocytes, CD-3, CD-4, and
CD8-positive lymphocytes in peripheral blood However, RT did not chan
ge the per centages of lymphocytes and its subsets. Radiation therapy
increased the percentage of interleukin 2 (IL-2) receptor-positive lym
phocytes, and RT significantly decreased in vitro lymphoblast transfor
mation by PHA, PPD, or monoclonal antibodies to T-cell surface antigen
s (anti-CD2 or anti-CD3). In vitro incubation with IL-2 did not increa
se lymphoblast transformation by anti-CD3 before RT but significantly
increased after RT. In conclusion, we suggest that one of the fine mec
hanisms behind the RT-induced suppression of immune responsiveness of
patients with lung cancer is a defect in IL-2 synthesis by lymphocytes
.