Colin J. Dunn, PhD; Nigel D. Stake, PhD; Marilyn M. Hardee, MS
To the Editor: The results of studies of patients with cancer have shown that significant T-lymphocyte tumor infiltration, increased HLA-DR expression, and tumor regression can be achieved after the infusion of high doses of interleukin-2 and lymphokine-activated killer cells (1, 2). A major concern, however, with this therapy is the incidence of severe side effects (1, 3). One alternative to high-dose cytokine therapy would be the use of a locally implanted polymer, which would allow the slow release of interleukin and the infiltration of a tumor by lymphoid cells without systemic side effects.
We have recently reported (4) a localized
Colin J. Dunn, Nigel D. Stake, Marilyn M. Hardee. Slow Release of Interleukin-2 from Polymer Implants. Ann Intern Med. 1988;109:761–762. doi: 10.7326/0003-4819-109-9-761_2
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Published: Ann Intern Med. 1988;109(9):761-762.
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