Wr. Carroll et al., PERILESIONAL INTERLEUKIN-2 IN THE VX-2 CARCINOMA IN RABBITS - A PRELIMINARY INVESTIGATION, Otolaryngology and head and neck surgery, 112(3), 1995, pp. 430-436
Immune system amplification by perilesional injection of interleukin-2
is a promising adjuvant approach for treating squamous cell carcinoma
of the head and neck. A pilot study was designed to develop an animal
model bearing squamous cell carcinoma in which to test the efficacy o
f perilesional interleukin-2. Rabbits were inoculated intramuscularly
with the papilloma virus-induced squamous carcinoma VX-2 cell line. Tu
mor regression and host lymphatic response after perilesional interleu
kin-2 were measured. Variable responses were found. Growth of tumor ce
lls implanted from cell culture was rapid in most animals. Tumor growt
h was prevented in animals receiving 10,000 units of interleukin-2 per
injection initiated 9 days after tumor inoculation. This inhibition a
pproached statistical significance when compared with growth of saline
controls. Histologic responses consisted primarily of plasma cell and
eosinophil infiltration. The intensity of the inflammatory response d
id not correlate with interleukin-2 dose. A trend toward enhanced tumo
r growth was seen with lower doses of interleukin-2 and when interleuk
in-a therapy was initiated simultaneously with tumor inoculation. Thes
e findings suggest that high-dose recombinant interleukin-2 can preven
t tumor growth if initiated after tumor inoculation. Whether this effe
ct was caused by direct tumor cytotoxicity or mediated by the immune s
ystem is unclear. These preliminary results underscore the importance
of understanding the effects of dose and schedule in the design of imm
unotherapy models before clinical use.