M. Takizawa et al., AUGMENTATION OF HOST-DEFENSE MECHANISMS AGAINST TUMOR BY SPERABILLIN POLYMERS, NEW BASIC PEPTIDYL BIOPOLYMERS, IN MICE, International journal of immunopharmacology, 16(1), 1994, pp. 67-74
Sperabillin polymers, which have been shown recently to have antitumor
activity, are new basic peptidyl polymers composed of a pseudo-peptid
e antibiotic, sperabillin A. The polymers, HP-2 (MW 9990), AP-2 (MW 20
,100) and AB-2 (MW 35,000), were found to potently activate murine per
itoneal macrophages The phagocytosis-dependent respiratory burst and F
cgamma receptor expression of peritoneal macrophages from C57BL/6 mice
were enhanced after in vitro cultivation with these polymers. When HP
-2, a representative of these polymers, was intraperitoneally injected
into mice, the number of peritoneal exudate cells increased and phago
cytosis-dependent respiratory burst and class II (I-A) antigen express
ion of peritoneal macrophages were augmented. These macrophages showed
strong inhibitory activity against the growth of murine tumor cell li
nes such as EL4 lymphoma and B16 melanoma. Nitrogen oxide, tumor necro
sis factor (TNF) and interleukin 1 (IL-1) might be required for this i
nhibitory activity. Moreover, in mice treated with HP-2, splenocyte co
unts also increased and non-specific killer activity of the splenocyte
s was augmented. These results indicate that sperabillin polymers are
new macrophage activators.