Gs. Kaklij et Sm. Kelkar, TUMOR-SPECIFIC TRANSPLANTATION RESISTANCE IN MICE AFTER TREATMENT OF INITIAL TUMORS WITH STREPTOCOCCUS-THERMOPHILUS, Microbiology and immunology, 40(1), 1996, pp. 55-58
Antitumor activity observed by treatment with Streptococcus thermophil
us was further investigated. The mice cured from fibrosarcoma by treat
ment with heat-killed preparation of S. thermophilus, when challenged
with fibrosarcoma failed to take up the tumor. However, these cured mi
ce when challenged with sarcoma-180 or Ehrlich ascites carcinoma, did
not show significant changes in tumor take and/or survival compared to
their respective controls. Similarly, mice cured from sarcoma-180 wer
e challenged with fibrosarcoma, sarcoma-180 or Ehrlich ascites carcino
ma. Though there was no change in the mean survival time (MST) of the
dying mice regarding sarcoma-180 or Ehrlich ascites carcinoma, there w
as 50 and 30% increase in the number of mice that showed total regress
ion respectively over controls. However, there was no difference in th
e growth rate of fibrosarcoma. Similar observations were made with mic
e cured from Ehrlich ascites carcinoma, challenged with these tumors.
These findings thus suggest that the antitumor response was tumor-spec
ific and that tumor-associated antigens may have a role in imparting t
his specificity. Bacterial treatment non-specifically augmented this p
rimary response.