• 제목/요약/키워드: responsiveness to recombinant IL-2

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Lewis Lung Carcinoma(LLC) 이식 생쥐에 있어서 천연운지 단백 다당체(Copolang)의 면역조절활성 (Immunomodulating Activities of Copolang, a Proteopolysaccharide from Coriolus versicolor in Lewis Lung Carcinoma (LLC) Bearing mice)

  • 문창규;임철홍;목명수;양경미;한혜승;최재영
    • 약학회지
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    • 제37권1호
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    • pp.9-17
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    • 1993
  • Immune functions of mice bearing Lewis Lung Carcinoma (LLC) were significantly suppressed when evaluated with mitogen responsiveness, IL-2 production and non-specific suppressor activity. Based on these immunosuppressive characteristics of LLC bearing mice, immunomodulating activates of Copolang were investigated in this model. After 15 days of LLC inoculation, Copolang was intraperitoneally administered for 7 consecutive days with doses of 20 or 200 mg/kg. Immune functions were evaluated 3 days after the final administration of Copolang. The results showed that the growth of LLC solid tumor was not inhibited by Copolang. But, mitogens-induced proliferation, IL-2 production and responsiveness to recombinant IL-2 of splenocytes were significantly augmented by the treatment of Copolang. However suppressor cell activity was not affected by Copolang. These results indicate that Copolang expresses potent immunomodulating activates through the augmentations of IL-2 production and responsiveness to recombinant IL-2, which have been generally known to be suppressed in tumor bearing mice, without affecting the growth of tumor.

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Immunomodulating Activities of Brazilin in vitro

  • Moon, Chang-Kiu;Mock, Myung-Soo;Yang, Kyung-Mee;Han, Hye-Seung;Won, Hyeon-Soon;Kim, Ji-Young;Chung, Jin-Ho;Moon, Chang-Hyun
    • Archives of Pharmacal Research
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    • 제15권4호
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    • pp.283-288
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    • 1992
  • This work was performed to investigate the effects of brazilin in vitro on mitrogen-induced proliferation, ConA-induced TCGF release and responsiveness to recombinant-induced proliferation, ConA-induced TCGF release and responsiveness to recombinant IL-2 using splenocytes from C57BL/6 female mice. Brazilin (29-80 ng/ml) caused a noticeable increase in TCGF production of splenocytes, but did not affect responsivness to recombinant IL-2, the expression of ConA-induced high affinity IL-2 receptor and mitogen-induced proliferation of splenocytes.

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