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논문 기본 정보

자료유형
학술저널
저자정보
Lalani Yatawara (Kochi Medical School) Susiji Wickramasinghe (Kochi Medical School) Mitsuru Nagataki (Kochi Medical School) Misa Takamoto (Sophy Incorporation) Haruka Nomura (Kochi Medical School) Yasunori Ikeue (Sophy Incorporation) Yoshiya Watanabe (Sophy Incorporation) Takeshi Agatsuma (Kochi Medical School)
저널정보
대한기생충학열대의학회 Parasites, Hosts and Diseases The Korean Journal of Parasitology Vol.47 No.4
발행연도
2009.10
수록면
345 - 351 (7page)

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The β-glucans derived from yeast cell walls have been reported for having many immunomodulatory activities in vivo and in vitro. In this study, Aureobasidium-derived soluble branched (1,3-1,6) b-glucan (Sophy β-glucan) was checked for natural killer (NK) activity and for the production of IFN-g and IL-4 in Leishmania amazonensis infection. The main experiment was performed with a group of female C57BL/6 and BALB/c mice, orally supplemented with 5% of Sophy β-glucan and infected with promastogotes of L. amazonensis (1 × 10<SUP>7</SUP>) into the footpad. Increase in the footpad thickness with time was observed in BALB/c mice in spite of the oral Sophy b-glucan supplement, but it was less in C57BL/6 mice. The difference in overall mean footpad thickness between ‘infection only’ versus ‘infection + glucan’ groups was statistically significant (P < 0.001). High NK activity in C57BL/6 than BALB/c mice was observed in ‘glucan only’ group compared to the control group and also in ‘infection + glucan’ group compared to ‘infection only’ group. The difference in the NK activity among these groups was significant (P < 0.05). The IFN-g level increased at weeks 7 and 8 post-infection in C57BL/6 mice and was significantly high in ‘infection + glucan’ group compared to the ‘infection only’ group (P < 0.05). IL-4 levels did not increase up to detectable levels throughout the study. The results led a conclusion that Sophy β-glucan enhances NK activity and cellular immunity in L. amazonensis-infected mice.

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Abstract
INTRODUCTION
MATERIALS AND METHODS
RESULTS
DISCUSSION
REFERENCES

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UCI(KEPA) : I410-ECN-0101-2014-510-002532205