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Inhibition of tumor metastasis and immunotherapy by a microbial polysaccharaide

Research Project

Project/Area Number 11650816
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field 生物・生体工学
Research InstitutionNagoya University

Principal Investigator

MIYAKE Katsuhide  Dept.of Biotechnol., Grad.School of Eng., Nagoya Univ., Assist.Prof., 工学研究科, 助手 (90252254)

Co-Investigator(Kenkyū-buntansha) NISHIJIMA Kenichi  Dept.of Biotechnol, Grad.School of Eng., Nagoya Univ., Assis.Prof., 工学研究科, 助手 (10262891)
Project Period (FY) 1999 – 2000
Project Status Completed (Fiscal Year 2000)
Budget Amount *help
¥3,400,000 (Direct Cost: ¥3,400,000)
Fiscal Year 2000: ¥1,600,000 (Direct Cost: ¥1,600,000)
Fiscal Year 1999: ¥1,800,000 (Direct Cost: ¥1,800,000)
KeywordsStreptococcus agalactiae / Sialyllactosamine / Sialyl Lewis carbohydrate / L-selectin / MEL-14 / セレクチン / 微生物多糖
Research Abstract

Structure of type specific capsular polysaccharide from group B streptococci, Streptococcus agalactiae type Ia and Ib have branched sialyl lactosamines linked to a lactose polymer. This structure is very similar to those of sugar chains, which are expressed in mammalian cells. Sialyl Lewis carbohydrates and several gangliosides expressed in cancer and hematopoietic cells have the sialyl lactosamine structure. These mammalian sugar chains are known to play important roles in metastasis and activation of immune system. In this study, we investigated effects of the capsular polysaccharide from S.agalactiae on hematopoietic cells. These polysaccharides showed activation effect on T-cells. This effect was inhibited by addition of anti-capsular polysaccharide antisera. This fact indicated that the effects caused by the type specific polysaccharide was due to sugar chain, because this antisera recognizes only sugar chain. We next studied targets of the polysaccharides on T-cells. T-cells are known to express L-selectin which binds sialyl Lewis carbohydrates. By using anti-L-selectin antibody (NEL-14), we analyzed reaction of T-cells to the signals caused by MEL-14. MEL-14 did not show any stimulation of T-cells, but this antibody showed similar effects to capsular polysaccharides in the presence of other signals such as CD3 and CD28 stimulation. These facts suggested that the bacterial specific capsular polysaccharide may bind to L-selectin and other unknown receptors.

Report

(3 results)
  • 2000 Annual Research Report   Final Research Report Summary
  • 1999 Annual Research Report

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Published: 1999-04-01   Modified: 2016-04-21  

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