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2016 Fiscal Year Final Research Report

The effect of quantitative T-cell receptor down-modulation in antibody reponses and its application for autoimnune diseases

Research Project

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Project/Area Number 15H06374
Research Category

Grant-in-Aid for Research Activity Start-up

Allocation TypeSingle-year Grants
Research Field Collagenous pathology/Allergology
Research InstitutionOsaka University

Principal Investigator

Mizui Masayuki  大阪大学, 医学系研究科, 助教 (30423106)

Project Period (FY) 2015-08-28 – 2017-03-31
Keywords全身性エリテマトーデス / 自己免疫疾患 / T細胞受容体 / 制御性T細胞 / 抗CD3抗体
Outline of Final Research Achievements

For quantitative down-modulation of T-cell receptor, we used anti-CD3 F(ab')2 antibody. In vivo injection of the antibody resulted in the temporal reduction of TCR intensity (around 20% vs controls) by flow cytometric analysis. When wild-type mice were immunized with NP-CGG, formation of germinal center B cells were significantly reduced, however, follicular helper T cell number were comparable in antibody-treated group. Notably, we found that the number of regulatory T cells (Tregs) were significantly increased by F(ab')2 antibody treatment. To address whether the reduction of antibody responses is due to direct inhibition of Tfh induction or through the induction of Treg, we will use Treg depletion models and/or Treg transfer models using Foxp3-DTR mice and/or Foxp3-GFP mice.

Free Research Field

免疫学、腎臓病学

URL: 

Published: 2018-03-22  

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