Literature DB >> 12731084

Induction of T cell tolerance to a protein expressed in the cytoplasm through retroviral-mediated gene transfer.

Chaorui Tian1, Jessamyn Bagley, Joel Kaye, John Iacomini.   

Abstract

BACKGROUND: Host immune responses to foreign gene products have been shown to lead to the elimination of genetically modified cells, and are a major barrier to successful therapeutic gene therapy. We have shown that immunological tolerance to retrovirally transduced cell surface proteins can be induced by expressing the gene encoding these products in bone marrow derived cells. Here, we investigate if expression of foreign gene products in bone marrow derived cells can be used to induce tolerance to cytoplasmic proteins.
METHODS: Balb/c mice were reconstituted with syngeneic bone marrow cells transduced with retrovirus carrying the gene encoding enhanced green fluorescent protein (eGFP), or mock-transduced bone marrow cells. After reconstitution, mice were immunized with cells expressing eGFP, and T cells were tested for the ability to kill eGFP-expressing targets in in vitro cytotoxic T lymphocyte (CTL) assays.
RESULTS: T cells from Balb/c mice reconstituted with mock-transduced bone marrow were able to kill target cells expressing eGFP. In contrast, T cells from mice reconstituted with eGFP-transduced bone marrow were unable to kill targets expressing eGFP. In addition, we observed that T cell responses to eGFP in C57BL/6 mice were minimal even under highly immunogenic conditions.
CONCLUSIONS: These data suggest that expression of foreign gene products in bone marrow derived cells is capable of inducing T cell tolerance to proteins expressed exclusively in the cytoplasm. Copyright 2003 John Wiley & Sons, Ltd.

Entities:  

Mesh:

Substances:

Year:  2003        PMID: 12731084     DOI: 10.1002/jgm.363

Source DB:  PubMed          Journal:  J Gene Med        ISSN: 1099-498X            Impact factor:   4.565


  6 in total

1.  Retinoic acid suppresses growth of lesions, inhibits peritoneal cytokine secretion, and promotes macrophage differentiation in an immunocompetent mouse model of endometriosis.

Authors:  Friedrich Wieser; Juanjuan Wu; Zhaoju Shen; Robert N Taylor; Neil Sidell
Journal:  Fertil Steril       Date:  2012-03-28       Impact factor: 7.329

2.  Visualization and manipulation of neural activity in the developing vertebrate nervous system.

Authors:  Jiayi Zhang; James B Ackman; Onkar S Dhande; Michael C Crair
Journal:  Front Mol Neurosci       Date:  2011-11-18       Impact factor: 5.639

3.  Development of Gene Transfer for Induction of Antigen-specific Tolerance.

Authors:  Brandon K Sack; Roland W Herzog; Cox Terhorst; David M Markusic
Journal:  Mol Ther Methods Clin Dev       Date:  2014-04-30       Impact factor: 6.698

Review 4.  Immunoresponse to Gene-Modified Hematopoietic Stem Cells.

Authors:  Claire M Drysdale; John F Tisdale; Naoya Uchida
Journal:  Mol Ther Methods Clin Dev       Date:  2019-10-31       Impact factor: 6.698

5.  Tolerance to MHC class II disparate allografts through genetic modification of bone marrow.

Authors:  P T Jindra; S Tripathi; C Tian; J Iacomini; J Bagley
Journal:  Gene Ther       Date:  2012-07-26       Impact factor: 5.250

6.  The site of allergen expression in hematopoietic cells determines the degree and quality of tolerance induced through molecular chimerism.

Authors:  Ulrike Baranyi; Martina Gattringer; Andreas M Farkas; Karin Hock; Nina Pilat; John Iacomini; Rudolf Valenta; Thomas Wekerle
Journal:  Eur J Immunol       Date:  2013-07-15       Impact factor: 5.532

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.