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Publication : Effect of CpG Depletion of Vector Genome on CD8(+) T Cell Responses in AAV Gene Therapy.

First Author  Bertolini TB Year  2021
Journal  Front Immunol Volume  12
Pages  672449 PubMed ID  34135899
Mgi Jnum  J:335607 Mgi Id  MGI:6729324
Doi  10.3389/fimmu.2021.672449 Citation  Bertolini TB, et al. (2021) Effect of CpG Depletion of Vector Genome on CD8(+) T Cell Responses in AAV Gene Therapy. Front Immunol 12:672449
abstractText  Adeno associated viral (AAV) vectors have emerged as a preferred platform for in vivo gene replacement therapy and represent one of the most promising strategies to treat monogenetic disorders such as hemophilia. However, immune responses to gene transfer have hampered human gene therapy in clinical trials. Over the past decade, it has become clear that innate immune recognition provides signals for the induction of antigen-specific responses against vector or transgene product. In particular, TLR9 recognition of the vector's DNA genome in plasmacytoid dendritic cells (pDCs) has been identified as a key factor. Data from clinical trials and pre-clinical studies implement CpG motifs in the vector genome as drivers of immune responses, especially of CD8(+) T cell activation. Here, we demonstrate that cross-priming of AAV capsid-specific CD8(+) T cells depends on XCR1(+) dendritic cells (which are likely the main cross-presenting cell that cooperates with pDCs to activate CD8(+) T cells) and can be minimized by the elimination of CpG motifs in the vector genome. Further, a CpG-depleted vector expressing human coagulation factor IX showed markedly reduced (albeit not entirely eliminated) CD8(+) T cell infiltration upon intramuscular gene transfer in hemophilia B mice when compared to conventional CpG(+) vector (comprised of native sequences), resulting in better preservation of transduced muscle fibers. Therefore, this deimmunization strategy is helpful in reducing the potential for CD8(+) T cell responses to capsid or transgene product. However, CpG depletion had minimal effects on antibody responses against capsid or transgene product, which appear to be largely independent of CpG motifs.
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