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Yunji Park

Researcher at Pohang University of Science and Technology

Publications -  41
Citations -  3483

Yunji Park is an academic researcher from Pohang University of Science and Technology. The author has contributed to research in topics: Cytotoxic T cell & Immune system. The author has an hindex of 19, co-authored 40 publications receiving 3104 citations. Previous affiliations of Yunji Park include La Jolla Institute for Allergy and Immunology.

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Reciprocal TH17 and regulatory T cell differentiation mediated by retinoic acid.

TL;DR: The vitamin A metabolite retinoic acid is identified as a key regulator of TGF-β–dependent immune responses, capable of inhibiting the IL-6–driven induction of proinflammatory TH17 cells and promoting anti-inflammatory Treg cell differentiation, indicating that a common metabolite can regulate the balance between pro- and anti- inflammatory immunity.
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Transcriptional reprogramming of mature CD4+ helper T cells generates distinct MHC class II-restricted cytotoxic T lymphocytes

TL;DR: It is found that the helper T cell fate was not fixed and that mature, antigen-stimulated CD4+ T cells terminated expression of the gene encoding ThPOK and reactivated genes of the CD8 lineage, resulting in the post-thymic termination of the helpers T cell program and the functional differentiation of distinct MHC class II–restrictedCD4+ cytotoxic T lymphocytes.
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Cutting Edge: CpG DNA inhibits dendritic cell apoptosis by up-regulating cellular inhibitor of apoptosis proteins through the phosphatidylinositide-3'-OH kinase pathway.

TL;DR: It is indicated that CpG DNA provides a survival signal to DCs, which might be one of mechanisms by which bacterial DNA stimulates and maintains the innate immune responses.
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Functional Dichotomy between OX40 and 4-1BB in Modulating Effector CD8 T Cell Responses

TL;DR: This study compares the role of two closely related TNFR family molecules, OX40 and 4-1BB, in generating effector CD8 T cells to Ag delivered by adenovirus and suggests that they can have a clear functional dichotomy in modulating effectorCD8 T cell responses.
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Effects of a hexameric deoxyriboguanosine run conjugation into CpG oligodeoxynucleotides on their immunostimulatory potentials.

TL;DR: The conjugation of consecutive deoxyriboguanosine residues, called a dG run, at the 3′ terminus of phosphodiester CpG ODNs significantly enhanced TNF-α and IL-12 production from mouse splenic dendritic cells (DCs).