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논문 기본 정보

자료유형
학술저널
저자정보
Seung Min Jung (The Catholic University of Korea) Wan-Uk Kim (The Catholic University of Korea)
저널정보
대한면역학회 Immune Network Immune Network Vol.22 No.1
발행연도
2022.2
수록면
150 - 172 (23page)

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In the past few decades, biological drugs and small molecule inhibitors targeting inflammatory cytokines, immune cells, and intracellular kinases have become the standard-of-care to treat autoimmune diseases. Inhibition of TNF, IL-6, IL-17, and IL-23 has revolutionized the treatment of autoimmune diseases, such as rheumatoid arthritis, ankylosing spondylitis, and psoriasis. B cell depletion therapy using anti-CD20 mAbs has shown promising results in patients with neuroinflammatory diseases, and inhibition of B cell survival factors is approved for treatment of systemic lupus erythematosus. Targeting co-stimulatory molecules expressed on Ag-presenting cells and T cells is also expected to have therapeutic potential in autoimmune diseases by modulating T cell function. Recently, small molecule kinase inhibitors targeting the JAK family, which is responsible for signal transduction from multiple receptors, have garnered great interest in the field of autoimmune and hematologic diseases. However, there are still unmet medical needs in terms of therapeutic efficacy and safety profiles. Emerging therapies aim to induce immune tolerance without compromising immune function, using advanced molecular engineering techniques.

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ABSTRACT
INTRODUCTION
INFLAMMATION IN AUTOIMMUNE DISEASES
CYTOKINE-TARGETED THERAPY
CELL-TARGETED THERAPY
KINASE-TARGETED THERAPY
EMERGING IMMUNOTHERAPY
CONCLUSION
REFERENCES

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