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논문 기본 정보

자료유형
학술저널
저자정보
Kathryne E. Marks (Rosalind Franklin University of Medicine and Science) Kaylin Cho (Rosalind Franklin University of Medicine and Science) Courtney Stickling (Rosalind Franklin University of Medicine and Science) Joseph M. Reynolds (Rosalind Franklin University of Medicine and Science)
저널정보
대한면역학회 Immune Network Immune Network Vol.21 No.3
발행연도
2021.6
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1 - 13 (13page)

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초록· 키워드

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TLR signaling is critical for broad scale immune recognition of pathogens and/or danger molecules. TLRs are particularly important for the activation and the maturation of cells comprising the innate immune response. In recent years it has become apparent that several different TLRs regulate the function of lymphocytes as well, albeit to a lesser degree compared to innate immunity. TLR2 heterodimerizes with either TLR1 or TLR6 to broadly recognize bacterial lipopeptides as well as several danger-associated molecular patterns. In general, TLR2 signaling promotes immune cell activation leading to tissue inflammation, which is advantageous for combating an infection. Conversely, inappropriate or dysfunctional TLR2 signaling leading to an overactive inflammatory response could be detrimental during sterile inflammation and autoimmune disease. This review will highlight and discuss recent research advances linking TLR2 engagement to autoimmune inflammation.

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ABSTRACT
INTRODUCTION
TLR2 EXPRESSION AND LIGATION
LOSS OF TLR2 SIGNALING IN MODELS OF AUTOIMMUNE INFLAMMATION AND HUMAN CORRELATIONS
INNATE ROLES OF TLR2 IN DRIVING AUTOIMMUNE INFLAMMATION
INTRINSIC TLR2 SIGNALING IN B CELL AND T CELLS CONTRIBUTES TO AUTOIMMUNE DISEASE PATHOGENESIS
CONCLUDING REMARKS
REFERENCES

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