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논문 기본 정보

자료유형
학술저널
저자정보
Mehdi Najar (Institut Jules Bordet, Université Libre de Bruxelles (ULB)) Mohammad Krayem (Institut Jules Bordet, Université Libre de Bruxelles) Nathalie Meuleman (Institut Jules Bordet, Université Libre de Bruxelles (ULB)) Dominique Bron (Institut Jules Bordet, Université Libre de Bruxelles (ULB)) Laurence Lagneaux (Institut Jules Bordet, Université Libre de Bruxelles (ULB))
저널정보
대한면역학회 Immune Network Immune Network Vol.17 No.2
발행연도
2017.4
수록면
89 - 102 (14page)

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초록· 키워드

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Mesenchymal Stromal Cells (MSCs) are potential cellular candidates for several immunotherapy purposes. Their multilineage potential and immunomodulatory properties make them interesting tools for the treatment of various immunological diseases. However, depending on the local microenvironment, diverse biological functions of MSCs can be modulated. Indeed, during infections such as obtained following TLR-agonist engagement (called as TLR priming), the phenotype, multilineage potential, hematopoietic support and immunomodulatory capacity of MSCs can present critical changes, which could further affect their therapeutic potential. Thus, for appropriate clinical application of MSCs, it is important to well know and understand these effects in particular during infectious episodes and to find the suitable experimental settings to study that. Pre-stimulation of MSCs with a specific TLR ligand may serve as an effective priming step to modulate one of its function to achieve a desired therapeutic issue.

목차

Mesenchymal stromal cells
Sensitivity to infection
Toll-Like Receptors
TLR signaling
MSC and TLR expression
MSC phenotype and TLR-priming
MSC multilineage potential and TLR-priming
MSC hematopoietic support and TLR-priming
MSC immunomodulation and TLR-priming
Conclusions & perspectives
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