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Abstract The cellular basis for site-specific inflammation remains unclear. In human fingers, proximal interphalangeal (PIP) joints are preferentially affected by inflammatory arthritis, whereas distal interphalangeal joints are spared, providing a model to investigate the predilection of inflammation to distinct sites.
Abstract The current concept is that the eye is an immune privileged site endowed with innate immune regulatory networks to maintain organ function. We now have evidence that resident T cells occupy intraocular tissues. In immune-mediated inflammatory diseases, such as psoriasis and rheumatoid arthritis, tissue resident T cells trigger disease flares in the skin and joints.
Supporting Information Filename Description art70123-sup-0001-Disclosureform.pdfPDF document, 647.7 KB Disclosure Form art70123-sup-0002-FigureS1.tifTIFF image, 5.8 MB Supplementary Data Fig 1. Demonstration of mouse siPAM efficiency in N2A cells A) Western blot and B) densitometry of PAM protein in N2A cells following a 72 h transfection with siNTC or siPAM. Treatment with siPAM knocked down PAM expression 67% (10 nM) and 51% (30 nM).
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