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               <dc:title>Increase of Circulating Monocyte-Platelet Conjugates in Rheumatoid Arthritis Responders to IL-6 Blockage</dc:title>
               <dc:creator>Mariscal, Anaís</dc:creator>
               <dc:creator>Zamora, Carlos</dc:creator>
               <dc:creator>Díaz Torne, César</dc:creator>
               <dc:creator>Ortiz, M. Àngels</dc:creator>
               <dc:creator>De Agustin, Juan Jose</dc:creator>
               <dc:creator>Reina, Delia</dc:creator>
               <dc:creator>Estrada, Paula</dc:creator>
               <dc:creator>Moya, Patricia</dc:creator>
               <dc:creator>Corominas, Hèctor</dc:creator>
               <dc:creator>Vidal, Silvia</dc:creator>
               <dc:subject>Platelets</dc:subject>
               <dc:subject>Monocytes</dc:subject>
               <dc:subject>Rheumatoid arthritis</dc:subject>
               <dc:subject>Tocilizumab</dc:subject>
               <dc:subject>Immune modulation</dc:subject>
               <dc:subject>Inflammation</dc:subject>
               <dc:subject>Immunity</dc:subject>
               <dc:description>Platelets (PLT) bind to a significant percentage of circulating monocytes and this im-munomodulatory interaction is increased in several inflammatory and autoimmune conditions. The therapeutic blockage of IL-6 with Tocilizumab (TCZ) alters PLT and the phenotype and function of monocytes in rheumatoid arthritis (RA). However, the relationship between monocyte-PLT conjugates (CD14+PLT+) and clinical and immunological variables and the regulation of this interaction by IL-6 blockage are still unknown. Here, we compared the presence of monocyte-PLT conjugates (CD14+PLT+) and membrane CD162 expression using flow cytometry, and, by ELISA, the markers of PLT activation (sCD62P and sCD40L) in healthy donors (HD) and patients with long-standing RA before TCZ (baseline). We found higher percentages and absolute counts of CD14+PLT+, and higher plasmatic levels of sCD62P and sCD40L but lower CD162 expression on monocytes from RA patients than those from HD. Additionally, the levels of CD14+PLT+ inversely correlated with inflammatory parameters. Interestingly, 95% of patients with lower percentages of CD14+PLT+ and only 63% of patients with higher percentages of CD14+PLT+ achieved a EULAR-defined response at four weeks (p = 0.036). After TCZ, the percentage of CD14+PLT+ increased in 92% of RA patients who achieved 12 w-remission (p &lt; 0.001). Our results suggest that the binding of PLTs has a modulatory effect, accentuated by the increased binding of PLTs to monocytes in response to the therapeutic blockage of IL-6.</dc:description>
               <dc:date>2022</dc:date>
               <dc:type>Article</dc:type>
               <dc:relation>Instituto de Salud Carlos III PI17/00072</dc:relation>
               <dc:relation>Instituto de Salud Carlos III PI20/00184</dc:relation>
               <dc:relation>International journal of molecular sciences ; Vol. 23 Núm. 10 (May 2022), p. 5748</dc:relation>
               <dc:rights>open access</dc:rights>
               <dc:rights>Aquest document està subjecte a una llicència d'ús Creative Commons. Es permet la reproducció total o parcial, la distribució, la comunicació pública de l'obra i la creació d'obres derivades, fins i tot amb finalitats comercials, sempre i quan es reconegui l'autoria de l'obra original.</dc:rights>
               <dc:rights>https://creativecommons.org/licenses/by/4.0/</dc:rights>
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