95 research outputs found

    Eyelid fat grafting: indications, operative technique and complications; a systematic review

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    International audienceIntroduction - Many recent studies concerning autologous fat grafting in the eyelids have been published, mostly consisting of case reports and retrospective case series. However, no study on the overall complication or satisfaction rate associated with the various grafting techniques exists. We performed a comprehensive literature review to determine the outcomes and complications of eyelid fat grafting, as well as patient satisfaction.Methods - A systematic review of the literature using the PRISMA criteria was conducted. This protocol was registered at the Prospective Register of Systematic Reviews at the National Institute for Health Research.Results - Sixteen studies, representing 1,159 patients and published between June 2004 and December 2014, were included. Satisfactory results, judged by clinical examination, were observed in all studies. Few postoperative complications were reported.Conclusions - We demonstrated that the procedures were easy to perform, and achieved satisfactory and sustainable results with few complications in both reconstructive and cosmetic surgery. However, a wide disparity exists in the various fat harvesting, fat purification, and reinjection techniques. Further studies are required to assess the long-term outcomes. Our conclusions should be accepted cautiously due to the small number of articles and the lack of evidence in published studies.<br

    KDM6B drives epigenetic reprogramming associated with lymphoid stromal cell early commitment and immune properties

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    Mature lymphoid stromal cells (LSCs) are key organizers of immune responses within secondary lymphoid organs. Similarly, inflammation-driven tertiary lymphoid structures depend on immunofibroblasts producing lymphoid cytokines and chemokines. Recent studies have explored the origin and heterogeneity of LSC/immunofibroblasts, yet the molecular and epigenetic mechanisms involved in their commitment are still unknown. This study explored the transcriptomic and epigenetic reprogramming underlying LSC/immunofibroblast commitment. We identified the induction of lysine demethylase 6B (KDM6B) as the primary epigenetic driver of early immunofibroblast differentiation. In addition, we observed an enrichment for KDM6B gene signature in murine inflammatory fibroblasts and pathogenic stroma of patients with autoimmune diseases. Last, KDM6B was required for the acquisition of LSC/immunofibroblast functional properties, including the up-regulation of CCL2 and the resulting recruitment of monocytes. Overall, our results reveal epigenetic mechanisms that participate in the early commitment and immune properties of immunofibroblasts and support the use of epigenetic modifiers as fibroblast-targeting strategies in chronic inflammation

    KDM6B drives epigenetic reprogramming associated with lymphoid stromal cell early commitment and immune properties

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    Mature lymphoid stromal cells (LSCs) are key organizers of immune responses within secondary lymphoid organs. Similarly, inflammation-driven tertiary lymphoid structures depend on immunofibroblasts producing lymphoid cytokines and chemokines. Recent studies have explored the origin and heterogeneity of LSC/immunofibroblasts, yet the molecular and epigenetic mechanisms involved in their commitment are still unknown. This study explored the transcriptomic and epigenetic reprogramming underlying LSC/immunofibroblast commitment. We identified the induction of lysine demethylase 6B (KDM6B) as the primary epigenetic driver of early immunofibroblast differentiation. In addition, we observed an enrichment for KDM6B gene signature in murine inflammatory fibroblasts and pathogenic stroma of patients with autoimmune diseases. Last, KDM6B was required for the acquisition of LSC/immunofibroblast functional properties, including the up-regulation of CCL2 and the resulting recruitment of monocytes. Overall, our results reveal epigenetic mechanisms that participate in the early commitment and immune properties of immunofibroblasts and support the use of epigenetic modifiers as fibroblast-targeting strategies in chronic inflammation

    VCA supercooling in a swine partial hindlimb model

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    Vascularized composite allotransplantations are complex procedures with substantial functional impact on patients. Extended preservation of VCAs is of major importance in advancing this field. It would result in improved donor-recipient matching as well as the potential for ex vivo manipulation with gene and cell therapies. Moreover, it would make logistically feasible immune tolerance induction protocols through mixed chimerism. Supercooling techniques have shown promising results in multi-day liver preservation. It consists of reaching sub-zero temperatures while preventing ice formation within the graft by using various cryoprotective agents. By drastically decreasing the cell metabolism and need for oxygen and nutrients, supercooling allows extended preservation and recovery with lower ischemia–reperfusion injuries. This study is the first to demonstrate the supercooling of a large animal model of VCA. Porcine hindlimbs underwent 48 h of preservation at − 5 °C followed by recovery and normothermic machine perfusion assessment, with no issues in ice formation and favorable levels of injury markers. Our findings provide valuable preliminary results, suggesting a promising future for extended VCA preservation

    Machine Perfusion Enables 24-h Preservation of Vascularized Composite Allografts in a Swine Model of Allotransplantation

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    The current gold standard for preserving vascularized composite allografts (VCA) is 4°C static cold storage (SCS), albeit muscle vulnerability to ischemia can be described as early as after 2 h of SCS. Alternatively, machine perfusion (MP) is growing in the world of organ preservation. Herein, we investigated the outcomes of oxygenated acellular subnormothermic machine perfusion (SNMP) for 24-h VCA preservation before allotransplantation in a swine model. Six partial hindlimbs were procured on adult pigs and preserved ex vivo for 24 h with either SNMP (n = 3) or SCS (n = 3) before heterotopic allotransplantation. Recipient animals received immunosuppression and were followed up for 14 days. Clinical monitoring was carried out twice daily, and graft biopsies and blood samples were regularly collected. Two blinded pathologists assessed skin and muscle samples. Overall survival was higher in the SNMP group. Early euthanasia of 2 animals in the SCS group was linked to significant graft degeneration. Analyses of the grafts showed massive muscle degeneration in the SCS group and a normal aspect in the SNMP group 2 weeks after allotransplantation. Therefore, this 24-h SNMP protocol using a modified Steen solution generated better clinical and histological outcomes in allotransplantation when compared to time-matched SCS

    Adipose tissu : improvement of knowledge of adipose tissu and stromal vascular fraction, advantage in the field of plastic surgery

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    L’objectif de cette thĂšse Ă©tait d’amĂ©liorer les connaissances fondamentales sur le tissu adipeux, organe qui est au cƓur de la pratique des chirurgiens plasticiens. En effet, ce tissu peut ĂȘtre transplantĂ© de façon autologue afin de combler une perte de substance (rĂŽle volumateur des adipocytes) mais Ă©galement servir Ă  des fins de rĂ©gĂ©nĂ©ration tissulaire en lien avec les cellules de la fraction vasculaire stromale (FVS) et tout particuliĂšrement des cellules stromales mĂ©senchymateuses (CSM). Ces cellules s’obtiennent aprĂšs lipoaspiration du tissu par une digestion enzymatique de la graisse obtenue. Il s’avĂšre que les connaissances disponibles sur ces CSM sont essentiellement issues d’études in vitro aprĂšs une phase de culture cellulaire plus ou moins longue et ainsi les propriĂ©tĂ©s in vivo sont mal connues. Ce travail a donc consistĂ© Ă  caractĂ©riser l’hĂ©tĂ©rogĂ©nĂ©itĂ© du compartiment stromal natif du tissu adipeux obtenu aprĂšs digestion enzymatique. Nous avons isolĂ© deux populations stromales natives distinctes : les ASC (CD34+), en grande majoritĂ©, et des cellules pĂ©ricytaires (CD146+). Ces 2 types cellulaires diffĂ©raient dans leurs phĂ©notypes, leurs potentiels de clonogĂ©nĂ©citĂ© et leurs propriĂ©tĂ©s immunomodulatrices in vitro et in vivo. Nous avons ensuite comparĂ© la digestion enzymatique du tissu aux techniques de digestion mĂ©canique utilisable au sein de nos blocs opĂ©ratoires. Nous avons dĂ©montrĂ© que ces nouvelles techniques permettaient bien de produite les cellules de la FVS dont des CSM, cellules particuliĂšrement intĂ©ressante pour des gestes de rĂ©gĂ©nĂ©ration tissulaire. De plus, l’ensemble des techniques de laboratoire acquise au cours de ce travail nous ont permis d’investiguer le rĂŽle des techniques de lipoaspiration utilisĂ© en chirurgie plastique sur le tissu adipeux. Nous avons dĂ©montrĂ© par cytomĂ©trie de flux et par immunofluorescence in situ qu’une partie de la trame microvasculaire Ă©tait conservĂ©e. L’ensemble de ces rĂ©sultats viennent s’ajouter aux donnĂ©es cliniques dĂ©montrant que la lipoaspiration du tissu est un geste permettant d’ĂȘtre plus conservateur pour le tissu et pourrait expliquer des taux de complications moindre aprĂšs chirurgie de contour de la silhouette.The aim of this work was to improve the knowledge on adipose tissue, organ that is at the heart of the practice of plastic surgeons. Indeed, this tissue can be transplanted autologously in order to fill a defect (volumizing role of the adipocytes) but also to be used for tissue regeneration in connection with the cells of the stromal vascular fraction (SVF) and especially the mesenchymal stromal cells (MSCs). These cells are obtained after liposuction of the tissue by enzymatic digestion of the extracellular matrix. It turns out that the knowledge available on these CSM is essentially derived from in vitro studies after a cell culture phase and thus the in vivo properties are poorly known. This work consisted in characterizing the heterogeneity of the native stromal compartment of adipose tissue obtained after enzymatic digestion. We isolated two distinct native stromal populations: the ASC (CD34 +), for the most part, and the pericyte cells (CD146 +). These 2 cell types differed in their phenotypes, their clonogenecity potentials and their immunomodulatory properties in vitro and in vivo. We then compared the enzymatic digestion of the tissue with the techniques of mechanical digestion usable within our operating room. We have demonstrated that these new techniques made it possible to produce the cells of the FVS including MSC, cells particularly interesting for regenerative surgery. In addition, all the laboratory techniques acquired during this work allowed us to investigate the role of liposuction techniques used in plastic surgery on adipose tissue. We have demonstrated by flow cytometry and confocal microscopy, that part of the microvasculature framework is conserved after liposuction. All of these results are in addition to clinical data demonstrating that liposuction of the tissue is a gesture to be more conservative for the tissue and could explain lower rates of complications after contour surgery

    Les cellules stromales natives du tissu adipeux (isolement, caractérisation phénotypique et propriétés immunomodulatrices)

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    Le traitement conservateur du cancer du sein peut aboutir Ă  des sĂ©quelles morphologiques importantes. Actuellement, le transfert de tissu adipeux utilisĂ© comme produit de comblement reprĂ©sente souvent la seule possibilitĂ© de correction chirurgicale de ces dĂ©formations. Ce traitement pose aujourd'hui question du fait de la prĂ©sence de cellules stromales mĂ©senchymateuses au sein du tissu nommĂ©es adipose-derived stromal cells (ADSC). Ces cellules connues pour leurs propriĂ©tĂ©s immunosuppressives ont montrĂ© dans plusieurs Ă©tudes rĂ©alisĂ©es chez l'animal qu'elles peuvent favoriser la croissance tumorale, sans qu'un lien entre les 2 phĂ©nomĂšnes n'ait Ă©tĂ© formellement dĂ©montrĂ©. En effet, il s'avĂšre que les connaissances disponibles sur ces ADSC sont essentiellement issues d'Ă©tudes in vitro aprĂšs une phase de culture cellulaire plus ou moins longue et ainsi les propriĂ©tĂ©s des cellules stromales mĂ©senchymateuses du tissu adipeux in vivo sont mal connues. Ce travail a donc consistĂ© Ă  caractĂ©riser l'hĂ©tĂ©rogĂ©nĂ©itĂ© phĂ©notypique du compartiment stromal natif du tissu adipeux en comparaison avec des ADSC cultivĂ©es standard. GrĂące Ă  une analyse par cytomĂ©trie en flux multi-couleurs du tissu adipeux, nous avons isolĂ© deux populations stromales natives distinctes: les ADSC, en grande majoritĂ©, mas aussi une autre prĂ©sentant un phĂ©notype de cellules pĂ©ricytaires. Ces 2 types cellulaires diffĂ©raient dans leur expression de marqueurs stromaux mais aussi de molĂ©cules permettant les interactions avec les cellules immunitaires. De mĂȘme, en culture, ces cellules avaient aussi une morphologie diffĂ©rente et les ADSC natives possĂ©daient un potentiel d'autorenouvellement supĂ©rieur attestĂ© par des tests de clonogĂ©nicitĂ©. Enfin, grĂące Ă  des tests d'inhibition de la prolifĂ©ration de lymphocytes T activĂ©s en prĂ©sence de ces cellules, il est apparu que les ADSC natives montraient un pouvoir immunosuppresseur puissant, supĂ©rieur Ă  celui des pĂ©ricytes. Cette inhibition de prolifĂ©ration dĂ©pendait de l'activitĂ© de l'enzyme immunosuppressive indolĂ©amine-2,3 dioxygĂ©nase dont la synthĂšse Ă©tait dĂ©clenchĂ©e par la prĂ©sence d'une cytokine inflammatoire, l'interfĂ©ron gamma. Le tissu adipeux Ă  l'Ă©tat natif contient donc 2 types de cellules stromales aux propriĂ©tĂ©s biologiques diffĂ©rentes, en particulier envers le systĂšme immunitaire. Leur capacitĂ© immunosupressive vis-Ă -vis des lymphocytes T, qui sont des acteurs majeurs de la surveillance immunitaire cellulaire anti-tumorale les rend potentiellement dangereuses en reconstruction mammaire aprĂšs cancer, ce qui renforce les recommandations de prudence sur les indications opĂ©ratoires. Il est donc nĂ©cessaire de poursuivre l'amĂ©lioration des connaissances sur les cellules stromales natives du tissu adipeux afin de mieux dĂ©finir la balance bĂ©nĂ©fices/risques des transferts graisseux en reconstruction mammaires.RENNES1-BU SantĂ© (352382103) / SudocSudocFranceF

    Comment on &quot;Augmentation mammaplasty by superolateral thoracic flap: a case report&quot;

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    Vertical Body Lift: Surgical Technique and Comparison with the Inferior Body Lift Technique

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