Dr Mathieu-Benoit VoisinSenior Lecturer in Immunology Centre: Microvascular Research Email: m.b.voisin@qmul.ac.ukTelephone: +44(0) 20 7882 3909ProfileResearchPublicationsSponsorsCollaboratorsNewsProfileORCID iD: 0000-0003-3001-0894 Mathieu-Benoit Voisin graduated in 2000 from the University of Bordeaux II (France) in Biological Sciences with a specialisation in Immunology. He obtained his PhD from the University of Tours (France) in 2003 and conducted post-doctoral research at Imperial College London. In 2007, he relocated with Prof Nourshargh to the William Harvey Research Institute to investigate the mechanisms of leukocyte diapedesis through blood vessels, developing new imaging techniques to visualise the responses. His work lead him to receive the Werner Risau New Investigator Award in Vascular Biology in 2010. In 2012 he was the recipient of the prestigious Versus Arthritis Career Development Fellowship to establish his own independent research programme studying neutrophil migration and functions in the lymphatic & lymphoid system. Since 2017, Dr Voisin is a Principal Investigator and Senior Lecturer in Immunology at the Centre for Microvascular Research. ResearchGroup members Researcher/Staff: Dr Jonathon Alexis Coates; Ms Julia Dielesen (PhD Student) Summary Neutrophils are key effectors of the innate immune response but can also contribute to the development of many acute inflammatory diseases. There is also evidence for neutrophil involvement in the regulation of the adaptive immunity and the pathogenesis of numerous chronic inflammatory conditions such as rheumatoid arthritis. The precise role of neutrophils in this autoimmune disorder is unclear and the focus of my research is to elucidate the mechanisms of neutrophil migration into lymphatic vessels and lymph nodes following antigen-induced arthritis and their role in the regulation of the acquired immunity. The main hypothesis is that neutrophil entry into lymphatic vessels plays an important role in the initiation of autoimmune diseases by changes in their phenotypes and their entry to the lymphatic vascular system. The project thus aims to characterize the mechanisms of neutrophil/lymphatic vessel interactions in vivo as analyzed by intravital confocal microscopy and the implications of this response to the development of arthritis. Collectively, the project will address a previously unexplored aspect of leukocyte biology and chronic disorders thus making a significant and novel contribution to the field of inflammation. Publications Rolas L, Stein M, Barkaway A et al. (2024). Senescent endothelial cells promote pathogenic neutrophil trafficking in inflamed tissues. nameOfConference DOI: 10.1038/s44319-024-00182-x QMRO: https://qmro.qmul.ac.uk/xmlui/handle/123456789/98188 Caxaria S, Bharde S, Fuller AM et al. (2023). Neutrophils infiltrate sensory ganglia and mediate chronic widespread pain in fibromyalgia. nameOfConference DOI: 10.1073/pnas.2211631120 QMRO: https://qmro.qmul.ac.uk/xmlui/handle/123456789/86231 Joulia R, Guerrero-Fonseca IM, Girbl T et al. (publicationYear). Neutrophil breaching of the blood vessel pericyte layer during diapedesis requires mast cell-derived IL-17A. nameOfConference DOI: 10.1038/s41467-022-34695-7 QMRO: https://qmro.qmul.ac.uk/xmlui/handle/123456789/82420 Iqbal AJ, Krautter F, Blacksell IA et al. (2022). Galectin‐9 mediates neutrophil capture and adhesion in a CD44 and β2 integrin‐dependent manner. nameOfConference DOI: 10.1096/fj.202100832r QMRO: https://qmro.qmul.ac.uk/xmlui/handle/123456789/76220 Reglero-Real N, Pérez-Gutiérrez L, Yoshimura A et al. (2021). Autophagy modulates endothelial junctions to restrain neutrophil diapedesis during inflammation. nameOfConference DOI: 10.1016/j.immuni.2021.07.012 QMRO: https://qmro.qmul.ac.uk/xmlui/handle/123456789/74480 Barkaway A, Rolas L, Joulia R et al. (2021). Age-related changes in the local milieu of inflamed tissues cause aberrant neutrophil trafficking and subsequent remote organ damage. nameOfConference DOI: 10.1016/j.immuni.2021.04.025 QMRO: https://qmro.qmul.ac.uk/xmlui/handle/123456789/72327 Topping LM, Thomas BL, Rhys HI et al. (2020). Targeting Extracellular Vesicles to the Arthritic Joint Using a Damaged Cartilage-Specific Antibody. nameOfConference DOI: 10.3389/fimmu.2020.00010 QMRO: https://uat2-qmro.qmul.ac.uk/xmlui/handle/123456789/63161 Owen-Woods C, Joulia R, Barkaway A et al. (2020). Local microvascular leakage promotes trafficking of activated neutrophils to remote organs. nameOfConference DOI: 10.1172/JCI133661 QMRO: https://uat2-qmro.qmul.ac.uk/xmlui/handle/123456789/62838 Arokiasamy S, King R, Boulaghrasse H et al. (2019). Heparanase-dependent Remodelling of Initial Lymphatic Glycocalyx 1 Regulates Tissue-fluid Drainage during Acute Inflammation in vivo. nameOfConference DOI: 10.3389/fimmu.2019.02316 QMRO: https://uat2-qmro.qmul.ac.uk/xmlui/handle/123456789/60002 VOISIN M, leoni G, WOODFIN A et al. (2019). Neutrophil elastase plays a non-redundant role in remodeling the venular basement membrane and neutrophil diapedesis post ischemia/reperfusion injury. nameOfConference DOI: 10.1002/path.5234 QMRO: https://uat2-qmro.qmul.ac.uk/xmlui/handle/123456789/54857 Voisin M, Nourshargh S (2019). Neutrophil trafficking to lymphoid tissues: physiological and pathological implications. nameOfConference DOI: 10.1002/path.5227 QMRO: https://uat2-qmro.qmul.ac.uk/xmlui/handle/123456789/54509 GIRBL T, Lenn T, Perez L et al. (publicationYear). Distinct compartmentalization of the chemokines CXCL1 and CXCL2 and the atypical receptor ACKR1 determine discrete stages of neutrophil diapedesis. nameOfConference DOI: 10.1016/j.immuni.2018.09.018 QMRO: https://uat2-qmro.qmul.ac.uk/xmlui/handle/123456789/50484 Macdougall CE, Wood EG, Loschko J et al. (2018). Visceral Adipose Tissue Immune Homeostasis Is Regulated by the Crosstalk between Adipocytes and Dendritic Cell Subsets. nameOfConference DOI: 10.1016/j.cmet.2018.02.007 QMRO: https://uat2-qmro.qmul.ac.uk/xmlui/handle/123456789/36587 Arokiasamy S, Nourshargh S, Wang W et al. (2017). Characterisation of the lymphatic endothelium glycocalyx and its regulation during acute inflammation in vivo. NA DOI: doi QMRO: qmroHref Barkaway A, Rolas L, Morrell S et al. (2017). Aged Vasculature Supports Enhanced and Aberrant Neutrophil-Vessel Wall Interactions in vivo. 2nd Joint Meeting of the European-Society-for-Microcirculation (ESM) and European-Vascular-Biology-Organisation (EVBO) DOI: doi QMRO: qmroHref King R, Morrell S, Nedospasov S et al. (2017). An Investigation Into the Role of Neutrophil-Derived TNF in Pathophysiological Microvascular Hyperpermeability. 2nd Joint Meeting of the European-Society-for-Microcirculation (ESM) and European-Vascular-Biology-Organisation (EVBO) DOI: doi QMRO: qmroHref Voisin MB (2017). TNF-alpha drives the migration and crawling of neutrophils into afferent lymphatic vessels during antigen challenge in vivo. 51st Annual Scientific Meeting of the European Society for Clinical Investigation DOI: doi QMRO: qmroHref VOISIN M (2017). Endogenous TNFα orchestrates the trafficking of neutrophils into and within lymphatic vessels during acute inflammation. nameOfConference DOI: 10.1038/srep44189 QMRO: https://uat2-qmro.qmul.ac.uk/xmlui/handle/123456789/23723 Herrera C, Voisin M-B, Escalante T et al. (2016). Effects of PI and PIII Snake Venom Haemorrhagic Metalloproteinases on the Microvasculature: A Confocal Microscopy Study on the Mouse Cremaster Muscle.. nameOfConference DOI: 10.1371/journal.pone.0168643 QMRO: https://uat2-qmro.qmul.ac.uk/xmlui/handle/123456789/18945 Pickworth CM, Beal R, Reglero N et al. (2016). Microvascular endothelial cells can exhibit autophagy in vivo: Role in neutrophil transendothelial cell migration?. Experimental Biology Meeting DOI: 10.1096/fasebj.30.1_supplement.165.8 QMRO: qmroHref Schnoor M, Alcaide P, Voisin M-B et al. (2016). Recruitment of Immune Cells into Inflamed Tissues: Consequences for Endothelial Barrier Integrity and Tissue Functionality. nameOfConference DOI: 10.1155/2016/1561368 QMRO: https://uat2-qmro.qmul.ac.uk/xmlui/handle/123456789/18621 Woodfin A, Beyrau M, Voisin M-B et al. (2016). ICAM-1–expressing neutrophils exhibit enhanced effector functions in murine models of endotoxemia. nameOfConference DOI: 10.1182/blood-2015-08-664995 QMRO: https://uat2-qmro.qmul.ac.uk/xmlui/handle/123456789/13894 Schnoor M, Alcaide P, Voisin M-B et al. (2015). Crossing the Vascular Wall: Common and Unique Mechanisms Exploited by Different Leukocyte Subsets during Extravasation. nameOfConference DOI: 10.1155/2015/946509 QMRO: https://uat2-qmro.qmul.ac.uk/xmlui/handle/123456789/18513 Herrera C, Escalante T, Voisin M-B et al. (publicationYear). Tissue Localization and Extracellular Matrix Degradation by PI, PII and PIII Snake Venom Metalloproteinases: Clues on the Mechanisms of Venom-Induced Hemorrhage. nameOfConference DOI: 10.1371/journal.pntd.0003731 QMRO: https://uat2-qmro.qmul.ac.uk/xmlui/handle/123456789/9775 Finsterbusch M, Voisin M-B, Beyrau M et al. (2014). Neutrophils recruited by chemoattractants in vivo induce microvascular plasma protein leakage through secretion of TNF.. nameOfConference DOI: 10.1084/jem.20132413 QMRO: https://uat2-qmro.qmul.ac.uk/xmlui/handle/123456789/13892 Colom B, Bodkin J, Voisin MB et al. (2013). Junctional adhesion molecule (JAM)-C can be cleaved by neutrophil elastase at sites of inflammation in vivo. nameOfConference DOI: doi QMRO: qmroHref Voisin M-B, Nourshargh S (2013). Neutrophil transmigration: emergence of an adhesive cascade within venular walls.. nameOfConference DOI: 10.1159/000346659 QMRO: qmroHref Proebstl D, Voisin M-B, Woodfin A et al. (2012). Pericytes support neutrophil subendothelial cell crawling and breaching of venular walls in vivo.. nameOfConference DOI: 10.1084/jem.20111622 QMRO: https://uat2-qmro.qmul.ac.uk/xmlui/handle/123456789/14750 Woodfin A, Voisin M-B, Beyrau M et al. (2011). The junctional adhesion molecule JAM-C regulates polarized transendothelial migration of neutrophils in vivo.. nameOfConference DOI: 10.1038/ni.2062 QMRO: https://uat2-qmro.qmul.ac.uk/xmlui/handle/123456789/19663 Leoni G, Voisin M-B, Carlson K et al. (2010). The melanocortin MC(1) receptor agonist BMS-470539 inhibits leucocyte trafficking in the inflamed vasculature.. nameOfConference DOI: 10.1111/j.1476-5381.2010.00688.x QMRO: qmroHref Woodfin A, Voisin M-B, Colom B et al. (2010). An investigation into the profile and dynamics of neutrophil transendothelial cell migration (TEM) using high resolution in vivo real-time confocal imaging. nameOfConference DOI: 10.1096/fasebj.24.1_supplement.232.2 QMRO: qmroHref Woodfin A, Voisin M-B, Nourshargh S (2010). Recent developments and complexities in neutrophil transmigration.. nameOfConference DOI: 10.1097/MOH.0b013e3283333930 QMRO: qmroHref Voisin M-B, Pröbstl D, Nourshargh S (2010). Venular basement membranes ubiquitously express matrix protein low-expression regions: characterization in multiple tissues and remodeling during inflammation.. nameOfConference DOI: 10.2353/ajpath.2010.090510 QMRO: qmroHref Scheiermann C, Colom B, Meda P et al. (2009). Junctional adhesion molecule-C mediates leukocyte infiltration in response to ischemia reperfusion injury.. nameOfConference DOI: 10.1161/ATVBAHA.109.187559 QMRO: qmroHref Voisin M-B, Woodfin A, Nourshargh S (2009). Monocytes and neutrophils exhibit both distinct and common mechanisms in penetrating the vascular basement membrane in vivo.. nameOfConference DOI: 10.1161/ATVBAHA.109.187450 QMRO: qmroHref Woodfin A, Voisin MB, Imhof BA et al. (2009). Endothelial cell activation leads to neutrophil transmigration as supported by the sequential roles of ICAM-2, JAM-A, and PECAM-1. nameOfConference DOI: 10.1182/blood-2008-11188375 QMRO: qmroHref Woodfin A, Voisin M-B, Imhof BA et al. (2009). Endothelial cell activation leads to neutrophil transmigration as supported by the sequential roles of ICAM-2, JAM-A, and PECAM-1.. nameOfConference DOI: 10.1182/blood-2008-11-188375 QMRO: qmroHref Proebstl D, Voisin M-B, Nourshargh S (2009). Pericytes facilitate leukocyte transmigration in vivo. nameOfConference DOI: 10.1096/fasebj.23.1_supplement.360.1 QMRO: qmroHref Woodfin A, Voisin M-B, Nourshargh S (2007). PECAM-1: a multi-functional molecule in inflammation and vascular biology.. nameOfConference DOI: 10.1161/ATVBAHA.107.151456 QMRO: qmroHref Woodfin A, Reichel CA, Khandoga A et al. (2007). JAM-A mediates neutrophil transmigration in a stimulus-specific manner in vivo: evidence for sequential roles for JAM-A and PECAM-1 in neutrophil transmigration.. nameOfConference DOI: 10.1182/blood-2006-09-047431 QMRO: qmroHref Young RE, Voisin M-B, Wang S et al. (2007). Role of neutrophil elastase in LTB4-induced neutrophil transmigration in vivo assessed with a specific inhibitor and neutrophil elastase deficient mice.. nameOfConference DOI: 10.1038/sj.bjp.0707267 QMRO: qmroHref Voisin MB, Woodfin A, Nourshargh S (2007). Neutrophil and monocyte transmigration elicited by ischemia/reperfusion (I/R) injury and CCL2 is associated with remodelling of the venular basement membrane (BM) in vivo. nameOfConference DOI: 10.1096/fasebj.21.5.a127-a QMRO: qmroHref Wang S, Voisin M-B, Larbi KY et al. (2006). Venular basement membranes contain specific matrix protein low expression regions that act as exit points for emigrating neutrophils.. nameOfConference DOI: 10.1084/jem.20051210 QMRO: https://uat2-qmro.qmul.ac.uk/xmlui/handle/123456789/18599 Voisin MB, Woodfin A, Dawes T et al. (2006). Neutrophil elastase (NE) deficient mice exhibit reduced leukocyte transmigration in response to ischaemia/reperfusion (I/R) injury. nameOfConference DOI: 10.1096/fasebj.20.5.a1083-c QMRO: qmroHref Voisin MB, Wang SJ, Larbi K et al. (2006). Neutrophils play a direct role in enhancing the size of venular basement membrane (BM) matrix protein low expression regions. nameOfConference DOI: 10.1096/fasebj.20.5.a1322-b QMRO: qmroHref Voisin MB, Young R, Dangerfield J et al. (2005). LTB4 is a potent inducer of cell surface neutrophil elastase (NE), a response that appears to play a role in LTB4-induced neutrophil transmigration in vivo. nameOfConference DOI: doi QMRO: qmroHref Wang SJ, Dangerfield J, Voisin MB et al. (2005). Pre-formed matrix protein "low expression" regions act as exit points for leukocytes migrating through the venular perivascular basement membrane. nameOfConference DOI: doi QMRO: qmroHref Voisin M-B, Buzoni-Gatel D, Bout D et al. (2004). Both expansion of regulatory GR1+ CD11b+ myeloid cells and anergy of T lymphocytes participate in hyporesponsiveness of the lung-associated immune system during acute toxoplasmosis.. nameOfConference DOI: 10.1128/IAI.72.9.5487-5492.2004 QMRO: qmroHref Voisin M-B, Bitard J, Daburon S et al. (2002). Separate functions for the two modules of the membrane-proximal cytokine binding domain of glycoprotein 190, the leukemia inhibitory factor low affinity receptor, in ligand binding and receptor activation.. nameOfConference DOI: 10.1074/jbc.M111624200 QMRO: qmroHref Sponsors British Heart Foundation William Harvey Research Foundation Versus Arthritis (Formerly Arthritis Research UK) CollaboratorsInternal Prof S. Nourshargh (WHRI) Prof C. Pitzalis (WHRI) Prof M. Perretti (WHRI) Dr P Longhi (WHRI) Prof A Nissim (WHRI) Prof F Marelli-Berg (WHRI) Dr M. Capasso (BCI) Dr Esther Castellano Sanchez (BCI) External Prof Q. Sattentau (Oxford) Prof R Chambers (UCL) Prof J Greenwood (UCL) Prof J. Gutierrez (Costa Rica) Prof Ed Rainger (University of Birmingham) News Dr. Mathieu-Benoit Voisin awarded Arthritis Research UK Fellowship (January 2012). Dr. Mathieu-Benoit Voisin awarded Young Investigator Award (Best oral presentation) at the international meeting of “Neutrophil in Immunity”, Quebec, Canada (June 2012). Back to top