User menu

Accès à distance ? S'identifier sur le proxy UCLouvain

Regenerative immunology: the immunological reaction to biomaterials.

  1. Orlando Giuseppe, Soker Shay, Stratta Robert J., Organ Bioengineering and Regeneration as the New Holy Grail for Organ Transplantation : , 10.1097/sla.0b013e31829c79cf
  2. Hynes R. O., The Extracellular Matrix: Not Just Pretty Fibrils, 10.1126/science.1176009
  3. Meng Fan Wei, Slivka Peter F., Dearth Christopher L., Badylak Stephen F., Solubilized extracellular matrix from brain and urinary bladder elicits distinct functional and phenotypic responses in macrophages, 10.1016/j.biomaterials.2014.12.044
  4. Morris Aaron H., Stamer D.K., Kyriakides T.R., The host response to naturally-derived extracellular matrix biomaterials, 10.1016/j.smim.2017.01.002
  5. Leifer Cynthia A., Dendritic cells in host response to biologic scaffolds, 10.1016/j.smim.2017.01.001
  6. Galili Uri, Avoiding Detrimental Human Immune Response Against Mammalian Extracellular Matrix Implants, 10.1089/ten.teb.2014.0392
  7. Bharat Ankit, Mohanakumar T., Immune Responses to Tissue-Restricted Nonmajor Histocompatibility Complex Antigens in Allograft Rejection, 10.1155/2017/6312514
  8. Mano J.F., Silva G.A., Azevedo H.S., Malafaya P.B., Sousa R.A., Silva S.S., Boesel L.F., Oliveira J.M., Santos T.C., Marques A.P., Neves N.M., Reis R.L., Natural origin biodegradable systems in tissue engineering and regenerative medicine: present status and some moving trends, 10.1098/rsif.2007.0220
  9. Kim Jaeyun, Li Weiwei Aileen, Choi Youngjin, Lewin Sarah A, Verbeke Catia S, Dranoff Glenn, Mooney David J, Injectable, spontaneously assembling, inorganic scaffolds modulate immune cells in vivo and increase vaccine efficacy, 10.1038/nbt.3071
  10. Singh Ankur, Peppas Nicholas A., Hydrogels and Scaffolds for Immunomodulation, 10.1002/adma.201402105
  11. Shao Kun, Singha Santiswarup, Clemente-Casares Xavier, Tsai Sue, Yang Yang, Santamaria Pere, Nanoparticle-Based Immunotherapy for Cancer, 10.1021/nn5062029
  12. Anderson James M., Rodriguez Analiz, Chang David T., Foreign body reaction to biomaterials, 10.1016/j.smim.2007.11.004
  13. Velnar, Bosn J Basic Med Sci, 16, 82 (2016)
  14. Diegelmann Robert, F., Wound healing: an overview of acute, fibrotic and delayed healing, 10.2741/1184
  15. Hunt, Adv Skin Wound Care, 13, 6 (2000)
  16. Silva Joana M., Zupancic Eva, Vandermeulen Gaëlle, Oliveira Vanessa G., Salgado Ana, Videira Mafalda, Gaspar Manuela, Graca Luis, Préat Véronique, Florindo Helena F., In vivo delivery of peptides and Toll-like receptor ligands by mannose-functionalized polymeric nanoparticles induces prophylactic and therapeutic anti-tumor immune responses in a melanoma model, 10.1016/j.jconrel.2014.11.033
  17. Hubbell Jeffrey A., Thomas Susan N., Swartz Melody A., Materials engineering for immunomodulation, 10.1038/nature08604
  18. Rayahin Jamie E., Gemeinhart Richard A., Activation of Macrophages in Response to Biomaterials, Results and Problems in Cell Differentiation (2017) ISBN:9783319540894 p.317-351, 10.1007/978-3-319-54090-0_13
  19. Platz Joseph, Bonenfant Nicholas R., Uhl Franziska E., Coffey Amy L., McKnight Tristan, Parsons Charles, Sokocevic Dino, Borg Zachary D., Lam Ying-Wai, Deng Bin, Fields Julia G., DeSarno Michael, Loi Roberto, Hoffman Andrew M., Bianchi John, Dacken Brian, Petersen Thomas, Wagner Darcy E., Weiss Daniel J., Comparative Decellularization and Recellularization of Wild-Type and Alpha 1,3 Galactosyltransferase Knockout Pig Lungs: A Model forEx VivoXenogeneic Lung Bioengineering and Transplantation, 10.1089/ten.tec.2016.0109
  20. Duisit Jérôme, Orlando Giuseppe, Debluts Donovan, Maistriaux Louis, Xhema Daela, de Bisthoven Yann-Alex J., Galli Cesare, Peloso Andrea, Behets Catherine, Lengelé Benoît, Gianello Pierre, Decellularization of the Porcine Ear Generates a Biocompatible, Nonimmunogenic Extracellular Matrix Platform for Face Subunit Bioengineering : , 10.1097/sla.0000000000002181
  21. Gifford Sheyna, Zambon Joao Paulo, Orlando Giuseppe, Recycling organs – growing tailor-made replacement kidneys, 10.2217/rme.15.60
  22. Peloso Andrea, Petrosyan Astgik, Da Sacco Stefano, Booth Christopher, Zambon Joao Paulo, OʼBrien Timothy, Aardema Charles, Robertson John, De Filippo Roger E, Soker Shay, Stratta Robert J, Perin Laura, Orlando Giuseppe, Renal Extracellular Matrix Scaffolds From Discarded Kidneys Maintain Glomerular Morphometry and Vascular Resilience and Retains Critical Growth Factors : , 10.1097/tp.0000000000000811
  23. Peloso Andrea, Dhal Abritee, Zambon Joao P, Li Peng, Orlando Giuseppe, Atala Anthony, Soker Shay, Current achievements and future perspectives in whole-organ bioengineering, 10.1186/s13287-015-0089-y
  24. Ren Xi, Moser Philipp T, Gilpin Sarah E, Okamoto Tatsuya, Wu Tong, Tapias Luis F, Mercier Francois E, Xiong Linjie, Ghawi Raja, Scadden David T, Mathisen Douglas J, Ott Harald C, Engineering pulmonary vasculature in decellularized rat and human lungs, 10.1038/nbt.3354
  25. Guyette Jacques P., Charest Jonathan M., Mills Robert W., Jank Bernhard J., Moser Philipp T., Gilpin Sarah E., Gershlak Joshua R., Okamoto Tatsuya, Gonzalez Gabriel, Milan David J., Gaudette Glenn R., Ott Harald C., Bioengineering Human Myocardium on Native Extracellular MatrixNovelty and Significance, 10.1161/circresaha.115.306874
  26. Mazza Giuseppe, Rombouts Krista, Rennie Hall Andrew, Urbani Luca, Vinh Luong Tu, Al-Akkad Walid, Longato Lisa, Brown David, Maghsoudlou Panagiotis, Dhillon Amar P., Fuller Barry, Davidson Brian, Moore Kevin, Dhar Dipok, De Coppi Paolo, Malago Massimo, Pinzani Massimo, Decellularized human liver as a natural 3D-scaffold for liver bioengineering and transplantation, 10.1038/srep13079
  27. Zhou Qian, Li Lanjuan, Li Jun, Stem cells with decellularized liver scaffolds in liver regeneration and their potential clinical applications, 10.1111/liv.12581
  28. Macchiarini Paolo, Jungebluth Philipp, Go Tetsuhiko, Asnaghi M Adelaide, Rees Louisa E, Cogan Tristan A, Dodson Amanda, Martorell Jaume, Bellini Silvia, Parnigotto Pier Paolo, Dickinson Sally C, Hollander Anthony P, Mantero Sara, Conconi Maria Teresa, Birchall Martin A, Clinical transplantation of a tissue-engineered airway, 10.1016/s0140-6736(08)61598-6
  29. Wilshaw Stacy-Paul, Kearney John, Fisher John, Ingham Eileen, Biocompatibility and Potential of Acellular Human Amniotic Membrane to Support the Attachment and Proliferation of Allogeneic Cells, 10.1089/tea.2007.0145
  30. Muhamed Jaseer, Revi Deepa, Rajan Akhila, Geetha Surendran, Anilkumar Thapasimuthu V., Biocompatibility and Immunophenotypic Characterization of a Porcine Cholecyst–derived Scaffold Implanted in Rats, 10.1177/0192623314550722
  31. Orlando Giuseppe, Farney Alan C., Iskandar Samy S., Mirmalek-Sani Sayed-Hadi, Sullivan David C., Moran Emma, AbouShwareb Tamer, De Coppi Paolo, Wood Kathryn J., Stratta Robert J., Atala Anthony, Yoo James J., Soker Shay, Production and Implantation of Renal Extracellular Matrix Scaffolds From Porcine Kidneys as a Platform for Renal Bioengineering Investigations : , 10.1097/sla.0b013e31825a02ab
  32. Tondreau Maxime Y., Laterreur Véronique, Vallières Karine, Gauvin Robert, Bourget Jean-Michel, Tremblay Catherine, Lacroix Dan, Germain Lucie, Ruel Jean, Auger Francois A., In VivoRemodeling of Fibroblast-Derived Vascular Scaffolds Implanted for 6 Months in Rats, 10.1155/2016/3762484
  33. Summers Charlotte, Rankin Sara M., Condliffe Alison M., Singh Nanak, Peters A. Michael, Chilvers Edwin R., Neutrophil kinetics in health and disease, 10.1016/j.it.2010.05.006
  34. Smith, J Leukoc Biol, 56, 672 (1994)
  35. Chistiakov Dimitry A., Bobryshev Yuri V., Orekhov Alexander N., Neutrophil's weapons in atherosclerosis, 10.1016/j.yexmp.2015.11.011
  36. Brinkmann V., Neutrophil Extracellular Traps Kill Bacteria, 10.1126/science.1092385
  37. HERNIGOU PH., MATHIEU G., POIGNARD A., MANICOM O., BEAUJEAN F., ROUARD H., Percutaneous Autologous Bone-Marrow Grafting for Nonunions : Surgical Technique, 10.2106/00004623-200609001-00015
  38. Soehnlein O., Multiple Roles for Neutrophils in Atherosclerosis, 10.1161/circresaha.111.257535
  39. Murray Peter J., Allen Judith E., Biswas Subhra K., Fisher Edward A., Gilroy Derek W., Goerdt Sergij, Gordon Siamon, Hamilton John A., Ivashkiv Lionel B., Lawrence Toby, Locati Massimo, Mantovani Alberto, Martinez Fernando O., Mege Jean-Louis, Mosser David M., Natoli Gioacchino, Saeij Jeroen P., Schultze Joachim L., Shirey Kari Ann, Sica Antonio, Suttles Jill, Udalova Irina, van Ginderachter Jo A., Vogel Stefanie N., Wynn Thomas A., Macrophage Activation and Polarization: Nomenclature and Experimental Guidelines, 10.1016/j.immuni.2014.06.008
  40. MANTOVANI A, SICA A, SOZZANI S, ALLAVENA P, VECCHI A, LOCATI M, The chemokine system in diverse forms of macrophage activation and polarization, 10.1016/j.it.2004.09.015
  41. Gordon Siamon, Taylor Philip R., Monocyte and macrophage heterogeneity, 10.1038/nri1733
  42. Pinto M.L., Rios E., Silva A.C., Neves S.C., Caires H.R., Pinto A.T., Durães C., Carvalho F.A., Cardoso A.P., Santos N.C., Barrias C.C., Nascimento D.S., Pinto-do-Ó P., Barbosa M.A., Carneiro F., Oliveira M.J., Decellularized human colorectal cancer matrices polarize macrophages towards an anti-inflammatory phenotype promoting cancer cell invasion via CCL18, 10.1016/j.biomaterials.2017.02.004
  43. Mimura Kallyne K. O., Moraes Andréia R., Miranda Aline C., Greco Rebecca, Ansari Tahera, Sibbons Paul, Greco Karin V., Oliani Sonia M., Mechanisms underlying heterologous skin scaffold-mediated tissue remodeling, 10.1038/srep35074
  44. Brown Bryan N., Ratner Buddy D., Goodman Stuart B., Amar Salomon, Badylak Stephen F., Macrophage polarization: An opportunity for improved outcomes in biomaterials and regenerative medicine, 10.1016/j.biomaterials.2012.02.034
  45. Badylak Stephen F., Gilbert Thomas W., Immune response to biologic scaffold materials, 10.1016/j.smim.2007.11.003
  46. Wolf Matthew T., Dearth Christopher L., Ranallo Christian A., LoPresti Samuel T., Carey Lisa E., Daly Kerry A., Brown Bryan N., Badylak Stephen F., Macrophage polarization in response to ECM coated polypropylene mesh, 10.1016/j.biomaterials.2014.04.115
  47. Petrosyan Astgik, Da Sacco Stefano, Tripuraneni Nikita, Kreuser Ursula, Lavarreda-Pearce Maria, Tamburrini Riccardo, De Filippo Roger E., Orlando Giuseppe, Cravedi Paolo, Perin Laura, A step towards clinical application of acellular matrix: A clue from macrophage polarization, 10.1016/j.matbio.2016.08.009
  48. Fishman J. M., Lowdell M. W., Urbani L., Ansari T., Burns A. J., Turmaine M., North J., Sibbons P., Seifalian A. M., Wood K. J., Birchall M. A., De Coppi P., Immunomodulatory effect of a decellularized skeletal muscle scaffold in a discordant xenotransplantation model, 10.1073/pnas.1213228110
  49. Bollyky P. L., Wu R. P., Falk B. A., Lord J. D., Long S. A., Preisinger A., Teng B., Holt G. E., Standifer N. E., Braun K. R., Xie C. F., Samuels P. L., Vernon R. B., Gebe J. A., Wight T. N., Nepom G. T., ECM components guide IL-10 producing regulatory T-cell (TR1) induction from effector memory T-cell precursors, 10.1073/pnas.1017360108
  50. Bollyky P. L., Falk B. A., Wu R. P., Buckner J. H., Wight T. N., Nepom G. T., Intact extracellular matrix and the maintenance of immune tolerance: high molecular weight hyaluronan promotes persistence of induced CD4+CD25+ regulatory T cells, 10.1189/jlb.0109001
  51. Thomas, Exp Biol Med (Maywood), 232, 406 (2007)
  52. Hall B. M., T Cells: Soldiers and Spies--The Surveillance and Control of Effector T Cells by Regulatory T Cells, 10.2215/cjn.06620714
  53. Gordon Siamon, Alternative activation of macrophages, 10.1038/nri978
  54. Allman Amy J., McPherson Timothy B., Badylak Stephen F., Merrill Lisa C., Kallakury Bhaskar, Sheehan Christine, Raeder Roberta H., Metzger Dennis W., XENOGENEIC EXTRACELLULAR MATRIX GRAFTS ELICIT A TH2-RESTRICTED IMMUNE RESPONSE1 : , 10.1097/00007890-200106150-00024
  55. Aachoui Youssef, Ghosh Swapan K., Extracellular Matrix from Porcine Small Intestinal Submucosa (SIS) as Immune Adjuvants, 10.1371/journal.pone.0027083
  56. Peloso Andrea, Urbani Luca, Cravedi Paolo, Katari Ravi, Maghsoudlou Panagiotis, Fallas Mario Enrique Alvarez, Sordi Valeria, Citro Antonio, Purroy Carolina, Niu Guoguang, McQuilling John P., Sittadjody Sivanandane, Farney Alan C., Iskandar Samy S., Zambon Joao P., Rogers Jeffrey, Stratta Robert J., Opara Emmanuel C., Piemonti Lorenzo, Furdui Cristina M., Soker Shay, De Coppi Paolo, Orlando Giuseppe, The Human Pancreas as a Source of Protolerogenic Extracellular Matrix Scaffold for a New-generation Bioartificial Endocrine Pancreas : , 10.1097/sla.0000000000001364
  57. Mirmalek-Sani Sayed-Hadi, Sullivan David C., Zimmerman Cynthia, Shupe Thomas D., Petersen Bryon E., Immunogenicity of Decellularized Porcine Liver for Bioengineered Hepatic Tissue, 10.1016/j.ajpath.2013.05.002
  58. Sun Lei, Yi Shounan, O'Connell Philip J, IL-10 is required for human CD4+CD25+ regulatory T cell-mediated suppression of xenogeneic proliferation, 10.1038/icb.2009.117
  59. Wu Jingjing, Yi Shounan, Ouyang Li, Jimenez Elvira, Simond Denbigh, Wang Wei, Wang Yiping, Hawthorne Wayne J., OʼConnell Philip J., In Vitro Expanded Human CD4+CD25+ Regulatory T Cells are Potent Suppressors of T-Cell-Mediated Xenogeneic Responses : , 10.1097/tp.0b013e3181734793
  60. Oh S. A., Li M. O., TGF- : Guardian of T Cell Function, 10.4049/jimmunol.1301843
  61. Tazelaar Henry D., Byrne Guerard W., McGregor Christopher G. A., Comparison of Gal and Non-Gal-Mediated Cardiac Xenograft Rejection : , 10.1097/tp.0b013e318212c7fe
  62. Chen Gang, Qian Hua, Starzl Thomas, Sun Hongtao, Garcia Bertha, Wang Ximo, Wise Yishai, Liu Yuanqing, Xiang Ying, Copeman Laura, Liu Weihua, Jevnikar Anthony, Wall William, Cooper David K C, Murase Noriko, Dai Yifan, Wang Wanyu, Xiong Yuliang, White David J, Zhong Robert, Acute rejection is associated with antibodies to non-Gal antigens in baboons using Gal-knockout pig kidneys, 10.1038/nm1330
  63. Galili U., Human natural anti-alpha-galactosyl IgG. II. The specific recognition of alpha (1----3)-linked galactose residues, 10.1084/jem.162.2.573
  64. Galili, J Biol Chem, 263, 17755 (1988)
  65. Galili Uri, Interaction of the natural anti-Gal antibody with α-galactosyl epitopes: a major obstacle for xenotransplantation in humans, 10.1016/0167-5699(93)90261-i
  66. Maruyama, Kidney Int, 57, 655 (2000)
  67. Park Seongsik, Kim Woong-Han, Choi Sun-Young, Kim Yong-Jin, Removal of Alpha-Gal Epitopes from Porcine Aortic Valve and Pericardium using Recombinant Human Alpha Galactosidase A, 10.3346/jkms.2009.24.6.1126
  68. Xu Hui, Wan Hua, Zuo Wenqi, Sun Wendell, Owens Rick T., Harper John R., Ayares David L., McQuillan David J., A Porcine-Derived Acellular Dermal Scaffold That Supports Soft Tissue Regeneration: Removal of Terminal Galactose-α-(1,3)-Galactose and Retention of Matrix Structure, 10.1089/ten.tea.2008.0384
  69. Wong Maelene L., Griffiths Leigh G., Immunogenicity in xenogeneic scaffold generation: Antigen removal vs. decellularization, 10.1016/j.actbio.2014.01.028
  70. Galili Uri, Anti-Gal: an abundant human natural antibody of multiple pathogeneses and clinical benefits, 10.1111/imm.12110
Bibliographic reference Cravedi, Paolo ; Farouk, Samira ; Angeletti, Andrea ; Edgar, Lauren ; Tamburrini, Riccardo ; et. al. Regenerative immunology: the immunological reaction to biomaterials.. In: Transplant International, Vol. 30, no. 12, p. 1199-1208 (2017)
Permanent URL http://hdl.handle.net/2078.1/191380