Update on the mechanisms of action of anti‑TNF-α antibodies and their clinical implications in inflammatory bowel disease.

The mechanisms of action of antitumor necrosis factor α (anti-TNF-α) antibodies in the therapy of inflammatory bowel disease (IBD) are not completely understood. Binding of antibodies to transmembrane TNF-α seems to be crucial for the induction of several cellular responses, including complement-dependent cytotoxicity, antibody-dependent cellular cytotoxicity, and reverse signaling. However, these processes alone do not fully explain the diversity of responses to anti-TNF-α therapy seen in different patients. Thus, the present review aimed to discuss the current role of anti-TNF-α antibodies in treatment algorithms for IBD as well as the current knowledge on the mechanisms of action of these antibodies, particularly the less well known aspects of anti-TNF-α blockade. We also discussed a complex role of particular macrophage subpopulations, T regulatory cells, and intestinal endothelial cells, as well as presented new data on the clinical relevance of anti-inflammatory responses attributed to the Fc region of anti-TNF-α antibodies.

[1]  I. Krela-kaźmierczak,et al.  An increase in serum tumour necrosis factor-α during anti-tumour necrosis factor-α therapy for Crohn's disease - A paradox or a predictive index? , 2016, Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver.

[2]  G. R. van den Brink,et al.  Mechanism of Action of Anti-TNF Therapy in Inflammatory Bowel Disease. , 2016, Journal of Crohn's & colitis.

[3]  P. Rutgeerts,et al.  Maintenance of Efficacy and Continuing Safety of Golimumab for Active Ulcerative Colitis: PURSUIT-SC Maintenance Study Extension Through 1 Year , 2016, Clinical and Translational Gastroenterology.

[4]  Luca Tiano,et al.  Anti-TNF-α treatment modulates SASP and SASP-related microRNAs in endothelial cells and in circulating angiogenic cells , 2016, Oncotarget.

[5]  G. D'Haens,et al.  Autophagy Contributes to the Induction of Anti-TNF Induced Macrophages. , 2016, Journal of Crohn's & colitis.

[6]  R. Cohen,et al.  Approach to Optimize Anti-TNF-α Therapy in Patients With IBD , 2016, Current Treatment Options in Gastroenterology.

[7]  Frank I. Scott,et al.  Advances in Therapeutic Drug Monitoring of Biologic Therapies in Inflammatory Bowel Disease: 2015 in Review , 2016, Current Treatment Options in Gastroenterology.

[8]  G. D'Haens,et al.  Optimization of anti-TNF therapy in patients with Inflammatory Bowel Disease , 2016, Expert review of clinical pharmacology.

[9]  Minhu Chen,et al.  Optimizing biologic treatment in IBD: objective measures, but when, how and how often? , 2015, BMC Gastroenterology.

[10]  A. Szymczak,et al.  Association of serum VEGF with clinical response to anti-TNFα therapy for Crohn's disease. , 2015, Cytokine.

[11]  L. Guidi,et al.  Paradoxical psoriasis in a large cohort of patients with inflammatory bowel disease receiving treatment with anti‐TNF alpha: 5‐year follow‐up study , 2015, Alimentary pharmacology & therapeutics.

[12]  L. Peyrin-Biroulet,et al.  Biologic agents for IBD: practical insights , 2015, Nature Reviews Gastroenterology &Hepatology.

[13]  A. Bitton,et al.  Risk of Lymphoma, Colorectal and Skin Cancer in Patients with IBD Treated with Immunomodulators and Biologics: A Quebec Claims Database Study , 2015, Inflammatory bowel diseases.

[14]  M. Neurath,et al.  Immunopathogenesis of inflammatory bowel diseases: functional role of T cells and T cell homing. , 2015, Clinical and experimental rheumatology.

[15]  M. Allez,et al.  Complications of biologics in inflammatory bowel disease , 2015, Current opinion in gastroenterology.

[16]  P. Eder,et al.  Angiogenesis-related proteins--their role in the pathogenesis and treatment of inflammatory bowel disease. , 2015, Current protein & peptide science.

[17]  A. Berger,et al.  Soluble CD163 is an indicator of liver inflammation and fibrosis in patients chronically infected with the hepatitis B virus , 2015, Journal of viral hepatitis.

[18]  R. Fausel,et al.  Biologics in the management of ulcerative colitis – comparative safety and efficacy of TNF-α antagonists , 2015, Therapeutics and clinical risk management.

[19]  K. Thorlund,et al.  Adalimumab versus infliximab for the treatment of moderate to severe ulcerative colitis in adult patients naïve to anti-TNF therapy: an indirect treatment comparison meta-analysis. , 2014, Journal of Crohn's & colitis.

[20]  C. Bain,et al.  Macrophages in intestinal homeostasis and inflammation , 2014, Immunological reviews.

[21]  Wolfgang Uter,et al.  In vivo imaging using fluorescent antibodies to tumor necrosis factor predicts therapeutic response in Crohn's disease , 2014, Nature Medicine.

[22]  L. Guidi,et al.  Dermatological adverse reactions during anti-TNF treatments: focus on inflammatory bowel disease. , 2013, Journal of Crohn's & colitis.

[23]  P. Rutgeerts,et al.  Recent advances: personalised use of current Crohn's disease therapeutic options , 2013, Gut.

[24]  L. Biancone,et al.  Lesional Accumulation of CD163-Expressing Cells in the Gut of Patients with Inflammatory Bowel Disease , 2013, PloS one.

[25]  G. Lichtenstein Comprehensive review: antitumor necrosis factor agents in inflammatory bowel disease and factors implicated in treatment response , 2013, Therapeutic advances in gastroenterology.

[26]  D. Conte,et al.  Reduction of CD68+ Macrophages and Decreased IL-17 Expression in Intestinal Mucosa of Patients with Inflammatory Bowel Disease Strongly Correlate With Endoscopic Response and Mucosal Healing following Infliximab Therapy , 2013, Inflammatory bowel diseases.

[27]  P. Taylor,et al.  Raised circulating tenascin-C in rheumatoid arthritis , 2012, Arthritis Research & Therapy.

[28]  A. Foussat,et al.  Safety and efficacy of antigen-specific regulatory T-cell therapy for patients with refractory Crohn's disease. , 2012, Gastroenterology.

[29]  S. Vermeire,et al.  Paradoxical inflammation induced by anti-TNF agents in patients with IBD , 2012, Nature Reviews Gastroenterology &Hepatology.

[30]  G. Rogler,et al.  Fc Gamma Receptor CD64 Modulates the Inhibitory Activity of Infliximab , 2012, PloS one.

[31]  G. Frühbeck,et al.  Increased tenascin C and Toll-like receptor 4 levels in visceral adipose tissue as a link between inflammation and extracellular matrix remodeling in obesity. , 2012, The Journal of clinical endocrinology and metabolism.

[32]  O. Dewit,et al.  Endoscopic improvement of mucosal lesions in patients with moderate to severe ileocolonic Crohn's disease following treatment with certolizumab pegol , 2012, Gut.

[33]  P. Rutgeerts,et al.  Regulatory macrophages induced by infliximab are involved in healing in vivo and in vitro , 2012, Inflammatory bowel diseases.

[34]  M. Serghini,et al.  [Efficacy and safety of Adalimumab in Crohn's disease]. , 2012, La Tunisie medicale.

[35]  Xin Chen,et al.  Contrasting effects of TNF and anti‐TNF on the activation of effector T cells and regulatory T cells in autoimmunity , 2011, FEBS letters.

[36]  R. Kiesslich,et al.  Antibodies against tumor necrosis factor (TNF) induce T-cell apoptosis in patients with inflammatory bowel diseases via TNF receptor 2 and intestinal CD14⁺ macrophages. , 2011, Gastroenterology.

[37]  S. Schreiber Certolizumab pegol for the treatment of Crohn’s disease , 2011, Therapeutic advances in gastroenterology.

[38]  H. Møller,et al.  Soluble macrophage-derived CD163 is a marker of disease activity and progression in early rheumatoid arthritis. , 2011, Clinical and experimental rheumatology.

[39]  G. Rogler,et al.  Efficacy and safety of certolizumab pegol in an unselected crohn's disease population: 26‐week data of the FACTS II survey , 2011, Inflammatory bowel diseases.

[40]  S. Rutella,et al.  Infliximab Therapy Inhibits Inflammation-Induced Angiogenesis in the Mucosa of Patients With Crohn's Disease , 2011, The American Journal of Gastroenterology.

[41]  J Michael Mathis,et al.  Role of the endothelium in inflammatory bowel diseases. , 2011, World journal of gastroenterology.

[42]  S. Benoit,et al.  Tumor necrosis factor alpha blockade exacerbates murine psoriasis-like disease by enhancing Th17 function and decreasing expansion of Treg cells. , 2010, Arthritis and rheumatism.

[43]  L. Dieleman,et al.  Long-term response rates to infliximab therapy for Crohn's disease in an outpatient cohort. , 2009, Canadian journal of gastroenterology = Journal canadien de gastroenterologie.

[44]  G. Porro,et al.  Biologic targeting in the treatment of inflammatory bowel diseases , 2009, Biologics : targets & therapy.

[45]  O. Shibolet,et al.  Infliximab in ulcerative colitis , 2008, Biologics : targets & therapy.

[46]  Takahiko Horiuchi,et al.  Mechanisms for cytotoxic effects of anti-tumor necrosis factor agents on transmembrane tumor necrosis factor alpha-expressing cells: comparison among infliximab, etanercept, and adalimumab. , 2008, Arthritis and rheumatism.

[47]  M. Vos,et al.  Early combined immunosuppression or conventional management in patients with newly diagnosed Crohn's disease: an open randomised trial , 2008, The Lancet.

[48]  P. Tak,et al.  Tumor necrosis factor antagonist mechanisms of action: a comprehensive review. , 2008, Pharmacology & therapeutics.

[49]  A. Griffiths,et al.  Induction and maintenance infliximab therapy for the treatment of moderate-to-severe Crohn's disease in children. , 2007, Gastroenterology.

[50]  I. Rosner,et al.  Increased Spontaneous Apoptosis of CD4+CD25+ T Cells in Patients with Active Rheumatoid Arthritis Is Reduced by Infliximab , 2005, Annals of the New York Academy of Sciences.

[51]  J. Belaiche,et al.  Association between polymorphism in IgG Fc receptor IIIa coding gene and biological response to infliximab in Crohn's disease , 2004, Alimentary pharmacology & therapeutics.

[52]  M. Cottone,et al.  Maintenance infliximab for Crohn's disease , 2002, The Lancet.

[53]  I. Mikaelian,et al.  Fc Receptor-mediated Effector Function Contributes to the Therapeutic Response of Anti-TNF Monoclonal Antibodies in a Mouse Model of Inflammatory Bowel Disease. , 2016, Journal of Crohn's & colitis.

[54]  L. Öhman,et al.  Response to infliximab therapy in ulcerative colitis is associated with decreased monocyte activation, reduced CCL2 expression and downregulation of Tenascin C. , 2015, Journal of Crohn's & colitis.

[55]  A. Szymczak,et al.  Calcium and phosphate metabolism in patients with inflammatory bowel diseases. , 2015, Polskie Archiwum Medycyny Wewnetrznej.

[56]  M. Neurath,et al.  Mongersen , an Oral SMAD 7 Antisense Oligonucleotide , and Crohn ’ s Disease , 2015 .

[57]  E. Kraszewska,et al.  Rising hospitalization rates for inflammatory bowel disease in Poland. , 2014, Polskie Archiwum Medycyny Wewnetrznej.

[58]  J. Mercera,et al.  Atg 16 L 1 T 300 A variant decreases selective autophagy resulting in altered cytokine signaling and decreased antibacterial defense Citation , 2014 .

[59]  D. Hommes,et al.  Anti-tumor necrosis factor-α antibodies induce regulatory macrophages in an Fc region-dependent manner. , 2011, Gastroenterology.

[60]  M. Picco Long-term safety of infliximab for the treatment of inflammatory bowel disease: a single-centre cohort study , 2009 .

[61]  H. A. Blair A review , 1940 .

[62]  L. Guidi,et al.  Clinical and Experimental Gastroenterology Dovepress Update on the Management of Inflammatory Bowel Disease: Specific Role of Adalimumab , 2022 .