Intestinal Organoids as a Tool for Inflammatory Bowel Disease Research

被引:48
作者
Angus, Hamish C. K. [1 ]
Butt, A. Grant [2 ]
Schultz, Michael [3 ]
Kemp, Roslyn A. [1 ]
机构
[1] Univ Otago, Dept Microbiol & Immunol, Dunedin, New Zealand
[2] Univ Otago, Dept Physiol, Dunedin, New Zealand
[3] Univ Otago, Dept Med, Dunedin, New Zealand
关键词
Inflammatory Bowel Disease; immunology; organoid; T cells; cytokines; regulation; diagnostics; CROHNS-DISEASE; CLINICAL-RESPONSE; BARRIER FUNCTION; HUMAN-COLON; STEM-CELLS; IFN-GAMMA; MODEL; ATG16L1; SUSCEPTIBILITY; MAINTENANCE;
D O I
10.3389/fmed.2019.00334
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Inflammatory Bowel Diseases (IBD) are difficult to model as freshly acquired tissues are short-lived, provide data as a snapshot in time, and are not always accessible. Many patients with IBD are non-responders to first-line treatments, and responders are prone to developing resistance to treatment over time-resulting in reduced patient quality of life, increased time to remission, and potential relapse. IBD is heterogenous and we are yet to fully understand the mechanisms of disease; thus, our ability to diagnose and prescribe optimal treatment remains ineffective. Intestinal organoids are derived from patient tissues expanded in vitro. Organoids offer unique insight into individual patient disease and are a potential route to personalized treatments. However, organoid models do not contain functional microbial and immune cell components. In this review, we discuss immune cell subsets in the context of IBD, and the requirement of immune cell and microbial components in organoid models for IBD research.
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页数:9
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共 80 条
[1]   Metabolic Functions of Gut Microbes Associate With Efficacy of Tumor Necrosis Factor Antagonists in Patients With Inflammatory Bowel Diseases [J].
Aden, Konrad ;
Rehman, Ateequr ;
Waschina, Silvio ;
Pan, Wei-Hung ;
Walker, Alesia ;
Lucio, Marianna ;
Nunez, Alejandro Mena ;
Bharti, Richa ;
Zimmerman, Johannes ;
Bethge, Johannes ;
Schulte, Berenice ;
Schulte, Dominik ;
Franke, Andre ;
Nikolaus, Susanna ;
Schroeder, Johann Oltmann ;
Vandeputte, Doris ;
Raes, Jeroen ;
Szymczak, Silke ;
Waetzig, Georg H. ;
Zeuner, Rainald ;
Schmitt-Kopplin, Philippe ;
Kaleta, Christoph ;
Schreiber, Stefan ;
Rosenstiel, Philip .
GASTROENTEROLOGY, 2019, 157 (05) :1279-+
[2]   Influence of immunogenicity on the long-term efficacy of infliximab in Crohn's disease [J].
Baert, F ;
Noman, M ;
Vermeire, S ;
Van Assche, G ;
D'Haens, G ;
Carbonez, A ;
Rutgeerts, P .
NEW ENGLAND JOURNAL OF MEDICINE, 2003, 348 (07) :601-608
[3]   Clinical response to adalimumab: relationship to anti-adalimumab antibodies and serum adalimumab concentrations in rheumatoid arthritis [J].
Bartelds, Geertje M. ;
Wijbrandts, Carla A. ;
Nurmohamed, Michael T. ;
Stapel, Steven ;
Lems, Willem F. ;
Aarden, Lucien ;
Dijkmans, Ben A. C. ;
Tak, Paul Peter ;
Wolbink, Gerrit Jan .
ANNALS OF THE RHEUMATIC DISEASES, 2007, 66 (07) :921-926
[4]   Morphological characterisation of Crohn's disease fistulae [J].
Bataille, F ;
Klebl, F ;
Rümmele, P ;
Schroeder, J ;
Farkas, S ;
Wild, PJ ;
Fürst, A ;
Hofstädter, F ;
Schölmerich, J ;
Herfarth, H ;
Rogler, G .
GUT, 2004, 53 (09) :1314-1321
[5]   Discovery and mechanism of ustekinumab A human monoclonal antibody targeting interleukin-12 and interleukin-23 for treatment of immune-mediated disorders [J].
Benson, Jacqueline M. ;
Peritt, David ;
Scallon, Bernard J. ;
Heavner, George A. ;
Shealy, David J. ;
Giles-Komar, Jill M. ;
Mascelli, Mary Ann .
MABS, 2011, 3 (06) :535-545
[6]   Rectal Organoids Enable Personalized Treatment of Cystic Fibrosis [J].
Berkers, Gitte ;
van Mourik, Peter ;
Vonk, Annelotte M. ;
Kruisselbrink, Evelien ;
Dekkers, Johanna F. ;
de Winter-de Groot, Karin M. ;
Arets, Hubertus G. M. ;
Marck-van der Wilt, Rozemarijn E. P. ;
Dijkema, Jasper S. ;
Vanderschuren, Maaike M. ;
Houwen, Roderick H. J. ;
Heijerman, Harry G. M. ;
van de Graaf, Eduard A. ;
Elias, Sjoerd G. ;
Majoor, Christof J. ;
Koppelman, Gerard H. ;
Roukema, Jolt ;
Bakker, Marleen ;
Janssens, Hettie M. ;
van der Meer, Renske ;
Vries, Robert G. J. ;
Clevers, Hans C. ;
de Jonge, Hugo R. ;
Beekman, Jeffrey M. ;
van der Ent, Cornelis K. .
CELL REPORTS, 2019, 26 (07) :1701-+
[7]   ALPHA-4-BETA-7-INTEGRIN MEDIATES LYMPHOCYTE BINDING TO THE MUCOSAL VASCULAR ADDRESSIN MADCAM-1 [J].
BERLIN, C ;
BERG, EL ;
BRISKIN, MJ ;
ANDREW, DP ;
KILSHAW, PJ ;
HOLZMANN, B ;
WEISSMAN, IL ;
HAMANN, A ;
BUTCHER, EC .
CELL, 1993, 74 (01) :185-195
[8]   Microbial Anti-Inflammatory Molecule (MAM) from Faecalibacterium prausnitzii Shows a Protective Effect on DNBS and DSS-Induced Colitis Model in Mice through Inhibition of NF-κB Pathway [J].
Breyner, Natalia M. ;
Michon, Cristophe ;
de sousa, Cassiana S. ;
Boas, Priscilla B. Vilas ;
Chain, Florian ;
Azevedo, Vasco A. ;
Langella, Philippe ;
Chatel, Jean M. .
FRONTIERS IN MICROBIOLOGY, 2017, 8
[9]   Intestinal CD103- dendritic cells migrate in lymph and prime effector T cells [J].
Cerovic, V. ;
Houston, S. A. ;
Scott, C. L. ;
Aumeunier, A. ;
Yrlid, U. ;
Mowat, A. M. ;
Milling, S. W. F. .
MUCOSAL IMMUNOLOGY, 2013, 6 (01) :104-113
[10]   A porous defense: the leaky epithelial barrier in intestinal disease [J].
Clayburgh, DR ;
Shen, L ;
Turner, JR .
LABORATORY INVESTIGATION, 2004, 84 (03) :282-291