Immunologists' Perspectives on Monogenic Inflammatory Bowel Diseases

被引:0
作者
Osman, Maryiam Jama Ali [1 ,2 ]
Aydogdu, Emine Selva [3 ]
Mackeh, Rafah [2 ]
Ozen, Ahmet [4 ,5 ,6 ]
Lo, Bernice [1 ,2 ]
机构
[1] Hamad Bin Khalifa Univ, Coll Hlth & Life Sci, Fac Med, Doha, Qatar
[2] Sidra Med, Res Branch, Doha, Qatar
[3] Marmara Univ, Fac Med, Istanbul, Turkiye
[4] Marmara Univ, Fac Med, Dept Pediat, Div Allergy & Immunol, Istanbul, Turkiye
[5] Istanbul Jeffrey Modell Diag Ctr Primary Immunode, Istanbul, Turkiye
[6] Isil Berat Barlan Ctr Translat Med, Istanbul, Turkiye
来源
TURKISH JOURNAL OF IMMUNOLOGY | 2024年 / 12卷
关键词
Inflammatory bowel diseases; monogenic defects; immune system; multidisciplinary approach; personalized medicine; HERMANSKY-PUDLAK-SYNDROME; STEM-CELL TRANSPLANTATION; HOYERAAL-HREIDARSSON-SYNDROME; MEVALONATE KINASE-DEFICIENCY; OF-FUNCTION MUTATIONS; IMMUNE DYSREGULATION; ULCERATIVE-COLITIS; CLINICAL-FEATURES; CROHNS-DISEASE; OMENN-SYNDROME;
D O I
10.4274/tji.galenos.2023.09327
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Inflammatory bowel diseases (IBD) encompass a group of chronic inflammatory disorders primarily impacting the gastrointestinal system, and they may also affect other organ systems. While common forms of IBD typically arise from multifactorial causes, there exists a subset of patients with single gene defects known as monogenic IBD (mIBD). Over 100 genes have been associated with mIBD, spanning various biological pathways which affect various tissues; the immune system is the most commonly involved, but more rarely, the intestinal epithelium is the primarily affected compartment. Timely diagnosis hinges on awareness and the application of contemporary molecular techniques. Due to the diverse range of causes, managing mIBD requires a multidisciplinary approach. Conventional treatments often fall short, necessitating a personalized strategy that considers the multifaceted nature of mIBD presentations and the diverse etiologic factors. In recent times, novel therapies have emerged, targeting specific causative genes or affected pathways. This discussion delves into the fundamental aspects of mIBD, with particular emphasis on recent breakthroughs in the field, encompassing newly identified gene defects and innovative management strategies.
引用
收藏
页码:17 / 36
页数:20
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共 256 条
[1]   BACH2 immunodeficiency illustrates an association between super-enhancers and haploinsufficiency [J].
Afzali, Behdad ;
Gronholm, Juha ;
Vandrovcova, Jana ;
O'Brien, Charlotte ;
Sun, Hong-Wei ;
Vanderleyden, Ine ;
Davis, Fred P. ;
Khoder, Ahmad ;
Zhang, Yu ;
Hegazy, Ahmed N. ;
Villarino, Alejandro V. ;
Palmer, Ira W. ;
Kaufman, Joshua ;
Watts, Norman R. ;
Kazemian, Majid ;
Kamenyeva, Olena ;
Keith, Julia ;
Sayed, Anwar ;
Kasperaviciute, Dalia ;
Mueller, Michael ;
Hughes, Jason D. ;
Fuss, Ivan J. ;
Sadiyah, Mohammed F. ;
Montgomery-Recht, Kim ;
McElwee, Joshua ;
Restifo, Nicholas P. ;
Strober, Warren ;
Linterman, Michelle A. ;
Wingfield, Paul T. ;
Uhlig, Holm H. ;
Roychoudhuri, Rahul ;
Aitman, Timothy J. ;
Kelleher, Peter ;
Lenardo, Michael J. ;
O'Shea, John J. ;
Cooper, Nichola ;
Laurence, Arian D. J. .
NATURE IMMUNOLOGY, 2017, 18 (07) :813-+
[2]   Pathogenesis and treatment of gastrointestinal disease in antibody deficiency syndromes [J].
Agarwal, Shradha ;
Mayer, Lloyd .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2009, 124 (04) :658-664
[3]   Characterization of Crohn disease in X-linked inhibitor of apoptosis-deficient male patients and female symptomatic carriers [J].
Aguilar, Claire ;
Lenoir, Christelle ;
Lambert, Nathalie ;
Begue, Bernadette ;
Brousse, Nicole ;
Canioni, Danielle ;
Berrebi, Dominique ;
Roy, Maryline ;
Gerart, Stephane ;
Chapel, Helen ;
Schwerd, Tobias ;
Siproudhis, Laurent ;
Schaeppi, Michela ;
Al-Ahmari, Ali ;
Mori, Masaaki ;
Yamaide, Akiko ;
Galicier, Lionel ;
Neven, Benedicte ;
Routes, John ;
Uhlig, Holm H. ;
Koletzko, Sibylle ;
Patel, Smita ;
Kanegane, Hirokazu ;
Picard, Capucine ;
Fischer, Alain ;
Bensussan, Nadine Cerf ;
Ruemmele, Frank ;
Hugot, Jean-Pierre ;
Latour, Sylvain .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2014, 134 (05) :1131-+
[4]   Human AGR2 Deficiency Causes Mucus Barrier Dysfunction and Infantile Inflammatory Bowel Disease [J].
Al-Shaibi, Ahmad A. ;
Abdel-Motal, Ussama M. ;
Hubrack, Satanay Z. ;
Bullock, Alex N. ;
Al-Marri, Amna A. ;
Agrebi, Nourhen ;
Al-Subaiey, Abdulrahman A. ;
Ibrahim, Nazira A. ;
Charles, Adrian K. ;
Elawad, Mamoun ;
Uhlig, Holm H. ;
Lo, Bernice .
CELLULAR AND MOLECULAR GASTROENTEROLOGY AND HEPATOLOGY, 2021, 12 (05) :1809-1830
[5]   LPS-responsive beige-like anchor (LRBA) gene mutation in a family with inflammatory bowel disease and combined immunodeficiency [J].
Alangari, Abdullah ;
Alsultan, Abdulrahman ;
Adly, Nouran ;
Massaad, Michel J. ;
Kiani, Iram Shakir ;
Aljebreen, Abdulrahman ;
Raddaoui, Emad ;
Almomen, Abdul-Kareem ;
Al-Muhsen, Saleh ;
Geha, Raif S. ;
Alkuraya, Fowzan S. .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2012, 130 (02) :481-+
[6]   Role of the Intestinal Epithelium and Its Interaction With the Microbiota in Food Allergy [J].
Ali, Ayesha ;
Tan, HuiYing ;
Kaiko, Gerard E. .
FRONTIERS IN IMMUNOLOGY, 2020, 11
[7]   Exaggerated follicular helper T-cell responses in patients with LRBA deficiency caused by failure of CTLA4-mediated regulation [J].
Alroqi, Fayhan J. ;
Charbonnier, Louis-Marie ;
Baris, Safa ;
Kiykim, Ayca ;
Chou, Janet ;
Platt, Craig D. ;
Algassim, Abdulrahman ;
Keles, Sevgi ;
Al Saud, Bandar K. ;
Alkuraya, Fowzan S. ;
Jordan, Michael ;
Geha, Raif S. ;
Chatila, Talal A. .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2018, 141 (03) :1050-+
[8]   Hermansky-Pudlak syndrome type 4 (HPS-4): clinical and molecular characteristics [J].
Anderson, PD ;
Huizing, M ;
Claassen, DA ;
White, J ;
Gahl, WA .
HUMAN GENETICS, 2003, 113 (01) :10-17
[9]   A homozygous loss-of-function mutation leading to CYBC1 deficiency causes chronic granulomatous disease [J].
Arnadottir, Gudny A. ;
Norddahl, Gudmundur L. ;
Gudmundsdottir, Steinunn ;
Agustsdottir, Arna B. ;
Sigurdsson, Snaevar ;
Jensson, Brynjar O. ;
Bjarnadottir, Kristbjorg ;
Theodors, Fannar ;
Benonisdottir, Stefania ;
Ivarsdottir, Erna V. ;
Oddsson, Asmundur ;
Kristjansson, Ragnar P. ;
Sulem, Gerald ;
Alexandersson, Kristjan F. ;
Juliusdottir, Thorhildur ;
Gudmundsson, Kjartan R. ;
Saemundsdottir, Jona ;
Jonasdottir, Adalbjorg ;
Jonasdottir, Aslaug ;
Sigurdsson, Asgeir ;
Manzanillo, Paolo ;
Gudjonsson, Sigurjon A. ;
Thorisson, Gudmundur A. ;
Magnusson, Olafur Th. ;
Masson, Gisli ;
Orvar, Kjartan B. ;
Holm, Hilma ;
Bjornsson, Sigurdur ;
Arngrimsson, Reynir ;
Gudbjartsson, Daniel F. ;
Thorsteinsdottir, Unnur ;
Jonsdottir, Ingileif ;
Haraldsson, Asgeir ;
Sulem, Patrick ;
Stefansson, Kari .
NATURE COMMUNICATIONS, 2018, 9
[10]   Identification of Variants in Genes Associated with Single-gene Inflammatory Bowel Disease by Whole-exome Sequencing [J].
Ashton, James J. ;
Andreoletti, Gaia ;
Coelho, Tracy ;
Haggarty, Rachel ;
Batra, Akshay ;
Afzal, Nadeem A. ;
Beattie, R. Mark ;
Ennis, Sarah .
INFLAMMATORY BOWEL DISEASES, 2016, 22 (10) :2317-2327