Somatic Mutations and Autoimmunity

被引:6
作者
Alriyami, Maha [1 ]
Polychronakos, Constantin [2 ]
机构
[1] Sultan Qaboos Univ, Coll Med & Hlth Sci, Dept Biochem, Muscat 123, Oman
[2] McGill Univ, Hlth Ctr Res Inst, Dept Pediat, Child Hlth & Human Dev Program,Endocrine Genet La, Montreal, PQ H4A 3J1, Canada
基金
加拿大健康研究院;
关键词
somatic mutations; autoimmunity; lymphocytes; DETECTABLE CLONAL MOSAICISM; NON-HODGKIN-LYMPHOMA; T-CELLS; LYMPHOPROLIFERATIVE SYNDROME; RHEUMATOID-ARTHRITIS; POSITIVE SELECTION; FAS MUTATIONS; DOUBLE-BLIND; RISK; AGE;
D O I
10.3390/cells10082056
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Autoimmune diseases are among the most common chronic illness caused by a dysregulated immune response against self-antigens. Close to 5% of the general population in Western countries develops some form of autoimmunity, yet its underlying causes, although intensively studied, are still not fully known, and no curative therapies exist. It is well established that autoimmune diseases have common mechanisms and are caused by both genetic and non-genetic risk factors. One novel risk factor that can contribute to autoimmunity is somatic mutations, in a role parallel to their role in cancer. Somatic mutations are stochastic, de novo, non-inherited mutations. In this hypothesis, the persistent proliferation of self-reactive lymphocytes (that is usually hindered by a series of checkpoints) is permitted, due to somatic mutations in these expanding cells, allowing them to bypass multiple regulatory checkpoints, causing autoimmunity. This novel concept of the contribution of these mutations in non-malignant diseases has recently started to be explored. It proposes a novel paradigm for autoimmunity etiology and could be the missing piece of the autoimmunity puzzle.
引用
收藏
页数:14
相关论文
共 86 条
[1]   Somatic copy number mosaicism in human skin revealed by induced pluripotent stem cells [J].
Abyzov, Alexej ;
Mariani, Jessica ;
Palejev, Dean ;
Zhang, Ying ;
Haney, Michael Seamus ;
Tomasini, Livia ;
Ferrandino, Anthony F. ;
Belmaker, Lior A. Rosenberg ;
Szekely, Anna ;
Wilson, Michael ;
Kocabas, Arif ;
Calixto, Nathaniel E. ;
Grigorenko, Elena L. ;
Huttner, Anita ;
Chawarska, Katarzyna ;
Weissman, Sherman ;
Urban, Alexander Eckehart ;
Gerstein, Mark ;
Vaccarino, Flora M. .
NATURE, 2012, 492 (7429) :438-+
[2]   T-CELL CLONING TO DETECT THE MUTANT 6-THIOGUANINE-RESISTANT LYMPHOCYTES PRESENT IN HUMAN PERIPHERAL-BLOOD [J].
ALBERTINI, RJ ;
CASTLE, KL ;
BORCHERDING, WR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1982, 79 (21) :6617-6621
[3]   T-CELLS RESPONSIVE TO MYELIN BASIC-PROTEIN IN PATIENTS WITH MULTIPLE-SCLEROSIS [J].
ALLEGRETTA, M ;
NICKLAS, JA ;
SRIRAM, S ;
ALBERTINI, RJ .
SCIENCE, 1990, 247 (4943) :718-721
[4]   Clonal copy-number mosaicism in autoreactive T lymphocytes in diabetic NOD mice [J].
Alriyami, Maha ;
Marchand, Luc ;
Li, Quan ;
Du, Xiaoyu ;
Olivier, Martin ;
Polychronakos, Constantin .
GENOME RESEARCH, 2019, 29 (12) :1951-1961
[5]   Population-based study of autoimmune conditions and the risk of specific lymphoid malignancies [J].
Anderson, Lesley A. ;
Gadalla, Shahinaz ;
Morton, Lindsay M. ;
Landgren, Ola ;
Pfeiffer, Ruth ;
Warren, Joan L. ;
Berndt, Sonja I. ;
Ricker, Winnie ;
Parsons, Ruth ;
Engels, Eric A. .
INTERNATIONAL JOURNAL OF CANCER, 2009, 125 (02) :398-405
[6]  
[Anonymous], 1959, CLONAL SELECTION THE
[7]  
[Anonymous], 1961, JAMA-J AM MED ASSOC, V176, P50, DOI [10.1001/jama.1961.03040140052017, DOI 10.1001/JAMA.1961.03040140052017]
[8]  
[Anonymous], 1900, ANN I PASTEUR PARIS
[9]   The rate of spontaneous mutations in human myeloid cells [J].
Araten, David J. ;
Krejci, Ondrej ;
DiTata, Kimberly ;
Wunderlich, Mark ;
Sanders, Katie J. ;
Zamechek, Leah ;
Mulloy, James C. .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 2013, 749 (1-2) :49-57
[10]   A quantitative measurement of the human somatic mutation rate [J].
Araten, DJ ;
Golde, DW ;
Zhang, RH ;
Thaler, HT ;
Gargiulo, L ;
Notaro, R ;
Luzzatto, L .
CANCER RESEARCH, 2005, 65 (18) :8111-8117