Somatic mosaicism in inborn errors of immunity: Current knowledge, challenges, and future perspectives

被引:15
作者
Aluri, Jahnavi [1 ]
Cooper, Megan A. [1 ,2 ]
机构
[1] Washington Univ St Louis, Dept Pediat, Div Rheumatol Immunol, St Louis, MO 63110 USA
[2] 660 S Euclid Ave,Box 8208, St Louis, MO 63110 USA
关键词
Inborn errors of immunity; Primary immunodeficiency; Genetics; Immunity; Mosaicism; Somatic; Next -generation sequencing; AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME; VEXAS SYNDROME; PERIODIC SYNDROMES; CLINICAL-FEATURES; NLRP3; MUTATION; ONSET; CANCER; DISEASE; PATIENT; IMMUNODEFICIENCY;
D O I
10.1016/j.smim.2023.101761
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Inborn errors of immunity (IEI) are a diverse group of monogenic disorders of the immune system due to germline variants in genes important for the immune response. Over the past decade there has been increasing recognition that acquired somatic variants present in a subset of cells can also lead to immune disorders or 'phenocopies' of IEI. Discovery of somatic mosaicism causing IEI has largely arisen from investigation of seemingly sporadic cases of IEI with predominant symptoms of autoinflammation and/or autoimmunity in which germline disease-causing variants are not detected. Disease-causing somatic mosaicism has been identified in genes that also cause germline IEI, such as FAS, and in genes without significant corresponding germline disease, such as UBA1 and TLR8. There are challenges in detecting low-level somatic variants, and it is likely that the extent of the somatic mosaicism causing IEI is largely uncharted. Here we review the field of somatic mosaicism leading to IEI and discuss challenges and methods for somatic variant detection, including diagnostic approaches for molecular diagnoses of patients.
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页数:11
相关论文
共 107 条
[1]   The Candidate Cancer Gene Database: a database of cancer driver genes from forward genetic screens in mice [J].
Abbott, Kenneth L. ;
Nyre, Erik T. ;
Abrahante, Juan ;
Ho, Yen-Yi ;
Vogel, Rachel Isaksson ;
Starr, Timothy K. .
NUCLEIC ACIDS RESEARCH, 2015, 43 (D1) :D844-D848
[2]  
Adzhubei Ivan, 2013, Curr Protoc Hum Genet, VChapter 7, DOI 10.1002/0471142905.hg0720s76
[3]   Immunodeficiency and bone marrow failure with mosaic and germline TLR8 gain of function [J].
Aluri, Jahnavi ;
Bach, Alicia ;
Kaviany, Saara ;
Paracatu, Luana Chiquetto ;
Kitcharoensakkul, Maleewan ;
Walkiewicz, Magdalena A. ;
Putnam, Christopher D. ;
Shinawi, Marwan ;
Saucier, Nermina ;
Rizzi, Elise M. ;
Harmon, Michael T. ;
Keppel, Molly P. ;
Ritter, Michelle ;
Similuk, Morgan ;
Kulm, Elaine ;
Joyce, Michael ;
de Jesus, Adriana A. ;
Goldbach-Mansky, Raphaela ;
Lee, Yi-Shan ;
Cella, Marina ;
Kendall, Peggy L. ;
Dinauer, Mary C. ;
Bednarski, Jeffrey J. ;
Bemrich-Stolz, Christina ;
Canna, Scott W. ;
Abraham, Shirley M. ;
Demczko, Matthew M. ;
Powell, Jonathan ;
Jones, Stacie M. ;
Scurlock, Amy M. ;
De Ravin, Suk See ;
Bleesing, Jack J. ;
Connelly, James A. ;
Rao, V. Koneti ;
Schuettpelz, Laura G. ;
Cooper, Megan A. .
BLOOD, 2021, 137 (18) :2450-2462
[4]   Somatic NOD2 mosaicism in Blau syndrome [J].
不详 .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2015, 136 (02) :484-+
[5]   Spontaneous in vivo reversion of an inherited mutation in the Wiskott-Aldrich syndrome [J].
Ariga, T ;
Kondoh, T ;
Yamaguchi, K ;
Yamada, M ;
Sasaki, S ;
Nelson, DL ;
Ikeda, H ;
Kobayashi, K ;
Moriuchi, H ;
Sakiyama, Y .
JOURNAL OF IMMUNOLOGY, 2001, 166 (08) :5245-5249
[6]  
Arlet JB, 2021, NEW ENGL J MED, V384, P2163, DOI 10.1056/NEJMc2102124
[7]   A Somatic NLRP3 Mutation as a Cause of a Sporadic Case of Chronic Infantile Neurologic, Cutaneous, Articular Syndrome/Neonatal-Onset Multisystem Inflammatory Disease Novel Evidence of the Role of Low-Level Mosaicism as the Pathophysiologic Mechanism Underlying Mendelian Inherited Diseases [J].
Arostegui, Juan I. ;
Lopez Saldana, Ma Dolores ;
Pascal, Mariona ;
Clemente, Daniel ;
Aymerich, Marta ;
Balaguer, Francesc ;
Goel, Ajay ;
Fournier del Castillo, Concepcion ;
Rius, Josefa ;
Plaza, Susana ;
Lopez Robledillo, Juan Carlos ;
Juan, Manel ;
Ibanez, Mercedes ;
Yaguee, Jordi .
ARTHRITIS AND RHEUMATISM, 2010, 62 (04) :1158-1166
[8]   Adenosine deaminase deficiency with mosaicism for a "second-site suppressor" of a splicing mutation: decline in revertant T lymphocytes during enzyme replacement therapy [J].
Arredondo-Vega, FX ;
Santisteban, I ;
Richard, E ;
Bali, P ;
Koleilat, M ;
Loubser, M ;
Al-Ghonaium, A ;
Al-Helali, M ;
Hershfield, MS .
BLOOD, 2002, 99 (03) :1005-1013
[9]   VEXAS syndrome in a woman [J].
Barba, Thomas ;
Jamilloux, Yvan ;
Durel, Cecile-Audrey ;
Bourbon, Estelle ;
Mestrallet, Fanelie ;
Sujobert, Pierre ;
Hot, Arnaud .
RHEUMATOLOGY, 2021, 60 (11) :E402-E403
[10]  
Barnell E.K., 2021, JCO PRECIS ONCOL, P5