Birds of a feather Common variable immune deficiencies

被引:17
作者
Romberg, Neil [1 ,2 ]
Lawrence, Monica G. [3 ]
机构
[1] Childrens Hosp Philadelphia, Div Allergy & Immunol, Philadelphia, PA 19104 USA
[2] Univ Penn, Perelman Sch Med, Dept Pediat, Philadelphia, PA 19104 USA
[3] Univ Virginia, Dept Med, Div Asthma Allergy, Charlottesville, VA USA
关键词
ANTIBODY-DEFICIENCY; B-CELLS; GERMLINE MUTATIONS; IMMUNODEFICIENCY; TACI; DYSREGULATION; IL-21; DISORDERS; SPECTRUM; DISEASE;
D O I
10.1016/j.anai.2019.07.027
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Objective: To update the reader on recently proposed common variable immune deficiency (CVID) diagnostic criteria, newly uncovered CVID pathobiology, freshly identified CVID-related genes, and novel CVID therapies. Data Sources: PubMed Central. Study Selections: We selected 60 clinical and translational research articles that have shaped CVID diagnostic criteria, introduced personalized therapies, and advanced our understanding of CVID biology and genetics. We have incorporated recent articles and older published work that are foundational to the modern understanding of this protean disease. Results: CVID has proven to be a heterogenous group of antibody deficiency diseases driven by defects in diverse biologic processes, including B-cell development, activation, tolerance, class-switch recombination, somatic hypermutation, and lymphoproliferation. Recent genetic advances have enabled identification of several CVID-related gene defects that may contribute to patients' infectious and noninfectious symptoms. Conclusion: Improved understanding of the aberrant biologic processes that drive CVID and the disease's genetic basis may be useful in directing therapeutic decisions, especially in cases complicated by autoimmune, lymphoproliferative, and inflammatory features. (C) 2019 American College of Allergy, Asthma & Immunology. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:461 / 467
页数:7
相关论文
共 63 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]   Treatment of hypogammaglobulinemia in adults: A scoring system to guide decisions on immunoglobulin replacement [J].
Agarwal, Shradha ;
Cunningham-Rundles, Charlotte .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2013, 131 (06) :1699-1701
[3]   Spectrum of Phenotypes Associated with Mutations in LRBA [J].
Alkhairy, Omar K. ;
Abolhassani, Hassan ;
Rezaei, Nima ;
Fang, Mingyan ;
Andersen, Kasper Krogh ;
Chavoshzadeh, Zahra ;
Mohammadzadeh, Iraj ;
El-Rajab, Mariam A. ;
Massaad, Michel ;
Chou, Janet ;
Aghamohammadi, Asghar ;
Geha, Raif S. ;
Hammarstrom, Lennart .
JOURNAL OF CLINICAL IMMUNOLOGY, 2016, 36 (01) :33-45
[4]   New diagnostic criteria for common variable immune deficiency (CVID), which may assist with decisions to treat with intravenous or subcutaneous immunoglobulin [J].
Ameratunga, R. ;
Woon, S. -T. ;
Gillis, D. ;
Koopmans, W. ;
Steele, R. .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2013, 174 (02) :203-211
[5]   Phosphoinositide 3-Kinase δ Gene Mutation Predisposes to Respiratory Infection and Airway Damage [J].
Angulo, Ivan ;
Vadas, Oscar ;
Garcon, Fabien ;
Banham-Hall, Edward ;
Plagnol, Vincent ;
Leahy, Timothy R. ;
Baxendale, Helen ;
Coulter, Tanya ;
Curtis, James ;
Wu, Changxin ;
Blake-Palmer, Katherine ;
Perisic, Olga ;
Smyth, Deborah ;
Maes, Mailis ;
Fiddler, Christine ;
Juss, Jatinder ;
Cilliers, Deirdre ;
Markelj, Gasper ;
Chandra, Anita ;
Farmer, George ;
Kielkowska, Anna ;
Clark, Jonathan ;
Kracker, Sven ;
Debre, Marianne ;
Picard, Capucine ;
Pellier, Isabelle ;
Jabado, Nada ;
Morris, James A. ;
Barcenas-Morales, Gabriela ;
Fischer, Alain ;
Stephens, Len ;
Hawkins, Phillip ;
Barrett, Jeffrey C. ;
Abinun, Mario ;
Clatworthy, Menna ;
Durandy, Anne ;
Doffinger, Rainer ;
Chilvers, Edwin R. ;
Cant, Andrew J. ;
Kumararatne, Dinakantha ;
Okkenhaug, Klaus ;
Williams, Roger L. ;
Condliffe, Alison ;
Nejentsev, Sergey .
SCIENCE, 2013, 342 (6160) :866-871
[6]   Agammaglobulinemia: causative mutations and their implications for novel therapies [J].
Berglof, Anna ;
Turunen, Janne J. ;
Gissberg, Olof ;
Bestas, Burcu ;
Blomberg, K. Emelie M. ;
Smith, C. I. Edvard .
EXPERT REVIEW OF CLINICAL IMMUNOLOGY, 2013, 9 (12) :1205-1221
[7]   International Consensus Document (ICON): Common Variable Immunodeficiency Disorders [J].
Bonilla, Francisco A. ;
Barlan, Isil ;
Chapel, Helen ;
Costa-Carvalho, Beatriz T. ;
Cunningham-Rundles, Charlotte ;
de la Morena, M. Teresa ;
Espinosa-Rosales, Francisco J. ;
Hammarstrom, Lennart ;
Nonoyama, Shigeaki ;
Quinti, Isabella ;
Routes, John M. ;
Tang, Mimi L. K. ;
Warnatz, Klaus .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY-IN PRACTICE, 2016, 4 (01) :38-59
[8]   CLASSIFICATION OF PATIENTS WITH COMMON VARIABLE IMMUNODEFICIENCY BY B-CELL SECRETION OF IGM AND IGG IN RESPONSE TO ANTI-IGM AND INTERLEUKIN-2 [J].
BRYANT, A ;
CALVER, NC ;
TOUBI, E ;
WEBSTER, ADB ;
FARRANT, J .
CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY, 1990, 56 (02) :239-248
[9]   Bach2 regulates AID-mediated immunoglobulin gene conversion and somatic hypermutation in DT40 B cells [J].
Budzynska, Paulina M. ;
Kylaniemi, Minna K. ;
Kallonen, Teemu ;
Soikkeli, Anni I. ;
Nera, Kalle-Pekka ;
Lassila, Olli ;
Alinikula, Jukka .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2017, 47 (06) :993-1001
[10]   TACI is mutant in common variable immunodeficiency and IgA deficiency [J].
Castigli, E ;
Wilson, SA ;
Garibyan, L ;
Rachid, R ;
Bonilla, F ;
Schneider, L ;
Geha, RS .
NATURE GENETICS, 2005, 37 (08) :829-834