Literature DB >> 31568798

Diagnostic interpretation of genetic studies in patients with primary immunodeficiency diseases: A working group report of the Primary Immunodeficiency Diseases Committee of the American Academy of Allergy, Asthma & Immunology.

Ivan K Chinn1, Alice Y Chan2, Karin Chen3, Janet Chou4, Morna J Dorsey2, Joud Hajjar5, Artemio M Jongco6, Michael D Keller7, Lisa J Kobrynski8, Attila Kumanovics9, Monica G Lawrence10, Jennifer W Leiding11, Patricia L Lugar12, Jordan S Orange13, Kiran Patel8, Craig D Platt4, Jennifer M Puck2, Nikita Raje14, Neil Romberg15, Maria A Slack16, Kathleen E Sullivan15, Teresa K Tarrant17, Troy R Torgerson18, Jolan E Walter19.   

Abstract

Genetic testing has become an integral component of the diagnostic evaluation of patients with suspected primary immunodeficiency diseases. Results of genetic testing can have a profound effect on clinical management decisions. Therefore clinical providers must demonstrate proficiency in interpreting genetic data. Because of the need for increased knowledge regarding this practice, the American Academy of Allergy, Asthma & Immunology Primary Immunodeficiency Diseases Committee established a work group that reviewed and summarized information concerning appropriate methods, tools, and resources for evaluating variants identified by genetic testing. Strengths and limitations of tests frequently ordered by clinicians were examined. Summary statements and tables were then developed to guide the interpretation process. Finally, the need for research and collaboration was emphasized. Greater understanding of these important concepts will improve the diagnosis and management of patients with suspected primary immunodeficiency diseases.
Copyright © 2019 American Academy of Allergy, Asthma & Immunology. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Chromosomal microarray; Mendelian; Sanger sequencing; exome sequencing; gene panel; genetic testing; genome sequencing; primary immunodeficiency; tools; variant interpretation

Year:  2019        PMID: 31568798     DOI: 10.1016/j.jaci.2019.09.009

Source DB:  PubMed          Journal:  J Allergy Clin Immunol        ISSN: 0091-6749            Impact factor:   10.793


  21 in total

Review 1.  How to evaluate for immunodeficiency in patients with autoimmune cytopenias: laboratory evaluation for the diagnosis of inborn errors of immunity associated with immune dysregulation.

Authors:  Roshini S Abraham
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2020-12-04

2.  Undetectable NK Cells due to the FCGR3A Variant, L66H, Which May Not Be Directly Disease-Causing.

Authors:  Maurice R G O'Gorman; Joseph A Church; Neema Izadi; Miao Sun; Emily M Mace
Journal:  J Clin Immunol       Date:  2021-08-26       Impact factor: 8.317

3.  Absent B cells, agammaglobulinemia, and hypertrophic cardiomyopathy in folliculin-interacting protein 1 deficiency.

Authors:  Francesco Saettini; Cecilia Poli; Jaime Vengoechea; Sonia Bonanomi; Julio C Orellana; Grazia Fazio; Fred H Rodriguez; Loreani P Noguera; Claire Booth; Valentina Jarur-Chamy; Marissa Shams; Maria Iascone; Maja Vukic; Serena Gasperini; Manuel Quadri; Amairelys Barroeta Seijas; Elizabeth Rivers; Mario Mauri; Raffaele Badolato; Gianni Cazzaniga; Cristina Bugarin; Giuseppe Gaipa; Wilma G M Kroes; Daniele Moratto; Monique M van Oostaijen-Ten Dam; Frank Baas; Silvère van der Maarel; Rocco Piazza; Zeynep H Coban-Akdemir; James R Lupski; Bo Yuan; Ivan K Chinn; Lucia Daxinger; Andrea Biondi
Journal:  Blood       Date:  2021-01-28       Impact factor: 22.113

4.  Disseminated Talaromyces marneffei Infection in a Non-HIV Infant With a Homozygous Private Variant of RELB.

Authors:  Xiaofang Ding; Han Huang; Lili Zhong; Min Chen; Fang Peng; Bing Zhang; Xinyu Cui; Xiu-An Yang
Journal:  Front Cell Infect Microbiol       Date:  2021-03-15       Impact factor: 5.293

5.  Late diagnosis and advances in genetics of chronic granulomatous disease.

Authors:  G Di Matteo; A Finocchi
Journal:  Clin Exp Immunol       Date:  2020-12-13       Impact factor: 4.330

6.  Characterization of Infants with Idiopathic Transient and Persistent T Cell Lymphopenia Identified by Newborn Screening-a Single-Center Experience in New York State.

Authors:  Artemio M Jongco; Robert Sporter; Elise Hon; Omer Elshaigi; Shouling Zhang; Foysal Daian; Emily Bae; Amanda Innamorato; Catherine Capo; Brianne Navetta-Modrov; David W Rosenthal; Vincent R Bonagura
Journal:  J Clin Immunol       Date:  2021-01-07       Impact factor: 8.317

7.  Primary Immunodeficiencies in India: Molecular Diagnosis and the Role of Next-Generation Sequencing.

Authors:  Arun Kumar Arunachalam; Madhavi Maddali; Fouzia N Aboobacker; Anu Korula; Biju George; Vikram Mathews; Eunice Sindhuvi Edison
Journal:  J Clin Immunol       Date:  2020-11-23       Impact factor: 8.317

8.  Efficacy and economics of targeted panel versus whole-exome sequencing in 878 patients with suspected primary immunodeficiency.

Authors:  Craig D Platt; Fatima Zaman; Wayne Bainter; Kelsey Stafstrom; Abuarahman Almutairi; Margot Reigle; Sabrina Weeks; Raif S Geha; Janet Chou
Journal:  J Allergy Clin Immunol       Date:  2020-09-02       Impact factor: 10.793

Review 9.  Beyond monogenetic rare variants: tackling the low rate of genetic diagnoses in predominantly antibody deficiency.

Authors:  Emily S J Edwards; Julian J Bosco; Samar Ojaimi; Robyn E O'Hehir; Menno C van Zelm
Journal:  Cell Mol Immunol       Date:  2020-08-17       Impact factor: 11.530

10.  Efficacy, Safety and Tolerability of a New 10% Intravenous Immunoglobulin for the Treatment of Primary Immunodeficiencies.

Authors:  Elena E Perez; Jacques Hébert; Anne K Ellis; Oral Alpan; William R Lumry; Ralph Shapiro; Daniel Suez; J Fernando Mandujano; Richard L Wasserman
Journal:  Front Immunol       Date:  2021-07-08       Impact factor: 7.561

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