Literature DB >> 32462469

Jeffrey's insights: Jeffrey Modell Foundation's global genetic sequencing pilot program to identify specific primary immunodeficiency defects to optimize disease management and treatment.

Jessica Quinn1, Vicki Modell1, Jennifer Holle2, Rebecca Truty2, Swaroop Aradhya2, Britt Johnson2, Jordan Orange1, Fred Modell3.   

Abstract

Primary immunodeficiencies (PI) are genetic defects of the immune system that result in chronic and often life-threatening infections and/or life-threatening autoimmunity if not diagnosed and treated. Patients with a suspected PI, but without a genetic diagnosis, commonly undergo a diagnostic odyssey that is costly, time-consuming, and arduous. This delay in diagnosis prevents appropriate disease management and treatment, contributing to prolonged suffering and decreased quality of life. Although next generation sequencing (NGS) can provide these patients with relief from such a diagnostic odyssey, it is often unavailable, mainly due to cost and inaccessibility. In January 2019, the Jeffrey Modell Foundation (JMF) launched a free genetic sequencing pilot program for Jeffrey Modell Centers Network (JMCN) patients clinically diagnosed with an underlying PI. A total of 21 sites within the JMCN were invited to participate. JMF collaborated with Invitae, and testing was comprised of Invitae's Primary Immunodeficiency Panel, which currently includes 207 genes. A questionnaire was disseminated to each participating physician to evaluate barriers to access to genetic sequencing and changes in disease management and treatment after testing. One hundred fifty-eight patients and 29 family members were tested in this pilot study. Twenty-one percent of patients with a suspected monogenic disorder received a molecular diagnosis, and others received potentially useful diagnostic leads. Based on the results of genetic sequencing, clinical diagnosis was altered in 45% of patients, disease management was altered in 40%, treatment was altered in 36%, and genetic counseling was altered in 62%. The results of this pilot program demonstrate the utility, cost-efficiency, and critical importance of NGS for PI and make the case for broad scale sequence-based diagnostics for PI patients when requested by expert immunologists.

Entities:  

Keywords:  Gene sequencing; Genetic sequencing; Jeffrey Modell Centers Network (JMCN); Jeffrey Modell Foundation (JMF); Next generation sequencing (NGS); Primary immunodeficiency (PI); Sequencing

Year:  2020        PMID: 32462469     DOI: 10.1007/s12026-020-09131-x

Source DB:  PubMed          Journal:  Immunol Res        ISSN: 0257-277X            Impact factor:   2.829


  8 in total

1.  Global Expansion of Jeffrey's Insights: Jeffrey Modell Foundation's Genetic Sequencing Program for Primary Immunodeficiency.

Authors:  Jessica Quinn; Vicki Modell; Britt Johnson; Sarah Poll; Swaroop Aradhya; Jordan S Orange; Fred Modell
Journal:  Front Immunol       Date:  2022-06-10       Impact factor: 8.786

2.  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

3.  Growth in diagnosis and treatment of primary immunodeficiency within the global Jeffrey Modell Centers Network.

Authors:  Jessica Quinn; Vicki Modell; Jordan S Orange; Fred Modell
Journal:  Allergy Asthma Clin Immunol       Date:  2022-03-04       Impact factor: 3.406

Review 4.  Druggable monogenic immune defects hidden in diverse medical specialties: Focus on overlap syndromes.

Authors:  Valentina Boz; Chiara Zanchi; Laura Levantino; Guglielmo Riccio; Alberto Tommasini
Journal:  World J Clin Pediatr       Date:  2022-03-09

5.  Genetic Testing in Egyptian Patients with Inborn Errors of Immunity: a Single-Center Experience.

Authors:  Rabab E El Hawary; Safa S Meshaal; Dalia S Abd Elaziz; Radwa Alkady; Sohilla Lotfy; Alia Eldash; Aya Erfan; Engy A Chohayeb; Mai M Saad; Rania K Darwish; Jeannette A Boutros; Nermeen M Galal; Aisha M Elmarsafy
Journal:  J Clin Immunol       Date:  2022-04-28       Impact factor: 8.542

6.  Clinical Utility of Whole Exome Sequencing and Targeted Panels for the Identification of Inborn Errors of Immunity in a Resource-Constrained Setting.

Authors:  Clair Engelbrecht; Michael Urban; Mardelle Schoeman; Brandon Paarwater; Ansia van Coller; Deepthi Raju Abraham; Helena Cornelissen; Richard Glashoff; Monika Esser; Marlo Möller; Craig Kinnear; Brigitte Glanzmann
Journal:  Front Immunol       Date:  2021-05-21       Impact factor: 7.561

7.  Immunity and Genetics at the Revolving Doors of Diagnostics in Primary Immunodeficiencies.

Authors:  Francesco Rispoli; Erica Valencic; Martina Girardelli; Alessia Pin; Alessandra Tesser; Elisa Piscianz; Valentina Boz; Flavio Faletra; Giovanni Maria Severini; Andrea Taddio; Alberto Tommasini
Journal:  Diagnostics (Basel)       Date:  2021-03-16

8.  Consensus Middle East and North Africa Registry on Inborn Errors of Immunity.

Authors:  Asghar Aghamohammadi; Nima Rezaei; Reza Yazdani; Samaneh Delavari; Necil Kutukculer; Ezgi Topyildiz; Ahmet Ozen; Safa Baris; Elif Karakoc-Aydiner; Sara Sebnem Kilic; Hulya Kose; Nesrin Gulez; Ferah Genel; Ismail Reisli; Kamel Djenouhat; Azzeddine Tahiat; Rachida Boukari; Samir Ladj; Reda Belbouab; Yacine Ferhani; Brahim Belaid; Reda Djidjik; Nadia Kechout; Nabila Attal; Khalissa Saidani; Ridha Barbouche; Aziz Bousfiha; Ali Sobh; Ragheed Rizk; Marwa H Elnagdy; Mona Al-Ahmed; Salem Al-Tamemi; Gulnara Nasrullayeva; Mehdi Adeli; Maryam Al-Nesf; Amel Hassen; Cybel Mehawej; Carla Irani; Andre Megarbane; Jessica Quinn; László Maródi; Vicki Modell; Fred Modell; Waleed Al-Herz; Raif S Geha; Hassan Abolhassani
Journal:  J Clin Immunol       Date:  2021-05-29       Impact factor: 8.317

  8 in total

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