Literature DB >> 32615565

Monogenic Primary Immunodeficiency Disorder Associated with Common Variable Immunodeficiency and Autoimmunity.

Mohammad Hossein Asgardoon1, Gholamreza Azizi2, Reza Yazdani1,3, Mahsa Sohani1, Salar Pashangzadeh1, Arash Kalantari4, Mansoureh Shariat5, Alireza Shafiei6, Fereshte Salami1, Mahnaz Jamee2, Seyed Erfan Rasouli2, Javad Mohammadi7, Gholamreza Hassanpour8, Marziyeh Tavakol2, Zahra Chavoshzadeh9, Seyed Alireza Mahdaviani10, Tooba Momen11, Nasrin Behniafard12, Mohammad Nabavi13, Mohammad Hassan Bemanian13, Saba Arshi13, Rasol Molatefi14, Roya Sherkat15, Afshin Shirkani16, Soheila Alyasin17, Farahzad Jabbari-Azad18, Javad Ghaffari19, Mehrnaz Mesdaghi20, Hamid Ahanchian18, Maryam Khoshkhui18, Mohammad Hossein Eslamian21, Taher Cheraghi22, Abbas Dabbaghzadeh23, Rasoul Nasiri Kalmarzi24, Hossein Esmaeilzadeh17, Javad Tafaroji25, Abbas Khalili26, Mahnaz Sadeghi-Shabestari27, Sepideh Darougar9, Mojgan Moghtaderi17, Akefeh Ahmadiafshar28, Behzad Shakerian29, Marzieh Heidarzadeh30, Babak Ghalebaghi22, Seyed Mohammad Fathi31, Behzad Darabi32, Morteza Fallahpour13, Azam Mohsenzadeh33, Sarehsadat Ebrahimi34, Samin Sharafian34, Ahmad Vosughimotlagh34, Mitra Tafakoridelbari34, Maziyar Rahimi Haji-Abadi34, Parisa Ashournia34, Anahita Razaghian34, Arezou Rezaei1, Samaneh Delavari1, Paniz Shirmast1, Fateme Babaha1, Ashraf Samavat35, Setareh Mamishi36, Hossein Ali Khazaei37, Babak Negahdari38, Nima Rezaei1, Hassan Abolhassani3,39,40, Asghar Aghamohammadi41,42.   

Abstract

BACKGROUND: Common variable immunodeficiency (CVID) is the most frequent primary immunodeficiency disorder mainly characterized by recurrent bacterial infections besides other immunological defects including loss of or dysfunction of B cells and decreased immunoglobulin levels. In this study, our aim is to evaluate clinical, immunological, and molecular data of patients with a primary clinical diagnosis of CVID and autoimmune phenotype with a confirmed genetic diagnosis.
METHODS: Among 297 patients with CVID, who were registered in the Iranian Primary Immunodeficiency Registry at Children's Medical Center Hospital in Iran, 83 patients have been genetically examined and 27 patients with autoimmunity and confirmed genetic mutations were selected for analysis. Whole-exome sequencing and confirmatory Sanger sequencing methods were used for the study population. A questionnaire was retrospectively filled for all patients to evaluate demographic, laboratory, clinical, and genetic data.
RESULTS: In the 27 studied patients, 11 different genetic defects were identified, and the most common mutated gene was LRBA, reported in 17 (63.0%) patients. Two patients (7.7%) showed autoimmune complications as the first presentation of immunodeficiency. Eleven patients (40.7%) developed one type of autoimmunity, and 16 patients (59.3%) progressed to poly-autoimmunity. Most of the patients with mono-autoimmunity (n = 9, 90.0%) primarily developed infectious complications, while in patients with poly-autoimmunity, the most common first presentation was enteropathy (n = 6, 37.6%). In 13 patients (61.9%), the diagnosis of autoimmune disorders preceded the diagnosis of primary immunodeficiency. The most frequent autoimmune manifestations were hematologic (40.7%), gastrointestinal (48.1%), rheumatologic (25.9%), and dermatologic (22.2%) disorders. Patients with poly-autoimmunity had lower regulatory T cells than patients with mono-autoimmunity.
CONCLUSION: In our cohort, the diagnosis of autoimmune disorders preceded the diagnosis of primary immunodeficiency in most patients. This association highlights the fact that patients referring with autoimmune manifestations should be evaluated for humoral immunity.
© 2020 S. Karger AG, Basel.

Entities:  

Keywords:  Autoimmunity; Common variable immunodeficiency; Primary immunodeficiency; Sanger sequencing; Whole-exome sequencing

Year:  2020        PMID: 32615565     DOI: 10.1159/000508817

Source DB:  PubMed          Journal:  Int Arch Allergy Immunol        ISSN: 1018-2438            Impact factor:   2.749


  3 in total

1.  Primary antibody deficiencies in Turkey: molecular and clinical aspects.

Authors:  Sinem Firtina; Yuk Yin Ng; Ozden H Ng; Ayca Kiykim; Esra Yucel Ozek; Manolya Kara; Elif Aydiner; Serdar Nepesov; Yildiz Camcioglu; Esra H Sayar; Ezgi Yalcin Gungoren; Ismail Reisli; Selda H Torun; Sule Haskologlu; Tuba Cogurlu; Aysenur Kaya; Sukru Cekic; Safa Baris; Ugur Ozbek; Ahmet Ozen; Muge Sayitoglu
Journal:  Immunol Res       Date:  2021-10-07       Impact factor: 2.829

Review 2.  Autoimmune Cytopenias in Common Variable Immunodeficiency Are a Diagnostic and Therapeutic Conundrum: An Update.

Authors:  Sanchi Chawla; Prabal Barman; Rahul Tyagi; Ankur Kumar Jindal; Saniya Sharma; Amit Rawat; Surjit Singh
Journal:  Front Immunol       Date:  2022-06-20       Impact factor: 8.786

Review 3.  The pediatric common variable immunodeficiency - from genetics to therapy: a review.

Authors:  Aleksandra Szczawinska-Poplonyk; Eyal Schwartzmann; Ewelina Bukowska-Olech; Michal Biernat; Stanislaw Gattner; Tomasz Korobacz; Filip Nowicki; Monika Wiczuk-Wiczewska
Journal:  Eur J Pediatr       Date:  2021-12-23       Impact factor: 3.860

  3 in total

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