Literature DB >> 28627729

The immune deficiency of chromosome 22q11.2 deletion syndrome.

Megan Morsheimer1, Terri F Brown Whitehorn2, Jennifer Heimall2, Kathleen E Sullivan2.   

Abstract

The syndrome originally described by Dr. Angelo DiGeorge had immunodeficiency as a central component. When a 22q11.2 deletion was identified as the cause in the majority of patients with DiGeorge syndrome, the clinical features of 22q11.2 deletion syndrome became so expansive that the immunodeficiency became less prominent in our thinking about the syndrome. This review will focus on the immune system and the changes in our understanding over the past 50 years. Initially characterized as a pure defect in T cell development, we now appreciate that many of the clinical features related to the immunodeficiency are well downstream of the limitation imposed by a small thymus. Dysfunctional B cells presumed to be secondary to compromised T cell help, issues related to T cell exhaustion, and high rates of atopy and autoimmunity are aspects of management that require consideration for optimal clinical care and for designing a cogent monitoring approach. New data on atopy are presented to further demonstrate the association.
© 2017 Wiley Periodicals, Inc.

Entities:  

Keywords:  DiGeorge; IgG; T cells; allergy; malignancy

Mesh:

Year:  2017        PMID: 28627729     DOI: 10.1002/ajmg.a.38319

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  17 in total

1.  FOXN1 compound heterozygous mutations cause selective thymic hypoplasia in humans.

Authors:  Qiumei Du; Larry K Huynh; Fatma Coskun; Erika Molina; Matthew A King; Prithvi Raj; Shaheen Khan; Igor Dozmorov; Christine M Seroogy; Christian A Wysocki; Grace T Padron; Tyler R Yates; M Louise Markert; M Teresa de la Morena; Nicolai Sc van Oers
Journal:  J Clin Invest       Date:  2019-11-01       Impact factor: 14.808

Review 2.  Imaging Features of Primary Immunodeficiency Disorders.

Authors:  Jose A Rodriguez; Tami J Bang; Carlos S Restrepo; Daniel B Green; Lorna P Browne; Daniel Vargas
Journal:  Radiol Cardiothorac Imaging       Date:  2021-03-25

3.  Inherited TNFSF9 deficiency causes broad Epstein-Barr virus infection with EBV+ smooth muscle tumors.

Authors:  Benjamin Fournier; Akihiro Hoshino; Anne-Sophie Defachelles; Bénédicte Neven; Julie Bruneau; Camille Bachelet; Mathieu Fusaro; Roman Klifa; Romain Lévy; Christelle Lenoir; Claire Soudais; Capucine Picard; Stéphane Blanche; Martin Castelle; Despina Moshous; Thierry Molina; Sylvain Latour
Journal:  J Exp Med       Date:  2022-06-03       Impact factor: 17.579

4.  Common Variable Immunodeficiency and Neurodevelopmental Delay Due to a 13Mb Deletion on Chromosome 4 Including the NFKB1 Gene: A Case Report.

Authors:  Clara Franco-Jarava; Irene Valenzuela; Jacques G Riviere; Marina Garcia-Prat; Mónica Martínez-Gallo; Romina Dieli-Crimi; Neus Castells; Laura Batlle-Masó; Pere Soler-Palacin; Roger Colobran
Journal:  Front Immunol       Date:  2022-06-17       Impact factor: 8.786

Review 5.  Immune and Genetic Features of the Chromosome 22q11.2 Deletion (DiGeorge Syndrome).

Authors:  Caroline Y Kuo; Rebecca Signer; Sulagna C Saitta
Journal:  Curr Allergy Asthma Rep       Date:  2018-10-30       Impact factor: 4.806

Review 6.  Variable immune deficiency related to deletion size in chromosome 22q11.2 deletion syndrome.

Authors:  Blaine Crowley; Melanie Ruffner; Donna M McDonald McGinn; Kathleen E Sullivan
Journal:  Am J Med Genet A       Date:  2018-01-17       Impact factor: 2.802

Review 7.  Newborn Screening for Severe Combined Immunodeficiency.

Authors:  John Routes; James Verbsky
Journal:  Curr Allergy Asthma Rep       Date:  2018-05-10       Impact factor: 4.806

8.  Relationship Between Severity of T Cell Lymphopenia and Immune Dysregulation in Patients with DiGeorge Syndrome (22q11.2 Deletions and/or Related TBX1 Mutations): a USIDNET Study.

Authors:  Deepti R Deshpande; Yesim Y Demirdag; Rebecca A Marsh; Kathleen E Sullivan; Jordan S Orange
Journal:  J Clin Immunol       Date:  2020-09-19       Impact factor: 8.317

Review 9.  Molecular Insights Into the Causes of Human Thymic Hypoplasia With Animal Models.

Authors:  Pratibha Bhalla; Christian A Wysocki; Nicolai S C van Oers
Journal:  Front Immunol       Date:  2020-05-05       Impact factor: 7.561

10.  Long-term robustness of a T-cell system emerging from somatic rescue of a genetic block in T-cell development.

Authors:  Patrick Kury; Marita Führer; Sebastian Fuchs; Myriam R Lorenz; Orlando Bruno Giorgetti; Shahrzad Bakhtiar; Andreas P Frei; Paul Fisch; Thomas Boehm; Klaus Schwarz; Carsten Speckmann; Stephan Ehl
Journal:  EBioMedicine       Date:  2020-08-22       Impact factor: 8.143

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