Literature DB >> 26246517

Cowden's syndrome with immunodeficiency.

Michael J Browning1, Anita Chandra2, Valentina Carbonaro3, Klaus Okkenhaug3, Julian Barwell4.   

Abstract

BACKGROUND: Cowden's syndrome is a rare, autosomal dominant disease caused by mutations in the phosphoinositide 3-kinase and phosphatase and tensin homolog (PTEN) gene. It is associated with hamartomatous polyposis of the gastrointestinal tract, mucocutaneous lesions and increased risk of developing certain types of cancer. In addition to increased risk of tumour development, mutations in PTEN have also been associated with autoimmunity in both mice and humans. Until now, however, an association between Cowden's syndrome and immune deficiency has been reported in a single patient only. METHODS AND
RESULTS: Two patients with Cowden's syndrome and an increased frequency of infections were investigated for possible underlying immunodeficiency. In one patient, hypogammaglobulinaemia with a functional antibody deficiency was identified, while the other patient had a persisting CD4+ T cell lymphopenia (with normal antibody production).
CONCLUSIONS: Our data indicate that Cowden's syndrome may be associated with both T cell and B cell immune dysfunction. We recommend that patients with Cowden's syndrome and an increased frequency of infections are investigated for associated immunodeficiency. Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/

Entities:  

Keywords:  Cell biology; Genetics; Immunology (including allergy); Infection

Mesh:

Substances:

Year:  2015        PMID: 26246517      PMCID: PMC4661225          DOI: 10.1136/jmedgenet-2015-103266

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  20 in total

1.  Mutations in PIK3CD can cause hyper IgM syndrome (HIGM) associated with increased cancer susceptibility.

Authors:  M C Crank; J K Grossman; S Moir; S Pittaluga; C M Buckner; L Kardava; A Agharahimi; H Meuwissen; J Stoddard; J Niemela; H Kuehn; S D Rosenzweig
Journal:  J Clin Immunol       Date:  2014-03-08       Impact factor: 8.317

2.  Cowden's disease associated with immunodeficiency.

Authors:  P J Ruschak; Y C Kauh; H A Luscombe
Journal:  Arch Dermatol       Date:  1981-09

3.  Impaired Fas response and autoimmunity in Pten+/- mice.

Authors:  A Di Cristofano; P Kotsi; Y F Peng; C Cordon-Cardo; K B Elkon; P P Pandolfi
Journal:  Science       Date:  1999-09-24       Impact factor: 47.728

4.  Regulation of class-switch recombination and plasma cell differentiation by phosphatidylinositol 3-kinase signaling.

Authors:  Sidne A Omori; Matthew H Cato; Amy Anzelon-Mills; Kamal D Puri; Miriam Shapiro-Shelef; Kathryn Calame; Robert C Rickert
Journal:  Immunity       Date:  2006-09-28       Impact factor: 31.745

5.  Functional evaluation of PTEN missense mutations using in vitro phosphoinositide phosphatase assay.

Authors:  S Y Han; H Kato; S Kato; T Suzuki; H Shibata; S Ishii; K Shiiba; S Matsuno; R Kanamaru; C Ishioka
Journal:  Cancer Res       Date:  2000-06-15       Impact factor: 12.701

6.  Pten inactivation alters peripheral B lymphocyte fate and reconstitutes CD19 function.

Authors:  Amy N Anzelon; Hong Wu; Robert C Rickert
Journal:  Nat Immunol       Date:  2003-02-03       Impact factor: 25.606

Review 7.  Regulation of T-cell responses by PTEN.

Authors:  Jodi L Buckler; Xiaohe Liu; Laurence A Turka
Journal:  Immunol Rev       Date:  2008-08       Impact factor: 12.988

Review 8.  Assessment and clinical interpretation of polysaccharide antibody responses.

Authors:  Kenneth Paris; Ricardo U Sorensen
Journal:  Ann Allergy Asthma Immunol       Date:  2007-11       Impact factor: 6.347

9.  Critical roles of Pten in B cell homeostasis and immunoglobulin class switch recombination.

Authors:  Akira Suzuki; Tsuneyasu Kaisho; Minako Ohishi; Manae Tsukio-Yamaguchi; Takeshi Tsubata; Pandelakis A Koni; Takehiko Sasaki; Tak Wah Mak; Toru Nakano
Journal:  J Exp Med       Date:  2003-03-03       Impact factor: 14.307

10.  The effect of deleting p110delta on the phenotype and function of PTEN-deficient B cells.

Authors:  Michelle L Janas; Daniel Hodson; Zania Stamataki; Sue Hill; Katie Welch; Laure Gambardella; Lloyd C Trotman; Pier Paolo Pandolfi; Elena Vigorito; Martin Turner
Journal:  J Immunol       Date:  2008-01-15       Impact factor: 5.422

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  19 in total

Review 1.  Immune Dysregulation and Disease Pathogenesis due to Activating Mutations in PIK3CD-the Goldilocks' Effect.

Authors:  Stuart G Tangye; Julia Bier; Anthony Lau; Tina Nguyen; Gulbu Uzel; Elissa K Deenick
Journal:  J Clin Immunol       Date:  2019-03-25       Impact factor: 8.317

Review 2.  Common variable immune deficiency: Dissection of the variable.

Authors:  Charlotte Cunningham-Rundles
Journal:  Immunol Rev       Date:  2019-01       Impact factor: 12.988

3.  Intermediate uveitis in a child with phosphatase and tensin homolog gene mutation and Bannayan-Riley-Ruvalcaba syndrome.

Authors:  Daphna Prat; Iris Ben Bassat Mizrachi; Vicktoria Vishnevskia-Dai
Journal:  BMJ Case Rep       Date:  2019-02-12

4.  Multidisciplinary surgical management of Cowden syndrome: Report of a case.

Authors:  Romeo Patini; Edoardo Staderini; Patrizia Gallenzi
Journal:  J Clin Exp Dent       Date:  2016-10-01

5.  Clinical impact of a targeted next-generation sequencing gene panel for autoinflammation and vasculitis.

Authors:  Ebun Omoyinmi; Ariane Standing; Annette Keylock; Fiona Price-Kuehne; Sonia Melo Gomes; Dorota Rowczenio; Sira Nanthapisal; Thomas Cullup; Rodney Nyanhete; Emma Ashton; Claire Murphy; Megan Clarke; Helena Ahlfors; Lucy Jenkins; Kimberly Gilmour; Despina Eleftheriou; Helen J Lachmann; Philip N Hawkins; Nigel Klein; Paul A Brogan
Journal:  PLoS One       Date:  2017-07-27       Impact factor: 3.240

6.  Identification of mutations in the PI3K-AKT-mTOR signalling pathway in patients with macrocephaly and developmental delay and/or autism.

Authors:  Kit San Yeung; Winnie Wan Yee Tso; Janice Jing Kun Ip; Christopher Chun Yu Mak; Gordon Ka Chun Leung; Mandy Ho Yin Tsang; Dingge Ying; Steven Lim Cho Pei; So Lun Lee; Wanling Yang; Brian Hon-Yin Chung
Journal:  Mol Autism       Date:  2017-12-20       Impact factor: 7.509

7.  De Novo PTEN Mutation in a Young Boy with Cutaneous Vasculitis.

Authors:  Angela Mauro; Ebun Omoyinmi; Neil James Sebire; Angela Barnicoat; Paul Brogan
Journal:  Case Rep Pediatr       Date:  2017-04-24

Review 8.  PI3Kδ and primary immunodeficiencies.

Authors:  Carrie L Lucas; Anita Chandra; Sergey Nejentsev; Alison M Condliffe; Klaus Okkenhaug
Journal:  Nat Rev Immunol       Date:  2016-09-12       Impact factor: 53.106

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.  Two Monogenetic Disorders, Activated PI3-Kinase-δ Syndrome 2 and Smith-Magenis Syndrome, in One Patient: Case Report and a Literature Review of Neurodevelopmental Impact in Primary Immunodeficiencies Associated With Disturbed PI3K Signaling.

Authors:  Nidia Moreno-Corona; Loïc Chentout; Lucie Poggi; Romane Thouenon; Cecile Masson; Melanie Parisot; Lou Le Mouel; Capucine Picard; Isabelle André; Marina Cavazzana; Laurence Perrin; Anne Durandy; Saba Azarnoush; Sven Kracker
Journal:  Front Pediatr       Date:  2021-06-24       Impact factor: 3.418

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