Literature DB >> 10898506

Diagnosis of X-linked lymphoproliferative disease by analysis of SLAM-associated protein expression.

K C Gilmour1, T Cranston, A Jones, E G Davies, D Goldblatt, A Thrasher, C Kinnon, K E Nichols, H B Gaspar.   

Abstract

X-linked lymphoproliferative disease (XLP) is an inherited immunodeficiency in which affected boys show abnormal responses to Epstein-Barr virus infection. The gene defective in XLP has been identified and designated SH2D1A and encodes a protein termed SLAM-associated protein (SAP). Mutation analysis in individuals with typical XLP presentations and family histories has only detected abnormalities in approximately 60% of patients. Thus, genetic analysis alone cannot confirm a diagnosis of XLP We have developed a SAP expression assay that can be used as a diagnostic indicator of XLP We show that SAP is constitutively expressed in normal individuals, in patients with severe sepsis and in patients with other primary immunodeficiencies. In six XLP patients, four with classical and two with atypical presentations, SAP expression was absent. In the latter two, who were previously assigned as having common variable immunodeficiency (CVID), the diagnosis of XLP was initially made using the protein expression assay. In two further patients in whom no mutation could be detected by genetic analysis, lack of SAP expression strongly suggests that these individuals have XLP. We therefore suggest that XLP should be suspected in certain boys previously diagnosed as having CVID and recommend that patients are investigated both by genetic analysis of SH2D1A and by expression of SAP protein.

Entities:  

Mesh:

Substances:

Year:  2000        PMID: 10898506     DOI: 10.1002/1521-4141(200006)30:6<1691::AID-IMMU1691>3.0.CO;2-K

Source DB:  PubMed          Journal:  Eur J Immunol        ISSN: 0014-2980            Impact factor:   5.532


  17 in total

Review 1.  X-linked lymphoproliferative syndrome.

Authors:  D L Nelson; C Terhorst
Journal:  Clin Exp Immunol       Date:  2000-12       Impact factor: 4.330

2.  X-linked lymphoproliferative disease due to SAP/SH2D1A deficiency: a multicenter study on the manifestations, management and outcome of the disease.

Authors:  Claire Booth; Kimberly C Gilmour; Paul Veys; Andrew R Gennery; Mary A Slatter; Helen Chapel; Paul T Heath; Colin G Steward; Owen Smith; Anna O'Meara; Hilary Kerrigan; Nizar Mahlaoui; Marina Cavazzana-Calvo; Alain Fischer; Despina Moshous; Stephane Blanche; Jana Pachlopnik Schmid; Jana Pachlopnick-Schmid; Sylvain Latour; Genevieve de Saint-Basile; Michael Albert; Gundula Notheis; Nikolaus Rieber; Brigitte Strahm; Henrike Ritterbusch; Arjan Lankester; Nico G Hartwig; Isabelle Meyts; Alessandro Plebani; Annarosa Soresina; Andrea Finocchi; Claudio Pignata; Emilia Cirillo; Sonia Bonanomi; Christina Peters; Krzysztof Kalwak; Srdjan Pasic; Petr Sedlacek; Janez Jazbec; Hirokazu Kanegane; Kim E Nichols; I Celine Hanson; Neena Kapoor; Elie Haddad; Morton Cowan; Sharon Choo; Joanne Smart; Peter D Arkwright; Hubert B Gaspar
Journal:  Blood       Date:  2010-10-06       Impact factor: 22.113

3.  Prevalence of SAP gene defects in male patients diagnosed with common variable immunodeficiency.

Authors:  D Eastwood; K C Gilmour; K Nistala; C Meaney; H Chapel; Z Sherrell; A D Webster; E G Davies; A Jones; H B Gaspar
Journal:  Clin Exp Immunol       Date:  2004-09       Impact factor: 4.330

4.  Defective B cell responses in the absence of SH2D1A.

Authors:  Massimo Morra; Robert A Barrington; Ana C Abadia-Molina; Susumo Okamoto; Aimee Julien; Charles Gullo; Anuj Kalsy; Matthew J Edwards; Gang Chen; Rosanne Spolski; Warren J Leonard; Brigitte T Huber; Persephone Borrow; Christine A Biron; Abhay R Satoskar; Michael C Carroll; Cox Terhorst
Journal:  Proc Natl Acad Sci U S A       Date:  2005-03-17       Impact factor: 11.205

5.  Structural basis for the interaction of the free SH2 domain EAT-2 with SLAM receptors in hematopoietic cells.

Authors:  M Morra; J Lu; F Poy; M Martin; J Sayos; S Calpe; C Gullo; D Howie; S Rietdijk; A Thompson; A J Coyle; C Denny; M B Yaffe; P Engel; M J Eck; C Terhorst
Journal:  EMBO J       Date:  2001-11-01       Impact factor: 11.598

6.  X-linked lymphoproliferative disease: three atypical cases.

Authors:  K Nistala; K C Gilmour; T Cranston; E G Davies; D Goldblatt; H B Gaspar; A M Jones
Journal:  Clin Exp Immunol       Date:  2001-10       Impact factor: 4.330

7.  Clinical and genetic characteristics of XIAP deficiency in Japan.

Authors:  Xi Yang; Hirokazu Kanegane; Naonori Nishida; Toshihiko Imamura; Kazuko Hamamoto; Ritsuko Miyashita; Kohsuke Imai; Shigeaki Nonoyama; Kazunori Sanayama; Akiko Yamaide; Fumiyo Kato; Kozo Nagai; Eiichi Ishii; Menno C van Zelm; Sylvain Latour; Xiao-Dong Zhao; Toshio Miyawaki
Journal:  J Clin Immunol       Date:  2012-01-08       Impact factor: 8.317

8.  X-Linked Lymphoproliferative Syndrome Presenting as Adult-Onset Multi-Infarct Dementia.

Authors:  Patrick R Blackburn; Wen-Lang Lin; David A Miller; Oswaldo Lorenzo-Betancor; Emily S Edwards; Michael T Zimmermann; Luca P Farrugia; William D Freeman; Alexandra I Soto; Ronald L Walton; Eric W Klee; Paldeep S Atwal; Roshini S Abraham; Daniel D Billadeau; Owen A Ross; Dennis W Dickson; James F Meschia
Journal:  J Neuropathol Exp Neurol       Date:  2019-05-01       Impact factor: 3.685

9.  Immunological and genetic analysis of 65 patients with a clinical suspicion of X linked hyper-IgM.

Authors:  K C Gilmour; D Walshe; S Heath; G Monaghan; S Loughlin; T Lester; G Norbury; C M Cale
Journal:  Mol Pathol       Date:  2003-10

10.  The value of DNA storage and pedigree analysis in rare diseases: a 17-year-old boy with X-linked lymphoproliferative disease (XLP) caused by a de novo SH2D1A mutation.

Authors:  E Overwater; Y Smulders; M van der Burg; M P Lombardi; H E Meijers-Heijboer; T W Kuijpers; A C Houweling
Journal:  Eur J Pediatr       Date:  2014-04-12       Impact factor: 3.183

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.