Literature DB >> 16611257

A91V perforin variation in healthy subjects and FHLH patients.

R Busiello1, G Fimiani, M G Miano, M Aricò, A Santoro, M V Ursini, C Pignata.   

Abstract

Familial haemophagocytic lymphohistiocytosis (FHLH) is a heterogeneous autosomal recessive disorder characterized by hyperactivation of monocytes/macrophages. Perforin (PRF1) gene alterations have been documented in 40% of patients with FHLH. Although several mutations have been identified, a clear correlation between the individual molecular alteration and the phenotypic expression of the disease is still unclear. In particular, the role that the A91V substitution plays in the pathogenesis of the disease is still controversial. In the effort to make a conclusive remark to this issue, we here report on the frequency of the A91V mutation in a group of unrelated healthy families obtained from the "Centre d'Etude du Polymorphisme Humain" (CEPH), which are considered representative of the worldwide population. This frequency was compared to that observed in FHLH patients recruited through the Italian National Registry. The frequency in CEPH healthy subjects is 3.7%, thus indicating that the alteration represents a polymorphism. However, the frequency of this alteration in FHLH patients associated with PRF1 mutation is much higher than that observed in controls (26.2%, P = 0.0002), suggesting that the alteration is an important genetic susceptibility factor.

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Year:  2006        PMID: 16611257     DOI: 10.1111/j.1744-313X.2006.00582.x

Source DB:  PubMed          Journal:  Int J Immunogenet        ISSN: 1744-3121            Impact factor:   1.466


  6 in total

1.  Functional and genetic testing in adults with HLH reveals an inflammatory profile rather than a cytotoxicity defect.

Authors:  Julien Carvelli; Christelle Piperoglou; Catherine Farnarier; Frédéric Vely; Karin Mazodier; Sandra Audonnet; Patrick Nitschke; Christine Bole-Feysot; Mohamed Boucekine; Audrey Cambon; Mohamed Hamidou; Jean-Robert Harle; Geneviève de Saint Basile; Gilles Kaplanski
Journal:  Blood       Date:  2020-07-30       Impact factor: 22.113

2.  Hypomorphic mutations in PRF1, MUNC13-4, and STXBP2 are associated with adult-onset familial HLH.

Authors:  Kejian Zhang; Michael B Jordan; Rebecca A Marsh; Judith A Johnson; Diane Kissell; Jarek Meller; Joyce Villanueva; Kimberly A Risma; Qian Wei; Peter S Klein; Alexandra H Filipovich
Journal:  Blood       Date:  2011-08-31       Impact factor: 22.113

3.  Hemophagocytic lymphohistiocytosis in adults: collaborative analysis of 137 cases of a nationwide German registry.

Authors:  Sebastian Birndt; Thomas Schenk; Babett Heinevetter; Frank M Brunkhorst; Georg Maschmeyer; Frank Rothmann; Thomas Weber; Markus Müller; Jens Panse; Olaf Penack; Roland Schroers; Jan Braess; Norbert Frickhofen; Stephan Ehl; Gritta Janka; Kai Lehmberg; Mathias W Pletz; Andreas Hochhaus; Thomas Ernst; Paul La Rosée
Journal:  J Cancer Res Clin Oncol       Date:  2020-02-20       Impact factor: 4.553

4.  The R156H variation in IL-12Rβ1 is not a mutation.

Authors:  Esther van de Vosse; Jaap T van Dissel; Loredana Palamaro; Giuliana Giardino; Francesca Santamaria; Rosa Romano; Anna Fusco; Silvia Montella; Mariacarolina Salerno; Matilde Valeria Ursini; Claudio Pignata
Journal:  Ital J Pediatr       Date:  2013-02-14       Impact factor: 2.638

5.  Perforin gene variant A91V in young patients with severe COVID-19.

Authors: 
Journal:  Haematologica       Date:  2020-07-23       Impact factor: 9.941

Review 6.  Digenic Inheritance: Evidence and Gaps in Hemophagocytic Lymphohistiocytosis.

Authors:  Erica A Steen; Michelle L Hermiston; Kim E Nichols; Lauren K Meyer
Journal:  Front Immunol       Date:  2021-11-17       Impact factor: 8.786

  6 in total

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