Literature DB >> 26596586

Molecular Characteristics, Clinical and Immunologic Manifestations of 11 Children with Omenn Syndrome in East Slavs (Russia, Belarus, Ukraine).

Svetlana O Sharapova1, Irina E Guryanova2, Olga E Pashchenko3, Irina V Kondratenko3, Larisa V Kostyuchenko4, Yulia A Rodina5, Tatjana V Varlamova5, Anastasiia V Bondarenko6, Liudmyla I Chernyshova5, Marina N Gyseva7, Mikhail V Belevtsev2, Nina V Minakovskaya2, Olga V Aleinikova2.   

Abstract

BACKGROUND: Omenn syndrome [Mendelian Inheritance (OMIM 603554)] is a genetic disease of the immune system, characterized by the presence of fatal generalized severe erythroderma, lymphoadenopathy, eosinophilia and profound immunodeficiency.
OBJECTIVE: We studied clinical and immunologic presentation of the disease manifestation among East Slavs population with genetically confirmed Omenn syndrome.
RESULTS: We collected clinical and immunologic data of 11 patients (1 from Belarus, 5--Ukraine, 5--Russia): 6 females, 5 males. The age of Omenn syndrome manifestation varied from the 1st day of life to 1 year and 1 month, the age of diagnosis--20 days to 1 year and 10 months. Nine out of 11 patients had classic immunologic phenotype T(+/-)B-NK+, 1 pt had TlowB + NK+ with CD3 + TCRgd + expansion and 1 had TlowB+/-NK+ phenotype. Eight out of 11 pts had mutation in RAG1 gene, 4 out of 8 had c.368-369delAA (p.K86fsX118) in homozygous state or heterozygous compound. In our cohort of patients, we also described two new mutations in RAG genes (p.E722Q in RAG1 and p.M459R in RAG2). At present, 7/11 were transplanted and 5 out of the transplanted are alive.
CONCLUSION: This study demonstrates that the most popular genetic abnormality in East Slavs children with Omenn syndrome is c.368-369delAA (p.K86fs118) in RAG1 gene, which may be connected with more favorable prognosis because 4/4 patients survived after hematopoietic stem cells transplantation.

Entities:  

Keywords:  East Slavs children; Omenn syndrome; RAG1/2 genes; mutations

Mesh:

Substances:

Year:  2015        PMID: 26596586     DOI: 10.1007/s10875-015-0216-7

Source DB:  PubMed          Journal:  J Clin Immunol        ISSN: 0271-9142            Impact factor:   8.317


  32 in total

1.  Omenn syndrome is associated with mutations in DNA ligase IV.

Authors:  Eyal Grunebaum; Andrea Bates; Chaim M Roifman
Journal:  J Allergy Clin Immunol       Date:  2008-10-09       Impact factor: 10.793

Review 2.  Clinical and immunological manifestations of patients with atypical severe combined immunodeficiency.

Authors:  Kerstin Felgentreff; Ruy Perez-Becker; Carsten Speckmann; Klaus Schwarz; Krzysztof Kalwak; Gasper Markelj; Tadej Avcin; Waseem Qasim; E G Davies; Tim Niehues; Stephan Ehl
Journal:  Clin Immunol       Date:  2011-05-30       Impact factor: 3.969

3.  BCG vaccination in patients with severe combined immunodeficiency: complications, risks, and vaccination policies.

Authors:  Beatriz E Marciano; Chiung-Yu Huang; Gyan Joshi; Nima Rezaei; Beatriz Costa Carvalho; Zoe Allwood; Aydan Ikinciogullari; Shereen M Reda; Andrew Gennery; Vojtech Thon; Francisco Espinosa-Rosales; Waleed Al-Herz; Oscar Porras; Anna Shcherbina; Anna Szaflarska; Şebnem Kiliç; Jose L Franco; Andrea C Gómez Raccio; Persio Roxo; Isabel Esteves; Nermeen Galal; Anete Sevciovic Grumach; Salem Al-Tamemi; Alisan Yildiran; Julio C Orellana; Masafumi Yamada; Tomohiro Morio; Diana Liberatore; Yoshitoshi Ohtsuka; Yu-Lung Lau; Ryuta Nishikomori; Carlos Torres-Lozano; Juliana T L Mazzucchelli; Maria M S Vilela; Fabiola S Tavares; Luciana Cunha; Jorge A Pinto; Sara E Espinosa-Padilla; Leticia Hernandez-Nieto; Reem A Elfeky; Tadashi Ariga; Heike Toshio; Figen Dogu; Funda Cipe; Renata Formankova; M Enriqueta Nuñez-Nuñez; Liliana Bezrodnik; Jose Gonçalo Marques; María I Pereira; Viviana Listello; Mary A Slatter; Zohreh Nademi; Danuta Kowalczyk; Thomas A Fleisher; Graham Davies; Bénédicte Neven; Sergio D Rosenzweig
Journal:  J Allergy Clin Immunol       Date:  2014-04       Impact factor: 10.793

4.  Skin infiltration of CD56(bright) CD16(-) natural killer cells in a case of X-SCID with Omenn syndrome-like manifestations.

Authors:  Fumie Shibata; Tomoko Toma; Taizo Wada; Masayuki Inoue; Yumi Tone; Kazuhide Ohta; Yoshihito Kasahara; Fumie Sano; Mitsuaki Kimura; Mitsuru Ikeno; Shoichi Koizumi; Akihiro Yachie
Journal:  Eur J Haematol       Date:  2007-07       Impact factor: 2.997

5.  Mutations in CHD7 in patients with CHARGE syndrome cause T-B + natural killer cell + severe combined immune deficiency and may cause Omenn-like syndrome.

Authors:  A R Gennery; M A Slatter; J Rice; L H Hoefsloot; D Barge; A McLean-Tooke; T Montgomery; J A Goodship; A D Burt; T J Flood; M Abinun; A J Cant; D Johnson
Journal:  Clin Exp Immunol       Date:  2008-05-26       Impact factor: 4.330

6.  Recombinase-activating gene 1 immunodeficiency: different immunological phenotypes in three siblings.

Authors:  Srdjan Pasic; Slavisa Djuricic; Goran Ristic; Bojana Slavkovic
Journal:  Acta Paediatr       Date:  2009-02-24       Impact factor: 2.299

Review 7.  The genetic and biochemical basis of Omenn syndrome.

Authors:  S Santagata; A Villa; C Sobacchi; P Cortes; P Vezzoni
Journal:  Immunol Rev       Date:  2000-12       Impact factor: 12.988

8.  Omenn syndrome in an infant with IL7RA gene mutation.

Authors:  Silvia Giliani; Carmen Bonfim; Genevieve de Saint Basile; Gaetana Lanzi; Nicole Brousse; Adriana Koliski; Mariester Malvezzi; Alain Fischer; Luigi D Notarangelo; Francoise Le Deist
Journal:  J Pediatr       Date:  2006-02       Impact factor: 4.406

9.  Similar recombination-activating gene (RAG) mutations result in similar immunobiological effects but in different clinical phenotypes.

Authors:  Hanna IJspeert; Gertjan J Driessen; Michael J Moorhouse; Nico G Hartwig; Beata Wolska-Kusnierz; Krzysztof Kalwak; Anna Pituch-Noworolska; Irina Kondratenko; Joris M van Montfrans; Ester Mejstrikova; Arjan C Lankester; Anton W Langerak; Dik C van Gent; Andrew P Stubbs; Jacques J M van Dongen; Mirjam van der Burg
Journal:  J Allergy Clin Immunol       Date:  2014-01-11       Impact factor: 10.793

10.  A novel immunodeficiency associated with hypomorphic RAG1 mutations and CMV infection.

Authors:  Jean-Pierre de Villartay; Annick Lim; Hamoud Al-Mousa; Sophie Dupont; Julie Déchanet-Merville; Edith Coumau-Gatbois; Marie-Lise Gougeon; Arnaud Lemainque; Céline Eidenschenk; Emmanuelle Jouanguy; Laurent Abel; Jean-Laurent Casanova; Alain Fischer; Françoise Le Deist
Journal:  J Clin Invest       Date:  2005-11       Impact factor: 14.808

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  6 in total

1.  Phenotypical heterogeneity in RAG-deficient patients from a highly consanguineous population.

Authors:  S S Meshaal; R E El Hawary; D S Abd Elaziz; A Eldash; R Alkady; S Lotfy; A A Mauracher; L Opitz; J Pachlopnik Schmid; M van der Burg; J Chou; N M Galal; J A Boutros; R Geha; A M Elmarsafy
Journal:  Clin Exp Immunol       Date:  2018-11-04       Impact factor: 4.330

2.  Mutation c.256_257delAA in RAG1 Gene in Polish Children with Severe Combined Immunodeficiency: Diversity of Clinical Manifestations.

Authors:  Anna Szaflarska; Magdalena Rutkowska-Zapała; Monika Kotula; Anna Gruca; Agnieszka Grabowska; Marzena Lenart; Marta Surman; Elżbieta Trzyna; Anna Mordel; Anna Pituch-Noworolska; Maciej Siedlar
Journal:  Arch Immunol Ther Exp (Warsz)       Date:  2017-01-12       Impact factor: 4.291

3.  A Novel RAG1 Mutation in a Compound Heterozygous Status in a Child With Omenn Syndrome.

Authors:  Juan Shen; Li Jiang; Yifang Gao; Rongqiong Ou; Sifei Yu; Binyan Yang; Changyou Wu; Weiping Tan
Journal:  Front Genet       Date:  2019-10-02       Impact factor: 4.599

Review 4.  Proposal for a 6-step approach for differential diagnosis of neonatal erythroderma.

Authors:  E Cuperus; A Bygum; L Boeckmann; C Bodemer; M C Bolling; M Caproni; A Diociaiuti; S Emmert; J Fischer; A Gostynski; S Guez; M E van Gijn; K Hannulla-Jouppi; C Has; A Hernández-Martín; A E Martinez; J Mazereeuw-Hautier; M Medvecz; I Neri; V Sigurdsson; K Suessmuth; H Traupe; V Oji; S G M A Pasmans
Journal:  J Eur Acad Dermatol Venereol       Date:  2022-03-15       Impact factor: 9.228

5.  The Clinical and Genetic Spectrum of 82 Patients With RAG Deficiency Including a c.256_257delAA Founder Variant in Slavic Countries.

Authors:  Svetlana O Sharapova; Małgorzata Skomska-Pawliszak; Yulia A Rodina; Beata Wolska-Kuśnierz; Nel Dabrowska-Leonik; Bozena Mikołuć; Olga E Pashchenko; Srdjan Pasic; Tomáš Freiberger; Tomáš Milota; Renata Formánková; Anna Szaflarska; Maciej Siedlar; Tadej Avčin; Gašper Markelj; Peter Ciznar; Krzysztof Kalwak; Sylwia Kołtan; Teresa Jackowska; Katarzyna Drabko; Alenka Gagro; Małgorzata Pac; Elissaveta Naumova; Snezhina Kandilarova; Katarzyna Babol-Pokora; Dzmitry S Varabyou; Barbara H Barendregt; Elena V Raykina; Tatiana V Varlamova; Anna V Pavlova; Hana Grombirikova; Maruša Debeljak; Irina V Mersiyanova; Anastasiia V Bondarenko; Liudmyla I Chernyshova; Larysa V Kostyuchenko; Marina N Guseva; Jelena Rascon; Audrone Muleviciene; Egle Preiksaitiene; Christoph B Geier; Alexander Leiss-Piller; Yasuhiro Yamazaki; Tomoki Kawai; Jolan E Walter; Irina V Kondratenko; Anna Šedivá; Mirjam van der Burg; Natalia B Kuzmenko; Luigi D Notarangelo; Ewa Bernatowska; Olga V Aleinikova
Journal:  Front Immunol       Date:  2020-06-10       Impact factor: 7.561

6.  Primary Immunodeficiencies in Russia: Data From the National Registry.

Authors:  Anna A Mukhina; Natalya B Kuzmenko; Yulia A Rodina; Irina V Kondratenko; Andrei A Bologov; Tatiana V Latysheva; Andrei P Prodeus; Alexander N Pampura; Dmitrii N Balashov; Natalya I Ilyina; Elena A Latysheva; Ekaterina A Deordieva; Oksana A Shvets; Elena V Deripapa; Irina N Abramova; Olga E Pashenko; Svetlana S Vahlyarskaya; Natalya V Zinovyeva; Sergei B Zimin; Elena V Skorobogatova; Elena B Machneva; Daria S Fomina; Maria G Ipatova; Ludmila Yu Barycheva; Ludmila S Khachirova; Irina A Tuzankina; Michail A Bolkov; Natalya V Shakhova; Elena M Kamaltynova; Farida I Sibgatullina; Marina N Guseva; Raisa N Kuznetsova; Anzhelika M Milichkina; Areg A Totolian; Natalia M Kalinina; Evgenia A Goltsman; Ekatherina I Sulima; Anastasia Yu Kutlyanceva; Anna A Moiseeva; Anna L Khoreva; Zoya Nesterenko; Elena V Tymofeeva; A Ermakova; Dilyara D Proligina; Linara R Kalmetieva; Gulshat A Davletbaieva; Irina A Mirsayapova; Olga A Richkova; Ksenia P Kuzmicheva; Maria A Grakhova; Natalya B Yudina; Ekaterina A Orlova; Olga S Selezneva; Svetlana G Piskunova; Tatiana V Samofalova; Tatiana V Bukina; Anna D Pechkurova; N Migacheva; A Zhestkov; Elena V Barmina; Natalya A Parfenova; Svetlana N Isakova; Elena V Averina; Irina V Sazonova; Svetlana Yu Starikova; Tatiana V Shilova; Tatiana V Asekretova; Roman N Suprun; Elena I Kleshchenko; Vladimir V Lebedev; Elena V Demikhova; Valerii G Demikhov; Veronica A Kalinkina; Alla V Gorenkova; Svetlana N Duryagina; Tatiana B Pavlova; Vera M Shinkareva; Irina V Smoleva; Tatiana P Aleksandrova; Zema V Bambaeva; Marina A Philippova; Elena M Gracheva; Galina I Tcyvkina; Alexey V Efremenkov; D Mashkovskaya; Irina V Yarovaya; Valentina A Alekseenko; Ivan V Fisyun; Galina V Molokova; Ekatherina V Troitskya; Ludmila I Piatkina; Elena V Vlasova; O Ukhanova; Ekaterina G Chernishova; M Vasilieva; Olga M Laba; E Volodina; Ekaterina V Safonova; Kirill A Voronin; Maria V Gurkina; Alexander G Rumyantsev; Galina A Novichkova; Anna Yu Shcherbina
Journal:  Front Immunol       Date:  2020-08-06       Impact factor: 7.561

  6 in total

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