Genotype-phenotype study of familial haemophagocytic lymphohistiocytosis due to perforin mutations

A. Trizzino, U. Zur Stadt, I. Ueda, K. Risma, G. Janka, E. Ishii, K. Beutel, J. Sumegi, S. Cannella, D. Pende, A. Mian, J. I. Henter, G. Griffiths, A. Santoro, A. Filipovich, M. Aricò

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Abstract

Background: PRF1 gene mutations are associated with familial haemophagocytic lymphohistiocytosis type 2 (FHL2). Genotype-phenotype analysis, previously hampered by limited numbers of patients, was for the first time performed by data pooling from five large centres worldwide. Patients and methods: Members of the Histiocyte Society were asked to report cases of FHL2 on specific forms. Data were pooled in a common database and analysed. Results: The 124 patients had 63 different mutations (including 15 novel mutations): 11 nonsense, 10 frameshift, 38 missense and 4 in-frame deletions. Some mutations were found more commonly: 1122 G→A (W374X), associated with Turkish origin, in 32 patients; 50delT (L17fsX22) associated with African/African American origin, in 21 patients; and 1090-91delCT (L364fsX), in 7 Japanese patients. Flow cytometry showed that perforin expression was absent in 40, reduced in 6 and normal in 4 patients. Patients presented at a median age of 3 months (quartiles: 2, 3 and 13 months), always with fever, splenomegaly and thrombocytopenia. NK activity was absent in 36 (51%), ≤ 2% in 18 (26%), 3- ≤ 5% in 10 (14%), > 5% in 4 (6%), "reduced" in 2 (3%) (not reported, n = 54). Nonsense mutations were significantly associated with younger age at onset (p <0.001) and absent natural killer activity (p = 0.008). Conclusion: PRF1 mutations are spread over the functional domains. Specific mutations are strongly associated with Turkish, African American and Japanese ethnic groups. Later onset and residual cytotoxic function are observed in patients with at least one missense mutation.

Original languageEnglish
Pages (from-to)15-21
Number of pages7
JournalJournal of Medical Genetics
Volume45
Issue number1
DOIs
Publication statusPublished - Jan 2008

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Hemophagocytic Lymphohistiocytosis
Perforin
Genotype
Phenotype
Mutation
Nonsense Codon
African Americans
Histiocytes
Splenomegaly
Missense Mutation
Age of Onset
Ethnic Groups
Thrombocytopenia
Meta-Analysis
Flow Cytometry
Fever
Databases

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this

Trizzino, A., Zur Stadt, U., Ueda, I., Risma, K., Janka, G., Ishii, E., ... Aricò, M. (2008). Genotype-phenotype study of familial haemophagocytic lymphohistiocytosis due to perforin mutations. Journal of Medical Genetics, 45(1), 15-21. https://doi.org/10.1136/jmg.2007.052670

Genotype-phenotype study of familial haemophagocytic lymphohistiocytosis due to perforin mutations. / Trizzino, A.; Zur Stadt, U.; Ueda, I.; Risma, K.; Janka, G.; Ishii, E.; Beutel, K.; Sumegi, J.; Cannella, S.; Pende, D.; Mian, A.; Henter, J. I.; Griffiths, G.; Santoro, A.; Filipovich, A.; Aricò, M.

In: Journal of Medical Genetics, Vol. 45, No. 1, 01.2008, p. 15-21.

Research output: Contribution to journalArticle

Trizzino, A, Zur Stadt, U, Ueda, I, Risma, K, Janka, G, Ishii, E, Beutel, K, Sumegi, J, Cannella, S, Pende, D, Mian, A, Henter, JI, Griffiths, G, Santoro, A, Filipovich, A & Aricò, M 2008, 'Genotype-phenotype study of familial haemophagocytic lymphohistiocytosis due to perforin mutations', Journal of Medical Genetics, vol. 45, no. 1, pp. 15-21. https://doi.org/10.1136/jmg.2007.052670
Trizzino, A. ; Zur Stadt, U. ; Ueda, I. ; Risma, K. ; Janka, G. ; Ishii, E. ; Beutel, K. ; Sumegi, J. ; Cannella, S. ; Pende, D. ; Mian, A. ; Henter, J. I. ; Griffiths, G. ; Santoro, A. ; Filipovich, A. ; Aricò, M. / Genotype-phenotype study of familial haemophagocytic lymphohistiocytosis due to perforin mutations. In: Journal of Medical Genetics. 2008 ; Vol. 45, No. 1. pp. 15-21.
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abstract = "Background: PRF1 gene mutations are associated with familial haemophagocytic lymphohistiocytosis type 2 (FHL2). Genotype-phenotype analysis, previously hampered by limited numbers of patients, was for the first time performed by data pooling from five large centres worldwide. Patients and methods: Members of the Histiocyte Society were asked to report cases of FHL2 on specific forms. Data were pooled in a common database and analysed. Results: The 124 patients had 63 different mutations (including 15 novel mutations): 11 nonsense, 10 frameshift, 38 missense and 4 in-frame deletions. Some mutations were found more commonly: 1122 G→A (W374X), associated with Turkish origin, in 32 patients; 50delT (L17fsX22) associated with African/African American origin, in 21 patients; and 1090-91delCT (L364fsX), in 7 Japanese patients. Flow cytometry showed that perforin expression was absent in 40, reduced in 6 and normal in 4 patients. Patients presented at a median age of 3 months (quartiles: 2, 3 and 13 months), always with fever, splenomegaly and thrombocytopenia. NK activity was absent in 36 (51{\%}), ≤ 2{\%} in 18 (26{\%}), 3- ≤ 5{\%} in 10 (14{\%}), > 5{\%} in 4 (6{\%}), {"}reduced{"} in 2 (3{\%}) (not reported, n = 54). Nonsense mutations were significantly associated with younger age at onset (p <0.001) and absent natural killer activity (p = 0.008). Conclusion: PRF1 mutations are spread over the functional domains. Specific mutations are strongly associated with Turkish, African American and Japanese ethnic groups. Later onset and residual cytotoxic function are observed in patients with at least one missense mutation.",
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T1 - Genotype-phenotype study of familial haemophagocytic lymphohistiocytosis due to perforin mutations

AU - Trizzino, A.

AU - Zur Stadt, U.

AU - Ueda, I.

AU - Risma, K.

AU - Janka, G.

AU - Ishii, E.

AU - Beutel, K.

AU - Sumegi, J.

AU - Cannella, S.

AU - Pende, D.

AU - Mian, A.

AU - Henter, J. I.

AU - Griffiths, G.

AU - Santoro, A.

AU - Filipovich, A.

AU - Aricò, M.

PY - 2008/1

Y1 - 2008/1

N2 - Background: PRF1 gene mutations are associated with familial haemophagocytic lymphohistiocytosis type 2 (FHL2). Genotype-phenotype analysis, previously hampered by limited numbers of patients, was for the first time performed by data pooling from five large centres worldwide. Patients and methods: Members of the Histiocyte Society were asked to report cases of FHL2 on specific forms. Data were pooled in a common database and analysed. Results: The 124 patients had 63 different mutations (including 15 novel mutations): 11 nonsense, 10 frameshift, 38 missense and 4 in-frame deletions. Some mutations were found more commonly: 1122 G→A (W374X), associated with Turkish origin, in 32 patients; 50delT (L17fsX22) associated with African/African American origin, in 21 patients; and 1090-91delCT (L364fsX), in 7 Japanese patients. Flow cytometry showed that perforin expression was absent in 40, reduced in 6 and normal in 4 patients. Patients presented at a median age of 3 months (quartiles: 2, 3 and 13 months), always with fever, splenomegaly and thrombocytopenia. NK activity was absent in 36 (51%), ≤ 2% in 18 (26%), 3- ≤ 5% in 10 (14%), > 5% in 4 (6%), "reduced" in 2 (3%) (not reported, n = 54). Nonsense mutations were significantly associated with younger age at onset (p <0.001) and absent natural killer activity (p = 0.008). Conclusion: PRF1 mutations are spread over the functional domains. Specific mutations are strongly associated with Turkish, African American and Japanese ethnic groups. Later onset and residual cytotoxic function are observed in patients with at least one missense mutation.

AB - Background: PRF1 gene mutations are associated with familial haemophagocytic lymphohistiocytosis type 2 (FHL2). Genotype-phenotype analysis, previously hampered by limited numbers of patients, was for the first time performed by data pooling from five large centres worldwide. Patients and methods: Members of the Histiocyte Society were asked to report cases of FHL2 on specific forms. Data were pooled in a common database and analysed. Results: The 124 patients had 63 different mutations (including 15 novel mutations): 11 nonsense, 10 frameshift, 38 missense and 4 in-frame deletions. Some mutations were found more commonly: 1122 G→A (W374X), associated with Turkish origin, in 32 patients; 50delT (L17fsX22) associated with African/African American origin, in 21 patients; and 1090-91delCT (L364fsX), in 7 Japanese patients. Flow cytometry showed that perforin expression was absent in 40, reduced in 6 and normal in 4 patients. Patients presented at a median age of 3 months (quartiles: 2, 3 and 13 months), always with fever, splenomegaly and thrombocytopenia. NK activity was absent in 36 (51%), ≤ 2% in 18 (26%), 3- ≤ 5% in 10 (14%), > 5% in 4 (6%), "reduced" in 2 (3%) (not reported, n = 54). Nonsense mutations were significantly associated with younger age at onset (p <0.001) and absent natural killer activity (p = 0.008). Conclusion: PRF1 mutations are spread over the functional domains. Specific mutations are strongly associated with Turkish, African American and Japanese ethnic groups. Later onset and residual cytotoxic function are observed in patients with at least one missense mutation.

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