Genetic predisposition to immune cell malfunction and inflammation
Author: Torralba-Raga, Lamberto J
Date: 2021-10-01
Location: Erna Möllersalen, Neo Building, Karolinska Institutet, Flemingsberg
Time: 09.30
Department: Inst för medicin, Huddinge / Dept of Medicine, Huddinge
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Thesis (10.72Mb)
Abstract
Our genome contains all the instructions to control the synthesis of proteins, the development of cells and the interaction between body systems. We are armed with an immune system, made up of cells, chemical compounds and physical barriers, that protects us from invading pathogens. The fields of human genetics and human immunology noticeably intertwin with each other when faults in one system are phenotypically manifested as diseases in the other one. Primary immunodeficiencies represent a diverse group of genetically determined disorders characterized by functional defects in the immune system that display a wide range of clinical and immunological phenotypes. Among these phenotypes, hemophagocytic lymphohistiocytosis (HLH) involves a group of hyperinflammatory illnesses characterized by life-threatening, toxic activation of the immune system caused by mutations in diverse genes that impact the killing capacity of cytotoxic lymphocytes.
In this thesis, we have investigated and characterized novel gene variants associated with HLH or hyperinflammatory phenotypes in case reports (Papers I, II, IV, V and VI) and as well as in one comparative study (III). In Paper I, we identified a novel hemizygous SH2D1A variant in a 21-yearold man that succumbed to Epstein-Barr virus (EBV)-HLH/lymphoma diagnosis. Interestingly, the patient had three healthy siblings carrying that variant, suggesting incomplete penetrance for this variant in X-linked lymphoproliferative disease type-1. In Paper II, a patient with a disease-causing SH2D1A variant displayed central nervous system damage without ongoing EBV infection, supporting the notion that EBV might be dispensable for the observed central nervous vasculitis. In Paper III, we compared two UNC13D isoforms with distinct transcription start sites that presented different N-terminal domains and we confirmed that although their expression was differentially regulated, they were equally recruited to the immune synapse and similarly contributed to cytotoxicity. In Paper IV, we uncovered a novel homozygous RAB27A variant identified in a patient with adult-onset HLH. Interestingly, this study presents the first RAB27A variant with enhanced binding to Munc13-4, a key player of cytotoxicity. In Paper V, we identified two novel MVK variants in a newborn manifesting systemic inflammation and exaggerated mevalonate accumulation. In this case, we established an association between severe MVK deficiency and HLH phenotype. In Paper VI, we reported a novel homozygous ISG15 variant in a patient with viral susceptibility phenotype. Remarkably, ISG15 deficiency has been previously associated with mycobacterial susceptibility and excessive type I interferon responses, but not with viral immunity. Thus, our study underscores the role of ISGylation for viral protection in the human setting.
Overall, these studies expand our understanding of HLH and related hyperinflammatory disorders at the genetic level, since new gene variants and new associations were identified; at the protein and pathway interaction level, due to novel protein properties described, and at the phenotypic level since both uncommon and new manifestations were reported.
In this thesis, we have investigated and characterized novel gene variants associated with HLH or hyperinflammatory phenotypes in case reports (Papers I, II, IV, V and VI) and as well as in one comparative study (III). In Paper I, we identified a novel hemizygous SH2D1A variant in a 21-yearold man that succumbed to Epstein-Barr virus (EBV)-HLH/lymphoma diagnosis. Interestingly, the patient had three healthy siblings carrying that variant, suggesting incomplete penetrance for this variant in X-linked lymphoproliferative disease type-1. In Paper II, a patient with a disease-causing SH2D1A variant displayed central nervous system damage without ongoing EBV infection, supporting the notion that EBV might be dispensable for the observed central nervous vasculitis. In Paper III, we compared two UNC13D isoforms with distinct transcription start sites that presented different N-terminal domains and we confirmed that although their expression was differentially regulated, they were equally recruited to the immune synapse and similarly contributed to cytotoxicity. In Paper IV, we uncovered a novel homozygous RAB27A variant identified in a patient with adult-onset HLH. Interestingly, this study presents the first RAB27A variant with enhanced binding to Munc13-4, a key player of cytotoxicity. In Paper V, we identified two novel MVK variants in a newborn manifesting systemic inflammation and exaggerated mevalonate accumulation. In this case, we established an association between severe MVK deficiency and HLH phenotype. In Paper VI, we reported a novel homozygous ISG15 variant in a patient with viral susceptibility phenotype. Remarkably, ISG15 deficiency has been previously associated with mycobacterial susceptibility and excessive type I interferon responses, but not with viral immunity. Thus, our study underscores the role of ISGylation for viral protection in the human setting.
Overall, these studies expand our understanding of HLH and related hyperinflammatory disorders at the genetic level, since new gene variants and new associations were identified; at the protein and pathway interaction level, due to novel protein properties described, and at the phenotypic level since both uncommon and new manifestations were reported.
List of papers:
I. Diagnostic challenges for a novel SH2D1A mutation associated with X-linked lymphoproliferative disease. Lamberto Torralba-Raga, Bianca Tesi, Samuel C. C. Chiang, Heinrich Schlums, Magnus Nordenskjöld, AnnaCarin Horne, Jan-Inge Henter, Marie Meeths, Mohamed Abdelhaleem, Sheila Weitzman and Yenan T. Bryceson. Pediatr Blood Cancer. 2020 Apr;67(4):e28184.
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II. Fatal central nervous system lymphocytic vasculitis after treatment for Burkitt lymphoma in a patient with a SH2D1A Mutation. João Farela Neves, Lamberto Torralba Raga, Samuel C. C. Chiang, Bianca Tesi, José Pedro Vieira, Ana Isabel Cordeiro, Luis Borrego and Yenan T. Bryceson. Pediatr Infect Dis J. 2019 Feb;38(2):e29-e31.
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III. Alternative UNC13D promoter encodes a functional Munc13-4 isoform predominantly expressed in lymphocytes and platelets. Donatella Galgano, Tayebeh Soheili, Matthias Voss, Lamberto Torralba-Raga, Bianca Tesi, Frank Cichocki, Isabelle Andre, Jens Rettig, Marina Cavazzana and Yenan T. Bryceson. Front Immunol. 2020 Jun 9;11:1154.
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IV. A novel RAB27A variant associated with fatal hemophagocytic lymphohistiocytosis alters effector protein binding affinities. Timo C.E. Zondag*, Lamberto Torralba-Raga*, Jan A.M. Van Laar, Maud A.W. Hermans, Iris H.I.M. Hollink, P.M. Van Hagen, Deborah A. Briggs, Alistair N. Hume and Yenan T. Bryceson, PhD. *Shared first authorship. [Manuscript]
V. Mevalonate kinase deficiency: Hemophagocytic lymphohistiocytosis as a presenting feature of patients with mevalonic aciduria. Lamberto Torralba-Raga*, Gonçalo Padeira*, Laura E. Covill, Marta Conde, Ana Isabel Cordeiro, Marco Gattorno, Maura Faraci, Yenan T. Bryceson and João Farela Neves. *Shared first authorship. [Manuscript]
VI. A novel ISG15 missense variant in a patient with severe viral susceptibility. Lamberto Torralba-Raga, Tessa Campbell, Caroline Eriksson, Charlotte Engvall, Stefan Berg and Yenan T. Bryceson. [Manuscript]
I. Diagnostic challenges for a novel SH2D1A mutation associated with X-linked lymphoproliferative disease. Lamberto Torralba-Raga, Bianca Tesi, Samuel C. C. Chiang, Heinrich Schlums, Magnus Nordenskjöld, AnnaCarin Horne, Jan-Inge Henter, Marie Meeths, Mohamed Abdelhaleem, Sheila Weitzman and Yenan T. Bryceson. Pediatr Blood Cancer. 2020 Apr;67(4):e28184.
Fulltext (DOI)
Pubmed
View record in Web of Science®
II. Fatal central nervous system lymphocytic vasculitis after treatment for Burkitt lymphoma in a patient with a SH2D1A Mutation. João Farela Neves, Lamberto Torralba Raga, Samuel C. C. Chiang, Bianca Tesi, José Pedro Vieira, Ana Isabel Cordeiro, Luis Borrego and Yenan T. Bryceson. Pediatr Infect Dis J. 2019 Feb;38(2):e29-e31.
Fulltext (DOI)
Pubmed
View record in Web of Science®
III. Alternative UNC13D promoter encodes a functional Munc13-4 isoform predominantly expressed in lymphocytes and platelets. Donatella Galgano, Tayebeh Soheili, Matthias Voss, Lamberto Torralba-Raga, Bianca Tesi, Frank Cichocki, Isabelle Andre, Jens Rettig, Marina Cavazzana and Yenan T. Bryceson. Front Immunol. 2020 Jun 9;11:1154.
Fulltext (DOI)
Pubmed
View record in Web of Science®
IV. A novel RAB27A variant associated with fatal hemophagocytic lymphohistiocytosis alters effector protein binding affinities. Timo C.E. Zondag*, Lamberto Torralba-Raga*, Jan A.M. Van Laar, Maud A.W. Hermans, Iris H.I.M. Hollink, P.M. Van Hagen, Deborah A. Briggs, Alistair N. Hume and Yenan T. Bryceson, PhD. *Shared first authorship. [Manuscript]
V. Mevalonate kinase deficiency: Hemophagocytic lymphohistiocytosis as a presenting feature of patients with mevalonic aciduria. Lamberto Torralba-Raga*, Gonçalo Padeira*, Laura E. Covill, Marta Conde, Ana Isabel Cordeiro, Marco Gattorno, Maura Faraci, Yenan T. Bryceson and João Farela Neves. *Shared first authorship. [Manuscript]
VI. A novel ISG15 missense variant in a patient with severe viral susceptibility. Lamberto Torralba-Raga, Tessa Campbell, Caroline Eriksson, Charlotte Engvall, Stefan Berg and Yenan T. Bryceson. [Manuscript]
Institution: Karolinska Institutet
Supervisor: Bryceson, Yenan T.
Co-supervisor: Horne, AnnaCarin; Nordenskjöld, Magnus
Issue date: 2021-09-10
Rights:
Publication year: 2021
ISBN: 978-91-8016-332-3
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