Literature DB >> 29729943

Phenotype, penetrance, and treatment of 133 cytotoxic T-lymphocyte antigen 4-insufficient subjects.

Charlotte Schwab1, Annemarie Gabrysch1, Peter Olbrich2, Virginia Patiño3, Klaus Warnatz1, Daniel Wolff4, Akihiro Hoshino5, Masao Kobayashi6, Kohsuke Imai7, Masatoshi Takagi7, Ingunn Dybedal8, Jamanda A Haddock9, David M Sansom10, Jose M Lucena11, Maximilian Seidl12, Annette Schmitt-Graeff13, Veronika Reiser14, Florian Emmerich15, Natalie Frede1, Alla Bulashevska1, Ulrich Salzer1, Desirée Schubert16, Seiichi Hayakawa6, Satoshi Okada6, Maria Kanariou17, Zeynep Yesim Kucuk18, Hugo Chapdelaine19, Lenka Petruzelkova20, Zdenek Sumnik20, Anna Sediva21, Mary Slatter22, Peter D Arkwright23, Andrew Cant22, Hanns-Martin Lorenz24, Thomas Giese25, Vassilios Lougaris26, Alessandro Plebani26, Christina Price27, Kathleen E Sullivan28, Michel Moutschen29, Jiri Litzman30, Tomas Freiberger31, Frank L van de Veerdonk32, Mike Recher33, Michael H Albert34, Fabian Hauck34, Suranjith Seneviratne35, Jana Pachlopnik Schmid36, Antonios Kolios37, Gary Unglik38, Christian Klemann39, Carsten Speckmann40, Stephan Ehl1, Alan Leichtner41, Richard Blumberg42, Andre Franke43, Scott Snapper44, Sebastian Zeissig45, Charlotte Cunningham-Rundles46, Lisa Giulino-Roth47, Olivier Elemento48, Gregor Dückers49, Tim Niehues49, Eva Fronkova50, Veronika Kanderová50, Craig D Platt51, Janet Chou51, Talal A Chatila51, Raif Geha51, Elizabeth McDermott52, Su Bunn53, Monika Kurzai54, Ansgar Schulz55, Laia Alsina56, Ferran Casals57, Angela Deyà-Martinez56, Sophie Hambleton22, Hirokazu Kanegane5, Kjetil Taskén58, Olaf Neth2, Bodo Grimbacher59.   

Abstract

BACKGROUND: Cytotoxic T-lymphocyte antigen 4 (CTLA-4) is a negative immune regulator. Heterozygous CTLA4 germline mutations can cause a complex immune dysregulation syndrome in human subjects.
OBJECTIVE: We sought to characterize the penetrance, clinical features, and best treatment options in 133 CTLA4 mutation carriers.
METHODS: Genetics, clinical features, laboratory values, and outcomes of treatment options were assessed in a worldwide cohort of CTLA4 mutation carriers.
RESULTS: We identified 133 subjects from 54 unrelated families carrying 45 different heterozygous CTLA4 mutations, including 28 previously undescribed mutations. Ninety mutation carriers were considered affected, suggesting a clinical penetrance of at least 67%; median age of onset was 11 years, and the mortality rate within affected mutation carriers was 16% (n = 15). Main clinical manifestations included hypogammaglobulinemia (84%), lymphoproliferation (73%), autoimmune cytopenia (62%), and respiratory (68%), gastrointestinal (59%), or neurological features (29%). Eight affected mutation carriers had lymphoma, and 3 had gastric cancer. An EBV association was found in 6 patients with malignancies. CTLA4 mutations were associated with lymphopenia and decreased T-, B-, and natural killer (NK) cell counts. Successful targeted therapies included application of CTLA-4 fusion proteins, mechanistic target of rapamycin inhibitors, and hematopoietic stem cell transplantation. EBV reactivation occurred in 2 affected mutation carriers after immunosuppression.
CONCLUSIONS: Affected mutation carriers with CTLA-4 insufficiency can present in any medical specialty. Family members should be counseled because disease manifestation can occur as late as 50 years of age. EBV- and cytomegalovirus-associated complications must be closely monitored. Treatment interventions should be coordinated in clinical trials.
Copyright © 2018 American Academy of Allergy, Asthma & Immunology. All rights reserved.

Entities:  

Keywords:  Cytotoxic T-lymphocyte antigen 4; abatacept; autoimmunity; common variable immunodeficiency; hematopoietic stem cell transplantation; hypogammaglobulinemia; immune dysregulation; primary immunodeficiency; sirolimus

Mesh:

Substances:

Year:  2018        PMID: 29729943      PMCID: PMC6215742          DOI: 10.1016/j.jaci.2018.02.055

Source DB:  PubMed          Journal:  J Allergy Clin Immunol        ISSN: 0091-6749            Impact factor:   10.793


  41 in total

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