» Articles » PMID: 36228738

Monogenic Early-onset Lymphoproliferation and Autoimmunity: Natural History of STAT3 Gain-of-function Syndrome

Overview
Date 2022 Oct 13
PMID 36228738
Authors
Affiliations
Soon will be listed here.
Abstract

Background: In 2014, germline signal transducer and activator of transcription (STAT) 3 gain-of-function (GOF) mutations were first described to cause a novel multisystem disease of early-onset lymphoproliferation and autoimmunity.

Objective: This pivotal cohort study defines the scope, natural history, treatment, and overall survival of a large global cohort of patients with pathogenic STAT3 GOF variants.

Methods: We identified 191 patients from 33 countries with 72 unique mutations. Inclusion criteria included symptoms of immune dysregulation and a biochemically confirmed germline heterozygous GOF variant in STAT3.

Results: Overall survival was 88%, median age at onset of symptoms was 2.3 years, and median age at diagnosis was 12 years. Immune dysregulatory features were present in all patients: lymphoproliferation was the most common manifestation (73%); increased frequencies of double-negative (CD4-CD8-) T cells were found in 83% of patients tested. Autoimmune cytopenias were the second most common clinical manifestation (67%), followed by growth delay, enteropathy, skin disease, pulmonary disease, endocrinopathy, arthritis, autoimmune hepatitis, neurologic disease, vasculopathy, renal disease, and malignancy. Infections were reported in 72% of the cohort. A cellular and humoral immunodeficiency was observed in 37% and 51% of patients, respectively. Clinical symptoms dramatically improved in patients treated with JAK inhibitors, while a variety of other immunomodulatory treatment modalities were less efficacious. Thus far, 23 patients have undergone bone marrow transplantation, with a 62% survival rate.

Conclusion: STAT3 GOF patients present with a wide array of immune-mediated disease including lymphoproliferation, autoimmune cytopenias, and multisystem autoimmunity. Patient care tends to be siloed, without a clear treatment strategy. Thus, early identification and prompt treatment implementation are lifesaving for STAT3 GOF syndrome.

Citing Articles

Pulmonary Aspergillosis and Low HIES Score in a Family with STAT3 N-Terminal Domain Mutation.

Lima de Souza S, Asano T, Glumoff V, Keskitalo S, Pikkarainen K, Martelius T J Clin Immunol. 2025; 45(1):73.

PMID: 39928202 PMC: 11811237. DOI: 10.1007/s10875-025-01867-1.


Functional validation of a novel STAT3 'variant of unknown significance' identifies a new case of STAT3 GOF syndrome and reveals broad immune cell defects.

Mackie J, Suan D, McNaughton P, Haerynck F, OSullivan M, Guerin A Clin Exp Immunol. 2025; 219(1).

PMID: 39836489 PMC: 11791529. DOI: 10.1093/cei/uxaf005.


Beyond FAScinating: advances in diagnosis and management of autoimmune lymphoproliferative syndrome and activated PI3 kinase δ syndrome.

Rao V, Pittaluga S, Uzel G Hematology Am Soc Hematol Educ Program. 2024; 2024(1):126-136.

PMID: 39644063 PMC: 11665610. DOI: 10.1182/hematology.2024000537.


Large granular lymphocyte leukemia: a clonal disorder with autoimmune manifestations.

Marchand T, Pastoret C, Moignet A, Roussel M, Lamy T Hematology Am Soc Hematol Educ Program. 2024; 2024(1):143-149.

PMID: 39644019 PMC: 11665628. DOI: 10.1182/hematology.2024000539.


Common variable immunodeficiency: autoimmune cytopenias and advances in molecular diagnosis.

Cunningham-Rundles C, Casanova J, Boisson B Hematology Am Soc Hematol Educ Program. 2024; 2024(1):137-142.

PMID: 39643993 PMC: 11665743. DOI: 10.1182/hematology.2024000538.


References
1.
Forbes L, Vogel T, Cooper M, Castro-Wagner J, Schussler E, Weinacht K . Jakinibs for the treatment of immune dysregulation in patients with gain-of-function signal transducer and activator of transcription 1 (STAT1) or STAT3 mutations. J Allergy Clin Immunol. 2018; 142(5):1665-1669. PMC: 6322659. DOI: 10.1016/j.jaci.2018.07.020. View

2.
Mauracher A, Eekels J, Woytschak J, van Drogen A, Bosch A, Prader S . Erythropoiesis defect observed in STAT3 GOF patients with severe anemia. J Allergy Clin Immunol. 2019; 145(4):1297-1301. DOI: 10.1016/j.jaci.2019.11.042. View

3.
Velayos T, Martinez R, Alonso M, Garcia-Etxebarria K, Aguayo A, Camarero C . An Activating Mutation in Results in Neonatal Diabetes Through Reduced Insulin Synthesis. Diabetes. 2017; 66(4):1022-1029. DOI: 10.2337/db16-0867. View

4.
Singh J, Solomon D, Dougados M, Felson D, Hawker G, Katz P . Development of classification and response criteria for rheumatic diseases. Arthritis Rheum. 2006; 55(3):348-52. DOI: 10.1002/art.22003. View

5.
Nabhani S, Schipp C, Miskin H, Levin C, Postovsky S, Dujovny T . STAT3 gain-of-function mutations associated with autoimmune lymphoproliferative syndrome like disease deregulate lymphocyte apoptosis and can be targeted by BH3 mimetic compounds. Clin Immunol. 2017; 181:32-42. DOI: 10.1016/j.clim.2017.05.021. View