Distinct molecular response patterns of activating STAT3 mutations associate with penetrance of lymphoproliferation and autoimmunity

• Published in: Clinical immunology (Orlando, Fla.) Vol. 210; p. 108316
• Main Authors: Jägle, Sabine, Heeg, Maximilian, Grün, Sarah, Rensing-Ehl, Anne, Maccari, Maria Elena, Klemann, Christian, Jones, Neil, Lehmberg, Kai, Bettoni, Claudia, Warnatz, Klaus, Grimbacher, Bodo, Biebl, Ariane, Schauer, Uwe, Hague, Rosie, Neth, Olaf, Mauracher, Andrea, Pachlopnik Schmid, Jana, Fabre, Alexandre, Kostyuchenko, Larysa, Führer, Marita, Lorenz, Myriam Ricarda, Schwarz, Klaus, Rohr, Jan, Ehl, Stephan
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.01.2020
• ISSN: 1521-6616; 1521-7035
• DOI: 10.1016/j.clim.2019.108316

Germline STAT3 gain-of-function (GOF) mutations have been linked to poly-autoimmunity and lymphoproliferation with variable expressivity and incomplete penetrance. Here we studied the impact of 17 different STAT3 GOF mutations on the canonical STAT3 signaling pathway and correlated the molecular results with clinical manifestations. The mutations clustered in three groups. Group 1 mutants showed altered STAT3 phosphorylation kinetics and strong basal transcriptional activity. They were associated with the highest penetrance of lymphoproliferation and autoimmunity. Group 2 mutants showed a strongly inducible transcriptional reporter activity and were clinically less penetrant. Group 3 mutants were mostly located in the DNA binding domain and showed the strongest DNA binding affinity despite a poor transcriptional reporter response. Thus, the GOF effect of STAT3 mutations is determined by a heterogeneous response pattern at the molecular level. The correlation of response pattern and clinical penetrance indicates a significant contribution of mutation-determined effects on disease manifestations. •Germline STAT3 gain-of-function mutations differentially affect individual molecular steps in the STAT3 signaling cascade•Based on the pattern of molecular consequences, the mutations clustered in three functional groups.•The functional groups could be associated with disease penetrance of lymphoproliferation and autoimmunity.