From:  Selective IgG4 deficiency and autoimmune cytopenias

 Clinical, laboratory, and molecular data of patients with sIgG4D

No.Age (years)*Age (years)^SexDiseaseMedical history/Family historyIgG4 levels (mg/dL)#TNFRSF13B/TACI defects
155MAITNo/No1.0Wild-type
21816MAITNo/No< 1.0rs72553883-Heter (p.A181E)
rs8072293-Heter (p.T27=)
rs11078355-Heter (p.S277=)
rs2274892-Heter (intronic)
31818FAITNo/Mother with hereditary spherocytosis2.0Wild-type
43521FAITNo/Daughter with CVID1.0Wild-type
52727FAITNo/No2.0rs8072293-Heter (p.T27=)
rs11078355-Heter (p.S277=)
rs2274892-Heter (intronic)
67272FAHAUrticaria/Niece with CVID2.0rs8072293-Homo (p.T27=)
rs34562254-Heter (p.P251L)
rs2274892-Heter (intronic)
rs11652843-Heter (intronic)
rs11652811-Heter (intronic)
79084MAITDM/No1.0rs8072293-Heter (p.T27=)
rs11078355-Heter (p.S277=)
rs11652843-Heter (intronic)
rs11652811-Heter (intronic)
89087MAHAVitiligo/No2.0rs8072293-Heter (p.T27=)
rs2274892-Heter (intronic)

AIT: autoimmune thrombocytopenia; AHA: autoimmune hemolytic anemia; CVID: common variable immunodeficiency; DM: diabetes mellitus; F: female; M: male; sIgG4D: selective IgG4 deficiency; Heter: heterozygous; Homo: homozygous; *: age at enrolment; ^: age at emergence (diagnosis) of autoimmune cytopenia; #: normal range (8–140 mg/dL)