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. 2021 Mar 18;9:624116. doi: 10.3389/fped.2021.624116

Table 2.

Family members evaluated based on ALPS Criteria.

Subject
ALPS Criteria V-1 V-2 V-3 V-4 IV-1 IV-2
Required:
TCR αβDNTcs >2% or >68 cells/μL Present Present Present Absent N/A N/A
Clinical: LAD and/or Organomegaly Present Present Absent Absent Present Present
Primary accessory:
Genetic sequencing HMM HMM Declined Testing Declined Testing HMM HMM
FAS c.758 G>T (p. Gly253 Val) FAS c. 758 G>T (p. Gly253 Val) N/A N/A FAS c. 758 G>T (p. Gly253 Val) FAS c. 758 G>T (p. Gly253 Val)
Apoptosis assay (normal 68-93%) 38% N/A N/A N/A 41% N/A
Secondary accessory:
IL-18 (normal <540 pg/mL) 1513 958 714 260 N/A N/A
IL-10 (normal <2 pg/mL) 300 186 40.5 <1.6 N/A N/A
sFAS-L (normal 69-492 pg/mL) 5952 4825 1601 169 N/A N/A
Vitamin B12 (normal 200-1100 ng/mL) >2000 >2000 1892 675 N/A N/A
Clinical manifestations AIHA ITP Absent Absent History of anemia History of Anemia
Family history LP, AI LP, AI LP, AI LP,AI LP, AI LP, AI

AI, autoimmunity; AIHA, autoimmune hemolytic anemia; DNTCs, double negative T cells; HMM, heterozygous missense mutation; IL, interleukin; ITP, immune thrombocytopenia; LAD, lymphadenopathy; LP, lymphoproliferation; N/A, not applicable; sFAS-L, soluble FAS ligand.