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. 2016 Oct 7;18(5):290–303. doi: 10.1080/15384047.2016.1235669

Table 1.

Clinical data summary.

Patient other disease/information age sex TCR LGL phenotype and purity ANC STAT3 Treatment
T-LGLL#1 asymptomatic 71 F αβ CD3+CD4+ 90% 2690 K658F no
T-LGLL#2   20 M γδ CD3+CD8+ 24% 810 Y640F no
T-LGLL#3 celiac 69 F αβ CD3+CD8+ 81% 1090 WT no
T-LGLL#4   61 F αβ CD3+CD8+ 90% 620 D661Y no
T-LGLL#5 lupus 39 F αβ CD3+CD8+ 35%, CD3+76% 1000 WT no
T-LGLL#6 HA, transf/dep 58 M αβ CD3+CD8+ 74% 2130 Y640F CsA
T-LGLL#7   61, 59# F β CD8+ 43% 1800, 2100# WT no
T-LGLL#8   60 F + marrow CD3+CD8+CD57+ 15%, CD45+ bright 38% 490 WT no
T-LGLL#9   53, 55# F + CD3+CD8+ 24% 690, 250# WT no
T-LGLL#10 PRCA 45 M γ CD3+CD8+ 89% 700 WT MTX
T-LGLL#11   43 M αβ CD3+CD8+ 94% 1600 Y640F, prev I659L MTX
T-LGLL#12 agranulocytosis 38 M αβ, γδ CD3+CD8+ 65% 0 WT CsA, pred.
T-LGLL#13   70 F αβ CD3+ 86% 200 D661V no
T-LGLL#14 RA 56 F γδ CD3+CD8+ 84% 280 WT no
T-LGLL#15 transf/dep until CTX 64 M αβ CD2+CD3+CD8+ 67% 900 WT no; prev. on CTX
T-LGLL#16   69 F αβ CD3+CD8+ 55%, CD3+CD56+ 45% 980 WT no
T-LGLL#17 asymptomatic 61 M γ CD3+CD8+ 55% 7000 WT no
T-LGLL#18   51 F γ CD3+CD8+ 96%,CD3+CD57+ 67% 420 WT CsA
T-LGLL#19 asymptomatic 38 F αβ 20-30%, bone marrow 1200 Y640F no
T-LGLL#20   46 M αβ CD3+CD8+ 56%, CD3+CD16+ 34%, CD3+CD57+ 51% 1000 Y640F no
T-LGLL#21 RA 34 F * CD3+ 93%, CD8+ 32% 200 Y640F Plaquenil, pred.
T-LGLL#22 stable disease 64 F no data CD3+CD8+ 30% 3538 Y640F no
T-LGLL#23   23 F αβ CD3+CD8+ 63%, CD3+CD57+ 29% 1100 Y640F no
T-LGLL#24   65 F + CD3+CD8+ 93%, CD3+CD57+ 61% 730 D661Y no
T-LGLL#25 asymptomatic 79 M αβ CD3+CD8+CD57+ 44% 1623 Y640F no

Abbreviations: methotrexate (MTX), Cytoxan (CTX), cyclosporine A (CsA), prednisone (pred.), rheumatoid arthritis (RA), pure red cell aplasia (PRCA), hemolytic anemia (HA), transfusion dependent (transf/dep).

Age = patient age at the time of the sample collection.

Treatments listed include only immunosuppressants for LGLL and/or autoimmune disease. Other medications the patients may be taking are not listed.

Clinical data correspond to laboratory diagnostic tests performed on the date of blood collection or the closest date for which this information is available.

TCR and flow data are from peripheral blood unless otherwise specified.

*

TCR positivity is sometimes there, sometimes not # data correlate to A, B samples respectively in Fig. 1.