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. 2020 Dec 25;106(4):1763–1774. doi: 10.1210/clinem/dgaa958

Table 2.

Sequential immunofluorescence in a subset of samples

HLA class I STAT 1 PKR VP1
Chronic GD 1 Positive Negative Negative Negative
Chronic GD 2 Positive Positive Positive Positive
Chronic GD 3 Positive Negative Positive Positive
Chronic GD 4 Negative Negative Positive Positive
Chronic GD 5 Positive Negative Positive Positive
Chronic GD 6 Positive Positive Positive Positive
Chronic GD 7 Negative Negative Negative Negative
Chronic GD 8 Negative Negative Positive Positive
Chronic GD 9 Positive Positive Positive Positive
New GD 1 Positive Positive Positive Positive
New GD 2 Positive Positive Positive Positive
New GD 3 Positive Positive Positive Positive
New GD 4 Positive Positive Positive Positive
Control 1 Positive Positive Positive Positive
Control 2 Positive Positive Negative Negative
Control 3 Negative Negative Negative Negative
Control 4 Negative Negative Negative Negative

Seventeen samples were stained sequentially with immunofluorescence for HLA class I, STAT1, PKR, and VP1. The table shows that the majority of the GD samples were both HLA class I and STAT1 positive (shown in bold). All new GD samples stained positively for all proteins studied.

Abbreviations: GD, Graves disease; HLA, human leukocyte antigen; PKR, protein kinase R; STAT1, signal transducer and activator of transcription 1; VP1, enteroviral capsid protein 1.