Figure 3
PBMCs of patients with SS use distinct HS moieties to bind DC-HIL at high levels. PBMCs freshly isolated from patients with SS (Pt. 2 with Vβ+ cells at 93%, in which SD-4+ cells were 95%, and Pt. 3B with Vβ+ cells at 98.3%, in which SD-4+ cells were 96%) were assayed by flow cytometry for DC-HIL binding (A) and expression of HS epitopes (B) as in Figure 2. (C) DC-HIL binding by these cells was blocked by pretreatment with 40 μg/mL anti–HS mAb or control Ig (IgM plus IgG). DC-HIL binding is assessed by MFI left after subtracting MFI of control staining from MFI of positive staining (ΔMFI).

PBMCs of patients with SS use distinct HS moieties to bind DC-HIL at high levels. PBMCs freshly isolated from patients with SS (Pt. 2 with Vβ+ cells at 93%, in which SD-4+ cells were 95%, and Pt. 3B with Vβ+ cells at 98.3%, in which SD-4+ cells were 96%) were assayed by flow cytometry for DC-HIL binding (A) and expression of HS epitopes (B) as in Figure 2. (C) DC-HIL binding by these cells was blocked by pretreatment with 40 μg/mL anti–HS mAb or control Ig (IgM plus IgG). DC-HIL binding is assessed by MFI left after subtracting MFI of control staining from MFI of positive staining (ΔMFI).

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