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. 2018 Sep 13;19(9):2747. doi: 10.3390/ijms19092747

Table 4.

Comparison of key characteristics of DILS (diffuse infiltrative lymphocytosis syndrome) and SS (Sjögren’s syndrome). Both are characterized by focal lymphocytic sialoadenitis [146].

Category Diffuse Infiltrative Lymphocytosis Syndrome Sjögren’s Syndrome
association HIV/AIDS Autoimmune diseases
histology glandular CD8+ T cell infiltration primarily CD4+ T cell infiltration
(staining not usually performed)
clinical manifestations parotiditis
xerostomia
xerotoconjunctivitis sicca
hypergammaglobulinemia
possible extraglandular organ involvement
usually no parotiditis
xerostomia
keratoconjuncitivits sicca
hypergammaglobulinemia
possible extraglandular organ involvement
laboratory tests supporting diagnosis HIV seropositivity
autoantibodies rarely present
autoantibodies including ANA, SS-A (Ro), SS-B (La), RF
HLA association DR5 (DR11), DR6 (DR13) B8, DR2, DR3, DR4, DQ2, A1
treatment ART, corticosteroids, symptomatic treatment symptomatic treatment