Table 2.
Samples | Investigation | Localization/major findings | Ref. |
Duodenal biopsies from 16 children with newly diagnosed CD, 9 maintained on GFD, 10 controls | HSP72 mRNA expression, protein level and localization | HSP72 mRNA and protein are increased in CD, and decreased by GFD. HSP72 was localized in villous enterocytes of the epithelium and lamina propria immune cells | [102] |
Duodenal biopsy specimens from 30 HLA-DQ2 (+) NCGS and 15 CD patients maintained on GFD | HSP27 or HSP70 mRNA expression, before and after challenge with gluten-containing bread daily for 3 d | mRNA expression of HSP27 and HSP70 in the duodenal mucosa was not different in any of the groups | [103] |
Jejunal biopsies from 78 children with clinical suspicion of CD | Epithelial HSP65 expression | Increased mitochondrial HSP65 expression in the jejunal mucosa in 80% (16/20) of children with CD and in 24% (14/58) of non-CD patients. Strong correlation between HSP65, γδ + T-cells and serum IgA endomysial autoantibodies. HSP65 is a potential mucosal integrity modulator | [104] |
Duodenal biopsies from 12 patients with CD and 10 controls | Small HSP αB-crystallin expression and distribution | Increased αB-crystallin in CD, localized in the supra-nuclear region of enterocytes in the duodenal mucosa | [105] |
Blood samples from 128 patients with CD and 94 healthy individuals | HSPA1A gene (HSP70-1) polymorphism | Altered frequency of an intermediate HSPA1A allele in CD (64.5%) vs normal (37.2%). HSP70-1 gene is part of a high-risk haplotype for CD | [106] |
Blood samples from 19 families with CD patients and 95 healthy individuals | HLA-linked HSPA1B gene (HSP70-2) polymorphism | Altered HSPA1B allele frequencies in CD vs normal and non-affected MHC haplotypes | [107] |
CD: Coeliac disease; GFD: Gluten-free diet; HSP: Heat shock protein; NCGS: Non-coeliac gluten sensitivity; Ig: Immunoglobulin; HLA: Human leukocyte antigen; MHC: Major histocompatibility complex.