TY - JOUR
T1 - Serum cytokine elevations in celiac disease
T2 - Association with disease presentation
AU - Manavalan, John Sanil
AU - Hernandez, Lincoln
AU - Shah, Jayesh Girish
AU - Konikkara, John
AU - Naiyer, Afzal Jamal
AU - Lee, Anne Roland
AU - Ciaccio, Edward
AU - Minaya, Maria Theresa
AU - Green, Peter H.R.
AU - Bhagat, Govind
PY - 2010/1
Y1 - 2010/1
N2 - Celiac disease (CD) is an autoimmune disorder that is triggered by an immune response to gluten in genetically predisposed individuals. Although considered a primary gastrointestinal disease, CD is now known to have widespread systemic manifestations. We attempted to define the nature and role of systemic cytokine levels in the pathophysiology of CD. Multiplex cytokine assays were performed on four different groups of adult patients; patients with active CD (ACD), patients on a gluten-free diet (GFD) with positive TTG IgA antibodies, patients on a GFD with negative antibodies, and those with refractory CD (RCD). The results were compared with values in healthy adult controls. Patients with active CD and those on GFD with positive antibodies had significantly higher levels of proinflammatory cytokines, such as interferon-γ, interleukin (IL)-1β, tumor necrosis factor-α, IL-6 and IL-8, and also Th-2 cytokines such as IL-4 and IL-10, compared with normal controls and patients on GFD without antibodies. Interestingly patients on GFD for less than 1 year had significantly higher levels of both proinflammatory cytokines and Th2 cytokines compared with the patients on GFD for more than 1 year. In addition, a statistically significant correlation between levels of TTG IgA titers and serum levels of Th-2 cytokines IL-4 (p < 0.001), IL-10 (p < 0.001) and inflammatory cytokines such as IL-1α (p < 0.001), IL-1β (p < 0.005), and IL-8 (p < 0.05) was observed.
AB - Celiac disease (CD) is an autoimmune disorder that is triggered by an immune response to gluten in genetically predisposed individuals. Although considered a primary gastrointestinal disease, CD is now known to have widespread systemic manifestations. We attempted to define the nature and role of systemic cytokine levels in the pathophysiology of CD. Multiplex cytokine assays were performed on four different groups of adult patients; patients with active CD (ACD), patients on a gluten-free diet (GFD) with positive TTG IgA antibodies, patients on a GFD with negative antibodies, and those with refractory CD (RCD). The results were compared with values in healthy adult controls. Patients with active CD and those on GFD with positive antibodies had significantly higher levels of proinflammatory cytokines, such as interferon-γ, interleukin (IL)-1β, tumor necrosis factor-α, IL-6 and IL-8, and also Th-2 cytokines such as IL-4 and IL-10, compared with normal controls and patients on GFD without antibodies. Interestingly patients on GFD for less than 1 year had significantly higher levels of both proinflammatory cytokines and Th2 cytokines compared with the patients on GFD for more than 1 year. In addition, a statistically significant correlation between levels of TTG IgA titers and serum levels of Th-2 cytokines IL-4 (p < 0.001), IL-10 (p < 0.001) and inflammatory cytokines such as IL-1α (p < 0.001), IL-1β (p < 0.005), and IL-8 (p < 0.05) was observed.
KW - Celiac disease
KW - Cytokines
KW - TTg IgA antibodies
UR - http://www.scopus.com/inward/record.url?scp=71249096411&partnerID=8YFLogxK
U2 - 10.1016/j.humimm.2009.09.351
DO - 10.1016/j.humimm.2009.09.351
M3 - Article
C2 - 19735687
AN - SCOPUS:71249096411
SN - 0198-8859
VL - 71
SP - 50
EP - 57
JO - Human Immunology
JF - Human Immunology
IS - 1
ER -