TY - JOUR
T1 - Plasma sCD28, sCTLA-4 levels in neuromyelitis optica and multiple sclerosis during relapse
AU - Wang, Honghao
AU - Wang, Kai
AU - Zhong, Xiaonan
AU - Dai, Yongqiang
AU - Wu, Aimin
AU - Li, Ying
AU - Hu, Xueqiang
PY - 2012/2/29
Y1 - 2012/2/29
N2 - Background: Soluble forms of CD28 (sCD28) and CTLA-4 (sCTLA-4) were associated with many autoimmune diseases like Sjögren's syndrome, systemic lupus erythematosus, asthma, and autoimmune myasthenia gravis. However, sCD28 and sCTLA-4 in neuromyelitis optica (NMO) and multiple sclerosis (MS) patients were less studied. Objective: To measure the plasma sCD28, sCTLA-4 in NMO and MS patients, and investigate whether sCD28 and sCTLA-4 possible use as sensitive biomarkers for diseases activity. Methods: Plasma concentrations of sCD28, sCTLA-4 were measured by an enzyme-linked immunosorbent assay (ELISA) in NMO (n = 22), MS (n = 21) patients and controls (n = 18). Results: The concentration of sCD28 levels were higher in the inflammatory demyelinating diseases cohort compared with the controls (NMO, p = 0.034; MS, p = 0.026) and the levels of sCD28 were slightly higher in NMO compared with MS. The sCTLA-4 levels were lower in the MS subgroup compared with the controls (p = 0.032). Both sCD28 and sCTLA-4 did not show any correlation with EDSS score in NMO and MS patients. Conclusions: Our study revealed for the first time that the levels of increased plasma sCD28 and decreased plasma sCTLA-4 in NMO and MS patients, but had little correlation with clinical presentations.
AB - Background: Soluble forms of CD28 (sCD28) and CTLA-4 (sCTLA-4) were associated with many autoimmune diseases like Sjögren's syndrome, systemic lupus erythematosus, asthma, and autoimmune myasthenia gravis. However, sCD28 and sCTLA-4 in neuromyelitis optica (NMO) and multiple sclerosis (MS) patients were less studied. Objective: To measure the plasma sCD28, sCTLA-4 in NMO and MS patients, and investigate whether sCD28 and sCTLA-4 possible use as sensitive biomarkers for diseases activity. Methods: Plasma concentrations of sCD28, sCTLA-4 were measured by an enzyme-linked immunosorbent assay (ELISA) in NMO (n = 22), MS (n = 21) patients and controls (n = 18). Results: The concentration of sCD28 levels were higher in the inflammatory demyelinating diseases cohort compared with the controls (NMO, p = 0.034; MS, p = 0.026) and the levels of sCD28 were slightly higher in NMO compared with MS. The sCTLA-4 levels were lower in the MS subgroup compared with the controls (p = 0.032). Both sCD28 and sCTLA-4 did not show any correlation with EDSS score in NMO and MS patients. Conclusions: Our study revealed for the first time that the levels of increased plasma sCD28 and decreased plasma sCTLA-4 in NMO and MS patients, but had little correlation with clinical presentations.
KW - Multiple sclerosis
KW - Neuromyelitis optica
KW - SCD28
KW - SCTLA-4
UR - http://www.scopus.com/inward/record.url?scp=84856970594&partnerID=8YFLogxK
U2 - 10.1016/j.jneuroim.2011.11.010
DO - 10.1016/j.jneuroim.2011.11.010
M3 - Article
C2 - 22177277
SN - 0165-5728
VL - 243
SP - 52
EP - 55
JO - Journal of Neuroimmunology
JF - Journal of Neuroimmunology
IS - 1-2
ER -