TABLE 3.
Summary of findings supporting increased activation of immune responses in patients with tic disorders and Tourette syndrome
| References of studies supporting the finding | |
|---|---|
| Changes in gene expression | |
| Over-expression of genes modulating cytotoxicity and antigen presentation of NK and CD8+ T lymphocytes in PBMC | 40–42 |
| Over-expression of the D5 dopamine receptor gene in PBMC | 50 |
| Changes in lymphocyte subpopulation numbers | |
| Reduced percentage of CD4+CD25+ natural regulatory | 49a |
| T lymphocytes (Tregs) in moderate/severe patients | |
| Correlation of Tregs percentage with disease severity | 49a |
| Decreased percentage of β18+ CD8+ T lymphocytes in moderate/severe patients | 49a |
| Increased number of CD95+ T lymphocytes | 52 |
| Increased number of CD69+ B lymphocytes | 52 |
| Changes in the synthesis of effector molecules by immune competent cells | |
| Increased plasma levels of TNFα and IL-12 | 58a |
| Correlation of TNFα and IL-12 plasma levels with disease severity | 58a |
| Increased plasma levels of sVCAM-1 and sE-selectin | 61 |
| Increased plasma levels of neopterin | 13a |
| Increased synthesis of anti-neuronal antibodies (CONTROVERSIAL) | 11, 65, 67, 74, 76–80 |
| Increased density of Fc μ receptors (receptors for IgM) on B lymphocytes | 53 |
NK, natural killer cells; PBMC, peripheral blood mononuclear cells; TNFα, tumor necrosis factor-α; IL-12, interleukin-12; sVCAM-1, soluble vascular cell adhesion molecule-1; sE-selectin, soluble E-selectin; Fc, Fragment crystallizable; IgM, immunoglobulin M.
The study combined patients with Tourette’s syndrome (or other chronic tic disorder) and patients with pediatric-onset obsessive-compulsive disorder.