The symptoms of chronic fatigue syndrome (CFS) are consistent with cytokine dysregulation. This has led to the hypothesis of immune dysregulation as the cause of this illness. To further test this hypothesis, we did repeated blood sampling for cytokines while patients and matched healthy controls slept in the sleep lab. Because no one method for assaying cytokines is acknowledged to be better than another, we assayed for protein in serum, message in peripheral blood lymphocytes (PBLs), and function in resting and stimulated PBLs. We found no evidence of proinflammatory cytokine upregulation. Instead, in line with some of our earlier studies, we did find some evidence to support a role for an increase in interleukin-10, an antiinflammatory cytokine. Although the changes were small, they may contribute to the common complaint in CFS patients of disrupted sleep.Chronic fatigue syndrome (CFS) is a medically unexplained illness lasting at least 6 months and characterized by severe fatigue that produces a substantial reduction in activity accompanied by at least four of the following symptoms: sore throat, tender lymph nodes, headache, myalgia, arthralgia, unrefreshing sleep, difficulty concentrating, and the report of syndromic exacerbation following mild exertion (7). One major hypothesis for the cause of CFS is an immune dysregulation of unknown etiology with high levels of proinflammatory cytokines producing the CFS symptom complex. Two findings fostered this idea: first, approximately a third of CFS patients report a sudden, influenza-like onset of their illness (37), and second, administration of proinflammatory cytokines leads to many of the same symptoms seen in CFS (26). However, we recently reviewed the literature on this hypothesis and found relatively little empirical data to support it (20); a more recent small study did report higher levels of one such cytokine, serum transforming growth factor , in patients than in controls (35); however, another group did not confirm this result (30). Other work extending the research to cellular production of proinflammatory cytokines was also negative (1).However, a very different and alternative hypothesis focuses on the common complaint in CFS of unrefreshing sleep (4).Recent work suggests that sleep is under the control of a cytokine/sleep network where normal sleep follows a balanced secretion of pro-and anti-inflammatory cytokines (13). We hypothesized that CFS might result from an imbalance of this network in favor of the anti-inflammatory cytokines which are sleep disrupting (14). Supporting this possibility is the result of a recent study (28) in which we sampled blood for cytokines every 20 min across a 24-h day in patients with fibromyalgia (FM) (28), a medically unexplained, diffuse pain syndrome that has substantial overlap with CFS (5). Of several pro-and anti-inflammatory cytokines studied, the only one to show differences from controls, i.e., increases, was the anti-inflammatory cytokine interleukin-10 (IL-10), and that was true only for nocturnal dat...