IL1B and amyotrophic lateral sclerosis: Also, given our experience in characterising the inflammatory responses of primary human brain pericytes to some of the implicated cytokines (IL-1β, TNFα) [21, 37, 38], we reasoned that if ALS serum indeed harbours increased levels of these or other cytokines, then by chronically exposing human brain pericytes to ALS sera we might use these cells as biosensors of inflammation.