Significance
Individuals who suffer paralysis on one side of the body and then develop rheumatoid arthritis show joint inflammation only on the neurologically intact side. We successfully modeled hemiplegia-induced protection from arthritis by transferring arthritogenic serum from K/BxN mice into recipients that had undergone unilateral sciatic and femoral nerve transection. Protection from serum-transferred arthritis could not be achieved by inhibiting the sympathetic, parasympathetic, or sensory arms of the nervous system. However, nerve transection did inhibit the joint-localized, inflammation-enhancing vascular leak rapidly induced by arthritogenic immune complexes and suggestively altered the transcriptome of the ankle microvasculature.