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Central Nervous System Activation of the Indoleamine‐2,3‐Dioxygenase Pathway in Human T Cell Lymphotropic Virus Type I–Associated Myelopathy/Tropical Spastic Paraparesis
18
Citations
9
References
2000
Year
Nitric OxideImmunodeficienciesViral PathogenesisImmunologyPathologyImmune RegulationImmune SystemIndoleamine‐2,3‐dioxygenase PathwayJamaican Ham/tsp PatientsInflammationImmunopathologyNeuroimmunologyAutoimmune DiseaseAllergyNeurovirologyVirologyAutoimmunityImmune FunctionCytokineMolecular VirologyAntiviral ResponseVirus-host InteractionCentral Nervous SystemMedicineViral Immunity
Human T cell lymphotropic virus type I (HTLV-I) is associated with a chronic neurologic disease called HTLV-I-associated myelopathy/tropical spastic paraparesis (HAM/TSP). The potential mechanisms of HAM/TSP pathogenesis were assessed by examination of 2 pathways initiated by interferon-gamma, a predominant cytokine in HAM/TSP. Jamaican HAM/TSP patients (n=17) were compared with patients with other neurologic diseases (ONDs; n=13) with respect to cerebrospinal fluid levels of the following: neopterin; nitrite plus nitrate, a stable indicator of nitric oxide; and tryptophan and kynurenine, metabolites of the indoleamine-2,3-dioxygenase (IDO) pathway. HAM/TSP patients had significantly elevated levels of neopterin (P=.003) and kynurenine (P=.05) and a significantly decreased level of tryptophan (P=.003), compared with patients with ONDs. These results support immune activation within the central nervous system and activation of the IDO pathway. Thus, activation of the IDO pathway may play a role in HAM/TSP.
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