Research

TNF-α and IL-10 downregulation and marked oxidative stress in Neuromyelitis Optica

Giselle Pentón-Rol^1* , Majel Cervantes-Llanos^1* , Gregorio Martínez-Sánchez² , José A Cabrera-Gómez³ , Carmen M Valenzuela-Silva¹ , Omar Ramírez-Nuñez² , Mayté Casanova-Orta² , María A Robinson-Agramonte³ , Ileana Lopategui-Cabezas⁴ and Pedro A López-Saura¹

¹  Clinical Trials Division, Center for Biological Research, Havana, Cuba

²  Center for Research and Biological Evaluations, Institute of Pharmacy and Food Sciences, University of Havana, Havana, Cuba

³  International Center of Neurological Restoration, Havana, Cuba

⁴  Higher Institute of Medical Sciences "Victoria de Girón", Havana, Cuba

author email corresponding author email* Contributed equally

Journal of Inflammation 2009, 6:18doi:10.1186/1476-9255-6-18

Published:	2 June 2009

Abstract

Background

Neuromyelitis optica is a central nervous system demyelinating and inflammatory syndrome. The objective of this study is to identify cytokines related to the cellular immune response as well as blood brain barrier integrity and oxidative stress.

Methods

We performed a molecular characterization of cellular immune response and oxidative stress in serum from relapsing-NMO (R-NMO) patients and established the correlations between the clinical measurements and molecular parameters using the Bayesian approach.

Serum samples from 11 patients with R-NMO diagnosed according to Wingerchuk criteria and matched in terms of age, gender and ethnicity with the healthy controls were analyzed. The levels of TNF-α, IFN-γ, IL-10, MMP-9, TIMP-1 and oxidative stress markers: malondialdehyde, advanced oxidation protein products, peroxidation potential, superoxide dismutase, catalase, and total hydroperoxides were measured.

Results

We found almost undetectable levels of TNF-α, a decreased production of IL-10 and a significant up-regulation of every oxidative stress biomarker studied. The insufficient production of TNF-α and IL-10 in R-NMO patients, which are two important players of T cell mediated immunoregulation, suggest an effector – regulator imbalance. The overproduction of oxygen reactive species as a consequence of the chronic inflammatory milieu is reflected on the excess of oxidative damage mediators detected. Furthermore, Multidimensional Scaling and a Bayesian linear regression model revealed a significant linear dependence between Expanded Disability Status Scale Kurtzke and TIMP-1; pointing to a possible predictive or prognostic value of this clinical-molecular relationship.

Conclusion

These results suggest that there is a breakdown in immunoregulatory mechanisms and noteworthy pro-oxidant environment contributing to NMO pathogenesis.