Autoimmune syndrome in the tropical spastic paraparesis/myelopathy associated with human T-lymphotropic virus infections

Felipe García, Martha C. Domínguez, Miyerlandi Torres, Óscar Tamayo, William Criollo, Milton Quintana, Adalberto Sánchez, .

Keywords: paraparesis, spastic, human T-lymphotropic virus 1, primateT-lymphotropic virus 1, spinal cord, autoantibodies, autoimmunity, molecular mimicry

Abstract

Introduction. Previous reports have given evidence that in tropical spastic paraparesis (TSP)/ human T-lymphotrophic virus (HTLV-I)-associated myelopathy (HAM), an autoimmune process occurs as part of its pathogenesis.
Objective. The roles of autoimmunity and the molecular mimicry was evaluated in TSP/HAM
patients.
Materials and methods. Plasma samples were characterized from patients in the Pacific coastal region of Colombia. Thirty-seven were identified as TSP/HAM, 10 were diagnosed with adult Tcell leukemia virus, 22 were asymptomatic carriers but seropositive for HTLV-I and 20 were seronegative and served as negative controls. Plasmatic levels of the following were determined: antinuclear antibody (ANA) levels, anticardiolipine-2 (ACL_2), interferon- (IFN-??) and interleukin- 4 (IL-4). Using Western blot, the crossreactivity of the seropositive and seronegative samples was evaluated against proteins extracted from several central nervous system components of non infected Wistar rats. The HTLV-I seropositive plasmas were crossreacted with a monoclonal tax (LT4 anti-taxp40) from spinal cord neurons of non infected Wistar rats.
Results. Of the TSP/HAM patients, 70.2% were reactive against ANA and 83.8% against ACL- 2, in contrast with those ATL and asymptomatic seropositives subjects that were not reactive (P<0.001). Moreover, 70.3% had detectable levels of IFN and 43.2% had detectable IL-4. LT4 anti-taxp40 and plasma of TSP/HAM exhibited cross reactivity with a MW 33-35 kDa protein from the rat spinal cord nuclei. Conclusion. Support was provided for the existence of an autoimmune syndrome mediated by molecular mimicry; the syndrome was responsible for some of the axonal degeneration observed in TSP/HAM patients.

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  • Felipe García Laboratorio de Biología Molecular y Patogénesis, Departamento de Ciencias Fisiológicas, Escuela de Ciencias Básicas, Facultad de Salud, Universidad del Valle, Cali, Colombia
  • Martha C. Domínguez Laboratorio de Biología Molecular y Patogénesis, Departamento de Ciencias Fisiológicas, Escuela de Ciencias Básicas, Facultad de Salud, Universidad del Valle, Cali, Colombia
  • Miyerlandi Torres Laboratorio de Biología Molecular y Patogénesis, Departamento de Ciencias Fisiológicas, Escuela de Ciencias Básicas, Facultad de Salud, Universidad del Valle, Cali, Colombia
  • Óscar Tamayo Facultad de Medicina, Universidad Santiago de Cali, Cali, Colombia
  • William Criollo Sección de Farmacología, Departamento de Ciencias Fisiológicas, Facultad de Salud, Universidad del Valle, Cali, Colombia
  • Milton Quintana Facultad de Medicina, Universidad del Sinú, Montería, Córdoba, Colombia
  • Adalberto Sánchez Laboratorio de Biología Molecular y Patogénesis, Departamento de Ciencias Fisiológicas, Escuela de Ciencias Básicas, Facultad de Salud, Universidad del Valle, Cali, Colombia

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How to Cite
1.
García F, Domínguez MC, Torres M, Tamayo Óscar, Criollo W, Quintana M, et al. Autoimmune syndrome in the tropical spastic paraparesis/myelopathy associated with human T-lymphotropic virus infections. biomedica [Internet]. 2008 Dec. 1 [cited 2024 May 17];28(4):510-22. Available from: https://revistabiomedica.org/index.php/biomedica/article/view/56
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Original articles

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