Your browser doesn't support javascript.
loading
Mogamulizumab for Treatment of Human T-lymphotropic Virus Type 1-Associated Myelopathy/Tropical Spastic Paraparesis: A Single-Center US-based Series.
Meyerowitz, Eric A; Mukerji, Shibani S; Kyle Harrold, G; Erdil, Rachel M; Chen, Steven T; Rudmann, Emily A; Tsibris, Athe; Venna, Nagagopal; Robbins, Gregory K.
Afiliación
  • Meyerowitz EA; Division of Infectious Diseases, Montefiore Medical Center, Bronx, New York, USA.
  • Mukerji SS; Albert Einstein College of Medicine, Bronx, New York, USA.
  • Kyle Harrold G; Division of Neuroimmunology and Neuro-Infectious Diseases, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Erdil RM; Harvard Medical School, Boston, Massachusetts, USA.
  • Chen ST; Division of Neuroimmunology and Neuro-Infectious Diseases, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Rudmann EA; Harvard Medical School, Boston, Massachusetts, USA.
  • Tsibris A; Division of Geographic Medicine and Infectious Diseases, Tufts Medical Center, Boston, Massachusetts, USA.
  • Venna N; Harvard Medical School, Boston, Massachusetts, USA.
  • Robbins GK; Department of Dermatology, Massachusetts General Hospital, Boston, Massachusetts, USA.
Clin Infect Dis ; 77(6): 851-856, 2023 09 18.
Article en En | MEDLINE | ID: mdl-37157862
ABSTRACT

BACKGROUND:

Human T-lymphotropic virus type 1 (HTLV-1)-associated myelopathy/tropical spastic paraparesis (HAM/TSP) is a chronic neurological condition characterized by progressive myelopathic symptoms including spasticity, pain, weakness, and urinary symptoms, without proven treatments. Mogamulizumab (MOG) is a monoclonal antibody that binds CCR4 and leads to the clearance of HTLV-1-infected CCR4+ cells. A phase 1-2a study in Japan evaluated MOG for the treatment of HAM/TSP and reported decreases in HTLV-1 proviral load and neuroinflammatory markers, with clinical improvement in some participants.

METHODS:

We administered MOG 0.1 mg/kg every 8 weeks to individuals with HAM/TSP as a compassionate and palliative treatment. Patients who received MOG had (1) a positive peripheral HTLV-1 antibody, (2) progressive myelopathic symptoms, and (3) a diagnosis of HAM/TSP.

RESULTS:

Four female patients, ages 45-68, received MOG (range, 2-6 infusions) between 1 November 2019 and 30 November 2022. Two patients with <3 years of symptoms had milder disease, with Osame scores <4. The other 2, with >7 years of symptoms, had Osame scores >5. One patient, with 6 total treatments, received dose-reduced MOG after she developed a rash at the initial dose. The 2 patients with milder baseline disease reported symptomatic improvement and saw reductions in Osame and/or modified Ashworth scale scores during follow-up. The other 2 patients showed no improvement. All 4 developed rashes after receiving MOG-a treatment-limiting event in some cases.

CONCLUSIONS:

Clinical trials are needed including diverse patient populations to assess the potential role of MOG for HAM/TSP. Our findings may help inform the development of these trials.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Virus Linfotrópico T Tipo 1 Humano / Paraparesia Espástica Tropical / Exantema Tipo de estudio: Risk_factors_studies Límite: Female / Humans Idioma: En Revista: Clin Infect Dis Asunto de la revista: DOENCAS TRANSMISSIVEIS Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Virus Linfotrópico T Tipo 1 Humano / Paraparesia Espástica Tropical / Exantema Tipo de estudio: Risk_factors_studies Límite: Female / Humans Idioma: En Revista: Clin Infect Dis Asunto de la revista: DOENCAS TRANSMISSIVEIS Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos