Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8466870 | Cytotherapy | 2018 | 8 Pages |
Abstract
Virus-specific T-cell (VST) infusion becomes a promising alternative treatment for refractory viral infections after hematopoietic stem cell transplantation (HSCT). However, VSTs are often infused during an immunosuppressive treatment course, especially corticosteroids, which are a first-line curative treatment of graft-versus-host disease (GVHD). We were interested in whether corticosteroids could affect adenovirus (ADV)-VST functions. After interferon (IFN)-γ based immunomagnetic selection, ADV-VSTs were in vitro expanded according to three different culture conditions: without methylprednisolone (MP; nâ=â7), with a final concentration of MP 1âµg/mL (nâ=â7) or MP 2âµg/mL (nâ=â7) during 28â±â11 days. Efficacy and alloreactivity of expanded ADV-VSTs was controlled in vitro. MP transitorily inhibited ADV-VST early expansion. No impairment of specific IFN-γ secretion capacity and cytotoxicity of ADV-VSTs was observed in the presence of MP. However, specific proliferation and alloreactivity of ADV-VSTs were decreased in the presence of MP. Altogether, these results and the preliminary encouraging clinical experiences of co-administration of MP 1âmg/kg and ADV-VSTs will contribute to safe and efficient use of anti-viral immunotherapy.
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Authors
Arnaud Campidelli, Chongsheng Qian, Caroline Laroye, Véronique Decot, Loïc Reppel, Maud D'aveni, Danièle Bensoussan,