BTI-322 for acute rejection after renal transplantation

Mourad, Michel;Besse, T.;Malaise, Jacques;Baldi, A.;Squifflet, Jean-Paul;et.al.
(1997) Transplantation Proceedings — Vol. 29, n° 5, p. 2353 (1997)

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Authors
  • Mourad, MichelUCLouvain
    Author
  • Besse, T.
    Author
  • Malaise, JacquesUCLouvain
    Author
  • Baldi, A.
    Author
  • Latinne, DominiqueUCLouvain
    Author
  • Bazin, HervéUCLouvain
    Author
  • Pirson, YvesUCLouvain
    Author
  • Squifflet, Jean-PaulUCLouvain
    Author
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Abstract
BTI-322/LO-CD2a, a rat IgG2b, anti-CD2 monoclonal antibody which binds to all human T and natural killer (NK) cells, was first produced at our Institution1 and was first administered to patients on a compassionate-use basis in 1992. Four patients (three with renal allograft rejection and one with graft-versus-host-disease [GVHD]) resistant to standard therapies received treatment with LO-CD2a 10 mg/d intravenously (IV) for up to 12 days, plus steroids. In all cases, the drug was well tolerated, with no evidence of undesirable side effects; significant clinical benefit was demonstrated in each case. In 1993, LO-CD2a was successfully produced in vitro and became known as BTI-322. A study was initiated to evaluate the safety and determine the minimally effective dose of BTI-322 for treatment of either the first episode of acute renal allograft rejection (group AR) or uncontrolled rejection (rescue therapy; group RT).
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Citations

Mourad, M., Besse, T., Malaise, J., Baldi, A., Latinne, D., Bazin, H., Pirson, Y., Hope, J., & Squifflet, J.-P. (1997). BTI-322 for acute rejection after renal transplantation. Transplantation Proceedings, 29(5), 2353. https://doi.org/10.1016/s0041-1345(97)00398-9 (Original work published 1997)