Murine monoclonal anti-T cell antibodies for treatment of steroid-resistant acute graft-versus-host disease.

Published

Journal Article

Four different murine monoclonal anti-T cell antibodies were administered to 15 patients with severe steroid resistant graft versus host disease (GVHD) in a phase I clinical trial in order to evaluate feasibility and toxicity. Antibodies 9.6 (IgG2a) and 35.1 (IgG2a) bind to separate epitopes on the E receptor (Tp50); antibody 10.2 (IgG2a) binds to the murine Lyt-1 homolog (Tp67); and antibody 12.1 (IgG2a) binds to a cell surface antigen with a molecular weight of approximately 100,000 daltons (Tp100). A total of 151 infusions were given, ranging in dose from one to 20 mg, each administered over a one to four hour period. One patient received a total of 259 mg of antibody over a period of 45 days. Six infusions (4%) in two patients were associated with fever or fever and chills. By decreasing the infusion rate, subsequent infusions to these two patients were accomplished without additional reactions. Although most of the patients treated with monoclonal antibodies required platelet support, the number of platelet units given was not significantly different from similar patients not receiving monoclonal antibodies. Six of ten patients receiving intermediate to high doses (5-20 mg) antibody therapy had evidence of at least partial improvement in GVHD in at least one involved organ system. None of the patients became immunized to mouse immunoglobulin. Our results suggest that therapy of GVHD with murine monoclonal anti-T cell antibodies is feasible and that these antibodies apparently can be administered to marrow transplant patients without significant toxicity. Further studies are required to determine which antibodies or combinations of antibodies have optimal anti-GVHD effect.

Full Text

Duke Authors

Cited Authors

  • Remlinger, K; Martin, PJ; Hansen, JA; Doney, KC; Smith, A; Deeg, HJ; Sullivan, K; Storb, R; Thomas, ED

Published Date

  • January 1, 1984

Published In

Volume / Issue

  • 9 / 1

Start / End Page

  • 21 - 35

PubMed ID

  • 6198309

Pubmed Central ID

  • 6198309

International Standard Serial Number (ISSN)

  • 0198-8859

Language

  • eng

Conference Location

  • United States