Expression of CD134 (0X‐40) on T cells during the first 100 days following allogeneic bone marrow transplantation as a marker for lymphocyte activation and therapy‐resistant graft‐versus‐host disease

CD134 (OX‐40) is an activation‐associated antigen which functions as a costimulatory receptor for CD4+ T cells. In order to determine the expression of CD134 during immune recovery following allogeneic bone marrow transplantation (BMT), we measured its expression on T cells and T cell subsets during...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Cytometry (New York, N.Y.) N.Y.), 1999-10, Vol.38 (5), p.238-243
Hauptverfasser: Lamb, L.S., Abhyankar, S.A., Hazlett, L., O'Neal, W., Folk, R.S., Vogt, S., Parrish, R.S., Bridges, K., Henslee‐Downey, P.J., Gee, Adrian P.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:CD134 (OX‐40) is an activation‐associated antigen which functions as a costimulatory receptor for CD4+ T cells. In order to determine the expression of CD134 during immune recovery following allogeneic bone marrow transplantation (BMT), we measured its expression on T cells and T cell subsets during the first 100 days following BMT in 26 patients. CD4+CD134+ T could be seen approximately 14 days following BMT cells in patients who did not develop GvHD which required therapy (n = 20). The percentage of CD4+CD134+ cells continued to increase up to the fourth week following BMT to a maximum of 40–50% of CD4+ T cells (normal = 1–8%). Two patients who developed Grade I‐II GvHD and who responded to treatment with pulsed high‐dose methylprednisolone (MPD) showed a decline of approximately 40% in CD4+CD134+ T cells was seen within 48 hours of treatment. Four patients who developed GvHD that was not responsive to MPD and who later developed high IV GvHD showed increasing CD4+CD134+ T cells up to 85% of the CD4+ T cells. Additionally, rapid increases in CD134+ T cells following antibody‐based T cell therapy were associated with GvHD recurrence. In no cases was the percentage of CD134+ CD4+ T cells predictive of clinical GvHD. In this exploratory study, we have shown that CD134, although not predictive of the initial onset of GvHD, may be a useful tool for monitoring the response to early GvHD therapy and identification of patients at risk for reemergence of GvHD who may benefit from anti‐T cell therapy. Cytometry (Comm. Clin. Cytometry) 38: 238–243, 1999.  © 1999 Wiley‐Liss, Inc.
ISSN:0196-4763
1097-0320
DOI:10.1002/(SICI)1097-0320(19991015)38:5<238::AID-CYTO6>3.0.CO;2-O