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Mixed chimaerism is common at the time of acute graft-versus-host disease and disease response in patients receiving non-myeloablative conditioning and allogeneic stem cell transplantation.

Mattsson, Jonas, 1966 (författare)
Karolinska Institutet
Uzunel, M (författare)
Karolinska Institutet
Brune, Mats, 1950 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för invärtesmedicin, Avdelningen för internmedicin,Institute of Internal Medicine, Dept of Medicine
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Hentschke, P (författare)
Barkholt, L (författare)
Stierner, Ulrika, 1952 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för särskilda specialiteter, Avdelningen för onkologi,Institute of Selected Clinical Sciences, Department of Oncology
Aschan, J (författare)
Ringdén, O (författare)
Karolinska Institutet
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 (creator_code:org_t)
Wiley, 2001
2001
Engelska.
Ingår i: British journal of haematology. - : Wiley. - 0007-1048. ; 115:4, s. 935-44
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • We report the clinical outcome and results of chimaerism analysis in various cell lineages of 30 patients given non-myeloablative conditioning, followed by allogeneic stem cell transplantation (SCT). The commonest diagnoses were chronic myelogenous leukaemia (n = 11) and solid tumours (n = 11). Twenty-one patients received SCT from human leucocyte antigen (HLA)-identical siblings and nine from matched unrelated donors. Median patient age was 53 (28-77) years. Four non-myeloablative protocols were used, including fludarabine (30 mg/m2 x 3-6), busulphan (4 mg/kg x 2), cyclophosphamide (Cy) (30 mg/kg/day x 2) or total body irradiation (2 Gy), and anti-thymocyte globulin. The patients were analysed by polymerase chain reaction (PCR) analysis of minisatellites on days 14, 21 and 28, then every other week up to 3 months and monthly thereafter. All samples were cell separated for T, B and myeloid cells using immunomagnetic beads. Eighteen patients were alive at a median follow-up of 11 (6-20) months. Acute graft-versus-host disease (GVHD) occurred in 22 patients. Eighteen of the 22 patients with acute GVHD showed mixed chimaerism (MC) in the T-cell fraction at the time of acute GVHD. However, all patients with acute GVHD showed donor chimaerism (DC) in the T-cell fraction median 76 (7-414) days after onset versus three out of eight patients without acute GVHD, P < 0.001]. Disease response was diagnosed in 15 patients, median 100 (37-531) days after SCT. At the time of disease response, six out of 15 patients showed MC in the T-cell fraction. In conclusion, mixed chimaerism in the T-cell fraction is common at the time of acute GVHD and disease response in patients conditioned with non-myeloablative therapy.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

Nyckelord

Adult
Aged
Bone Marrow Cells
pathology
Busulfan
therapeutic use
Cell Count
Cyclophosphamide
therapeutic use
Female
Graft vs Host Disease
immunology
Hematopoietic Stem Cell Transplantation
Histocompatibility Testing
Humans
Immunosuppressive Agents
therapeutic use
Male
Middle Aged
T-Lymphocytes
pathology
Transplantation Conditioning
methods
Transplantation
Homologous
Treatment Outcome
Vidarabine
analogs & derivatives
therapeutic use
Whole-Body Irradiation

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