Influence of cytomegalovirus (CMV) sero-positivity on CMV infection, lymphocyte recovery and non-CMV infections following T-cell-depleted allogeneic stem cell transplantation: a comparison between two T-cell depletion regimens
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Chakrabarti, S
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机构:Bristol Royal Hosp Sick Children, Adult Bone Marrow Transplant Unit, Bristol, Avon, England
Chakrabarti, S
Milligan, DW
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机构:Bristol Royal Hosp Sick Children, Adult Bone Marrow Transplant Unit, Bristol, Avon, England
Milligan, DW
Brown, J
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机构:Bristol Royal Hosp Sick Children, Adult Bone Marrow Transplant Unit, Bristol, Avon, England
Brown, J
Osman, H
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机构:Bristol Royal Hosp Sick Children, Adult Bone Marrow Transplant Unit, Bristol, Avon, England
Osman, H
Vipond, IB
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机构:Bristol Royal Hosp Sick Children, Adult Bone Marrow Transplant Unit, Bristol, Avon, England
Vipond, IB
Pamphilon, DH
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机构:Bristol Royal Hosp Sick Children, Adult Bone Marrow Transplant Unit, Bristol, Avon, England
Pamphilon, DH
Marks, DI
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机构:Bristol Royal Hosp Sick Children, Adult Bone Marrow Transplant Unit, Bristol, Avon, England
Marks, DI
机构:
[1] Bristol Royal Hosp Sick Children, Adult Bone Marrow Transplant Unit, Bristol, Avon, England
[2] Bristol Royal Hosp Sick Children, Publ Hlth Labs, Bristol, Avon, England
[3] Birmingham Heartlands Hosp, Dept Haematol & Virol, Birmingham B9 5ST, W Midlands, England
We compared the incidence and outcome of preemptively treated cytomegalovirus (CMV) infection, lymphocyte recovery and non-CMV infections between two different TCD modalities, one employing CD34+ selection and T-cell add-back (TCAB), preceded by Campath-1H in vivo (CD34+/TCAB group, n = 29), and the other using grafts incubated with Campath-1H in vitro (Campath-1H in vitro group, n = 32). The probabilities of CMV reactivation and recurrence were 67 and 83.6% in the CD34+/TCAB group and 42.9 and 20% in the Campath-1H group (P = 0.07 and 0.02). Donor seropositivity reduced CMV reactivation in the Campath-1H group, but not in the CD34+/TCAB group. The durations of positive PCR/antigenemia positivity and antiviral therapy were also significantly longer in the CD34+/TCAB group. However, only two patients developed CMV disease in each group. The mean absolute lymphocyte counts (x 10(9)/l) at 30 days (0.27 vs 0.4, P = 0.03) and 100 days (0.77 vs 1.4, P = 0.01) were significantly lower in the CD34+/TCAB group along with a higher incidence of non-CMV infections in CMV at-risk patients, but not in the CMV low-risk group. These findings suggest that the modality of TCD should be tailored according to the CMV risk status, and CMV sero-positive patients should receive a less extensively T-cell-depleted graft and a CMV sero-positive graft if possible.