2008
DOI: 10.1016/j.bbmt.2007.12.401
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391: Rituximab Infusion after Allogeneic HCT Prevents Donor B Cell Reconstitution and Alloimmunity One Year Post Transplant

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Cited by 3 publications
(2 citation statements)
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“…(94) Thus, rituximab treatment post allogeneic HCT may potentially eliminate CD20+ alloreactive cells while leaving early pre and pro B cells to develop into nonalloreactive mature B cells. Rituximab therapy is well tolerated with relatively few infectious complications (91) because long-lived host plasma cells continue to secrete protective antimicrobial antibodies (95). …”
Section: Rationale For Rituximab Treatment Of Chronic Gvhdmentioning
confidence: 99%
“…(94) Thus, rituximab treatment post allogeneic HCT may potentially eliminate CD20+ alloreactive cells while leaving early pre and pro B cells to develop into nonalloreactive mature B cells. Rituximab therapy is well tolerated with relatively few infectious complications (91) because long-lived host plasma cells continue to secrete protective antimicrobial antibodies (95). …”
Section: Rationale For Rituximab Treatment Of Chronic Gvhdmentioning
confidence: 99%
“…However, use of rituximab posttransplantation risks delaying recovery of a donor-derived B cell immune response. Rituximab therapy 2 months after allo-HSCT prevents donor B cell reconstitution up to 1 year after transplantation [69,70]. The half-life of rituximab, despite the influence of the tumor burden, could range from several days to months.…”
Section: Time To Explore Preventive Strategies For Bos After Hsctmentioning
confidence: 99%