Rituxan in the treatment of cold agglutinin disease.
نویسندگان
چکیده
Dr Gyger and colleagues, in reply to our work on granulocyte colony-stimulating factor (G-CSF) bone marrow (BM) purging, have pointed out three aspects of the problem: the possible negative balance of marrow cells after short-term G-CSF administration, the need for at least two cytokines for priming BM stem cells (BMSC), and the probable contamination of BM harvest. Overall, we agree on each of these three points and we would like to stress that the misinterpretation of the term ‘‘priming’’ could be the origin of the observations made by Gyger et al. In fact this term was already used in previous reports1-3 on the same subject showing early expansion of CD341 BMSC and their mobilization. We agree that the term should be used only to mean ‘‘activation’’ of SC and not mobilization. To this purpose we have used the term priming to differentiate it from peripheral blood (PB) mobilization. On the other hand, our data overlap those of Dicke et al,4 where the term ‘‘activation’’ was used with the same meaning of our ‘‘priming.’’ As far as PB contamination, we have stressed this point in the discussion and confirm that the purpose of our study was essentially clinical: in other words, we wanted to show that short-term G-CSF can increase the BMSC, allowing for a positive engraftment compared with steady-state BM. The availability of an alternative source of SC with rapid engraftment may find clinical application in the pediatric and the allogeneic settings.
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ورودعنوان ژورنال:
- Blood
دوره 92 9 شماره
صفحات -
تاریخ انتشار 1998