Table 1

Peripheral blood myeloid progenitor cell–mobilizing effects of 300 mg intravenous natalizumab in 4 MS patients

BFU-E colonies, no.
CFU-G/-M/-GM colonies, no.
Before infusion1 h after infusion24 h after infusion48 h after infusion72 h after infusionBefore infusion1 h after infusion24 h after infusion48 h after infusion72 h after infusion
Patient 1 10 88 100* 100* 22 43 39 
Patient 2 34 100* 100* 100* 10 38 34 40 
Patient 3 10 100* 100* 100* 67 21 27 10 11 
Patient 4 50 100* 100* 100* 100* 44 25 18 20 
Median 67 100 100 100 15.5 26 26 29.5 
P — .08 .004 .005 .009 — .12 .005 .06 .05 
BFU-E colonies, no.
CFU-G/-M/-GM colonies, no.
Before infusion1 h after infusion24 h after infusion48 h after infusion72 h after infusionBefore infusion1 h after infusion24 h after infusion48 h after infusion72 h after infusion
Patient 1 10 88 100* 100* 22 43 39 
Patient 2 34 100* 100* 100* 10 38 34 40 
Patient 3 10 100* 100* 100* 67 21 27 10 11 
Patient 4 50 100* 100* 100* 100* 44 25 18 20 
Median 67 100 100 100 15.5 26 26 29.5 
P — .08 .004 .005 .009 — .12 .005 .06 .05 

Colony-forming activity was determined after plating 4×105 MNCs in 24-well plates before and 1, 24, 48, and 72 hours following the initial infusion of natalizumab.

— indicates not applicable.

*

In these particular culture plates, at least 100 single BFU-Es were discernible. In fact, the plating efficacy was unexpectedly higher, so that some of the BFU-E growth was not clearly attributable to individual colonies.

Statistical significance expressed as P value compared with baseline (time = before) using the 2-sided paired t test.

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