Table 2.
|
% F344 DSA-I |
||
---|---|---|---|
12 weeks | 24 weeks | P | |
NT | 54.3±19.9 | 86.1±2.284 | 0.043 |
BMC | 65.8±13.5 | 46.8±15.5a | NS |
MSC | 16.1±5.25b | 35.1±15.9a | NS |
|
% F344 DSA-II |
||
---|---|---|---|
12 weeks | 24 weeks | P | |
NT | 8.87±4.9 | 31.6±5.2 | 0.03 |
BMC | 22.4±6.6 | 17.1±6.1 | NS |
MSC | 1.6±1.2b | 15.5±7.1c | NS |
The presence of circulating DSA class-I and class-II was quantified on recipient serum samples incubated with kidney donor (F344) spleen cells and measured by flow cytometry. A fluorescence increase of 15% with regard to the negative control was considered positive. Results were expressed as a percentage of positive cells with regard to the total number of CD3+ spleen cells. DSA titters were analyzed by analysis of variance followed by Scheffe's test. MSC treatment protects from developing DSAs from 1 week after the injection (12 weeks) and at 24 weeks. The BMCs injection has a different reaction, increasing the DSAs at 1 week after cell transplantation and maintaining them along with time.
P≤0.04 versus NT, bP=0.06 versus BMC; cP=0.06 versus NT.
DSAs, donor specific antibodies.