Sentence examples for mice received naïve from inspiring English sources

Control mice received naïve rabbit serum.

Control mice received naïve CD25− cells on day −1 and either no pre-treatment or anti-CD4 mAbs alone (Fig. 5A) As shown in Fig. 5B, adoptive transfer control and anti-CD4 control mice rejected their skin allografts acutely (MST 19 days, n=6 and 19 days n=4, respectively).

Numbers of IFN-γ+ donor CD4 T cells were highest in those recipients that showed protective immunity, however, there were also significant numbers of cytokine-producing cells in mice receiving naïve T cells where there was no immunity (Fig. 3F).

In contrast all mice which received naïve serum or were in a control non-treated group died between 13 and 25 days.

Additionally, allografts transplanted to mice that received naïve T cells and anti-Gr-1 mAb also enjoyed prolonged survival (p<0.05) with the grafts rejected with the same kinetics as those placed on mice that received BM3 Tm and anti-Gr-1 mAb.

In order to identify parameters other than viral antigenic load that differ and could affect memory conversion of antiviral CD8 T cells, mice that had received naïve P14/GFP+ cells late were treated the day after the cell transfer with polyI C (100 µg/mouse), CpG (200 µg/mouse) or recombinant IFNγ (50 ng/mouse).

Furthermore, despite BM3 Tm undergoing similar levels of T-cell proliferation to that of naïve BM3 T cells, the absolute number of BM3 T cells present within the spleen, MLN, DLN and CLN of allograft recipients at 10 days after transplantation was significantly higher in mice that had received naïve (39147±13757 cells) compared to memory BM3 T cells (Fig. 2F, 14222±4972 cells, p<0.05).

Skin allografts taken 10 days after transplant from mice that had received BM3 Tm were found to harbour an extensive PMN infiltrate, whereas PMN were rarely found in the grafts of mice that had received naïve BM3 T cells (Fig. 5).

Mice that received BM3 Tm and a depleting anti-Gr-1 mAb on days 5, 10, 15 and 20 days i.p. post transplantation rejected skin allografts in a delayed fashion compared to Tm-mediated rejection without anti-Gr-1 mAb (Fig. 6A; p<0.05), but with the same tempo as mice that had received naïve BM3 T cells.

To this end, CBARAG−/− mice received 1×10 naïve or memory BM3 T cells i.v. before being transplanted with an H2Kb+ skin graft the day after cell transfer.

Naïve mice received pooled sera collected from different groups, as indicated in Figure 4C, in a 1∶100 dilution, by intraperitoneal route, 2 h before challenge.