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. 2010 Jan;159(1):100–108. doi: 10.1111/j.1365-2249.2009.04035.x

Table 3.

Normalized data for C3a and C5a levels using mouse and human sera.

Mouse sera (%) Human sera (%)
C3a levels
No mAb to factor B with:
Ca++ sufficient buffer (both CP and AP) 100 100
Ca++ deficient buffer (AP only) 76.6 ± 3.6* 88.9 ± 4.5*
(range) (33–106) (45–140)
mAb to factor B with:
Ca++ sufficient buffer (CP only) 60.5 ± 3.3** 71.0 ± 2.8**
(range) (33–91) (43–102)
Ca++ deficient buffer (no CP or AP) 0 5.3 ± 1.1
C5a levels
No mAb to factor B with:
Ca++ sufficient buffer (both CP and AP) 100 100
Ca++ deficient buffer (AP only) 79.1 ± 3.6*** 62.8 ± 3.8***
(range) (14–116) (18–110)
mAb to factor B with:
Ca++ sufficient buffer (CP only) 46.6 ± 2.8**** 74.3 ± 2.2****
(range) (4–92) (48–94)
Ca++ deficient buffer (no CP or AP) 0 0.8 ± 0.6

P-values for mouse versus human sera:

*

P = 0·04;

**

P = 0·02;

***

P = 0·003;

****

P < 0·0001.

The data for up to six experiments were normalized to 100% of the values obtained in the absence of monoclonal antibody (mAb) to factor using Ca++ sufficient buffer.

The data are expressed as mean ± standard error of the mean based on n = 34 human sera for both assays, n = 45 murine sera for C5a levels and n = 24 murine sera for C3a levels. AP, alternative pathway; CO, classical pathway.