The frequency of antigen-specific ASC was calculated as a percentage of total IgG-producing cells. The

limit of detection (LD) was found to be three spots per well. These three spots were used to calculate the LD as a percentage of total spots obtained for IgG-producing cells for each individual patient. We set up an in vitro culture system that is suitable for studying the regulation of FVIII-specific memory B cells [17,18]. For this purpose, we obtained spleen cells from haemophilic mice treated with human FVIII and depleted these spleen cells of CD138+ ASC. Thereby, we generated a CD138− spleen cell population that did not contain any anti-FVIII ASC (Fig. 1) but contained FVIII-specific memory B, T cells and other cells. When we stimulated this CD138− cell mixture with human FVIII, FVIII-specific memory B cells were re-stimulated and differentiated into Y-27632 solubility dmso anti-FVIII ASC that could be detected as soon as 3 days after re-stimulation (Fig. 1) [17]. The maximum of newly formed anti-FVIII ASC was observed 6 days selleck inhibitor after re-stimulation (Fig. 1) [17]. In further experiments, we found that the re-stimulation of FVIII-specific memory B cells in our in vitro culture system

strictly depended on the presence of activated T cells [17]. Furthermore, a direct cell-to-cell contact between FVIII-specific memory B cells and activated T cells was required [17]. Based on our finding that activated T cells are required to re-stimulate FVIII-specific memory B cells in our in vitro culture system, MCE公司 we wanted to identify the specific co-stimulatory interactions that would be necessary for this process. Furthermore, we were interested to find out whether blocking essential co-stimulatory interactions would prevent the re-stimulation of FVIII-specific memory B cells. We added blocking antibodies against CD40L, CD80 (B7-1), CD86 (B7-2), ICOSL or recombinant competitor proteins (mICOS/Fc, mCTLA-4/Fc) to the CD138− spleen cell cultures immediately before re-stimulation with FVIII to study the importance of the relevant ligand

receptor pairs. The blockade of B7-CD28 or CD40-CD40L interactions significantly inhibited the re-stimulation of FVIII-specific memory B cells (Fig. 2) [17]. Both CD80 (B7-1) and CD86 (B7-2) contributed to the required co-stimulatory interactions with CD28. Blockade of both molecules prevented the re-stimulation of memory cells almost completely, whereas the blockade of only one of the two molecules resulted in a partial blockade (Fig. 2) [17]. The negative control antibodies and human IgG1 (negative control for mCTLA-4/Fc) did not show any effect. In contrast to CD40-CD40L and B7-CD28 interactions, ICOS-ICOSL interactions did not contribute to the re-stimulation of FVIII-specific memory cells. Neither the addition of a blocking antibody against ICOSL nor the use of a recombinant competitor protein (mICOS/Fc) resulted in a significant alteration in the re-stimulation of memory B cells (Fig. 2) [17].