Fig. 2.
Fig. 2. Proliferative responses of β2GPI-specific CD4+ T-cell clones to 15 synthetic peptides covering the entire domain V. / The β2GPI-specific CD4+ T-cell clones OM2 and OM8 were cultured with autologous APCs for 3 days in medium alone or in medium supplemented with individual synthetic peptides (5 μg/mL), and peptide-induced T-cell proliferation was measured by3H-thymidine incorporation. GP-F, GP1, GP2, GP3, and MalBP (10 μg/mL) were also used as antigens for T-cell proliferation. Significant T-cell proliferation to domain V peptide or recombinant β2GPI in comparison with the respective controls is shown as an asterisk. Similar results were obtained in 4 independent experiments.

Proliferative responses of β2GPI-specific CD4+ T-cell clones to 15 synthetic peptides covering the entire domain V.

The β2GPI-specific CD4+ T-cell clones OM2 and OM8 were cultured with autologous APCs for 3 days in medium alone or in medium supplemented with individual synthetic peptides (5 μg/mL), and peptide-induced T-cell proliferation was measured by3H-thymidine incorporation. GP-F, GP1, GP2, GP3, and MalBP (10 μg/mL) were also used as antigens for T-cell proliferation. Significant T-cell proliferation to domain V peptide or recombinant β2GPI in comparison with the respective controls is shown as an asterisk. Similar results were obtained in 4 independent experiments.

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