Figure 4
Figure 4. Itch−/− αβ T cells are required for elevated IgM and autoimmune antibodies but dispensable for hyper-IgE. (A) No production of antinuclear antibodies was detected by ELISA in sera of TCRa−/− or TCRa−/− Itch−/− mice. Mice are divided in 2 age groups: 1 to 3 and 4 to 7 months of age. (B) Analysis of total Igs by ELISA from preimmune TCRa−/− WT, TCRa−/− Itch−/+, and TCRa−/− Itch−/− mice shows no significant difference among the groups for most of the isotypes. (C) However, IgE is substantially elevated in Itch−/− mice. (D) Ag-specific Igs in TCRa−/− WT, TCRa−/− Itch+/−, and TCRa−/− Itch−/− mice immunized with TNP-Ficoll were equivalent. (E) The average (± SD) numbers of total peritoneal B-cell subpopulations from TCRa−/− WT (□; n = 8), TCRa−/− Itch+/− (; n = 8), and TCRa−/− Itch−/− (■; n = 18) mice are shown. Subpopulations were identified by flow cytometry as follows: B2 = IgDhiIgMlo; B1 = IgMhiIgDlo; B1a = Mac1+CD5+; and B1b = Mac1+CD5−.

Itch−/− αβ T cells are required for elevated IgM and autoimmune antibodies but dispensable for hyper-IgE. (A) No production of antinuclear antibodies was detected by ELISA in sera of TCRa−/− or TCRa−/−Itch−/− mice. Mice are divided in 2 age groups: 1 to 3 and 4 to 7 months of age. (B) Analysis of total Igs by ELISA from preimmune TCRa−/− WT, TCRa−/−Itch−/+, and TCRa−/−Itch−/− mice shows no significant difference among the groups for most of the isotypes. (C) However, IgE is substantially elevated in Itch−/− mice. (D) Ag-specific Igs in TCRa−/− WT, TCRa−/−Itch+/−, and TCRa−/−Itch−/− mice immunized with TNP-Ficoll were equivalent. (E) The average (± SD) numbers of total peritoneal B-cell subpopulations from TCRa−/− WT (□; n = 8), TCRa−/−Itch+/− (; n = 8), and TCRa−/−Itch−/− (■; n = 18) mice are shown. Subpopulations were identified by flow cytometry as follows: B2 = IgDhiIgMlo; B1 = IgMhiIgDlo; B1a = Mac1+CD5+; and B1b = Mac1+CD5.

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