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Treg depletion or adoptive cell transfer to CD3−/− mice is not sufficient to restore an Ova-specific CD8+ T cell response.

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posted on 2013-02-20, 05:36 authored by Emilie Franck, Carole Bonneau, Laetitia Jean, Jean-Paul Henry, Yann Lacoume, Anna Salvetti, Olivier Boyer, Sahil Adriouch

(A) B6 (n = 3) and SM-Ova (n = 3) mice were injected i.p. at day −4 and day −1 with 250 µg of anti-CD25 (PC-61) antibody to inactivate endogenous Treg, or with PBS, followed by the injection of rAAV-Ova at day 0. Splenocytes from treated mice were collected 14 days after immunization and analyzed as before by flow cytometry for the presence of Ova-specific CD8+ cells using H-2Kb/Ova257–264 pentamer staining. Representative FACS profiles and bar graphs are shown and numbers correspond to percentages of cells positively stained with the H-2Kb/Ova257–264 pentamer in the gated CD8+ population. (B) 2×107 purified CD8+ T cells originating from B6 or SM-Ova donor mice were adoptively transferred into syngenic CD3−/− recipient mice (n = 6) together with 3×107 purified CD4+ T cells originating exclusively from B6 donors. Recipient CD3−/− mice were immunized with rAAV-Ova one day later and splenocytes were collected, enumerated and analyzed 14 days after by flow cytometry to evaluate the percentages and absolute numbers of Ova-specific CD8+ cells. Representative profiles gated on the CD8+ population are shown in the left panel and the total numbers of Ova-specific CD8+ per spleen are shown in the right bar graph.


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