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. 2023 Dec 4;92(1):e00421-23. doi: 10.1128/iai.00421-23

Fig 3.

Fig 3

Effect of IL-22-deficient CD4+ T cells as donor cells on pGP3-deficient C. muridarum spreading from small intestine into large intestine in Rag2−/− mice. Mice deficient in Rag2 (Rag2−/−) listed on the right as recipient mice were adoptively transferred without (panel a, n = 5) or with 1 × 106 donor CD4+ T cells purified from C57BL/6J (b, n = 5) or IL-22−/− (c, n = 4) mice. The transfer was performed via retro-orbital injection twice, 3 days before and 1 day after infection, respectively. Mice were infected via intrajejunal injection with 1 × 105 IFUs of CMpGP3S. Three days after inoculation, rectal swabs (Swb) were collected, and all mice were sacrificed for collecting gastrointestinal tissues as listed along the X-axis. Live CMpGP3S organisms were recovered from each sample and expressed as log10 IFUs per tissue or swab. The data came from two or three independent experiments. Note that IL-22-deficient CD4+ T cells were insufficient for rescuing Rag2−/− mice to block the spreading of live chlamydial organisms into the large intestine. * denotes an observed P-value <0.05, based on a Wilcoxon rank-sum test, comparison of the live chlamydial organisms in the colon and large intestinal tissues overall between panels b and c.