Viewing negative mentions of gene expression of Foxp3 (M. musculus) in T cells

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Bacchetta et al. (2006)FOXP3 proteinT cellsIn contrast, the suppressive function of CD4+ CD25high T cells from IPEX patients who do not express FOXP3 protein was profoundly impaired.
Guo et al. (2010)Foxp3T cellsThe present study shows that in Foxp3 transgenic (Foxp3-Tg) mice, in which the transgene is driven by the lck distal promoter, CD4+CD25- T cells that express the Foxp3 transgene do not upregulate the expression of CD25-, GITR, or CTLA-4, and do not have suppressive function; however, the Foxp3-Tg+CD4+CD25- T cells exhibit significantly reduced proliferative response to TCR engagement.
Haque et al. (2010)FoxP3T cellsHowever, the proliferation in CD4+ GFP- T cells was significantly suppressed by Tregs co-expressing FoxP3 and Bcl-xL as compared with cells expressing FoxP3 alone on day 4 but not day 2 (Figure 3c, d).
Sun et al. (2006)Foxp3T cellA remaining CD25- T cell population, which also became suppressive in response to OVA/CTB treatment, did not express Foxp3.
Fontenot et al. (2005)Foxp3T cellsIn contrast, Foxp3 was not expressed in thymocytes or peripheral T cells from Il2rg(-/-) mice.
Pandiyan and Lenardo (2008)Foxp3T cellsPrevious data has demonstrated that scurfy T cells do not express Foxp3, that they are CD25+ and that these cells do not have any Treg activity (Khattri, et. al.).
Efimova et al. (2011)FOXP3T cellsBecause a small percentage of CD4+CD25+ T cells are not Tregs and do not express FOXP3, the isolated Treg samples were never completely pure, based on FOXP3 expression, and ranged from approximately 80%–85% FOXP3 positive.
Chen et al. (2004)foxP3T cellsCD4(+) T cells in these mice expressed higher levels of CTLA-4 and glucocorticoid-induced TNF-related receptor than naive CD4(+) T cells, but only 3% of the recolonizing cells were CD25(+) and did not express significant foxP3 mRNA.
Xia et al. (2008)Foxp3T-cellIn vivo, alloAg-enriched, TGF-beta/IL-2-conditioned nT(reg) expressed high-level Foxp3 following infusion, effectively overcame acute rejection and induced long-term survival of donor but not third-party heart allografts in peritransplant host T-cell-depleted mice.
Zhou et al. (2008)FoxP3T cellsThe infiltrate was composed of both CD4+ and CD8+ T cells, not unlike what has been observed in other T reg cell–dependent lymphoproliferative diseases and FoxP3-deficient mice (Fig. 5 E).
Lochner et al. (2008)Foxp3T cellst+ T cells do not express Foxp3, but cells from WT mice protected the host from a scurfy phenotype (not depicted).
Jiang et al. (2007)Foxp3 mRNAT cellsAs shown in Figure 4, Foxp3 mRNA was not detectable in CD8+ T cells from OVA-stimulated and unstimulated ACAID mice, normal mice, or PBS-AC-injected mice.
Kuczma et al. (2009)Foxp3T cellsT(reg) cells expressing a high level of Foxp3 and TCRs not used by naive CD4(+) T cells present a stable suppressor phenotype and dominate the peripheral T(reg) population in unmanipulated mice.
Giuliani et al. (2008)Foxp3T cellIn view of these properties, we propose the terminology “NK-ireg” to define this NKPSG cells even if they do not express the transcription factor Foxp3 and they cannot inhibit CD3 dependent T cell expansion (data not shown).
Oida et al. (2010)Foxp3T cellsinduced surface LAP not only on T cells that converted to Foxp3+ but also on T cells in which Foxp3 was not expressed.
Fleissner et al. (2010)Foxp3T cellsInterestingly, allostimulated CD8+CD103+ T cells lacked Foxp3, CD25, LAG3, CTLA4, and GITR expression suggesting that these cells belong to another subtype of CD8+ Tregs.
Shafiani et al. (2010)Foxp3T cellsImportantly, the ESAT-6–specific CD4+ T cells were not T reg cells because they did not express Foxp3 (Fig.
Shafiani et al. (2010)Foxp3T cellsS2 shows that tetramer-binding Mtb-specific CD4+ T cells do not express Foxp3 during early Mtb infection.
Ghebeh et al. (2008)FOXP3T-lymphocytesThe cut off point for positive and negative for FOXP3, B7-H1 and PD-1 was 5% (5% of total CD3+ T-lymphocytes).
Wieten et al. (2009)Foxp3T cellsHowever, in the present study CD4+CD25+ T cells from HSP70 immunized mice did not increasingly express Foxp3, indicating the possible presence of distinct types of regulation in different models of inflammation.
Han et al. (2009)Foxp3T cellsOur results demonstrate that CD69(+)CD4(+)CD25(-) T cells act as a new subset of regulatory CD4(+) T cells, with distinct characteristics of negative expression of Foxp3, no secretion of IL-10, but high expression of CD122 and membrane-bound TGF-beta1.
Han et al. (2009)Foxp3T cellsDistinct from the previously described CD4(+) Treg cell subsets, CD69(+)CD4(+)CD25(-) T cells express high CD122, but they do not express Foxp3 and secrete IL-10, TGF-beta1, IL-2, and IFN-gamma.
Malemud (2009)FoxP3T-cells-expressing T-cells that also failed to express FoxP3 which showed marked proliferation in vitro compared to IL-7R?