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1 nd an invariant T-cell receptor-alpha chain (invariant NKT cells).
2 ionally similar to mammalian CD1d-restricted invariant NKT cells.
3 features with both the gammadelta T and the invariant NKT cells.
4 y impaired in the intrathymic development of invariant NKT cells.
5 lls have an innate-like phenotype similar to invariant NKT cells.
6 te CD8(+) T cell pool and the development of invariant NKT cells.
7 y stimulated alpha-galactosylceramide-primed invariant NKT cells.
8 FN-alpha was at least partially dependent on invariant NKT cells.
9 those of conventional NK cells, T cells, and invariant NKT cells.
10 d for presentation of autoantigens to murine invariant NKT cells.
11 s have been silenced, are unable to activate invariant NKT cells.
12 D56(+) T cells, and small numbers of classic invariant NKT cells.
13 cytokine GM-CSF in the thymic development of invariant NKT cells, a role that licenses these cells to
14 e protective later during infection than the invariant NKT cell agonist alpha-galactosylceramide.
15 wo potent variants of the highly stimulatory invariant NKT cell agonist alpha-galactosylceramide.
16 that innate T cells such as CD1d-restricted invariant NKT cells all underwent a phase of intense int
18 ein (SAP) is required for the development of invariant NKT cells and mediates signals from signaling
19 genic milieu through the interplay of Tregs, invariant NKT cells, and plasmacytoid dendritic cells, w
20 Moreover, CD1d tetramer staining shows that invariant NKT cells are activated in response to oral Sa
24 cellular mechanism by which IL-4(+)IL-13(+) invariant NKT cells are necessary for IL-4Ralpha signali
26 ciprocal interactions between CD8(+) DCs and invariant NKT cells are required for tolerance induction
28 s, effector T cells, regulatory T cells, and invariant NKT cells, as well as its impact on immune dis
29 dentified within GBM were not canonical, or "invariant," NKT cells, as they demonstrated diverse TCR
30 reveal that CCR7 controls the development of invariant NKT cells by enabling their access to IL-15 tr
31 ructing the function of the immunoregulatory invariant NKT cells can affect tumor cell survival is no
33 an anti-Valpha24-Jalpha18 Ab, human primary invariant NKT cells could be divided into Valpha24 low-
36 gesting that both Ag-specific CD4 T cell and invariant NKT cell effector responses to Salmonella-OVA
45 w that regulatory T cells (T(reg) cells) and invariant NKT cells (iNKT cells) perceived stronger TCR
50 populations of innate-like T cells including invariant NKT cells (iNKT), CD8alphaalphaTCRalphabeta sm
52 We found not only that mice deficient in invariant NKT cells (Jalpha18(-/-)) had a marked attenua
53 In contrast, the skins of UVB-irradiated invariant NKT cell-knockout (Jalpha18(-/-)) and NKT cell
55 ate T cells such as gammadelta TCR(+) cells, invariant NKT cells, mucosal-associated invariant T cell
57 tk and Rlk, leading to a 7-fold reduction in invariant NKT cell numbers in the thymus of Itk/Rlk-/- m
58 ant in this disease but does not involve the invariant NKT cell often associated with CD1d-restricted
59 dings suggest that the activation of hepatic invariant NKT cells plays a critical role in regulating
61 became clear that this cell does not express invariant NKT cell receptors characteristic of most NKT
65 Similar to polyclonal T-CD4 T cells and also invariant NKT cells, T3 CD4 T cell development is contro
67 18-deficient mice, which lack only type 1 or invariant NKT cells, the increase in the numbers of lung
68 d on a subset with semi-invariant TCR termed invariant NKT cells, the majority of CD1d-restricted lip
69 nd that, as has been suggested for mammalian invariant NKT cells, they may serve as immune regulators
73 bers of cotransferred gammadelta T cells and invariant NKT cells, whereas either cell type alone was
74 nd activation of a unique subset of T cells, invariant NKT cells, which express limited TCR diversity
75 largely absent in mice lacking CD1d-specific invariant NKT cells, with no effect on innate itk(-/-) C
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