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Intrinsic factors and CD1d1 but not CD1d2 expression levels control invariant natural killer T cell subset differentiation.
Amable L, Ferreira Martins LA, Pierre R, Do Cruseiro M, Chabab G, Sergé A, Kergaravat C, Delord M, Viret C, Jaubert J, Liu C, Karray S, Marie JC, Irla M, Georgiev H, Clave E, Toubert A, Lucas B, Klibi J, Benlagha K. Amable L, et al. Nat Commun. 2023 Dec 1;14(1):7922. doi: 10.1038/s41467-023-43424-7. Nat Commun. 2023. PMID: 38040679 Free PMC article.
Here, we show that the non-classical class I-like major histocompatibility complex CD1 molecules CD1d2, expressed in BALB/c and not in B6 mice, could not account for this difference. ...
Here, we show that the non-classical class I-like major histocompatibility complex CD1 molecules CD1d2, expressed in BALB/c and not i …
Expression of CD1d2 on thymocytes is not sufficient for the development of NK T cells in CD1d1-deficient mice.
Chen YH, Wang B, Chun T, Zhao L, Cardell S, Behar SM, Brenner MB, Wang CR. Chen YH, et al. J Immunol. 1999 Apr 15;162(8):4560-6. J Immunol. 1999. PMID: 10201995
Unlike CD1d1, which is expressed by all lymphocytes, CD1d2 can be detected only on the surface of thymocytes. To determine whether CD1d2 can select a unique subset of NK T cells, we compared the remnant population of NK T cells in CD1d1 degrees and CD1d1, CD1d2
Unlike CD1d1, which is expressed by all lymphocytes, CD1d2 can be detected only on the surface of thymocytes. To determine whether …
Differing roles of CD1d2 and CD1d1 proteins in type I natural killer T cell development and function.
Sundararaj S, Zhang J, Krovi SH, Bedel R, Tuttle KD, Veerapen N, Besra GS, Khandokar Y, Praveena T, Le Nours J, Matsuda JL, Rossjohn J, Gapin L. Sundararaj S, et al. Proc Natl Acad Sci U S A. 2018 Feb 6;115(6):E1204-E1213. doi: 10.1073/pnas.1716669115. Epub 2018 Jan 19. Proc Natl Acad Sci U S A. 2018. PMID: 29351991 Free PMC article.
Intriguingly, the T cell antigen receptor repertoire and phenotype of CD1d2-selected type I NKT cells in CD1D1(-/-) mice differed from CD1d1-selected type I NKT cells. ...Accordingly, CD1d2 molecules could not present glycolipid antigens with long acyl chains effici …
Intriguingly, the T cell antigen receptor repertoire and phenotype of CD1d2-selected type I NKT cells in CD1D1(-/-) mice differed fro …
Identification of a new mouse Cd1d2 allele.
Gozalbo-López B, Pérez-Rosado A, Parra-Cuadrado JF, Martínez-Naves E. Gozalbo-López B, et al. Eur J Immunogenet. 2004 Feb;31(1):1-3. doi: 10.1111/j.1365-2370.2004.00431.x. Eur J Immunogenet. 2004. PMID: 15009173
The function of the Cd1d2 gene has not been elucidated. Here we described a method to analyse variations in mouse Cd1 genes. We found a new allele for Cd1d2 characterized by a point mutation, resulting in a replacement of alanine at position 176 by a valine....
The function of the Cd1d2 gene has not been elucidated. Here we described a method to analyse variations in mouse Cd1 genes. We found …
Caveolin-mediated endocytosis of the Chlamydia M278 outer membrane peptide encapsulated in poly(lactic acid)-Poly(ethylene glycol) nanoparticles by mouse primary dendritic cells enhances specific immune effectors mediated by MHC class II and CD4+ T cells.
Dixit S, Sahu R, Verma R, Duncan S, Giambartolomei GH, Singh SR, Dennis VA. Dixit S, et al. Biomaterials. 2018 Mar;159:130-145. doi: 10.1016/j.biomaterials.2017.12.019. Epub 2017 Dec 26. Biomaterials. 2018. PMID: 29324305 Free PMC article.
Our results reveal that PPM triggered enhanced expression of effector cytokines and chemokines, surface activation markers (Cd1d2, Fcgr1), pathogen-sensing receptors (TLR2, Nod1), co-stimulatory (CD40, CD80, CD86) and MHC class I and II molecules. ...
Our results reveal that PPM triggered enhanced expression of effector cytokines and chemokines, surface activation markers (Cd1d2, Fc …
High doses of alpha-galactosylceramide potentiate experimental autoimmune encephalomyelitis by directly enhancing Th17 response.
Qian G, Qin X, Zang YQ, Ge B, Guo TB, Wan B, Fang L, Zhang JZ. Qian G, et al. Cell Res. 2010 Apr;20(4):480-91. doi: 10.1038/cr.2010.6. Epub 2010 Jan 19. Cell Res. 2010. PMID: 20084083
Furthermore, antigen-presenting cells (APCs) predominantly express CD1d1, whereas the majority of CD4(+) T cells express CD1d2. Knockdown of CD1d1 or CD1d2 gene expression by RNAi interfered with the activation of iNKT or Th17/Th1 cells, respectively. ...
Furthermore, antigen-presenting cells (APCs) predominantly express CD1d1, whereas the majority of CD4(+) T cells express CD1d2. Knock …
Regulation of CD1d expression by murine tumor cells: escape from immunosurveillance or alternate target molecules?
Fiedler T, Walter W, Reichert TE, Maeurer MJ. Fiedler T, et al. Int J Cancer. 2002 Mar 20;98(3):389-97. doi: 10.1002/ijc.10141. Int J Cancer. 2002. PMID: 11920590 Free article.
Only a limited number of CD1 antigens is retained in the mouse, i.e., the group II CD1 antigens, which are split into CD1D1 and CD1d2. Several T cell subsets have been shown to interact with murine CD1 antigens, including NK cells or "natural T cells" with the invariant V …
Only a limited number of CD1 antigens is retained in the mouse, i.e., the group II CD1 antigens, which are split into CD1D1 and CD1d2
Gene expression of cell surface antigens in the early phase of murine influenza pneumonia determined by a cDNA expression array technique.
Sakai S, Mantani N, Kogure T, Ochiai H, Shimada Y, Terasawa K. Sakai S, et al. Mediators Inflamm. 2002 Dec;11(6):359-61. doi: 10.1080/0962935021000051557. Mediators Inflamm. 2002. PMID: 12581500 Free PMC article.
RESULTS AND CONCLUSIONS: We focused on the expression of 46 mRNAs for cell surface antigens. Of these 46 mRNAs that we examined, four (CD1d2 antigen, CD39 antigen-like 1, CD39 antigen-like 3, CD68 antigen) were up-regulated and one (CD36 antigen) was down-regulated. ...
RESULTS AND CONCLUSIONS: We focused on the expression of 46 mRNAs for cell surface antigens. Of these 46 mRNAs that we examined, four (CD