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Dendritic cells immature

AQP7 is expressed in the proximal tubule of the kidney, testis, gastrointestinal tract, immature dendritic cells and ear. This glycerol channel is also highly expressed in adipocytes where it is thought to control the release of triglycerides. [Pg.216]

Yang D, Howard OMZ, Chen Q, Oppenheim JJ. Cutting edge Immature dendritic cells generated from monocytes in the presence of TGF-betal express functional C-C chemokine receptor 6. J Immunol 1999 163 1737-1741. [Pg.84]

Shellenberger TD, Wang M, Gujrati M, et al. BRAK/CXCL14 is a potent inhibitor of angiogenesis and is a chemotactic factor for immature dendritic cells. Cancer Res 2004 64 8262-8270. [Pg.334]

Takahashi, M. and Kobayashi, Y., Cytokine production in association with phagocytosis of apoptotic cells by immature dendritic cells, Cell. Immunol. 226, 2, 105, 2003. [Pg.322]

Mahnke K. Qian Y, Knop J, Enk AH Induction of CD4+/CD25+ regulatory T cells by targeting of antigens to immature dendritic cells. Blood 2003 101 4862-4869. [Pg.38]

Caron G, Delneste Y, Roelandts E Histamine induces CD86 expression and chemokine production by human immature dendritic cells. J Immunol 2001 166 6000-6006. [Pg.80]

First, we incubated immature dendritic cells (iDC) in the presence or absence of IRIV and could not observe upregulation of defined maturation markers. However, iDC incubation with supernatants harvested from IRIV stimulated PBMC cultures resulted in upregulation of CD86, human leukocyte antigen (HLA)-class I molecules, and, in most cases, also of CD83 (6). These results demonstrate that IRIV-induced cytokine secretion of PBMC indeed favors maturation of DC. [Pg.226]

Figure 6 Immunopotentiating reconstituted influenza virosomes (IRIV) adjuvant effects in the induction of tumor associated antigen-specific cytotoxic T cell. CD14-negative cells from a healthy donor peripheral blood mononuclear cells were cocultured with autologous immature dendritic cells (iDC) in the presence of Melan-A/Mart-l27-35, alone (A) or supplemented with either control liposomes (B) or IRIV (1 50, C). On day 7, culture cells were restimulated with Melan-A/MART-127-35 pulsed iDC and cultured for six further days [see Materials and Methods ]. On day 7 after restimulation cells were stained with fluorescein isothiocyanate-conjugated anti-CD8 and phosphatidylethanolamine-conjugated HL A-A0201 /Melan-A/MART -127-3 5 tetramers. Source From Ref. 6. Figure 6 Immunopotentiating reconstituted influenza virosomes (IRIV) adjuvant effects in the induction of tumor associated antigen-specific cytotoxic T cell. CD14-negative cells from a healthy donor peripheral blood mononuclear cells were cocultured with autologous immature dendritic cells (iDC) in the presence of Melan-A/Mart-l27-35, alone (A) or supplemented with either control liposomes (B) or IRIV (1 50, C). On day 7, culture cells were restimulated with Melan-A/MART-127-35 pulsed iDC and cultured for six further days [see Materials and Methods ]. On day 7 after restimulation cells were stained with fluorescein isothiocyanate-conjugated anti-CD8 and phosphatidylethanolamine-conjugated HL A-A0201 /Melan-A/MART -127-3 5 tetramers. Source From Ref. 6.
Figure 31-1 (A) Locations of the primary and secondary tissues of the immune system. The primary lymphoid organs are the thymus, which makes T cells, and the hone marrow, which forms B cells. After moving from these organs into the blood circulation the cells reach one of the secondary lymphoid organs, which include lymph nodes, spleen, tonsils, and Peyer s patches on the small intestine. Immature dendritic cells are found in body tissues including skin and mucous membranes and respond to foreign proteins by inducing attack by T lyphocytes and antibody formation by B cells. (B) Schematic drawing of a lymph node. From Nossal.1 Courtesy of Gustav J. V. Nossal. Figure 31-1 (A) Locations of the primary and secondary tissues of the immune system. The primary lymphoid organs are the thymus, which makes T cells, and the hone marrow, which forms B cells. After moving from these organs into the blood circulation the cells reach one of the secondary lymphoid organs, which include lymph nodes, spleen, tonsils, and Peyer s patches on the small intestine. Immature dendritic cells are found in body tissues including skin and mucous membranes and respond to foreign proteins by inducing attack by T lyphocytes and antibody formation by B cells. (B) Schematic drawing of a lymph node. From Nossal.1 Courtesy of Gustav J. V. Nossal.
Dendritic cells are very important APCs along with mononuclear phagocytes. They are distributed in small quantities in various tissues that come in contact with the external environment including the skin, inner lining of the nose, lungs, stomach and intestine. The blood contains immature dendritic cells. After activation, dendritic cells migrate to the lymphoid tissue to initiate an acquired response following their interaction with lymphoid cells, B and T cells. There are two most common types... [Pg.14]

THi cells via IL-12 production after they come in contact with a pathogen. The characteristics of mature and immature dendritic cells are further pointed out in Tables 1.5 and 1.6. [Pg.16]

VI. Vallin, H., Blomberg, S., Aim, G. V., Cederblad, B., and Ronnblom, L., Patients with systemic lupus erythematosus (SLE) have a circulating inducer of interferon-alpha (IFN-alpha) production acting on leucocytes resembling immature dendritic cells. Clin. Exp. Immunol. 115, 196—202 (1999). [Pg.171]

Multiple sclerosis patient was treated with a new cellular therapy - activated CD4+ T cells from this patient were isolated (based on the selection for CD25+), anergized in-vitro on immature dendritic cells and returned to the patient s blood stream. This patient has also colon cancer. Which one of the following statements is the most likely ... [Pg.671]

Cathelicidins and defensins induce histamine release from mast cells [182-184]. Human BD-2, -3 and -4 and a-defensins recruit monocytes, T cells (memory and naive) and immature dendritic cells [185-188] Cathelicidins (bovine, human, mouse and pig) are chemotactic for several subsets of peripheral blood cells in vitro [178,189] and in vivo [190]. For example, CRAMP (Cathelin-related antimicrobial peptide, the murine orthologue of human cathelicidin/LL-37), like LL-37, was chemotactic for human monocytes, neutrophils, macrophages, and for mouse peripheral blood leukocytes in vitro and in vivo [189]. These results suggest that host defense peptides recruit innate and adaptive immune cells for protective cellular and humoral responses to pathogens. [Pg.639]

Shared receptors are defined as able to bind more than one CK this concept is only valid inside each CK family. For example CCL20, alternatively named liver and activation-regulated CK (LARC), macrophage inflammatory protein-da (MIP-3a) or Exodus-1, is the only CK known to interact with CC CK receptor 6 (CCR6), a property shared with the antimicrobial (i-defensins. The ligand-receptor pair CCL20-CCR6 is responsible for the chemoattraction of immature dendritic cells, effector/memory T cells, and B cells and plays a role at skin and mucosal surfaces under homeostatic and... [Pg.718]

CCRl Activated T-cells, monocytes, eosinophils, immature dendritic cells, basophils MIP-Ia (CCL3), MIP-li3 (CCL4), MCP-3 (CCL7), RANTES (CCL5)... [Pg.133]

CCR6 T-cells, immature dendritic cells, B-cells MlP-3a/ljARC/exodus (CCL20)... [Pg.133]

Rigano R, Buttari B, Profumo E, Ortona E, Delunardo E, Margotti P, Mattel V, Teggi A, Sorice M, Siracusano A (2007) Echinococcus granulosus antigen B impairs human dendritic cell differentiation and polarizes immature dendritic cell maturation towards a Th2 cell response. Infect Immun 75 1667-1678... [Pg.378]


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