نتایج جستجو برای: intestinal mannose receptors

تعداد نتایج: 360309  

Journal: :Journal of controlled release : official journal of the Controlled Release Society 2015
Joana M Silva Eva Zupancic Gaëlle Vandermeulen Vanessa G Oliveira Ana Salgado Mafalda Videira Manuela Gaspar Luis Graca Véronique Préat Helena F Florindo

We hypothesized that the co-entrapment of melanoma-associated antigens and the Toll-like receptor (TLR) ligands Poly(I:C) and CpG, known to be Th1-immunopotentiators, in mannose-functionalized aliphatic polyester-based nanoparticles (NPs) could be targeted to mannose receptors on antigen-presenting cells and induce anti-tumor immune responses. High entrapment efficiencies of antigens and immuno...

2003
ALAN B. EZEKOWITZ ANB SIAMON GORDON

Infection of the mouse peritoneal cavity by bacillus Calmette-Gu6rin (BCG) 1 markedly alters the surface properties of macrophages (mob), compard with cells obtained from uninfected control animals or after injection of thioglycollate broth. BCG-activated peritoneal mob (BCG-PM) express enhanced Ia antigens (Ag), but reduced receptors for mannose-terminated glycoconjugates (MFR), Fc receptors, ...

Journal: :The Journal of infectious diseases 2002
Zhong Su Anny Fortin Philippe Gros Mary M Stevenson

Opsonin-independent macrophage phagocytosis was investigated as a possible mechanism of controlling early blood-stage Plasmodium chabaudi AS infection. Early during infection, peritoneal macrophages from resistant C57BL/6 (B6) mice exhibited increased phagocytosis of parasitized red blood cells (pRBCs) and free merozoites, which was absent in mice with deficient interferon (IFN)-gamma productio...

Journal: :The Journal of Experimental Medicine 2002
Daniel J. Campbell Eugene C. Butcher

Effector and memory T cells can be subdivided based on their ability to traffic through peripheral tissues such as inflamed skin and intestinal lamina propria, a property controlled by expression of 'tissue-specific' adhesion and chemoattractant receptors. However, little is known about the development of these selectively homing T cell subsets, and it is unclear whether activation in cutaneous...

Journal: :PLoS ONE 2009
Christopher J. Day Joe Tiralongo Regan D. Hartnell Carie-Anne Logue Jennifer C. Wilson Mark von Itzstein Victoria Korolik

The pathogenic clinical strain NCTC11168 was the first Campylobacter jejuni strain to be sequenced and has been a widely used laboratory model for studying C. jejuni pathogenesis. However, continuous passaging of C. jejuni NCTC11168 has been shown to dramatically affect its colonisation potential. Glycan array analysis was performed on C. jejuni NCTC11168 using the frequently passaged, non-colo...

Journal: :PLoS Pathogens 2007
Meimei Shan Per Johan Klasse Kaustuv Banerjee Antu K Dey Sai Prasad N Iyer Robert Dionisio Dustin Charles Lila Campbell-Gardener William C Olson Rogier W Sanders John P Moore

The human immunodeficiency virus type 1 (HIV-1) envelope glycoprotein gp120 is a vaccine immunogen that can signal via several cell surface receptors. To investigate whether receptor biology could influence immune responses to gp120, we studied its interaction with human, monocyte-derived dendritic cells (MDDCs) in vitro. Gp120 from the HIV-1 strain JR-FL induced IL-10 expression in MDDCs from ...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2004
Jonathan H LeBowitz Jeffrey H Grubb John A Maga Deborah H Schmiel Carole Vogler William S Sly

Enzyme-replacement therapy is an established means of treating lysosomal storage diseases. Infused therapeutic enzymes are targeted to lysosomes of affected cells by interactions with cell-surface receptors that recognize carbohydrate moieties, such as mannose and mannose 6-phosphate, on the enzymes. We have tested an alternative, peptide-based targeting system for delivery of enzymes to lysoso...

Journal: :The Biochemical journal 1990
B Smedsrød J Melkko L Risteli J Risteli

The fate of the circulating C-terminal propeptide of type I procollagen (PICP) was studied. Trace amounts of 125I-PICP administered intravenously to rats disappeared from the blood with an initial t1/2 of 6.1 min. After 45 min the radioactivity was distributed as follows: liver, 36%; blood, 23%; kidneys, 18%; urine, 20%; spleen, 1%; lungs, 2%; heart, 0.4%. To prevent escape of label from the si...

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