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1.
Immunol Lett ; 174: 28-36, 2016 06.
Article in English | MEDLINE | ID: mdl-27085380

ABSTRACT

Type 1 diabetes mellitus (T1DM) is a chronic autoimmune disease characterized by the destruction of insulin-secreting ß cells upon autoreactive T cell attack. Oral administration of autoantigens is an attractive approach to treating T1DM, but an effective carrier should be used in order to protect antigens. Lactococcus lactis, a safe engineering strain, was used for this task in the present study. Two recombinant L. lactis expressing protein HSP65-6IA2P2 were used and be investigated the effects and mechanisms against T1DM in NOD mice. Our findings demonstrate that recombinant L. lactis strains can successfully both deliver antigens to intestinal mucosa and maintain the epitopes for a long time in NOD mice. Oral administration of recombinant L. lactis could prevent hyperglycemia, improve glucose tolerance, and reduce insulitis by inhibiting antigen-specific proliferation of T cells, augmenting regulatory immune reactions, and balancing ratios of Th17/Tregs and Th1/Th2. These results prove that orally administrated L. lactis expressing HSP65-6IA2P2 is an effective approach for the prevention of T1DM in NOD mice.


Subject(s)
Bacterial Proteins/genetics , Chaperonin 60/genetics , Diabetes Mellitus, Type 1/prevention & control , Gene Expression , Lactococcus lactis/genetics , Probiotics/administration & dosage , Receptor-Like Protein Tyrosine Phosphatases, Class 8/genetics , Recombinant Fusion Proteins/genetics , Administration, Oral , Animals , Blood Glucose , Diabetes Mellitus, Type 1/blood , Diabetes Mellitus, Type 1/immunology , Diabetes Mellitus, Type 1/pathology , Female , Glucose Tolerance Test , Immunomodulation , Insulin/metabolism , Insulin Secretion , Interferon-gamma/biosynthesis , Intestinal Mucosa/microbiology , Islets of Langerhans/metabolism , Islets of Langerhans/pathology , Mice , Mice, Inbred NOD , Spleen/immunology , Spleen/metabolism , T-Lymphocyte Subsets/immunology , T-Lymphocyte Subsets/metabolism , Vaccines
2.
Int J Mol Sci ; 15(1): 574-87, 2014 Jan 06.
Article in English | MEDLINE | ID: mdl-24398982

ABSTRACT

Atrazine molecular imprinted polymers (MIPs) were comparatively synthesized using identical polymer formulation by far-infrared (FIR) radiation and ultraviolet (UV)-induced polymerization, respectively. Equilibrium binding experiments were carried out with the prepared MIPs; the results showed that MIP(uv) possessed specific binding to atrazine compared with their MIP(FIR) radiation counterparts. Scatchard plot's of both MIPs indicated that the affinities of the binding sites in MIPs are heterogeneous and can be approximated by two dissociation-constants corresponding to the high- and low-affinity binding sites. Moreover, several common pesticides including atrazine, cyromazine, metamitron, simazine, ametryn, terbutryn were tested to determine their specificity, similar imprinting factor (IF) and different selectivity index (SI) for both MIPs. Physical characterization of the polymers revealed that the different polymerization methods led to slight differences in polymer structures and performance by scanning electron microscope (SEM), Fourier transform infrared absorption (FT-IR), and mercury analyzer (MA). Finally, both MIPs were used as selective sorbents for solid phase extraction (SPE) of atrazine from lake water, followed by high performance liquid chromatography (HPLC) analysis. Compared with commercial C18 SPE sorbent (86.4%-94.8%), higher recoveries of atrazine in spiked lake water were obtained in the range of 90.1%-97.1% and 94.4%-101.9%, for both MIPs, respectively.


Subject(s)
Atrazine/chemistry , Molecular Imprinting , Polymers/chemistry , Adsorption , Atrazine/isolation & purification , Chromatography, High Pressure Liquid , Infrared Rays , Polymerization/radiation effects , Polymers/chemical synthesis , Solid Phase Extraction , Spectroscopy, Fourier Transform Infrared , Ultraviolet Rays , Water/chemistry
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