RÉSUMÉ
Immune checkpoint blockade (ICB) therapy has brought significant advancements to the field of oncology. However, the diverse responses among patients highlight the need for more accurate predictive tools. In this study, insights are drawn from tumor-immunology pathways, and a novel network-based ICB immunotherapeutic signature, termed ICBnetIS, is constructed. The signature is derived from advanced biological network-based computational strategies involving co-expression networks and molecular interactions networks. The efficacy of ICBnetIS is established through its association with enhanced patient survival and a robust immune response characterized by diverse immune cell infiltration and active anti-tumor immune pathways. The validation process positions ICBnetIS as an effective tool in predicting responses to ICB therapy, analyzing ICB data from a broad collection of over 700 samples from multiple cancer types of more than 15 datasets. It achieves an aggregated prediction AUC of 0.784, which outperforms the other nine renowned immunotherapeutic signatures, indicating the superior predictive capability of ICBnetIS. To sum up, the findings suggest ICBnetIS as a potent tool in predicting ICB therapy responses, offering significant implications for patient selection and treatment optimization in oncology. The study highlights the role of ICBnetIS in advancing personalized treatment strategies, potentially transforming the clinical landscape of ICB therapy.
RÉSUMÉ
A series of (S)-1-phenyl-3,4-dihydroisoquinoline-2(1H)-carboxamide derivatives was synthesized and evaluated for inhibitory activity against monoamine oxidase (MAO)-A and-B, acetylcholine esterase (AChE), and butyrylcholine esterase (BChE). Four compounds (2i, 2p, 2t, and 2v) showed good inhibitory activity against both MAO-A and MAO-B, and two compounds (2d and 2j) showed selective inhibitory activity against MAO-A, with IC50 values of 1.38 and 2.48 µM, respectively. None of the compounds showed inhibitory activity against AChE; however, 12 compounds showed inhibitory activity against BChE. None of the active compounds showed cytotoxicity against L929cells. Molecular docking revealed several important interactions between the active analogs and amino acid residues of the protein receptors. This research paves the way for further study aimed at designing MAO and ChE inhibitors for the treatment of depression and neurodegenerative disorders.
Sujet(s)
Cholinesterases , Monoamine oxidase , Monoamine oxidase/métabolisme , Cholinesterases/métabolisme , Inhibiteurs de la monoamine oxydase/pharmacologie , Simulation de docking moléculaire , Relation structure-activité , Anticholinestérasiques/composition chimique , Acetylcholinesterase/métabolismeRÉSUMÉ
Fragile X syndrome (FXS) is a common mental retardation syndrome. Anxiety and abnormal social behaviors are prominent features of FXS in humans. To better understand the effects of hyperbaric oxygen therapy (HBOT) on these behaviors, we analyzed anxiety-related and social behaviors in Fmr1 knockout mice treated by HBOT. In the open field test, HBOT group mice preferred the periphery to central areas and tended to run or walk along the wall. The results suggested that thigmotaxis was significantly increased in the HBOT group compared with the control group. In the elevated plus maze test, the percentage of distance traveled was significantly increased in the open arm and significantly decreased in the closed arm for HBOT group mice compared with control group mice. These results suggested that HBOT group mice displayed enhanced motor activity in the open arm and exhibited fewer anxiety-related behaviors. In the three-chambered social approach test, the HBOT group mice made more approaches to the wire cup containing an acquaintance mouse than control group mice in the sociability test and made more approaches to the wire cup containing a stranger mouse than control group mice in the social novelty preference test. The results suggested that HBOT group mice showed increased levels of social interaction and decreased "social anxiety" than the control group to partner mice in this test. Our findings indicated that HBOT resulted in altered anxiety and social behavior in Fmr1 knockout mice and could possibly be used as a treatment for FXS.
Sujet(s)
Syndrome du chromosome X fragile/thérapie , Oxygénation hyperbare/méthodes , Comportement social , Animaux , Anxiété/thérapie , Comportement animal , Protéine du syndrome X fragile/génétique , Syndrome du chromosome X fragile/génétique , Mâle , Apprentissage du labyrinthe , Souris , Souris de lignée C57BLRÉSUMÉ
E(rns) is an envelope glycoprotein of classical swine fever virus (CSFV) and has an unusual feature of RNase activity. In the present study, we demonstrate that E(rns) counteracts Newcastle disease virus (NDV)-mediated induction of IFN-beta. For this purpose, E(rns) fused to the enhanced green fluorescent protein (EGFP) was transiently expressed in porcine kidney 15 (PK15) cells. In luciferase activity assay, E(rns)-EGFP was found to prevent IFN-beta promoter-driven luciferase expression and block the induction of IFN-beta promoter mediated by NDV in a dosedependent manner. Through IFN-specific semi-quantitative RT-PCR detection, obvious decrease of IFN-beta mRNA in NDV-infected PK15 cells was observed in the presence of E(rns)-EGFP. In contrast, EGFP alone showed none of this block capacity. In addition, E(rns)-EGFP mutations with RNase inactivation were also found to block NDV-mediated induction of IFN-beta. These evidences establish a novel function for CSFV E(rns) glycoprotein in counteraction of the IFN-beta induction pathway.
Sujet(s)
Virus de la peste porcine classique/métabolisme , Interféron bêta/génétique , Virus de la maladie de Newcastle/physiologie , Protéines de l'enveloppe virale/métabolisme , Animaux , Lignée cellulaire , Virus de la peste porcine classique/génétique , Régulation de l'expression des gènes , Glycoprotéines/génétique , Glycoprotéines/métabolisme , Protéines à fluorescence verte/génétique , Protéines à fluorescence verte/métabolisme , Cinétique , Luciferases/génétique , Luciferases/métabolisme , Régions promotrices (génétique)/génétique , ARN messager/génétique , ARN messager/métabolisme , RT-PCR , Ribonucléases/métabolisme , Transduction du signal/génétique , Transduction du signal/physiologie , Suidae , Transfection , Protéines de l'enveloppe virale/génétiqueRÉSUMÉ
E(rns) is an envelope glycoprotein of classical swine fever virus (CSFV) with unusual RNase activity. Recently, E(rns) was found to have a new function of counteracting the beta-interferon (IFN-beta) induction pathway. In this study, wildtype ErnsSM and two mutated E(rns) proteins ErnsH297k and ErnsH346k were expressed in insect cells and purified for RNase activity and function analysis. RNase activity assay in vitro demonstrated that only wildtype E(rns) protein had RNase activity. However, both wildtype ErnsSM and the two mutated E(rns)ErnsH297k and ErnsH346k as exogenous proteins had a block effect on Newcastle disease virus (NDV)-mediated IFN-beta promoter induction.
Sujet(s)
Peste porcine classique/métabolisme , Protéines virales/métabolisme , Animaux , Séquence nucléotidique , Technique de Western , Lignée cellulaire , Amorces ADN , Escherichia coli/génétique , Technique d'immunofluorescence , Interféron bêta/biosynthèse , Ribonucléases/métabolisme , Protéines virales/composition chimique , Protéines virales/génétiqueRÉSUMÉ
A functional IP10-scFv fusion protein retaining the antibody specificity for acidic isoferritin and chemokine function was produced at high level in Esherichia coli (E. coli). IP10-scFv gene from the recombinant plasmid pc3IP104c9 was subcloned into pET28a fused to N-terminal His-tag sequence in frame and overexpressed in E. coli BL21(DE3). With an on-column refolding procedure based on Ni-chelating chromatography, the active fusion protein was recovered efficiently from inclusion bodies with a refolding yield of approximate 45% confirmed by spectrophotometer. The activity of refolded IP10-scFv was determined through sodium dodecyl sulfate-polyacrylamide gel electrophoresis, Western blotting and enzyme-linked immunosorbent assay. The results showed the fusion protein retains the specific binding activity to AIF with an affinity constant of 4.48x10(-8) M as well as the chemokine function of IP-10. The overall yield of IP10-scFv with bioactivity in E. coli flask culture was more than 40 mg/L.
Sujet(s)
Corps d'inclusion/composition chimique , Corps d'inclusion/génétique , Pliage des protéines , Récepteurs aux cytokines/génétique , Protéines de fusion recombinantes/isolement et purification , Animaux , Spécificité des anticorps , Lignée cellulaire tumorale , Mouvement cellulaire/génétique , Mouvement cellulaire/immunologie , Chromatographie d'affinité/méthodes , Clonage moléculaire , Escherichia coli/génétique , Escherichia coli/métabolisme , Femelle , Humains , Région variable d'immunoglobuline/génétique , Souris , Souris de lignée BALB C , Récepteurs aux cytokines/composition chimique , Récepteurs aux cytokines/isolement et purification , Protéines de fusion recombinantes/composition chimique , Protéines de fusion recombinantes/génétique , Lymphocytes T/immunologie , Cellules cancéreuses en cultureRÉSUMÉ
OBJECTIVE: To Establish a rapid and objective quantitative fluorogenic real-time PCR assay for early detection of human respiratory syncytial virus (hRSV). METHODS: Two pairs of primers and one TaqMan Fluorogenic probe that are specific for the recognition of the most conservative N gene of hRSV for virus detection with LighCycler PCR in 93 nasopharyngeal secretion specimens collected from infants and young children. The assay was compared with virus isolation, routine PCR, nested PCR, and enzyme-linked immunosorbent assay (ELISA). RESULTS: This TaqMan assay had a sensitivity of 1 x 10(2) cDNA copies/microl with a dynamic range between 1 x 10(2) and 1 x 10(7) cDNA copies/microl, which was the same as that of nested PCR, but 10 times more sensitive than routine PCR. The specificity of the assay was evaluated by comparing hRSV with polivirus type 1, coxsackie virus type 2, influenza A, influenza B and adenovirus type 7. A PCR product of the expected size (195 bp) was produced and fluorescence signal detected for hRSV, but not for any of the other viruses. The results in LightCycler and Rotor-Gene instrument were consistent. Forty-four specimens (43.9%) were hRSV-positive with this assay and 4 (4/93,4.3%) were hRSV-positive with ELISA, showing rather low correlation between the two methods. No visible relation was found between the concentration of hRSV RNA and severity of the disease. CONCLUSION: This assay is rapid, sensitive, specific and quantitative, and has the potential of wide application for early diagnosis of hRSV infection and evaluation of the therapeutic effect.
Sujet(s)
ARN viral/analyse , Infections à virus respiratoire syncytial/virologie , Virus respiratoire syncytial humain/isolement et purification , Enfant d'âge préscolaire , Humains , Nourrisson , Partie nasale du pharynx/virologie , Réaction de polymérisation en chaîne/méthodesRÉSUMÉ
To study the possible recombinant relationship among differently derived classical swine fever virus, the coding regions of 21 isolates were analyzed to detect recombination and breakpoints through gene trees comparison and quartet analyses. The results show nucleotide area corresponding to E0, E1 and E2 as a possible recombinant tract between ALD ( D49532) and GPE-(D49533) while NS5A-NS5B of the isolate 39 (AF407339) appears to be derived from a virulent Shimen strain (AF092448) sequence. This suggests that intertypic exchanges of genetic materials during mixed infections under natural or laboratorial conditions can lead classical swine fever virus to adapt to the changes of host environment.
Sujet(s)
Virus de la peste porcine classique/classification , Cadres ouverts de lecture , Phylogenèse , Alignement de séquences/méthodes , Virus de la peste porcine classique/génétique , Biologie informatique/méthodes , Évolution moléculaire , Fonctions de vraisemblance , Recombinaison génétiqueRÉSUMÉ
We combined the specificity of tumor-specific antibody with the chemokine function of interferon-gamma inducible protein 10 (IP-10) to recruit immune effector cells in the vicinity of tumor cells. A novel fusion protein of IP10-scFv was constructed by fusing mouse IP-10 to V(H) region of single-chain Fv fragment (scFv) against acidic isoferritin (AIF), and expressed in NS0 murine myeloma cells. The IP10-scFv fusion protein was shown to maintain the specificity of the antiAIF scFv with similar affinity constant, and bind to the human hepatocarcinoma SMMC 7721 cells secreting AIF as well as the activated mouse T lymphocytes expressing CXCR3 receptor. Furthermore, the IP10-scFv protein either in solution or bound on the surface of SMMC 7721 cells induced significant chemotaxis of mouse T cells in vitro. The results indicate that the IP10-scFv fusion protein possesses both bioactivities of the tumor-specific antibody and IP-10 chemokine, suggesting its possibility to induce an enhanced immune response against the residual tumor cells in vivo.
Sujet(s)
Spécificité des anticorps , Fragments d'immunoglobuline/métabolisme , Récepteurs aux cytokines/métabolisme , Protéines de fusion recombinantes/métabolisme , Animaux , Séquence nucléotidique , Lignée cellulaire , Amorces ADN , Vecteurs génétiques , Fragments d'immunoglobuline/génétique , Souris , Liaison aux protéines , Récepteurs aux cytokines/génétique , Récepteurs aux cytokines/immunologie , Protéines de fusion recombinantes/génétique , Protéines de fusion recombinantes/immunologie , Lymphocytes TRÉSUMÉ
Classical swine fever virus nonstructural protein 5B (NS5B) encodes an RNA-dependent RNA polymerase, a key enzyme of the viral replication complex. To better understand the initiation of viral RNA synthesis and to establish an in vitro replication system, a recombinant NS5B protein, lacking the C-terminal 24-amino acid hydrophobic domain, was expressed in Escherichia coli. The truncated fusion protein (NS5Bdelta24) was purified on a Ni-chelating HisTrap affinity column and demonstrated to initiate either plus- or minus-strand viral RNA synthesis de novo in a primer-independent manner but not by terminal nucleotidyle transferase activity. De novo RNA synthesis represented the preferred mechanism for initiation of classical swine fever virus RNA synthesis by RNA-dependent RNA polymerase in vitro. Both Mg2+ and Mn2+ supported de novo initiation, however, RNA synthesis was more efficient in the presence of Mn2+ than in the presence of Mg2+. De novo initiation of RNA synthesis was stimulated by preincubation with 0.5 mm GTP, and a 3'-terminal cytidylate on the viral RNA template was preferred for de novo initiation. Furthermore, the purified protein was also shown, by North-Western blot analysis, to specifically interact with the 3'-end of both plus- and minus-strand viral RNA templates.
Sujet(s)
Virus de la peste porcine classique/enzymologie , RNA replicase/composition chimique , ARN/composition chimique , Régions 3' non traduites , Technique de Northern , Technique de Western , Amorces ADN/composition chimique , Électrophorèse sur gel de polyacrylamide , Escherichia coli/métabolisme , Magnésium/composition chimique , Manganèse/composition chimique , Plasmides/métabolisme , Liaison aux protéines , Structure tertiaire des protéines , Protéines de fusion recombinantes/métabolisme , RT-PCR , TempératureRÉSUMÉ
A functional single-chain Fv antibody fragment (scFv) specific for acidic isoferritin (AIF) was produced at high level in Escherichia coli. The variable regions of heavy chain (V(H)) and light chain (V(L)) from the hybridoma 4c9 were connected with a flexible linker using an assembly polymerase chain reaction. The construct of V(H)-linker-V(L) was inserted into a phagemid pCANTAB 5 E followed by selection with the Recombinant Phage Antibody System (RPAS). Anti-AIF scFv gene from the recombinant phagemid pCAN4c9 was subcloned into pET28a fused to N-terminal His-tag sequence in frame and overexpressed in E. coli BL21(DE3). With an on-column refolding procedure based on Ni-chelating chromatography, the active anti-AIF scFv was recovered efficiently from inclusion bodies with a refolding yield of approximate 75% confirmed by spectrophotometer. The activity of refolded scFv was determined through sodium dodecyl sulfate-polyacrylamide gel electrophoresis, Western blotting and enzyme-linked immunosorbent assay. The results showed anti-AIF scFv retains the specific binding activity to AIF with an affinity constant of 7.29 x 10(-8) mol l(-1). The overall yield of anti-AIF scFv with bioactivity in E. coli flask culture was more than 60 mg l(-1).
Sujet(s)
Complexe antigène-anticorps/analyse , Escherichia coli/métabolisme , Ferritines/métabolisme , Hybridomes/métabolisme , Fragments d'immunoglobuline/biosynthèse , Fragments d'immunoglobuline/métabolisme , Ingénierie des protéines/méthodes , Animaux , Complexe antigène-anticorps/métabolisme , Marqueurs biologiques tumoraux/analyse , Marqueurs biologiques tumoraux/métabolisme , Lignée cellulaire , Test ELISA , Escherichia coli/génétique , Humains , Fragments d'immunoglobuline/génétique , Souris , Protéines de fusion recombinantes/biosynthèseRÉSUMÉ
We have refined entropy theory to explore the meaning of the increasing sequence data on nucleic acids and proteins more conveniently. The concept of selection constraint was not introduced, only the analyzed sequences themselves were considered. The refined theory serves as a basis for deriving a method to analyze non-coding regions (NCRs) as well as coding regions. Positions with maximal entropy might play the most important role in genome functions as opposed to positions with minimal entropy. This method was tested in the well-characterized coding regions of 12 strains of Classical Swine Fever Virus (CSFV) and non-coding regions of 20 strains of CSFV. It is suitable to analyze nucleic acid sequences of a complete genome and to detect sensitive positions for mutagenesis. As such, the method serves to formulate the basis for elucidating the functional mechanism.
Sujet(s)
Virus de la peste porcine classique/génétique , Modèles génétiques , Analyse de séquence d'ARN/méthodes , Algorithmes , Séquence nucléotidique , Théorème de Bayes , Bases de données d'acides nucléiques , Entropie , Génome viral , Informatique mathématique , Modèles statistiques , Données de séquences moléculaires , Protéines ribosomiques/génétiqueRÉSUMÉ
In order to explore the mechanism for the genomic replication of classical swine fever virus (CSFV), so as to make a basis for investigating its pathogenicity, an introduction of the information theory is presented in connection with the statistical mechanics, whence small-sample statistics appears naturally as a consequence of the Bayesian approach. Furthermore, a selection rule for identifying the pattern of a recognition site for an RNA-binding protein is proposed by means of the maximum entropy principle. Based on those, the information contents of 3'-untranslated regions (3'UTRs) of genomes of 20 CSFV strains and 5'-untranslated regions (5'UTRs) of genomes of 58 CSFV strains are analyzed with a computational algorithm in a reduction mode, and the 3'UTR sites of 20 strains and 5'UTR sites of 58 strains containing important motifs are extracted from the unaligned RNA sequences of unequal lengths. These sites, which have the patterns of sequence and structure similar to the putative cis elements related to the regulation of genomic replication, would be identified as the potential recognition sites in 3'UTRs and 5'UTRs for CSFV replicase responsible for classical swine fever virus genomic replication, and to some extent, this identification is supported by experimental evidence. Finally, information analysis allows a presumption to be made about the CSFV RNA replication initiation mechanism.