LIVIVO - The Search Portal for Life Sciences

zur deutschen Oberfläche wechseln
Advanced search

Search results

Result 1 - 10 of total 33

Search options

  1. Article ; Online: Designing a Novel di-epitope Diphtheria Vaccine: A Rational Structural Immunoinformatics Approach.

    Shadmani, Mahsa / Ghasemnejad, Atefeh / Bazmara, Samira / Bagheri, Kamran Pooshang

    Current computer-aided drug design

    2024  

    Abstract: Background: The design of an epitope-based vaccine against diphtheria toxin (DT) originated from the idea that many strong binder epitopes may be structurally located in the depth of DT. Subsequently, many ineffective antibodies may be produced by the ... ...

    Abstract Background: The design of an epitope-based vaccine against diphtheria toxin (DT) originated from the idea that many strong binder epitopes may be structurally located in the depth of DT. Subsequently, many ineffective antibodies may be produced by the presentation of those epitopes to T and B lymphocytes. The other critical issue is the population coverage of a vaccine that has been neglected in traditional vaccines.

    Objective: Given the issues above, our study aimed to design a peptide-based diphtheria vaccine, considering the issues of unwanted epitopes and population coverage.

    Methods: The frequencies of pre-determined HLA alleles were listed. A country in which almost all HLA alleles had been determined in almost all geographical distribution was selected. The epitopes within the sequence of diphtheria toxin were predicted by the NetMHCIIPan server based on the selected HLA alleles. Strong binder epitopes on the surface of diphtheria toxin were selected by structural epitope mapping. The epitopes, which cover almost all the human population for each of the HLA alleles in the candidate country, were then selected as epitopebased vaccines.

    Results: At first, 793 strong binder epitopes were predicted, of which 82 were surface epitopes. Nine surface epitopes whose amino acids had extruding side chains were selected. Finally, 2 epitopes had the most population coverage and were suggested as a di-epitope diphtheria vaccine. The population coverage of the di-epitope vaccine in France and the world was 100 and 99.24 %, respectively. HLA-DP had the most roles in epitope presentation.

    Conclusion: Our results indicated that 97.75 % of unwanted antibodies (791 epitopes) have been reduced. Achieving two immunodominant surface epitopes confirmed our rational filtration strategy for sequential reduction of unwanted epitopes. Our novel insight may pave a new way to designing novel peptide-based vaccines to avoid producing non-specific antibodies.
    Language English
    Publishing date 2024-04-25
    Publishing country United Arab Emirates
    Document type Journal Article
    ISSN 1875-6697
    ISSN (online) 1875-6697
    DOI 10.2174/0115734099294259240411073449
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  2. Article ; Online: Oxineur, a novel peptide from Caspian cobra Naja naja oxiana against HT-29 colon cancer.

    Sadat, Seyedeh Narjes / Bagheri, Kamran Pooshang / Maghsoudi, Hosein / Shahbazzadeh, Delavar

    Biochimica et biophysica acta. General subjects

    2022  Volume 1867, Issue 2, Page(s) 130285

    Abstract: Colon cancer ranks fourth in mortality. This cancer is still an important clinical challenge worldwide due to its high prevalence and poor prognosis. Proteomic studies revealed that snake venom is a diverse and variable mixture of enzymatic and non- ... ...

    Abstract Colon cancer ranks fourth in mortality. This cancer is still an important clinical challenge worldwide due to its high prevalence and poor prognosis. Proteomic studies revealed that snake venom is a diverse and variable mixture of enzymatic and non-enzymatic proteins and peptides. Despite the toxic effects of these molecules, several proteins and peptides have been isolated that have practical applications and appear to induce apoptosis and prevent cell metastasis. In this study, we worked on cytotoxic effects and anticancer activity of Naja naja oxiana (Iranian Caspian cobra) snake venom components on HT-29 cell line colon cancer. Separated Fraction-5 by FPLC indicated the high cytotoxicity on HT-29 cell line colon cancer by MTT test. Further isolation of F5 by HPLC showed that the purified peak 2, nominated as Oxineur that contains a cytotoxic effect on HT-29 cells and reduces cell viability at 8 μg/ml to 4% in 24 h. Oxineur has the least cytotoxic effect on HEK-293 normal cells. Further studies on Oxineur peptide confirmed the apoptotic effects with high expression of CASP9 gene and DNA fragmentation in cancerous cells. The partial sequence of Oxineur revealed 71% homology with the neurotoxin II from Naja naja oxiana. Since our target molecule is a peptide in the molecular weight range of 7 kDa, it has potentially a therapeutic value.
    MeSH term(s) Animals ; Humans ; Elapidae ; Naja naja ; Elapid Venoms/pharmacology ; Elapid Venoms/chemistry ; HT29 Cells ; Iran ; Proteomics ; HEK293 Cells ; Snake Venoms ; Antineoplastic Agents/pharmacology ; Peptides/pharmacology ; Colonic Neoplasms/drug therapy
    Chemical Substances Elapid Venoms ; Snake Venoms ; Antineoplastic Agents ; Peptides
    Language English
    Publishing date 2022-11-30
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 60-7
    ISSN 1872-8006 ; 1879-2596 ; 1879-260X ; 1879-2642 ; 1879-2618 ; 1879-2650 ; 0006-3002 ; 0005-2728 ; 0005-2736 ; 0304-4165 ; 0167-4838 ; 1388-1981 ; 0167-4889 ; 0167-4781 ; 0304-419X ; 1570-9639 ; 0925-4439 ; 1874-9399
    ISSN (online) 1872-8006 ; 1879-2596 ; 1879-260X ; 1879-2642 ; 1879-2618 ; 1879-2650
    ISSN 0006-3002 ; 0005-2728 ; 0005-2736 ; 0304-4165 ; 0167-4838 ; 1388-1981 ; 0167-4889 ; 0167-4781 ; 0304-419X ; 1570-9639 ; 0925-4439 ; 1874-9399
    DOI 10.1016/j.bbagen.2022.130285
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  3. Article ; Online: Improving bactericidal performance of implant composite coatings by synergism between Melittin and tetracycline.

    Zarghami, Vahid / Ghorbani, Mohammad / Bagheri, Kamran Pooshang / Shokrgozar, Mohammad Ali

    Journal of materials science. Materials in medicine

    2022  Volume 33, Issue 6, Page(s) 46

    Abstract: Methicillin resistance Staphylococcus aureus bacteria (MRSA) are serious hazards of bone implants. The present study was aimed to use the potential synergistic effects of Melittin and tetracycline to prevent MRSA associated bone implant infection. ... ...

    Abstract Methicillin resistance Staphylococcus aureus bacteria (MRSA) are serious hazards of bone implants. The present study was aimed to use the potential synergistic effects of Melittin and tetracycline to prevent MRSA associated bone implant infection. Chitosan/bioactive glass nanoparticles/tetracycline composite coatings were deposited on hydrothermally etched titanium substrate. Melittin was then coated on composite coatings by drop casting method. The surfaces were analyzed by FTIR, XRD, and SEM instruments. Tetracycline in coatings revealed multifunctional behaviors include bone regeneration and antibacterial activity. Releasing ALP enzyme from MC3T3 cells increased by tetracycline, so it is suitable candidate as osteoinductive and antibacterial agent in orthopedic implants coatings. Melittin increased the proliferation of MC3T3 cells. Composite coatings with combination of tetracycline and Melittin eradicate all MRSA bacteria, while coatings with one of them could no t eradicate all of the bacteria. In conclusion, chitosan/bioactive glass/tetracycline/Melittin coating can be suggested as a multifunctional bone implant coating because of its osteogenic and promising antibacterial activity. Graphical abstract.
    MeSH term(s) Anti-Bacterial Agents/pharmacology ; Chitosan/pharmacology ; Coated Materials, Biocompatible/pharmacology ; Melitten/pharmacology ; Methicillin-Resistant Staphylococcus aureus ; Tetracycline/pharmacology ; Titanium/pharmacology
    Chemical Substances Anti-Bacterial Agents ; Coated Materials, Biocompatible ; Melitten (20449-79-0) ; Chitosan (9012-76-4) ; Titanium (D1JT611TNE) ; Tetracycline (F8VB5M810T)
    Language English
    Publishing date 2022-05-21
    Publishing country United States
    Document type Journal Article
    ZDB-ID 1031752-1
    ISSN 1573-4838 ; 0957-4530
    ISSN (online) 1573-4838
    ISSN 0957-4530
    DOI 10.1007/s10856-022-06666-3
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  4. Article ; Online: Prevention the formation of biofilm on orthopedic implants by melittin thin layer on chitosan/bioactive glass/vancomycin coatings.

    Zarghami, Vahid / Ghorbani, Mohammad / Bagheri, Kamran Pooshang / Shokrgozar, Mohammad Ali

    Journal of materials science. Materials in medicine

    2021  Volume 32, Issue 7, Page(s) 75

    Abstract: Methicillin-resistant and Vancomycin-resistant Staphylococcus aureus bacteria (MRSA and VRSA, respectively) can seriously jeopardizes bone implants. This research aimed to examine the potential synergistic effects of Melittin and vancomycin in preventing ...

    Abstract Methicillin-resistant and Vancomycin-resistant Staphylococcus aureus bacteria (MRSA and VRSA, respectively) can seriously jeopardizes bone implants. This research aimed to examine the potential synergistic effects of Melittin and vancomycin in preventing MRSA and VRSA associated bone implant infections. Chitosan/bioactive glass nanoparticles/vancomycin composites were coated on hydrothermally etched titanium substrates by casting method. The composite coatings were coated by Melittin through drop casting technique. Melittin raised the proliferation of MC3T3 cells, making it an appropriate option as osteoinductive and antibacterial substance in coatings of orthopedic implants. Composite coatings having combined vancomycin and Melittin eliminated both planktonic and adherent MRSA and VRSA bacteria, whereas coatings containing one of them failed to kill the whole VRSA bacteria. Therefore, chitosan/bioactive glass/vancomycin/Melittin coating can be used as a bone implant coating because of its anti-infective properties.
    MeSH term(s) 3T3 Cells ; Animals ; Anti-Bacterial Agents/pharmacology ; Antimicrobial Peptides/pharmacology ; Bacterial Adhesion/drug effects ; Biofilms ; Bone Substitutes/chemistry ; Cell Proliferation ; Ceramics/chemistry ; Chitosan/chemistry ; Coated Materials, Biocompatible/chemistry ; Melitten/administration & dosage ; Melitten/chemistry ; Methicillin-Resistant Staphylococcus aureus/drug effects ; Mice ; Microscopy, Electron, Scanning ; Nanoparticles/chemistry ; Orthopedics ; Powders ; Prostheses and Implants ; Staphylococcus aureus/drug effects ; Surface Properties ; Titanium/chemistry ; Vancomycin/administration & dosage ; Vancomycin/chemistry ; Vancomycin Resistance/drug effects
    Chemical Substances Anti-Bacterial Agents ; Antimicrobial Peptides ; Bioglass ; Bone Substitutes ; Coated Materials, Biocompatible ; Powders ; Melitten (20449-79-0) ; Vancomycin (6Q205EH1VU) ; Chitosan (9012-76-4) ; Titanium (D1JT611TNE)
    Language English
    Publishing date 2021-06-22
    Publishing country United States
    Document type Journal Article
    ZDB-ID 1031752-1
    ISSN 1573-4838 ; 0957-4530
    ISSN (online) 1573-4838
    ISSN 0957-4530
    DOI 10.1007/s10856-021-06551-5
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  5. Article ; Online: Designing a New Multi-Epitope Pertussis Vaccine with Highly Population Coverage Based on a Novel Sequence and Structural Filtration Algorithm.

    Ghasemnejad, Atefeh / Bazmara, Samira / Shadmani, Mahsa / Bagheri, Kamran Pooshang

    IEEE/ACM transactions on computational biology and bioinformatics

    2021  Volume 18, Issue 5, Page(s) 1885–1892

    Abstract: Pertussis vaccine is produced from physicochemically inactivated toxin for many years. Recent advancements in immunoinformatics [N. Tomar and R. K. De, "Immunoinformatics: an integrated scenario," Immunology, vol. 131, no. 2, pp. 153-168, 2010] and ... ...

    Abstract Pertussis vaccine is produced from physicochemically inactivated toxin for many years. Recent advancements in immunoinformatics [N. Tomar and R. K. De, "Immunoinformatics: an integrated scenario," Immunology, vol. 131, no. 2, pp. 153-168, 2010] and structural bioinformatics can provide a new multidisciplinary approach to overcome the concerns including unwanted antibodies and incomplete population coverage. In this study we focused on solving the challenging issues by designing a multi-epitope vaccine (MEV) using rational bioinformatics analyses. The frequencies of All HLA DP, DQ, and DR alleles were evaluated in almost all countries. Strong binder surface epitopes on the pertussis toxin were selected based on our novel filtration strategy. Finally, the population coverage of MEV was determined in the candidate country. Filtration steps yielded 312 strong binder epitopes. Finally, 8 surface strong binder epitopes were selected as candidate epitopes. The population coverage of the MEV in France and the world was 98 and 100 percent, respectively. Our algorithm successfully filtered many unwanted strong binder epitopes. Considering the HLA type of all individuals in a country, we theoretically provided the maximum chance to all humans to be vaccinated efficiently. Application of a MEV would be led to production of highly efficient target specific antibodies, significant reduction of unwanted antibodies, and avoid possible raising of auto-antibodies as well.
    MeSH term(s) Algorithms ; Antibodies, Bacterial/immunology ; Computational Biology/methods ; Epitopes/chemistry ; Epitopes/genetics ; Epitopes/immunology ; Epitopes/metabolism ; Humans ; Models, Molecular ; Pertussis Toxin/chemistry ; Pertussis Toxin/genetics ; Pertussis Toxin/immunology ; Pertussis Toxin/metabolism ; Pertussis Vaccine/chemistry ; Pertussis Vaccine/genetics ; Pertussis Vaccine/immunology ; Pertussis Vaccine/metabolism
    Chemical Substances Antibodies, Bacterial ; Epitopes ; Pertussis Vaccine ; Pertussis Toxin (EC 2.4.2.31)
    Language English
    Publishing date 2021-10-07
    Publishing country United States
    Document type Journal Article
    ISSN 1557-9964
    ISSN (online) 1557-9964
    DOI 10.1109/TCBB.2019.2958803
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  6. Article ; Online: Prevention, inhibition, and degradation effects of melittin alone and in combination with vancomycin and rifampin against strong biofilm producer strains of methicillin-resistant Staphylococcus epidermidis.

    Mirzaei, Rasoul / Alikhani, Mohammad Yousef / Arciola, Carla Renata / Sedighi, Iraj / Yousefimashouf, Rasoul / Bagheri, Kamran Pooshang

    Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie

    2022  Volume 147, Page(s) 112670

    Abstract: Methicillin-resistant Staphylococcus epidermidis (MRSE) bacteria are being recognized as true pathogens as they are able to resist methicillin and commonly form biofilms. Recent studies have shown that antimicrobial peptides (AMPs) are promising agents ... ...

    Abstract Methicillin-resistant Staphylococcus epidermidis (MRSE) bacteria are being recognized as true pathogens as they are able to resist methicillin and commonly form biofilms. Recent studies have shown that antimicrobial peptides (AMPs) are promising agents against biofilm-associated bacterial infections. In this study, we aimed to explore the antibiofilm activity of melittin, either alone or in combination with vancomycin and rifampin, against biofilm-producing MRSE strains. Minimum biofilm preventive concentration (MBPC), minimum biofilm inhibition concentration (MBIC), and minimum biofilm eradication concentration (MBEC), as well as fractional biofilm preventive-, inhibitory-, and eradication concentrations (FBPCi, FBICi, and FBECi), were determined for the antimicrobial agents tested. Cytotoxicity and hemolytic activity of melittin at its synergistic concentration were examined on human embryonic kidney cells (HEK-293) and Red Blood Cells (RBCs), respectively. The effect of melittin on the downregulation of biofilm-associated genes was explored using Real-Time PCR. MBPC, MBIC, and MBEC values for melittin were in the range of 0.625-20, 0.625-20, and 10-40 μg/μL, respectively. Melittin showed high synergy (FBPCi, FBICi and FBECi < 0.5). The synergism resulted in a 64-512-fold, 2-16 and 2-8-fold reduction in melittin, rifampicin and vancomycin concentrations, respectively. The synergistic melittin concentration found to be effective did not manifest either cytotoxicity on HEK-293 or hemolytic activity on RBCs. Results showed that melittin downregulated the expression of biofilm-associated icaA, aap, and psm genes in all isolates tested, ranging from 0.04-folds to 2.11-folds for icaA and from 0.05 to 3.76-folds for aap and psm. The preventive and therapeutic indexes of melittin were improved 8-fold when combined with vancomycin and rifampin. Based on these findings, the combination of melittin with conventional antibiotics could be proposed for treating or preventing biofilm-associated MRSE infections.
    MeSH term(s) Anti-Bacterial Agents/administration & dosage ; Anti-Bacterial Agents/pharmacology ; Biofilms/drug effects ; Dose-Response Relationship, Drug ; Down-Regulation ; Drug Resistance, Multiple, Bacterial ; Drug Synergism ; Drug Therapy, Combination ; Genes, Bacterial ; HEK293 Cells ; Humans ; Melitten/administration & dosage ; Melitten/pharmacology ; Methicillin Resistance ; Microbial Sensitivity Tests ; Rifampin/administration & dosage ; Rifampin/pharmacology ; Staphylococcus epidermidis/drug effects ; Vancomycin/administration & dosage ; Vancomycin/pharmacology
    Chemical Substances Anti-Bacterial Agents ; Melitten (20449-79-0) ; Vancomycin (6Q205EH1VU) ; Rifampin (VJT6J7R4TR)
    Language English
    Publishing date 2022-02-03
    Publishing country France
    Document type Journal Article
    ZDB-ID 392415-4
    ISSN 1950-6007 ; 0753-3322 ; 0300-0893
    ISSN (online) 1950-6007
    ISSN 0753-3322 ; 0300-0893
    DOI 10.1016/j.biopha.2022.112670
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  7. Article ; Online: CTXP, The Major Cobra Toxin Peptide From Naja Naja Oxiana Venom; A Promising Target for Antivenom Agent Development.

    Chafi, Mohammad Hosseininejad / Eslamnezhad-Namin, Mohsen / Dastjerdeh, Mansoureh Shahbazi / Zareinejad, Mohammad Reza / Oghalaie, Akbar / Bagheri, Kamran Pooshang / Kazemi-Lomedasht, Fatemeh / Karimi, Gholamreza / Razzaghi-Abyaneh, Mehdi / Seyedjavadi, Sima Sadat / Behdani, Mahdi

    Current protein & peptide science

    2024  

    Abstract: Background and objective: Snakebite envenoming is a serious public health issue causing more than 135,000 annual deaths worldwide. Naja naja oxiana is one of the most clinically important venomous snakes in Iran and Central Asia. Conventional animal- ... ...

    Abstract Background and objective: Snakebite envenoming is a serious public health issue causing more than 135,000 annual deaths worldwide. Naja naja oxiana is one of the most clinically important venomous snakes in Iran and Central Asia. Conventional animal-derived polyclonal antibodies are the major treatment of snakebite envenoming. Characterization of venom components helps to pinpoint the toxic protein responsible for clinical manifestations in victims, which aids us in developing efficient antivenoms with minimal side effects. Therefore, the present study aimed to identify the major lethal protein of Naja naja oxiana by top-down proteomics.
    Methods: Venom proteomic profiling was performed using gel filtration (GF), reversed-phase (RP) chromatography, and intact mass spectrometry. The toxicity of GF-, and RP-eluted fractions was analyzed in BALB/c mice. The rabbit polyclonal antisera were produced against crude venom, GF fraction V (FV), and RP peak 1 (CTXP) and applied in neutralization assays.
    Results: Toxicity studies in BALB/c identified FV as the major toxic fraction of venom. Subsequently, RP separation of FV resulted in eight peaks, of which peak 1, referred to as "CTXP" (cobra toxin peptide), was identified as the major lethal protein. In vivo neutralization assays using rabbit antisera showed that polyclonal antibodies raised against FV and CTXP are capable of neutralizing at least 2-LD50s of crude venom, FV, and CTXP in all tested mice.
    Conclusion: Surprisingly, the Anti-CTXP antibody could neutralize 8-LD50 of the CTXP peptide. These results identified CTXP (a 7 kDa peptide) as a potential target for the development of novel efficient antivenom agents.
    Language English
    Publishing date 2024-01-23
    Publishing country United Arab Emirates
    Document type Journal Article
    ZDB-ID 2045662-1
    ISSN 1875-5550 ; 1389-2037
    ISSN (online) 1875-5550
    ISSN 1389-2037
    DOI 10.2174/0113892037277589231128103032
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  8. Article: Eradication of vancomycin-resistant Staphylococcus aureus on a mouse model of third-degree burn infection by melittin: an antimicrobial peptide from bee venom

    Bevalian, Parvaneh / Pashaei, Fatemeh / Akbari, Reza / Bagheri, Kamran Pooshang

    Toxicon. 2021 May 29,

    2021  

    Abstract: Third-degree burn infections caused by antibiotic-resistant bacteria are of high clinical concern. Chemical antibiotics are not promising in eradication of bacterial infections. In this challenging condition, antimicrobial peptides (AMPs) are recently ... ...

    Abstract Third-degree burn infections caused by antibiotic-resistant bacteria are of high clinical concern. Chemical antibiotics are not promising in eradication of bacterial infections. In this challenging condition, antimicrobial peptides (AMPs) are recently introduced as novel promising agents to overcome the issue. Accordingly, our study aimed to evaluate the efficiency of 'melittin' as natural peptide in bee venom, in eradicating vancomycin resistant Staphylococcus aureus (VRSA) on a mouse model of third-degree burn infection.In vitro pharmacological value of melittin was determined by examining its inhibitory and killing activities on VRSA isolates at different doses and time periods. The action mechanism of 'melittin' was evaluated by fluorescent release assay and Field Emission Scanning Electron Microscopy (FE-SEM) analyses. In vivo activity and toxicity of melittin were also examined on a mouse model of third-degree burn infection.The Minimum Inhibitory Concentration (MIC) and the Minimum Bactericidal Concentration (MBC) of melittin on all isolates ranged from ‘0.125 to 2 μg/mL’ and ‘0.125 to 4 μg/mL’, respectively. Rapid antibacterial activity of melittin on VRSA isolates was demonstrated by killing kinetics assays. Fluorometric and FE-SEM analyses indicated the membranolytic effects of melittin on VRSA isolates. The colonized VRSA bacteria were eradicated by melittin at 16 μg, in a single dose. No dermal toxicity and in vivo hemolysis were observed in the examined mice.The lack of in vivo toxicity of melittin along with its potent antibacterial activity indicated its promising therapeutic value as a topical drug against S. aureus associated third-degree burn infections.
    Keywords Staphylococcus aureus ; antibacterial properties ; antibiotic resistance ; antimicrobial peptides ; bee venoms ; dermal toxicity ; fluorescence ; fluorometry ; hemolysis ; melittin ; mice ; minimum inhibitory concentration ; therapeutics ; vancomycin
    Language English
    Dates of publication 2021-0529
    Publishing place Elsevier Ltd
    Document type Article
    Note NAL-AP-2-clean ; Pre-press version
    ZDB-ID 204479-1
    ISSN 1879-3150 ; 0041-0101
    ISSN (online) 1879-3150
    ISSN 0041-0101
    DOI 10.1016/j.toxicon.2021.05.015
    Database NAL-Catalogue (AGRICOLA)

    More links

    Kategorien

  9. Article ; Online: Bioinformatics analyses of immunogenic T-cell epitopes of LeIF and PpSP15 proteins from Leishmania major and sand fly saliva used as model antigens for the design of a multi-epitope vaccine to control leishmaniasis.

    Bordbar, Ali / Bagheri, Kamran Pooshang / Ebrahimi, Sahar / Parvizi, Parviz

    Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases

    2020  Volume 80, Page(s) 104189

    Abstract: Leishmaniasis is caused by protozoan parasites belonging to 20 Leishmania species. This infectious disease is transmitted by bites of infected phlebotomine sandflies, and is widespread in 97 countries throughout the world. No preventive or effective ... ...

    Abstract Leishmaniasis is caused by protozoan parasites belonging to 20 Leishmania species. This infectious disease is transmitted by bites of infected phlebotomine sandflies, and is widespread in 97 countries throughout the world. No preventive or effective vaccine has been developed yet. In this study, diverse computational methods were integrated to calculate evolutionary divergence, immunogenicity, IFN-γ production, epitope conservancy, and population coverage of protein fusion models of LeIF-SP15 namely SaLeish. Immunogenicity of LeIF of Leishmania species and SP15 of sandfly saliva has not been investigated in-silico in fusion form. A complete set of 9-mer MHC class I and 15-mer MHC class II peptides were identified with a high affinity for the antigenic epitopes of SaLeish inducing specific responses of CD8
    MeSH term(s) Amino Acid Sequence ; Animals ; Computational Biology/methods ; Disease Models, Animal ; Epitopes, T-Lymphocyte/chemistry ; Epitopes, T-Lymphocyte/immunology ; Histocompatibility Antigens Class I/chemistry ; Histocompatibility Antigens Class I/genetics ; Histocompatibility Antigens Class I/immunology ; Histocompatibility Antigens Class II/chemistry ; Histocompatibility Antigens Class II/genetics ; Histocompatibility Antigens Class II/immunology ; Humans ; Leishmania major/immunology ; Leishmaniasis Vaccines/immunology ; Leishmaniasis, Cutaneous/prevention & control ; Mice ; Peptide Initiation Factors/immunology ; Protozoan Proteins/immunology ; Psychodidae/immunology ; T-Lymphocyte Subsets/immunology ; T-Lymphocyte Subsets/metabolism
    Chemical Substances Epitopes, T-Lymphocyte ; Histocompatibility Antigens Class I ; Histocompatibility Antigens Class II ; LeIF protein, Leishmania ; Leishmaniasis Vaccines ; Peptide Initiation Factors ; Protozoan Proteins
    Language English
    Publishing date 2020-01-10
    Publishing country Netherlands
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2037068-4
    ISSN 1567-7257 ; 1567-1348
    ISSN (online) 1567-7257
    ISSN 1567-1348
    DOI 10.1016/j.meegid.2020.104189
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  10. Article ; Online: Development and characterization of human single chain antibody against Iranian Macrovipera lebetina snake venom.

    Eskafi, Ayda Hassanzadeh / Bagheri, Kamran Pooshang / Behdani, Mahdi / Yamabhai, Montarop / Shahbazzadeh, Delavar / Kazemi-Lomedasht, Fatemeh

    Toxicon : official journal of the International Society on Toxinology

    2021  Volume 197, Page(s) 106–113

    Abstract: Snakebite is an important public health problem in tropical and subtropical regions. Macrovipera lebetina is one of the most dangerous snakes in Iran. Envenoming by this snake can lead to respiratory distress, heart attack, bleeding, and death. The ... ...

    Abstract Snakebite is an important public health problem in tropical and subtropical regions. Macrovipera lebetina is one of the most dangerous snakes in Iran. Envenoming by this snake can lead to respiratory distress, heart attack, bleeding, and death. The specific treatment available is immunized equine serum, which has several side effects like serum sickness. Nowadays, single-chain fragment variable antibodies (scFvs) are one of the fast growing classes of monoclonal antibodies, which are suggested for treatment of envenoming. This study aimed to achieve a fully human scFv antibody against M. lebetina venom from human non-immune library. In this study, scFvs against M. lebetina venom were isolated by phage display technique. Using three rounds of biopanning, two specific scFvs (C37 and C69) with the highest affinity were selected. The selected scFvs purified by nickel affinity chromatography. The specific binding of purified antibodies were confirmed by enzyme-linked immunosorbent assay. The LD
    MeSH term(s) Animals ; Horses ; Humans ; Iran ; Lethal Dose 50 ; Mice ; Single-Chain Antibodies ; Snake Bites/drug therapy ; Snake Venoms ; Viperidae
    Chemical Substances Single-Chain Antibodies ; Snake Venoms
    Language English
    Publishing date 2021-04-24
    Publishing country England
    Document type Journal Article
    ZDB-ID 204479-1
    ISSN 1879-3150 ; 0041-0101
    ISSN (online) 1879-3150
    ISSN 0041-0101
    DOI 10.1016/j.toxicon.2021.04.017
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

To top