• Joe Tippens & the Fenbendazole Cancer Protocol
    As a prophylaxis against cancer, I am trying this myself due to several reasons; including the fact my Mother died from cancer.

    A former co-worker was diagnosed with stage 4 inoperable esophageal cancer over 2 years ago and told he had only weeks to live. Fast forward over 2 years later he is not only alive and well, but cancer free.

    Happy Healing Fenben® Tablets 222mg. Tablets.
    The prophylactic protocol is 3 tablets a week, then 4 days without it each week for 10 weeks. I'm in my second week of taking it without any side effects.
    https://thehappyhealingstore.com/product/fenben-222mg-tablets/
    The dosage is higher for someone who has actually been diagnosed with cancer.

    This Cancer Story Rocks! Joe Tippens And Fenbendazole
    https://www.youtube.com/live/PNzyuhXCgmQ?si=7C4LCGhVCsZ9P02c
    Joe Tippens & the Fenbendazole Cancer Protocol As a prophylaxis against cancer, I am trying this myself due to several reasons; including the fact my Mother died from cancer. A former co-worker was diagnosed with stage 4 inoperable esophageal cancer over 2 years ago and told he had only weeks to live. Fast forward over 2 years later he is not only alive and well, but cancer free. Happy Healing Fenben® Tablets 222mg. Tablets. The prophylactic protocol is 3 tablets a week, then 4 days without it each week for 10 weeks. I'm in my second week of taking it without any side effects. https://thehappyhealingstore.com/product/fenben-222mg-tablets/ The dosage is higher for someone who has actually been diagnosed with cancer. This Cancer Story Rocks! Joe Tippens And Fenbendazole https://www.youtube.com/live/PNzyuhXCgmQ?si=7C4LCGhVCsZ9P02c
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  • All too often lately I see stories posted about friends and loved ones passing because of cancer.

    Please watch this video. A friend I worked with at BNSF Railway in north Idaho was supposed to have died by a year ago last November from esophageal cancer. He did the Joe Tippins Protocol using dog dewormer described in the video below and is now alive and well and cancer free.

    All it takes is 1 gram of Fenbendazole a day for 2 weeks to kill most cancers! Knowledge is POWER. The Fenbendazole needed for this costs less than $150.00 and is safer than chemotherapy at a fraction of the cost.

    If I am ever diagnosed with cancer, guess what I will be using? Read the narrative below this video to find out how to get it.

    All too often lately I see stories posted about friends and loved ones passing because of cancer. Please watch this video. A friend I worked with at BNSF Railway in north Idaho was supposed to have died by a year ago last November from esophageal cancer. He did the Joe Tippins Protocol using dog dewormer described in the video below and is now alive and well and cancer free. All it takes is 1 gram of Fenbendazole a day for 2 weeks to kill most cancers! Knowledge is POWER. The Fenbendazole needed for this costs less than $150.00 and is safer than chemotherapy at a fraction of the cost. If I am ever diagnosed with cancer, guess what I will be using? Read the narrative below this video to find out how to get it.
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  • Good Day brothers and sisters. We have now come to Palm Sunday and the beginning of what is known as Holy Week. Our Lord was crucified and died during this week. It did not begin in a sad fashion though. It actually began in a very festive joyous way. Let’s see what the Smart Book says about it shall we?
    Luke 19:28-44 Amplified Bible
    The Triumphal Entry
    28 After saying these things, Jesus went on ahead [of them], going up to Jerusalem.
    29 When He approached Bethphage and Bethany, at the mount that is called Olivet, He sent two of the disciples, 30 saying, “Go into the village ahead of you; there, as you enter, you will find a [donkey’s] [a]colt tied, on which no one has ever sat. Untie it and bring it here. 31 If anybody asks you, ‘Why are you untying the colt?’ you will say, ‘The Lord needs it.’” 32 So those who were sent left and found the colt just as He had told them. 33 As they were untying the colt, its owners asked them, “Why are you untying the colt?” 34 They said, “The Lord needs it.” 35 They brought it to Jesus, and [b]they threw their robes over the colt and put Jesus on it. 36 As He rode along, people were spreading their coats on the road [as an act of homage before a king]. 37 As soon as He was approaching [Jerusalem], near the descent of the Mount of Olives, the entire multitude of the disciples [all those who were or claimed to be His followers] began praising God [adoring Him enthusiastically and] joyfully with loud voices for all the miracles and works of power that they had seen, 38 shouting,
    “BLESSED (celebrated, praised) IS THE KING WHO COMES IN THE NAME OF THE LORD!
    Peace in heaven and glory (majesty, splendor) in the highest [heaven]!”
    39 Some of the Pharisees from the crowd said to Him, “Teacher, rebuke Your disciples [for shouting these Messianic praises].” 40 Jesus replied, “I tell you, if these [people] keep silent, the stones will cry out [in praise]!”
    41 As He approached Jerusalem, He saw the city and wept over it [and the spiritual ignorance of its people], 42 saying, “If [only] you had known on this day [of salvation], even you, the things which make for peace [and on which peace depends]! But now they have been hidden from your eyes. 43 For a time [of siege] is coming when your enemies will put up a barricade [with pointed stakes] against you, and surround you [with armies] and hem you in on every side, 44 and they will level you to the ground, you [Jerusalem] and your children within you. They will not leave in you one stone on another, all because you did not [come progressively to] recognize [from observation and personal experience] the time of your visitation [when God was gracious toward you and offered you salvation].”
    John 12:12-16 King James Version
    12 On the next day much people that were come to the feast, when they heard that Jesus was coming to Jerusalem,13 Took branches of palm trees, and went forth to meet him, and cried, Hosanna: Blessed is the King of Israel that cometh in the name of the Lord.14 And Jesus, when he had found a young ass, sat thereon; as it is written,15 Fear not, daughter of Sion: behold, thy King cometh, sitting on an ass's colt.16 These things understood not his disciples at the first: but when Jesus was glorified, then remembered they that these things were written of him, and that they had done these things unto him.
    So yes, there was a prophecy of Jesus riding on an ass’s colt into Jerusalem and the people would be shouting Hosanna: Blessed is the King of Israel that cometh in the name of the Lord. Can you imagine the excitement of that day? The people of Israel had been waiting a long time for it to come. They recognized Him as the King of Israel for a day. Notice that even His Disciples didn’t really know what was going on until He was glorified. Their emotions had overwhelmed them. They were so excited with anticipation. They really thought He was going to rise up and defeat the Romans. He had come in on a meek and mild ass’s colt though and not a mighty white war horse. Jewish nobles rode on donkeys. They we’re recognizing Jesus as a noble king, but Jesus was coming in peace, not for war! Through His death and resurrection you can find remission for your sins and true peace can come into your life through Christ. You can be reborn. Make your choice for Christ today! Find true peace for your heart and life.
    The Lord bless and keep you, His face Shine upon you,
    Chaplain Loehne
    Good Day brothers and sisters. We have now come to Palm Sunday and the beginning of what is known as Holy Week. Our Lord was crucified and died during this week. It did not begin in a sad fashion though. It actually began in a very festive joyous way. Let’s see what the Smart Book says about it shall we? Luke 19:28-44 Amplified Bible The Triumphal Entry 28 After saying these things, Jesus went on ahead [of them], going up to Jerusalem. 29 When He approached Bethphage and Bethany, at the mount that is called Olivet, He sent two of the disciples, 30 saying, “Go into the village ahead of you; there, as you enter, you will find a [donkey’s] [a]colt tied, on which no one has ever sat. Untie it and bring it here. 31 If anybody asks you, ‘Why are you untying the colt?’ you will say, ‘The Lord needs it.’” 32 So those who were sent left and found the colt just as He had told them. 33 As they were untying the colt, its owners asked them, “Why are you untying the colt?” 34 They said, “The Lord needs it.” 35 They brought it to Jesus, and [b]they threw their robes over the colt and put Jesus on it. 36 As He rode along, people were spreading their coats on the road [as an act of homage before a king]. 37 As soon as He was approaching [Jerusalem], near the descent of the Mount of Olives, the entire multitude of the disciples [all those who were or claimed to be His followers] began praising God [adoring Him enthusiastically and] joyfully with loud voices for all the miracles and works of power that they had seen, 38 shouting, “BLESSED (celebrated, praised) IS THE KING WHO COMES IN THE NAME OF THE LORD! Peace in heaven and glory (majesty, splendor) in the highest [heaven]!” 39 Some of the Pharisees from the crowd said to Him, “Teacher, rebuke Your disciples [for shouting these Messianic praises].” 40 Jesus replied, “I tell you, if these [people] keep silent, the stones will cry out [in praise]!” 41 As He approached Jerusalem, He saw the city and wept over it [and the spiritual ignorance of its people], 42 saying, “If [only] you had known on this day [of salvation], even you, the things which make for peace [and on which peace depends]! But now they have been hidden from your eyes. 43 For a time [of siege] is coming when your enemies will put up a barricade [with pointed stakes] against you, and surround you [with armies] and hem you in on every side, 44 and they will level you to the ground, you [Jerusalem] and your children within you. They will not leave in you one stone on another, all because you did not [come progressively to] recognize [from observation and personal experience] the time of your visitation [when God was gracious toward you and offered you salvation].” John 12:12-16 King James Version 12 On the next day much people that were come to the feast, when they heard that Jesus was coming to Jerusalem,13 Took branches of palm trees, and went forth to meet him, and cried, Hosanna: Blessed is the King of Israel that cometh in the name of the Lord.14 And Jesus, when he had found a young ass, sat thereon; as it is written,15 Fear not, daughter of Sion: behold, thy King cometh, sitting on an ass's colt.16 These things understood not his disciples at the first: but when Jesus was glorified, then remembered they that these things were written of him, and that they had done these things unto him. So yes, there was a prophecy of Jesus riding on an ass’s colt into Jerusalem and the people would be shouting Hosanna: Blessed is the King of Israel that cometh in the name of the Lord. Can you imagine the excitement of that day? The people of Israel had been waiting a long time for it to come. They recognized Him as the King of Israel for a day. Notice that even His Disciples didn’t really know what was going on until He was glorified. Their emotions had overwhelmed them. They were so excited with anticipation. They really thought He was going to rise up and defeat the Romans. He had come in on a meek and mild ass’s colt though and not a mighty white war horse. Jewish nobles rode on donkeys. They we’re recognizing Jesus as a noble king, but Jesus was coming in peace, not for war! Through His death and resurrection you can find remission for your sins and true peace can come into your life through Christ. You can be reborn. Make your choice for Christ today! Find true peace for your heart and life. The Lord bless and keep you, His face Shine upon you, Chaplain Loehne
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  • https://www.sciencedirect.com/topics/immunology-and-microbiology/macrophage-activating-factor
    https://www.sciencedirect.com/topics/immunology-and-microbiology/macrophage-activating-factor
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  • First and foremost, NAC is beneficial to the body because of its antioxidant properties (1). Antioxidants — a group of compounds that include other well-known supplements like vitamin C, vitamin E, and astaxanthin — have the important job of helping fight free radical damage and preventing oxidative stress in the body. This is an important job, as oxidative stress has been linked to a wide range of diseases and dysfunctions, including cellular damage and cancer. (2)

    NAC acts as an antioxidant in its own right, but it also increases the production of other antioxidants such as glutathione. Glutathione is known as the “master antioxidant” and has demonstrated an ability to fight oxidative stress, support immune health (3), and offer protection from heavy metals (4), making it one of the most important — if not the most important — antioxidant in the body.

    NAC has also demonstrated strong anti-inflammatory properties; according to one study, published in Agents and Actions, it works by reducing the activity (5) of inflammatory cytokines and macrophages.
    First and foremost, NAC is beneficial to the body because of its antioxidant properties (1). Antioxidants — a group of compounds that include other well-known supplements like vitamin C, vitamin E, and astaxanthin — have the important job of helping fight free radical damage and preventing oxidative stress in the body. This is an important job, as oxidative stress has been linked to a wide range of diseases and dysfunctions, including cellular damage and cancer. (2) NAC acts as an antioxidant in its own right, but it also increases the production of other antioxidants such as glutathione. Glutathione is known as the “master antioxidant” and has demonstrated an ability to fight oxidative stress, support immune health (3), and offer protection from heavy metals (4), making it one of the most important — if not the most important — antioxidant in the body. NAC has also demonstrated strong anti-inflammatory properties; according to one study, published in Agents and Actions, it works by reducing the activity (5) of inflammatory cytokines and macrophages.
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  • All humans are born with a genetic defect. Our livers are missing a key enzyme, xl-gulono-§-lactone oxidase, which is required to synthesize ascorbic acid from glucose. The loss of this single gene prevents humans from making their own Vitamin C. The negative mutation of the so-called GULO gene has been well studied in both human and primate genomes. If this negative mutation could be corrected, most people would no longer need to supplement Vitamin C in their diets.
    Most living things today make their own Vitamin C and do not have to obtain it through food sources. They do this by converting glucuronic acid (C6H10O7), derived from glucose (C6H12O6), into ascorbic acid (C6H8O6). The exceptions that cannot make their own Vitamin C are guinea pigs, fruit eating bats, the red-vented bulbul bird, and higher primates, such as gorillas and humans.
    1 Vitamin C supports the production of interferons.
    Interferons are produced when the presence of pathogens is detected.
    They facilitate the ability of cells to initiate protective cellular defenses.
    2 Vitamin C enhances the function of phagocytes.
    Phagocytes are a kind of white blood cell that surrounds pathogens and other dangerous particles. Once the intruders are captured, they are digested and neutralized enzymatically.
    3 Vitamin C is mainly found in white blood cells.
    Some of these primary cells of the immune system have levels of vitamin C up to 80 times higher than the levels found in the plasma.
    4 Vitamin C supports the cellular immune response.
    There are 2 main ways that the body can respond to a pathogen: antibody immunity and cellular immunity. The cell-mediated response refers to the activation of macrophages, natural killer cells, and antigen-specific T-lymphocytes that attack anything that is perceived as a foreign agent.
    5 Vitamin C enhances cytokine production by white blood cells.
    Cytokines are communication proteins released from certain white blood cells and transmit information to other cells, thus promoting the immune response.
    6 Vitamin C inhibits the apoptosis of various forms of T-lymphocytes.
    T-lymphocytes are a type of white blood cell. They are an integral part of the cell-mediated immune defense system. Vitamin C helps to keep these important cells alive and viable.
    7 Vitamin C enhances the production of nitrogen oxide by phagocytes.
    Nitrogen oxide is produced in massive quantities in these cells, and is one of the factors that will kill captured pathogens.
    8 Vitamin C enhances the production of T-lymphocytes.
    These cells are essential for cell-mediated immune responses, and vitamin C helps to multiply in number.
    9 Vitamin C increases the production of B lymphocytes.
    These white blood cells produce the antibodies as part of the antibody-mediated immune response. These antibodies are formed in response to the initial introduction of an invading pathogen or antigen.
    10 Vitamin C inhibits the production of neuraminidase.
    Some pathogenic viruses and bacteria create neuraminidase, an enzyme that keeps them from being trapped in the mucus, one of the natural lines of body defense. By inhibiting neuraminidase, vitamin C helps to optimize this defense mechanism of the body.
    11 Vitamin C supports the production and activity of antibodies.
    Good antibody function is important for a healthy immune system.
    12 Vitamin C supports the activity of natural killer cells.
    Natural killer cells are small lymphocytes that can attack directly cells, such as cancer cells, and kill them
    13 Vitamin C favors the formation of prostaglandins.
    Prostaglandins are hormones - compounds that control a variety of physiological processes, including regulation of T-cell function.
    14 Vitamin C supports circular GMP levels in lymphocytes.
    Circular GMP plays a leading role in regulating various physiological responses, including immune responses. Circular GMP is important for normal reproduction and differentiation (specificity for specific purposes) of cells. Circular GMP also controls the action of many hormones, and appears to mediate relaxation of smooth muscle.
    All humans are born with a genetic defect. Our livers are missing a key enzyme, xl-gulono-§-lactone oxidase, which is required to synthesize ascorbic acid from glucose. The loss of this single gene prevents humans from making their own Vitamin C. The negative mutation of the so-called GULO gene has been well studied in both human and primate genomes. If this negative mutation could be corrected, most people would no longer need to supplement Vitamin C in their diets. Most living things today make their own Vitamin C and do not have to obtain it through food sources. They do this by converting glucuronic acid (C6H10O7), derived from glucose (C6H12O6), into ascorbic acid (C6H8O6). The exceptions that cannot make their own Vitamin C are guinea pigs, fruit eating bats, the red-vented bulbul bird, and higher primates, such as gorillas and humans. 1 Vitamin C supports the production of interferons. Interferons are produced when the presence of pathogens is detected. They facilitate the ability of cells to initiate protective cellular defenses. 2 Vitamin C enhances the function of phagocytes. Phagocytes are a kind of white blood cell that surrounds pathogens and other dangerous particles. Once the intruders are captured, they are digested and neutralized enzymatically. 3 Vitamin C is mainly found in white blood cells. Some of these primary cells of the immune system have levels of vitamin C up to 80 times higher than the levels found in the plasma. 4 Vitamin C supports the cellular immune response. There are 2 main ways that the body can respond to a pathogen: antibody immunity and cellular immunity. The cell-mediated response refers to the activation of macrophages, natural killer cells, and antigen-specific T-lymphocytes that attack anything that is perceived as a foreign agent. 5 Vitamin C enhances cytokine production by white blood cells. Cytokines are communication proteins released from certain white blood cells and transmit information to other cells, thus promoting the immune response. 6 Vitamin C inhibits the apoptosis of various forms of T-lymphocytes. T-lymphocytes are a type of white blood cell. They are an integral part of the cell-mediated immune defense system. Vitamin C helps to keep these important cells alive and viable. 7 Vitamin C enhances the production of nitrogen oxide by phagocytes. Nitrogen oxide is produced in massive quantities in these cells, and is one of the factors that will kill captured pathogens. 8 Vitamin C enhances the production of T-lymphocytes. These cells are essential for cell-mediated immune responses, and vitamin C helps to multiply in number. 9 Vitamin C increases the production of B lymphocytes. These white blood cells produce the antibodies as part of the antibody-mediated immune response. These antibodies are formed in response to the initial introduction of an invading pathogen or antigen. 10 Vitamin C inhibits the production of neuraminidase. Some pathogenic viruses and bacteria create neuraminidase, an enzyme that keeps them from being trapped in the mucus, one of the natural lines of body defense. By inhibiting neuraminidase, vitamin C helps to optimize this defense mechanism of the body. 11 Vitamin C supports the production and activity of antibodies. Good antibody function is important for a healthy immune system. 12 Vitamin C supports the activity of natural killer cells. Natural killer cells are small lymphocytes that can attack directly cells, such as cancer cells, and kill them 13 Vitamin C favors the formation of prostaglandins. Prostaglandins are hormones - compounds that control a variety of physiological processes, including regulation of T-cell function. 14 Vitamin C supports circular GMP levels in lymphocytes. Circular GMP plays a leading role in regulating various physiological responses, including immune responses. Circular GMP is important for normal reproduction and differentiation (specificity for specific purposes) of cells. Circular GMP also controls the action of many hormones, and appears to mediate relaxation of smooth muscle.
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  • The mechanism for anti-inflammatory action of Ivermectin was explained as inhibition of cytokine production by lipopolysaccharide challenged macrophages, blockade of activation of NF-kB, and the stress-activated MAP kinases JNK and p38, and inhibition of TLR4 signaling https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8203399/
    The mechanism for anti-inflammatory action of Ivermectin was explained as inhibition of cytokine production by lipopolysaccharide challenged macrophages, blockade of activation of NF-kB, and the stress-activated MAP kinases JNK and p38, and inhibition of TLR4 signaling https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8203399/
    WWW.NCBI.NLM.NIH.GOV
    The mechanisms of action of Ivermectin against SARS-CoV-2: An evidence-based clinical review article
    Considering the urgency of the ongoing COVID-19 pandemic, detection of various new mutant strains and future potential re-emergence of novel coronaviruses, repurposing of approved drugs such as Ivermectin could be worthy of attention. This evidence-based ...
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  • https://pubmed.ncbi.nlm.nih.gov/26814441/

    Nanoscale
    . 2016 Feb 14;8(6):3785-95. doi: 10.1039/c5nr09208f. Epub 2016 Jan 27.
    Functionalized graphene oxide serves as a novel vaccine nano-adjuvant for robust stimulation of cellular immunity
    Ligeng Xu 1, Jian Xiang, Ye Liu, Jun Xu, Yinchan Luo, Liangzhu Feng, Zhuang Liu, Rui Peng
    Affiliations collapse
    Affiliation
    1Institute of Functional Nano & Soft Materials (FUNSOM), Jiangsu Key Laboratory for Carbon-based Functional Materials & Devices, Soochow University, Suzhou, 215123, P.R. China. [email protected] [email protected].
    PMID: 26814441 DOI: 10.1039/c5nr09208f
    Free article
    Abstract
    Benefiting from their unique physicochemical properties, graphene derivatives have attracted great attention in biomedicine. In this study, we carefully engineered graphene oxide (GO) as a vaccine adjuvant for immunotherapy using urease B (Ure B) as the model antigen. Ure B is a specific antigen for Helicobacter pylori, which is a class I carcinogen for gastric cancer. Polyethylene glycol (PEG) and various types of polyethylenimine (PEI) were used as coating polymers. Compared with single-polymer modified GOs (GO-PEG and GO-PEI), certain dual-polymer modified GOs (GO-PEG-PEI) can act as a positive modulator to promote the maturation of dendritic cells (DCs) and enhance their cytokine secretion through the activation of multiple toll-like receptor (TLR) pathways while showing low toxicity. Moreover, this GO-PEG-PEI can serve as an antigen carrier to effectively shuttle antigens into DCs. These two advantages enable GO-PEG-PEI to serve as a novel vaccine adjuvant. In the subsequent in vivo experiments, compared with free Ure B and clinically used aluminum-adjuvant-based vaccine (Alum-Ure B), GO-PEG-PEI-Ure B induces stronger cellular immunity via intradermal administration, suggesting promising applications in cancer immunotherapy. Our work not only presents a novel, highly effective GO-based vaccine nano-adjuvant, but also highlights the critical roles of surface chemistry for the rational design of nano-adjuvants.

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    Front Immunol. 2017 Jun 13;8:673. doi: 10.3389/fimmu.2017.00673. eCollection 2017.
    https://pubmed.ncbi.nlm.nih.gov/26814441/ Nanoscale . 2016 Feb 14;8(6):3785-95. doi: 10.1039/c5nr09208f. Epub 2016 Jan 27. Functionalized graphene oxide serves as a novel vaccine nano-adjuvant for robust stimulation of cellular immunity Ligeng Xu 1, Jian Xiang, Ye Liu, Jun Xu, Yinchan Luo, Liangzhu Feng, Zhuang Liu, Rui Peng Affiliations collapse Affiliation 1Institute of Functional Nano & Soft Materials (FUNSOM), Jiangsu Key Laboratory for Carbon-based Functional Materials & Devices, Soochow University, Suzhou, 215123, P.R. China. [email protected] [email protected]. PMID: 26814441 DOI: 10.1039/c5nr09208f Free article Abstract Benefiting from their unique physicochemical properties, graphene derivatives have attracted great attention in biomedicine. In this study, we carefully engineered graphene oxide (GO) as a vaccine adjuvant for immunotherapy using urease B (Ure B) as the model antigen. Ure B is a specific antigen for Helicobacter pylori, which is a class I carcinogen for gastric cancer. Polyethylene glycol (PEG) and various types of polyethylenimine (PEI) were used as coating polymers. Compared with single-polymer modified GOs (GO-PEG and GO-PEI), certain dual-polymer modified GOs (GO-PEG-PEI) can act as a positive modulator to promote the maturation of dendritic cells (DCs) and enhance their cytokine secretion through the activation of multiple toll-like receptor (TLR) pathways while showing low toxicity. Moreover, this GO-PEG-PEI can serve as an antigen carrier to effectively shuttle antigens into DCs. These two advantages enable GO-PEG-PEI to serve as a novel vaccine adjuvant. In the subsequent in vivo experiments, compared with free Ure B and clinically used aluminum-adjuvant-based vaccine (Alum-Ure B), GO-PEG-PEI-Ure B induces stronger cellular immunity via intradermal administration, suggesting promising applications in cancer immunotherapy. Our work not only presents a novel, highly effective GO-based vaccine nano-adjuvant, but also highlights the critical roles of surface chemistry for the rational design of nano-adjuvants. Similar articles Alum-functionalized graphene oxide nanocomplexes for effective anticancer vaccination. Wang X, Cao F, Yan M, Liu Y, Zhu X, Sun H, Ma G. Acta Biomater. 2019 Jan 1;83:390-399. doi: 10.1016/j.actbio.2018.11.023. Epub 2018 Nov 15. PMID: 30448435 Synthesis of polymer-functionalized nanoscale graphene oxide with different surface charge and its cellular uptake, biosafety and immune responses in Raw264.7 macrophages. Wang B, Su X, Liang J, Yang L, Hu Q, Shan X, Wan J, Hu Z. Mater Sci Eng C Mater Biol Appl. 2018 Sep 1;90:514-522. doi: 10.1016/j.msec.2018.04.096. Epub 2018 May 1. PMID: 29853120 Immunostimulatory oligonucleotides-loaded cationic graphene oxide with photothermally enhanced immunogenicity for photothermal/immune cancer therapy. Tao Y, Ju E, Ren J, Qu X. Biomaterials. 2014 Dec;35(37):9963-9971. doi: 10.1016/j.biomaterials.2014.08.036. Epub 2014 Sep 15. PMID: 25224368 Recent progress of graphene oxide as a potential vaccine carrier and adjuvant. Cao W, He L, Cao W, Huang X, Jia K, Dai J. Acta Biomater. 2020 Aug;112:14-28. doi: 10.1016/j.actbio.2020.06.009. Epub 2020 Jun 10. PMID: 32531395 Review. Particulate formulations for the delivery of poly(I:C) as vaccine adjuvant. Hafner AM, Corthésy B, Merkle HP. Adv Drug Deliv Rev. 2013 Oct;65(10):1386-99. doi: 10.1016/j.addr.2013.05.013. Epub 2013 Jun 7. PMID: 23751781 Review. See all similar articles Cited by 7 articles Intranasal vaccination with influenza HA/GO-PEI nanoparticles provides immune protection against homo- and heterologous strains. Dong C, Wang Y, Gonzalez GX, Ma Y, Song Y, Wang S, Kang SM, Compans RW, Wang BZ. Proc Natl Acad Sci U S A. 2021 May 11;118(19):e2024998118. doi: 10.1073/pnas.2024998118. PMID: 33941704 Free PMC article. SPIO Enhance the Cross-Presentation and Migration of DCs and Anionic SPIO Influence the Nanoadjuvant Effects Related to Interleukin-1β. Liu H, Dong H, Zhou N, Dong S, Chen L, Zhu Y, Hu HM, Mou Y. Nanoscale Res Lett. 2018 Dec 20;13(1):409. doi: 10.1186/s11671-018-2802-0. PMID: 30570682 Free PMC article. Nanoparticle Vaccines Adopting Virus-like Features for Enhanced Immune Potentiation. Chattopadhyay S, Chen JY, Chen HW, Hu CJ. Nanotheranostics. 2017 Jun 9;1(3):244-260. doi: 10.7150/ntno.19796. eCollection 2017. PMID: 29071191 Free PMC article. Review. Single-cell mass cytometry and transcriptome profiling reveal the impact of graphene on human immune cells. Orecchioni M, Bedognetti D, Newman L, Fuoco C, Spada F, Hendrickx W, Marincola FM, Sgarrella F, Rodrigues AF, Ménard-Moyon C, Cesareni G, Kostarelos K, Bianco A, Delogu LG. Nat Commun. 2017 Oct 24;8(1):1109. doi: 10.1038/s41467-017-01015-3. PMID: 29061960 Free PMC article. Graphene and the Immune System: A Romance of Many Dimensions. Mukherjee SP, Bottini M, Fadeel B. Front Immunol. 2017 Jun 13;8:673. doi: 10.3389/fimmu.2017.00673. eCollection 2017.
    PUBMED.NCBI.NLM.NIH.GOV
    Functionalized graphene oxide serves as a novel vaccine nano-adjuvant for robust stimulation of cellular immunity - PubMed
    Benefiting from their unique physicochemical properties, graphene derivatives have attracted great attention in biomedicine. In this study, we carefully engineered graphene oxide (GO) as a vaccine adjuvant for immunotherapy using urease B (Ure B) as the model antigen. Ure B is a specific antigen for …
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  • Giant Viruses: Frank Aylward and the Beauty of Microbial Diversity.

    Frank Aylward is an assistant professor of biological sciences, at Virginia Tech. He specializes in microbial diversity and is fascinated by the abundance of microbes "that play critical roles in human health, the evolution of life on Earth, biogeochemical cycling, and the biosphere."

    Listen to it here: https://bit.ly/3eYtVGA

    Episode also available on Apple Podcasts: apple.co/30PvU9C
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    #Microbes #genome #Virus #bacteriophage #marinebacteira #microbial #genomics #bioinformatics #Findinggeniuspodcast #Healthpodcast #InternalMedicinepodcast #Biosciencespodcast
    Giant Viruses: Frank Aylward and the Beauty of Microbial Diversity. Frank Aylward is an assistant professor of biological sciences, at Virginia Tech. He specializes in microbial diversity and is fascinated by the abundance of microbes "that play critical roles in human health, the evolution of life on Earth, biogeochemical cycling, and the biosphere." Listen to it here: https://bit.ly/3eYtVGA Episode also available on Apple Podcasts: apple.co/30PvU9C . . . . #Microbes #genome #Virus #bacteriophage #marinebacteira #microbial #genomics #bioinformatics #Findinggeniuspodcast #Healthpodcast #InternalMedicinepodcast #Biosciencespodcast
    Giant Viruses: Frank Aylward and the Beauty of Microbial Diversity
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  • Dr. Sherri Tenpenny says this Covid vaccine is a well-designed killing tool. She says the vaccine kills type 2 macrophages in the body that usually act like firemen. She claims the jab can make antibodies that attack more than 25 organs in the body.
    https://www.trunews.com/stream/trunews-headlines-with-kerry-kinsey-march-8-2021
    Dr. Sherri Tenpenny says this Covid vaccine is a well-designed killing tool. She says the vaccine kills type 2 macrophages in the body that usually act like firemen. She claims the jab can make antibodies that attack more than 25 organs in the body. https://www.trunews.com/stream/trunews-headlines-with-kerry-kinsey-march-8-2021
    TruNews
    TruNews is the world's leading news source that reports, analyzes, and comments on global events and trends with a conservative, orthodox Christian worldview.
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