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GENLISA™ KITa - Kyushu Lung Cancer Antigen 1 (CXorf61) Detection Kit
The GENLISA™ KITa is an advanced enzyme immunoassay designed for the precise quantification of Kyushu Lung Cancer Antigen 1 (CXorf61) in various biological fluids. This kit can be used to measure CXorf61 levels in serum, plasma, tissue homogenates, and other related samples. CXorf61, a biomarker linked to lung cancer, plays a key role in early diagnosis and monitoring of the disease. The GENLISA™ KITa offers a reliable, sensitive, and efficient solution for research and clinical applications, facilitating enhanced understanding and management of lung cancer progression and patient prognosis.
#kyushu lung cancer antigen#Roledumab ELISA#panitumumab elisa#semaglutide elisa#golimumab elisa#ecoli hcp elisa#natalizumab elisa#mab-based elisa#dsrna j2 antibody#dsrna antibody j2
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saw this doll on the Lottie doll website 🥺
on April 28th I went to the hospital because within the span of a week I wasn't able to take care of myself or walk anymore.
when I got a CT scan the doctor told me it seemed like I had a brain disease. I was really scared, I didn't know what that meant, I didn't know if it was terminal or if it was cancer.
on April 30th I was out into the neurology ward and after getting an MRI, spinal tap, and x-ray the doctors there determined I have multiple sclerosis.
luckily it hadn't spread to my spinal cord yet so they put me on a strong dose of methylprednisolone for a few days, I started feeling much better and I was able to walk, eat, sleep on my back, and brush my teeth again!
it was very scary to know that if I had developed multiple sclerosis a decade or two earlier, there would be a good chance I wouldn't have survived.
but I was discharged from the hospital on May 6th and have been improving since! I already have started my treatment with natalizumab, I'm able to go back to work, able to walk to places by myself, able to shower and eat by myself, able to do all sorts of things again!
it has been a very difficult year for me, I lost all of my friends, it's overwhelming dealing with disability applications, dealing with ableism, dealing with having to call in sick often to work, feeling tired all the time, the brain fog and bad memory, but I am alive! >0<
but I think I would take that over not being able to eat or shower :')) it is awful when your tongue is numb and you can't taste anything... or when you have vertigo and double vision 24/7... or when you can't walk in a straight like and you keep falling over... 😵💫
I was able to celebrate my 25th birthday, go to the concerts with my dad that i had planned at the beginning of the year, I was able to go to the anime and comic book conventions with my brother, and I was able to eat my favourite foods again! >0<
I like this Lottie doll because having multiple sclerosis and going through all of these things by myself takes a lot of resilience. there is no cure for multiple sclerosis, and I have made peace with that. there's no guarantee that I will ever return to how I was before I went to the hospital.
but I am strong and brave, just like this Lottie doll! >0< she even looks like me ehehe
#dollblr#doll collector#dolls#fashion doll#my dolls#post#doll#lottie doll#lottie#multiple sclerosis#actually disabled#disability#disabled#RRMS#autoimmune disease
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The Future of Progressive Multifocal Leukoencephalopathy: Insights, Trends, and Projections for a Rare Neurological Condition
Introduction to Progressive Multifocal Leukoencephalopathy (PML)Progressive multifocal leukoencephalopathy (PML) is a rare, life-threatening demyelinating disorder of the central nervous system, triggered by the reactivation of the JC virus (John Cunningham virus). This condition predominantly impacts immunocompromised individuals, particularly those living with HIV/AIDS, patients undergoing immunosuppressive therapy for organ transplants, or those being treated for autoimmune diseases such as multiple sclerosis (MS). Given its severity, the medical community is increasingly focused on enhancing diagnostics, treatments, and prevention strategies. As our understanding of PML deepens, the market for related therapies has expanded, fueled by advancements in treatment options and ongoing research efforts.
Download the latest Progressive Multifocal Leukoencephalopathy Market Research Report to inform your strategic decisions with confidence.
Understanding PML and Market DynamicsPML arises when the dormant JC virus reactivates in an immunocompromised host, leading to a rapid and often fatal degeneration of the brain's white matter. Symptoms of PML include progressive weakness, vision problems, cognitive decline, and speech difficulties, often resulting in death within months if not treated. The critical nature of PML, coupled with the lack of effective therapies, creates a significant unmet need within the market.
Current treatments primarily focus on restoring immune function—such as antiretroviral therapy for HIV patients or halting immunosuppressive medications. However, the increasing prevalence of PML is driving demand for targeted and effective therapies, prompting further research and development (R&D) initiatives.
PML Market OutlookThe outlook for the PML market highlights a pressing need for innovative therapeutic strategies due to the grim prognosis associated with the disease. Companies and research institutions are prioritizing early diagnosis and personalized treatment plans to enhance patient outcomes. With PML being closely tied to biologic therapies, especially monoclonal antibodies (e.g., natalizumab for multiple sclerosis), regulatory agencies are paying closer attention to drug safety profiles, impacting the PML market landscape.
Explore the latest developments, pipeline therapies, and key market drivers influencing the PML market.
The global PML market is bolstered by an increasing number of immunocompromised patients resulting from conditions like HIV/AIDS, organ transplants, and autoimmune diseases. Additionally, the higher incidence of PML among multiple sclerosis patients receiving disease-modifying therapies underscores the urgent need for safer, more effective treatment options.
Current Market Insights and Pipeline DevelopmentsCurrent insights into the PML market reveal a limited range of treatment options that primarily target immune restoration. However, ongoing research is exploring new treatment modalities, including antiviral therapies, immune-modulating agents, and targeted biologics. Numerous companies are working to develop drugs that specifically target JC virus reactivation or enhance the immune response against the virus, offering hope to patients affected by this devastating condition.
Prominent players in the PML market are focusing on drug candidates designed to mitigate neurological damage associated with PML. Research is also aimed at improving early detection methods, as timely diagnosis is crucial for better treatment outcomes. Increased collaboration between pharmaceutical companies and academic institutions is expected to accelerate advancements in the PML market.
PML Market ForecastThe forecast for the PML market is promising, with expectations of a compound annual growth rate (CAGR) in the coming decade. Key drivers of this growth include:
Rising Prevalence of Immunocompromised Patients: The growing global incidence of HIV/AIDS, chemotherapy-related cancer patients, and individuals on long-term immunosuppressive therapies contribute to a larger population at risk for PML.
Advancements in Diagnostic Technologies: Innovations in imaging techniques, molecular diagnostics, and JC virus testing are enhancing detection capabilities for PML, allowing for earlier interventions that may slow disease progression and drive market growth.
Pipeline Developments and Novel Therapeutics: The emergence of new drugs and treatments targeting JC virus reactivation and immune dysregulation is pivotal for expanding the PML market. Ongoing clinical trials and pipeline products aimed at preventing or treating PML are anticipated to improve survival rates and quality of life for patients.
Strategic Collaborations: Partnerships between pharmaceutical companies and academic institutions are facilitating the rapid development of innovative therapies, which will likely lead to the commercialization of advanced treatments and further drive market expansion.
According to industry experts, the PML market forecast suggests substantial growth due to these factors, attracting attention from major pharmaceutical companies looking to address the unmet needs of this critical condition.
Challenges and Opportunities in the MarketDespite the positive developments within the PML market, challenges persist, including a limited understanding of JC virus reactivation mechanisms, a lack of curative therapies, and difficulties in managing PML in patients already facing other health issues.
Nevertheless, opportunities for growth abound. Increased awareness of PML risks among patients receiving immunosuppressive therapies is prompting more rigorous monitoring and early intervention strategies. Additionally, the shift towards personalized medicine is generating demand for therapies tailored to individual patient profiles, further enhancing the prospects of the PML market.
Conclusion: A Promising Horizon for the PML MarketIn summary, the PML market is evolving, driven by technological advancements, heightened awareness, and a focus on patient-centric treatment approaches. The outlook for the PML market indicates a future marked by improved diagnostics, innovative therapies, and enhanced patient outcomes.
The forecast for the PML market suggests robust growth, with key players diligently working to develop novel therapies to meet the unmet needs of PML patients. As the healthcare landscape shifts, the focus on rare diseases like PML is expected to increase, providing new hope for affected individuals and presenting meaningful opportunities for pharmaceutical companies to make a significant impact in this crucial area of neurology.
#PML#PML Market#PML Forecast#PML Companies#PML Drugs#PML Therapies#PML Epidemiology#PML Pipeline#PML Market Size#PML Market Trends
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Anvisa alerta sobre lotes falsificados de dois medicamentos
Tysabri é indicado para esclerose e Ozempic, para diabetes tipo 2 A Agência Nacional de Vigilância Sanitária (Anvisa) publicou, nesta sexta-feira (3), em seu site, um alerta aos profissionais de saúde e à população sobre lotes falsificados de dois medicamentos: Tysabri® (que contém a substância ativa natalizumabe), indicado para tratamento de formas mais ativas de esclerose múltipla, e…
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Anvisa alerta sobre lotes falsificados de dois medicamentos
A Agência Nacional de Vigilância Sanitária (Anvisa) publicou, nesta sexta-feira (3), em seu site, um alerta aos profissionais de saúde e à população sobre lotes falsificados de dois medicamentos: Tysabri® (que contém a substância ativa natalizumabe), indicado para tratamento de formas mais ativas de esclerose múltipla, e Ozempic® (o princípio ativo semaglutida), para tratar, em conjunto com dieta…
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Anvisa emite alerta sobre medicamentos Tysabri e Ozempic falsificados; veja os lotes
A Anvisa (Agência Nacional de Vigilância Sanitária) emitiu um alerta nesta sexta (3) a respeito da circulação de lotes falsificados do Tysabri (natalizumabe), para tratamento de esclerose múltipla, e Ozempic (semaglutida), indicado a adultos com diabetes tipo 2 -este último noticiado pela Folha em 25 de outubro. Leia mais (11/03/2023 – 16h33) Artigo Folha de S.Paulo – Equilíbrio e Saúde –…
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PROMISING THERAPIES AND POTENTIAL CURES FOR MULTIPLE SCLEROSIS
Multiple sclerosis (MS) is a chronic autoimmune disease that affects the central nervous system, specifically the brain and spinal cord. It is characterized by the immune system attacking the protective covering of nerve fibers, known as myelin, leading to inflammation, demyelination (loss of myelin), and a range of neurological symptoms. While there is currently no known cure for MS, there are several promising therapies and potential treatments that aim to manage symptoms, slow disease progression, and improve the quality of life for individuals with MS.
Disease-Modifying Therapies (DMTs): These treatments are designed to modify the course of the disease by reducing the frequency and severity of relapses, slowing down disability progression, and delaying the accumulation of new lesions in the brain and spinal cord. There are several classes of DMTs, including interferons, glatiramer acetate, oral immunomodulators, and monoclonal antibodies. Some examples of DMTs include:
Interferons: These are proteins that help regulate the immune system. They can reduce inflammation and the frequency of relapses. Examples include interferon beta-1a and interferon beta-1b.
Glatiramer Acetate: This is a synthetic protein that mimics myelin basic protein, helping to divert the immune system's attack away from the actual myelin.
Oral Immunomodulators: Drugs like fingolimod, siponimod, and teriflunomide modulate immune responses and reduce inflammation. They are taken orally.
Monoclonal Antibodies: Medications like ocrelizumab, alemtuzumab, and natalizumab target specific immune cells or molecules involved in the disease process.
Stem Cell Therapy: Stem cell transplantation involves replacing the immune system with healthy stem cells derived from the patient's own bone marrow or from a donor. This treatment aims to "reset" the immune system and halt the autoimmune attack on myelin. Autologous hematopoietic stem cell transplantation (aHSCT) has shown promising results in clinical trials for aggressive forms of relapsing-remitting MS.
B-cell Depletion: B cells are a type of immune cell that plays a role in the autoimmune response in MS. Monoclonal antibodies targeting CD20-positive B cells, such as ocrelizumab and rituximab, have been shown to reduce relapse rates and disability progression.
Neuroprotection and Remyelination: Some therapies focus on protecting nerve cells and promoting remyelination to repair damaged myelin. These approaches are still in experimental stages but show potential. Drugs like clemastine and opicinumab are being investigated for their ability to enhance remyelination.
Vitamin D Supplementation: There is evidence suggesting that vitamin D deficiency might play a role in MS development and progression. Some studies have shown that maintaining adequate levels of vitamin D through supplementation could have a positive impact on disease activity.
Anti-Inflammatory and Immunosuppressive Therapies: These treatments aim to control the immune response and reduce inflammation. Drugs like corticosteroids are often used to manage acute relapses and reduce inflammation in the central nervous system.
Myelin Repair Therapies: Researchers are exploring strategies to stimulate the repair and regrowth of damaged myelin. This includes promoting the differentiation of oligodendrocyte precursor cells into mature myelin-producing cells.
Personalized Medicine: With advancements in genetics and understanding of individual disease characteristics, personalized treatment plans are becoming more common. Tailoring therapies to the patient's specific disease profile could lead to better outcomes.
Mr. Jayesh Saini notes that, “The effectiveness of these therapies can vary from person to person, and treatment decisions should be made in consultation with a qualified healthcare provider. While significant progress has been made in the field of MS treatment, ongoing research is essential to continue improving therapies and potentially finding a cure in the future.”
#jayeshsaini #healthcare #LifeCareHospitals #Kenya #NHIF #NPS #TSC
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PROMISING THERAPIES AND POTENTIAL CURES FOR MULTIPLE SCLEROSIS
Multiple sclerosis (MS) is a chronic autoimmune disease that affects the central nervous system,
specifically the brain and spinal cord. It is characterized by the immune system attacking the
protective covering of nerve fibers, known as myelin, leading to inflammation, demyelination
(loss of myelin), and a range of neurological symptoms. While there is currently no known cure
for MS, there are several promising therapies and potential treatments that aim to manage
symptoms, slow disease progression, and improve the quality of life for individuals with MS.
Disease-Modifying Therapies (DMTs): These treatments are designed to modify the course of
the disease by reducing the frequency and severity of relapses, slowing down disability
progression, and delaying the accumulation of new lesions in the brain and spinal cord. There are
several classes of DMTs, including interferons, glatiramer acetate, oral immunomodulators, and
monoclonal antibodies. Some examples of DMTs include:
• Interferons: These are proteins that help regulate the immune system. They can reduce
inflammation and the frequency of relapses. Examples include interferon beta-1a and
interferon beta-1b.
• Glatiramer Acetate: This is a synthetic protein that mimics myelin basic protein, helping
to divert the immune system's attack away from the actual myelin.
• Oral Immunomodulators: Drugs like fingolimod, siponimod, and teriflunomide modulate
immune responses and reduce inflammation. They are taken orally.
• Monoclonal Antibodies: Medications like ocrelizumab, alemtuzumab, and natalizumab
target specific immune cells or molecules involved in the disease process.
Stem Cell Therapy: Stem cell transplantation involves replacing the immune system with healthy
stem cells derived from the patient's own bone marrow or from a donor. This treatment aims to
"reset" the immune system and halt the autoimmune attack on myelin. Autologous
hematopoietic stem cell transplantation (aHSCT) has shown promising results in clinical trials for
aggressive forms of relapsing-remitting MS.
B-cell Depletion: B cells are a type of immune cell that plays a role in the autoimmune response
in MS. Monoclonal antibodies targeting CD20-positive B cells, such as ocrelizumab and rituximab,
have been shown to reduce relapse rates and disability progression.
Neuroprotection and Remyelination: Some therapies focus on protecting nerve cells and
promoting remyelination to repair damaged myelin. These approaches are still in experimental
stages but show potential. Drugs like clemastine and opicinumab are being investigated for their
ability to enhance remyelination.
Vitamin D Supplementation: There is evidence suggesting that vitamin D deficiency might play a
role in MS development and progression. Some studies have shown that maintaining adequate
levels of vitamin D through supplementation could have a positive impact on disease activity.
Anti-Inflammatory and Immunosuppressive Therapies: These treatments aim to control the
immune response and reduce inflammation. Drugs like corticosteroids are often used to manage
acute relapses and reduce inflammation in the central nervous system.
Myelin Repair Therapies: Researchers are exploring strategies to stimulate the repair and
regrowth of damaged myelin. This includes promoting the differentiation of oligodendrocyte
precursor cells into mature myelin-producing cells.
Personalized Medicine: With advancements in genetics and understanding of individual disease
characteristics, personalized treatment plans are becoming more common. Tailoring therapies
to the patient's specific disease profile could lead to better outcomes.
Mr. Jayesh Saini notesthat, “The effectiveness of these therapies can vary from person to person,
and treatment decisions should be made in consultation with a qualified healthcare provider.
While significant progress has been made in the field of MS treatment, ongoing research is
essential to continue improving therapies and potentially finding a cure in the future.”
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Genetic Test Can Predict Predisposition to Drug-Induced Brain Infection PML
MedicalResearch.com Interview with:
Dr. Hatchwell Dr. Eli Hatchwell, MA MB BChir (Cantab) DPhil (Oxon) BA (OU) Chief Scientific Officer Population Bio UK, Inc. Begbroke Science Park Begbroke Hill Begbroke, Oxfordshire United Kingdom MedicalResearch.com: What is the background for this study? Response: Progressive Multifocal Leukoencephalopathy (PML) is a devastating condition that is associated with a number of clinical situations, including treatment with a variety of drugs. Of these, the best known is natalizumab (Tysabri), which is a very successful drug in the treatment of MS (multiple sclerosis). Only a small proportion of patients treated with natalizumab develop PML and this has always been a mystery. The study was based on a hypothesis that some individuals have an underlying susceptibility to developing PML, based on the presence of variants in genes that are important in the immune system. The study identified several of these variants. MedicalResearch.com: Where is the polyomavirus 2 found? Response: The polyoma 2 virus (aka JCV) has an estimated worldwide prevalence of 40–70%. More recent studies in Asian populations showed even higher rates, ranging from 70- 80%. In the body, the virus is found particularly in the kidneys in a dormant state but in PML, it is found at high levels in the brain. MedicalResearch.com: What are the main findings? Response: The study describes four variants that may account for 11% of drug-induced PML. Individuals with one or more of these variants are predicted to be at significantly higher risk of Progressive Multifocal Leukoencephalopathy compared to those who test negative. These variants are in genes with known roles in not only the immune system but also viral defense. MedicalResearch.com: What should readers take away from your report? Response: For the first time, a specific test is available that predicts an individual’s risk of Progressive Multifocal Leukoencephalopathy. The test should be implemented clinically to inform physicians and their patients of their individual risk for PML. Those who test positive are advised to avoid drugs with especially high risks of PML (in particular, Tysabri). MedicalResearch.com: What recommendations do you have for future research as a results of this study? Response: The insights gleaned from this study pave the way for future studies to expand the number of genes/variants that are implicated in Progressive Multifocal Leukoencephalopathy risk. Further, some of the insights may suggest interventions that will help treat PML. We view our study as a demonstration of the power of precision medicine in relation to drug adverse events. Disclosures: I am Chief Scientific Officer and co-founder of Population Bio. Citation: Progressive Multifocal Leukoencephalopathy Genetic Risk Variants for Pharmacovigilance Immunosuppressant Therapies Link to article: https://www.frontiersin.org/articles/10.3389/fneur.2022.1016377/full doi: 10.3389/fneur.2022.1016377 The information on MedicalResearch.com is provided for educational purposes only, and is in no way intended to diagnose, cure, or treat any medical or other condition. Always seek the advice of your physician or other qualified health and ask your doctor any questions you may have regarding a medical condition. In addition to all other limitations and disclaimers in this agreement, service provider and its third party providers disclaim any liability or loss in connection with the content provided on this website. Read the full article
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⭐️⭐️⭐️🔅🔅
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Do you look at yourself in the mirror regularly? I tend not to. 📸 Do you like taking selfies and splashing them over the soc-med? 🙋🏼♂️💁🏼♂️🙆🏼♂️🙅🏼♂️🤷🏼♂️🤦🏼♂️🙍🏼♂️🙎🏼♂️🧘🏼♂️⛷️🤸🤺🧙🐑🍧🍱🍹👫💏 I dont. I don't like being in pictures. This picture (all pictures actually) make me feel uncomfortable. But I took it to #BeUncomfortable And I'm on unlimited data 😜 I'm Feeling a bit tired today. I've been Teaching 6 days a week, plus all the other stuff, for a long time. Most of the time I am (have been) fine. Not a problem. But I'm noticing it a bit more; being tired. It is also week 3 in the Treatment cycle -next Wednesday is #tysabri time. So i will feel a bit more lively then 👊🏃 Now this isn't to have a moan or complain like 'oh my life is so bad' or 'feel sorry for me' to hell with that self-pitiest Pish! What I want is to train more. 💪🥋 I could run more because I don't need anyone for that. But #martialarts training I do (it's the way I am #lazybastard) There's isn't anyone close-by that is any good. That could push me. That could motivate me to try hard. . . . . . #autoimmunedisorder #autoimmunedisease #multiplesclerosis #ms #taekwondo #itf #taekwondotraining #itfinstructor #martialartsinstructor #kickmyass #tysabri #natalizumab #motivational #motivateme #autoimmunication #mswarrior #ihaterunning #redrunningshoes #redrunningshoesdiary #instagram #facebook #twitter #tumblr #hashtag (at Alton, Hampshire) https://www.instagram.com/p/B2HczuQgwX8/?igshid=14z16o6d9sd6q
#beuncomfortable#tysabri#martialarts#lazybastard#autoimmunedisorder#autoimmunedisease#multiplesclerosis#ms#taekwondo#itf#taekwondotraining#itfinstructor#martialartsinstructor#kickmyass#natalizumab#motivational#motivateme#autoimmunication#mswarrior#ihaterunning#redrunningshoes#redrunningshoesdiary#instagram#facebook#twitter#tumblr#hashtag
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3 anos do diagnóstico que me tirou do eixo que eu achava que tinha controle, tudo saiu do lugar e foi um tempo pra acontecer um reencontro com minha essência e aceitar a nova condição, o balancete desse último ano foi positivo, 1 ano sem surtos ( nome dado as crises de Esclerose Múltipla, não são surtos de "loucura"...rs), sem internações...Viva!!! Metade desse êxito provém dos bons especialistas que me acompanham, da medicação que tenho acesso, entretanto a outra metade é do meu esforço diário, terapia em dia, fisioterapia em dia, relações selecionadas, óleos essenciais, momentos só meus e massagens da Pretinha...rs E, assim entendi 'a pegada', que metade do sucesso a responsável SOU EU!!! Ontem fiz o passeio que prometi fazer todo dia 16/07... Sou boa em cumprir promessas, principalmente as que faço pra mim. . #multiplesclerosis #forçag35 #tysabri #natalizumabe #Repost @lilianandrereis ... https://www.instagram.com/p/CRaSeh4gX3c/?utm_medium=tumblr
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AI used to detect brain’s response to multiple sclerosis treatment
Combining artificial intelligence technology with MRI brain scans, researchers are able to detect the brain’s response to Natalizumab treatment for those with relapsing-remitting multiple sclerosis.
#ai#artificial intelligence#deep learning#machine learning#neurotech#neuroscience#science#health#medicine#neurology#multiple sclerosis
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