Recently I was doing scientific analyze of different vaccines, for my own development, being curious about this part of medicine, i was not so much in throughout my career. And found quite interesting things about Pneumococcal infections and vaccines against them. May be it is obvious for professionals and experts in this area, but from the point of view of clinical trials it was interesting to discover (for myself, for sure) the trend. Main struggle against IPDs (invasive pneumococcal diseases) started 20-30 years ago, when pneumococcal polysaccharide conjugate vaccines (PCVs) were developed globally by several pharma companies (first PCVs were made much earlier in 70th like PCV4 but main struggle was started later). First it was quite a few amount of serotypes in PCVs, which was reflected in its numbering - PCV7, PCV13, PCV16 etc. But later closer to current days - several pharma companies already registered vaccines like PCV20, PCV21. Now there are several trials ongoing where the very progressive high-end vaccines are under research - PCV26 and even PCV31. And that is fantastic development. However, I need to say, that generally there are about 100 (!) wild serotypes of Pneumacoccal infections existing in nature. Quite a lot, and we only now meeting the 1/4 of all serotypes numbers in our vaccines. There are a lot of reasons why, reasons what serotypes are included into PVCs and how it goes. But returning back to my own conclusion i got from all that research I was doing, reading many articles, study details and analytical reviews - this is all the race against time! Cause earlier researches found interesting trend - invention of vaccines with higher index (meaning PCV20, PCV30 etc) doesnt lead to win of humanity over IPDs but just partial success, because nature IMMEDIATELY replaces part of the vaccine serotypes (VT) by non-vaccine serotypes (NVT) in the pattern of morbidity globally. Obviously that race against time (human, and their vaccines against nature with her ~100 serotypes) possibly will end when humanity invents smth like "PCV100". But the issue here is in technology: results of the complexity of conjugate vaccine manufacturing, because only a fraction of these are currently included in the pneumococcal polysaccharide conjugate vaccines. In other words - we cannot do "PCV100" now, until we find proper carrier or vector to create that "PCV100". I wish all the researchers and companies success in this area, because this is THE VERY important area of medicine and struggles against disease, which may be fatal in many cases. Especially nowadays, when we have antibiotic resistent strains of bacterias, resistent serotypes and etc. Anyway it is very interesting to follow this topic and see how pharma industry develops. And be inside, doing clinical trials as professional makes me proud, being in the very edge of science and healthcare! #vaccines #virology #pneumococcaldiseases #clinicaltrials #modernapproach #PCV #opentowork
Stanislav Vartanov, MS’ Post
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Adjuvanted vs. Non-Adjuvanted Vaccines: What’s the Difference? 💉🧬 When we talk about flu and COVID-19 vaccines, one scientific detail that often gets overlooked is whether the vaccine contains an adjuvant. 🔹 What is an adjuvant? An adjuvant is a substance added to a vaccine to enhance the immune response. It helps the body “see” the vaccine antigen more clearly, making the response stronger and often longer-lasting. 🔹 Flu Vaccines Adjuvanted flu vaccines (like Fluad) are especially designed for older adults, whose immune systems may not respond as strongly. These vaccines trigger a more robust antibody response. Non-adjuvanted flu vaccines are effective as well but may not provide the same level of immune stimulation in high-risk populations. 🔹 COVID-19 Vaccines Most mRNA vaccines (Pfizer, Moderna) don’t contain traditional adjuvants — the lipid nanoparticles themselves help stimulate immunity. Protein-based vaccines (like Novavax) often use adjuvants (e.g., Matrix-M) to boost immune response. 💡 Why it matters: Adjuvants can improve protection in populations with weaker immune systems (older adults, immunocompromised). They may also reduce the amount of antigen needed per dose, helping scale global vaccine supply. As vaccine science continues to evolve, understanding these differences helps us see why certain vaccines are recommended for specific groups — and why innovation in adjuvants is just as important as innovation in vaccine platforms. https://lnkd.in/g2SYVB4r
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🌟 Advancements in Pertussis Vaccination: Optimizing Cationic Lipid-Based Adjuvants 🌟 I’m thrilled to share highlights from a recent study by Tavonga T. Mandava and colleagues that focuses on the design and evaluation of a novel cationic lipid nanoparticle-based pertussis vaccine. This research is pivotal in addressing the resurgence of pertussis cases globally, especially among vulnerable populations. 🔬 Key Insights: Innovative Approach: The study employed a Design-of-Experiments (DoE) methodology to optimize the lipid composition of a triple adjuvanted vaccine (L-TriAdj), enhancing its physicochemical properties and immunogenicity. Enhanced Immune Response: Results indicated that increasing the alkyl chain length of phosphatidylcholine lipids significantly improved cellular viability, uptake, and the induction of critical cytokines like IL-12 and IFN-γ. Importance of Lipid Composition: The findings underscore that varying the ratio of phosphoethanolamine and phosphatidylcholine lipids influences vaccine performance, with specific formulations leading to robust immune responses. 💡 Conclusion: This research not only provides valuable insights into the formulation of effective pertussis vaccines but also emphasizes the critical role of lipid composition in vaccine efficacy. Moving forward, in vivo studies will be essential to validate the protective capacity of these optimized formulations. Let's continue to innovate and improve our vaccine strategies for better public health outcomes! 💉✨ https://lnkd.in/eX9j-q_N #Vaccines #Immunology #CationicLipids #Pertussis #PublicHealth #Pharmaceuticals #Research
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United States Vaccines Market Size, Top 47 Vaccines Brand In-depth Analysis, Insights, and Forecasts to 2033 United States Vaccines Market Size and Trends The United States vaccines market size was valued at USD 29.5 billion in 2024 and is projected to hit around USD 60 billion by 2033, growing at a CAGR of 8.2% during the forecast period 2025 to 2033. United States Vaccine Market Growth Drivers One of the foremost factors influencing the expansion of the vaccine market in the United States is the rising prevalence of infectious diseases. With the emergence of new pathogens and variants, the demand for effective vaccines has surged. Additionally, advancements in biotechnology and genetic research are leading to the development of more effective and targeted vaccine formulations. Another critical catalyst is the robust investment in vaccine research and development. Government agencies and private organizations alike are funneling funds into vaccine projects, accelerating the pace of innovation. Moreover, regulatory support and streamlined approval processes have encouraged manufacturers to bring new vaccines to market more quickly. More Details @ https://lnkd.in/dTfaMzEP #vaccine #covid #coronavirus #vaccination #health #vaccines #pandemic #corona #trump #pfizer #lockdown #covidvaccine #healthcare #news #freedom #medicine #virus #moderna #science #flu #covidvacccine #india #influenza #memes #vaccineswork #doctor #staysafe #vaccinated #immunization #vaksin
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📢 Differences in immunogenicity to the recombinant zoster vaccine in IMID patients undergoing treatment with non-selective or selective JAK inhibitors 💬 In this study, we compared humoral and cellular responses to the recombinant herpes zoster vaccine (Shingrix™) across IMID patients receiving different immunosuppressive therapies. 🔹 JAK inhibitor–treated patients showed significantly reduced seroconversion and impaired CD4⁺ and CD8⁺ T-cell responses compared with those on anti-TNF or methotrexate. 🔹 Non-selective JAK-i (baricitinib, tofacitinib) were associated with the lowest responses, while selective JAK1-i (upadacitinib) performed comparatively better. 🔹 Anti-TNF/MTX patients retained more preserved vaccine-induced immunity. These findings underscore the impact of JAK pathway inhibition on vaccine immunogenicity and the importance of personalized vaccination strategies in immunosuppressed IMID populations. 📄 https://lnkd.in/dExcnuxS #Rheumatology #Vaccines #JAKinhibitors #IMIDs #SSc #SLE #RA #TranslationalImmunology #Shingrix #Autoimmunity
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A new industry article examines GeoVax's multi-antigen COVID-19 vaccine approach and its potential as a "game changer" for immunocompromised populations. The article highlights how GEO-CM04S1's dual-targeting of both spike and nucleocapsid proteins generated robust antibody and durable T-cell responses in patients who typically show subpar responses to single-antigen vaccines. Key findings discussed include Phase 2 data where GEO-CM04S1 outperformed an mRNA comparator in CLL patients, leading to the mRNA arm being halted for insufficient immunogenicity. The article also notes the broader industry shift away from single-antigen approaches, with federal health officials citing the need for longer-lasting and broader protection. Read the full article: https://lnkd.in/guZcVAAc #Vaccines #Immunology #Biotech
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Cavity Vaccine Update: Inside the Science, Safety Concerns, and Why It’s Still Not Ready for Your Patients Yet https://lnkd.in/gHyK7g3H There’s been a lot of interest in the idea of a cavity vaccine, one that targets the key player in caries, Streptococcus mutans, and two recent reviews give a clear status check. The first, “Dental caries vaccine: are we there yet?” (Patel, 2020) reports that research over the past 40 years has identified major virulence factors of S. mutans (Ag I/II adherence antigen, glucosyltransferases, glucan-binding proteins) that provoke antigen-specific immune responses. Animal studies have shown promising vaccines (e.g., recombinant multigenic DNA or mucosal delivery routes) and adjuvants, but the key takeaway is: despite decades of lab work, no vaccine is yet commercially available for human caries prevention. The author emphasizes the need for multicentre human clinical trials, safety and delivery system issues, and funding momentum. The second, “Developing a Vaccine for Dental Caries / Cavities” (Dental Didactics CE, 2022) complements this by describing the types of vaccine strategies attempted: whole-cell, subunit, synthetic peptides, and both active and passive immunisation. Notably, they highlight a major safety concern: antibodies raised against S. mutans in early trials showed reactivity with human heart and skeletal muscle tissues, a red flag for human application. They note that while animal data are strong, caries is not often considered a life-threatening disease and thus it has not attracted the same public-health funding priority as other vaccines. The science behind a caries vaccine is mature in the pre-clinical stage, we know targets, mechanisms, and delivery routes. But translation to safe, effective human use is not yet achieved. Until a human vaccine clears safety, efficacy and regulatory hurdles, prevention will continue to rely on fluoride, sealants, biofilm control, diet and risk-management. Dental caries vaccine: are we there yet? PubMed https://lnkd.in/gdVG2z4j Developing a Vaccine for Dental Caries / Cavities - Dental Didactics CE https://lnkd.in/gu227ZYi
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💡 Don’t miss this comprehensive review by Christian Marx and his co-workers, in collaboration with Thomas Schirrmann, on the crucial role of antibodies in effective pandemic preparedness and response.
The COVID-19 pandemic taught us a painful lesson: Vaccines alone are not enough! Until vaccines are widely available and used, our population remains vulnerable — and healthcare systems face immense pressure. During COVID-19 we already made progress in developing antibodies faster than ever, for example #YUMAB and #CORAT together with partners needed only 11 months from discovery to clinic, but that is still not fast enough. Together with Christian Marx and co-authors, we recently outline how neutralizing monoclonal antibodies play a crucial role in future pandemic response — for immediate protection and prophylaxis as well as for treatment, and even at later stages for people who cannot benefit from vaccination or for those who just do not want to get vaccinated for whatever reason. Our key message: Pandemic preparedness needs more than vaccines, it needs additional options for prophylaxis and treatment. We outline strategies, how to embed neutralizing antibodies into a larger concept including pre-development and stockpiling antibody candidates, building flexible manufacturing capacities, and fostering global collaboration to ensure rapid access when it’s needed most. Find our comprehensive review available online in mAbs here: https://lnkd.in/edDgB3np What lessons from COVID-19 do you think we still haven’t truly implemented? #PandemicPreparedness #Antibodies #PublicHealth #LifeSciences #YUMAB #CORAT
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This article captures an inflection point in vaccine development, the growing recognition that vulnerable populations need more than what first-generation single-antigen vaccines can provide. GeoVax Labs, Inc.’s GEO-CM04S1 data demonstrates that a multi-antigen MVA approach can generate both robust antibody and durable T-cell responses in immunocompromised patients. The Phase 2 results in CLL patients, where our vaccine succeeded while the mRNA comparator was halted, underscore why broader immune engagement matters for these populations. Worth reading for perspective on the evolving vaccine landscape and the shift toward next-generation platforms. Read the article: https://lnkd.in/esniG85d #Vaccines
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Unlocking Spirulina secrets to supercharge vaccines. James Cook University (JCU) researchers have found particles in popular ‘superfood’ Spirulina that could lead to huge advancements in vaccine production and effectiveness. Australia. December 2024 Excerpt: The research paper, led by Dr Farouq Sharifpour, DVM, PhD from JCU’s Australian Institute of Tropical Health & Medicine (AITHM), investigates Spirulina extracellular vesicles (SPEV) and their potential therapeutic benefits. While safely testing on mice, Dr Sharifpour and his team found that SPEV has huge potential as a new class of vaccine adjuvant (substances added to vaccines to make them more effective). Refer to the enclosed announcement to obtain additional information and to access the link to published research in Journal of Extracellular Biology 12 December 2024. https://lnkd.in/eSM9Mauw
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GeoVax Labs has presented compelling interim results for its multi-antigen COVID-19 vaccine, GEO-CM04S1, at the World Vaccine Congress Europe 2025, highlighting significant advancements for immunocompromised populations. Researchers demonstrated that the vaccine elicits strong T-cell responses to both Spike and Nucleocapsid antigens, potentially exceeding current mRNA booster performance. The Phase 2 trial focused on patients with hematologic malignancies showed a favorable safety profile with only mild-to-moderate adverse events. Dr. Mark J. Newman, Chief Scientific Officer, emphasized the limitations of existing 'one-size-fits-all' vaccines and presented data suggesting GEO-CM04S1 could provide broader, more durable immunity. The vaccine's unique design aims to address protection gaps for vulnerable patient groups. Interim safety results revealed no serious vaccine-related adverse events, with breakthrough infections remaining mild-to-moderate. These findings underscore the potential of GeoVax's MVA-vectored, multi-antigen approach to enhance COVID-19 vaccine strategies. CEO David Dodd expressed optimism about the vaccine's capacity to protect immunocompromised patients, highlighting the ongoing clinical trials evaluating its effectiveness across different patient populations.
GeoVax Demonstrates Promising COVID-19 Vaccine Potential for Immunocompromised Patients newsramp.com To view or add a comment, sign in
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