Category: Vaccine

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European prosecutors take over Belgian probe into Pfizergate – POLITICO Europe

April 6, 2024

Transparency campaigners and some political opponents have sought to put pressure on the Commission to discuss the case, but von der Leyen has so far avoided addressing it. In a reply to a direct question put to her by POLITICO about missing text messages, von der Leyen said: Everything necessary about that has been said and exchanged. And we will wait for the results.

In 2022, EPPO announced it was looking into the EUs vaccine procurement more generally, but this is the first time that the office has been linked with Pfizergate explicitly.

The case now being looked at by EPPO brings together several different legal, political and financial strands and it intersects with lawsuits that pharmaceutical giant Pfizer brought against Hungary and Poland.

Last year, Baldan, a 36-old Belgian lobbyist who is represented by the same lawyer that represents French vaccine-skeptic group Bon Sens, lodged a criminal complaint in Belgium in connection to von der Leyens role in the vaccine negotiations with Pfizer over what he alleges were acts of "interference in public functions, destruction of SMS, corruption and conflict of interest," according to legal information provided by his lawyer.Bon Sens hasput forward its own legal challenges in connection with Pfizergate.

The addition of European governments to his complaint adds weight to what might otherwise have been seen as a personal crusade. Hungary, led by Viktor Orbn, a steadfast opponent of von der Leyen, also filed a complaint in connection to the Commission presidents role in vaccine negotiations with Pfizer, according to two insiders with knowledge of the case, speaking on condition of anonymity because of its sensitivity.

Poland lodged its own complaint last November, a Polish government spokesperson confirmed. However, following the election of Tusk in December, the new government is working [to] withdraw Poland from these proceedings, the spokesperson said.

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European prosecutors take over Belgian probe into Pfizergate - POLITICO Europe

Polio vaccine shortage looms over India with Sanofi plants’ shutdown – The Economic Times

April 6, 2024

An unprecedented crisis looms over supplies of injectable poliomyelitis vaccine, or IPV - a crucial tool in India's efforts to eradicate polio - as French drugmaker Sanofi has shut down its manufacturing plants in the country, documents reviewed by ET showed. Sanofi - a leading supplier of the vaccine - ceased production of its IPV brand ShanIPV in December 2023, triggering concerns among health experts regarding an imminent supply disruption that may hobble the country's most ambitious immunisation campaign.

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IPV is manufactured by only two companies - Sanofi Pasteur and Serum Institute of India (SII). Pune-based SII started its supplies of the vaccine only in 2021. Sanofi is believed to cater to over 80% of India's IPV dose requirements.

"Having been a long-standing contributor to India's journey to become polio-free, we stay dedicated to supporting India's public health programme for polio eradication in alignment with the authorities." In September 2023, however, Sanofi had announced in a public notice that due to the discontinuation of the manufacturing and marketing, the product may not be available in the market. IPV is an integral part of India's Universal Immunization Programme (UIP) that provides free immunisation to children against 12 preventable diseases including measles, diphtheria, hepatitis B, and tuberculosis. IPV was introduced into UIP in 2015 as part of a global polio endgame strategy.

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"Time is running out to find alternate supply arrangements," a public health expert told ET on the condition of anonymity. "By now, the government should have floated tenders or placed additional orders to Serum. This shows the callousness as it will affect polio surveillance and polio control measures."

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Pune-based SII may need to ramp up its capacity to bridge the demand shortage, experts said. The IPV shots are administered to children at six weeks, 14 weeks and nine months. While oral polio drops are administered at birth and then at 6,10,14 months and 1.5 years. India was the first country to introduce fractional doses in 2016 to dissipate a shortage of IPV.

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Sanofi has made multiple submissions to the union health ministry, cautioning against the impending supply challenges and had sought relaxation of a condition for continuation of such supplies, the documents showed.

However, Sanofi at that time had maintained that supplies of the polio vaccines will remain unimpacted.

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Sanofi has made multiple submissions to the union health ministry, cautioning against the impending supply challenges and had sought relaxation of a condition for continuation of such supplies, the documents showed.

The company had noted that while its product (IPV vaccine) is fully compliant during the term of the tender with a residual shelf-life of less than 18 months, a second condition requires that the manufacturing date of the product does not exceed six months at the time of the supply.

Since ShanIPVs shelf life is 36 months, thus meeting the primary requirement of the tender, we would humbly request you to kindly consider relaxation of the second criteria, that is the product should not be older than six months at the time of supply, the company said in a letter sent in June last year.

It clearly stated that the company would not be able to adhere to the six-month shelf-life clause from May 2024 onwards. Such a relaxation would not in any way impact the clinical profile of the vaccine, it pointed out.

The deadline mentioned in the letter implies that the last date for production of the vaccine was in December 2023.

People aware of the matter said Sanofis vaccine supplies may not be impacted till the end of this month, but any further delay in making an alternate plan could hinder the shelf-life condition of its existing tender agreement.

Sanofi had also volunteered to make a one-time exception of extending half of the total volume of product that exceed six months from the manufacturing date at no extra cost.

As an alternative to ShanIPV, Sanofi is understood to have accelerated the process to seek regulatory approval for Imovax polio, a 10-dose IPV that it sells across the world.

Meanwhile, it is learned that Sanofi may sell its Medchal and Muppireddypally facilities to Gland Pharma, one of the largest generic injectables manufacturers. Gland was picked among two other shortlisted entities Bharat Biotech and SII. This, however, could not be confirmed from Gland Pharma.

Meanwhile, the health ministry is planning to hand over procurement of IPV to its central procurement agency CMSS, which may further delay the procurement of the polio vaccines.

Questions from ET sent to the health ministry remained unanswered.

A senior government official, though, said things are under control. If need be, we will use option clause, which gives the government the right to increase the quantity to be ordered up to 20-30% from the current supplier. In this case it will be Serum Institute of India, he said.

UIP is one of the largest public health drives of the government targeting over 27 million new-borns and 29 million pregnant women annually.

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Polio vaccine shortage looms over India with Sanofi plants' shutdown - The Economic Times

Gritstone ground down by phase 2 cancer vaccine fail, sparking race against cash to gather more data – Fierce Biotech

April 6, 2024

Gritstone bios gamble on a novel endpoint has backfired. The cancer vaccine failed to trigger hoped-for changes in circulating tumor DNA (ctDNA), causing the phase 2 trial to miss its primary endpoint and leaving the biotech clinging to immature survival data.

Investigators randomized 104 patients with metastatic microsatellite stable colorectal cancer to take one of two front-line therapies. All patients received induction and maintenance chemotherapy. Around half of the subjects also received Gritstones personalized neoantigen cancer vaccine, Bristol Myers Squibbs Yervoy and Roches Tecentriq during the maintenance phase.

The primary endpoint looked at changes in ctDNA. On that measure, Gritstones drug combination was numerically worse than chemotherapy alone, with the molecular responses in the vaccine and control arms coming in at 30% and 41.7%, respectively. Gritstone attributed the result to its misunderstanding of how ctDNA would change after treatment.

With regard to defining molecular response, we simply got it wrong, Gritstone CEO Andrew Allen, M.D., Ph.D., said in a statement. CtDNA levels in both arms decreased on chemotherapy for longer than we anticipated, generating similar short-term molecular response rates across arms and rendering our protocol measure of ctDNA change uninformative.

While the study missed its primary endpoint, Allen latched on to progression-free survival (PFS) data to contend that the results are highly encouraging. The PFS rate was higher in the vaccine group than in the control arm after six months and nine months. However, the lines crossed around the 12-month mark, creating a short period in which PFS probability was higher in the control arm.

The hazard ratio favored the vaccine regimen, clocking in at 0.82 in the overall population, but the wide confidence intervals make it impossible to draw firm conclusions. Gritstone reported a hazard ratio of 0.52 in a subgroup of high-risk patients. PFS data are more mature in the subgroup, leading Allen to call the result a striking signal, but, again, the confidence intervals are wide enough that the vaccine may be less effective than the control. Allen had discussed what would be a good PFS result at an event in March.

The separation [of the curves], of course, is likely and important, but the lifting of the tail is what we really care about, Allen said at the time. The CEO cited Bayers Stivarga as an example of a drug that shifted PFS by about two months [and is] not widely used because survival is basically no different.

Gritstone picked ctDNA, rather than the widely used and accepted PFS, as its primary endpoint because of concerns about pseudo progression. The term describes people whose tumors appear to grow after treatment but then shrink. That happens when T cells enter tumors and proliferate. Initially, this causes lesions to grow, but they then collapse as the immune cells wipe out the tumor.

Evidence of pseudo progression made Gritstone a little bit leery about PFS, Allen said, and led it to make ctDNA the primary endpoint. The hope was that ctDNA would provide a clear signal that the therapy is working and make the case for pushing ahead to an overall survival (OS) readout that will provide the truest test of efficacy.

Instead, the study missed the ctDNA endpoint, leaving Gritstone looking to immature PFS results that, at best, show trends favoring the vaccine to make the case for its therapy. The biotech expects to have mature PFS data in the third quarter of 2024, with OS data set to follow in the first half of next year.

The timing of the readouts is important, because Gritstones cash is running low. The biotech ended last year with $79.2 million, a sum it told investors would fund operations into the third quarter of 2024. Gritstone proposed a public offering in the immediate aftermath of the phase 2 data Monday and later priced a $32.5 million sale at $1.65 a share.

Gritstones share price has bounced between a low of $1.14 and high of $3.33 over the past year. The stock fell almost 33% in the wake of the updates Monday, falling to $1.58 in after-hours trading.

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Gritstone ground down by phase 2 cancer vaccine fail, sparking race against cash to gather more data - Fierce Biotech

Maternal RSV F Protein Vaccination Increases Risk of Preterm Birth, Reduces RSV Rates – Physician’s Weekly

April 6, 2024

Photo Credit: Peter Hansen

Study found a decreased risk of any and severe respiratory syncytial virus (RSV) lower respiratory disease in the group that received the vaccine compared to the group that received the placebo, and the vaccinated group had a higher risk of preterm birth than the placebo group.

Evidence Rating Level: 1 (Excellent)

Study Rundown: RSV is a major cause of respiratory tract infections in young children, particularly infants under six months. The virus particularly affects those living in low- and middle-income countries, where interventions are needed. Vaccinations for other viruses have shown to be effective in mothers, thus an RSV vaccine was proposed for maternal use, based on the RSV fusion (F) protein. A phase three trial (RSV MAT-009) was conducted as a double-blind, randomized control trial across 24 countries. The participants were assigned randomly using a 2:1 ratio to receive either one intramuscular injection of 120 g of RSVPreF3-Mat or the placebo. The primary outcomes included any medically assessed RSV-associated lower respiratory tract disease, and any RSV-associated tract disease in infants between birth to six months of age. The sites in low- and middle-income countries were mainly located in the southern hemisphere, whereas the sites in high-income countries were mainly in the northern hemisphere, making it impossible to understand geographic or socioeconomic factors that could have affected the results. Overall, the risk of any severe RSV-associated lower respiratory tract infection was lower in those receiving the RSVPreF3-Mat than in those receiving the placebo; however, the risk of preterm birth was higher in the RSVPreF3-Mat group comparatively.

Click to read the study in NEJM

In-Depth [randomized controlled trial]: Vaccination protecting against RSV during pregnancy may be beneficial for infants, but there has not been enough data on the vaccines safety. Thus, the studys main focus was the safety of infants between birth and 12 months of age and any or severe medically assessed RSV-associated lower respiratory tract infection in infants between birth and six months. Eligible participants included healthy women between the ages of 18 and 49 years of age with a singleton fetus between the gestational age of 24 weeks and 34 weeks with no known fetal abnormalities. In total, 5,328 pregnant women who met the criteria were vaccinated before enrollment and included in the study, along with 5,233 infants. Of these infants, 3426 were placed in the vaccine group and 1,711 in the placebo group. In the vaccinated group, there were 16 cases of RSV-associated lower respiratory tract infections, whereas in the placebo group, there were 24 cases of the disease (vaccine efficacy, 65.5%; 95% credible interval, 37.5 to 82.0). Also, the vaccinated group reported eight severe, medically assessed RSV-associated lower respiratory infections, while the placebo group reported 14 cases (vaccine efficacy, 69.0%; 95% credible interval, 33.0 to 87.6). Preterm birth occurred in 6.8% of infants in the vaccine group but only in 4.9% of infants in the placebo group (relative risk, 1.37; 95% confidence interval [CI], 1.08 to 1.74; P=0.01). In the vaccine group, 0.4% of infants (13 of 3494) died neonatally, whereas, in the placebo group, 0.2% of infants (3 of 1739) died neonatally (relative risk, 2.16; 95% CI, 0.62 to 7.56; p=0.23). Overall, the group who received RVPreF3-Mat had lower risks of any RSV-associated lower respiratory tract disease and severe RSV-associated lower respiratory tract disease when compared to the placebo group.

2024 2 Minute Medicine, Inc. All rights reserved. No works may be reproduced without expressed written consent from 2 Minute Medicine, Inc. Inquire about licensing here. No article should be construed as medical advice and is not intended as such by the authors or by 2 Minute Medicine, Inc.

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Maternal RSV F Protein Vaccination Increases Risk of Preterm Birth, Reduces RSV Rates - Physician's Weekly

Protecting Babies Against RSV Is Still Too Hard – The Atlantic

March 31, 2024

When a new RSV vaccine for pregnant people arrived last fall, Sarah Turner, a family-medicine physician at Lutheran Hospital, in Indiana, couldnt help but expect some pushback. At most, about half of her eligible pregnant patients opt to get a flu vaccine, she told me, and very few agree to the COVID shot.

But to Turners surprise, patients clamored for the RSV shotsome opting in even more eagerly than they did for Tdap, which protects newborns against pertussis and had previously been her easiest sell. For once, expectant parents were the ones starting conversations about immunizations.

Each year in the U.S., respiratory syncytial virus hospitalizes an estimated 58,000 to 80,000 kids under the age of 5; the risks are highest for infants, for whom the virus is enemy No. 1, says Sallie Permar, an immunologist and pediatrician in chief at NewYork-Presbyterian/Weill Cornell Medical Center. But this past season marked the first time that the U.S. had two tools that could substantially shrink that toll: a vaccine for pregnant people, who can then pass antibodies to their child, and a monoclonal antibody, known as nirsevimab, that is given directly to infants. Their arrival feels akin to the end of polio, Anne-Marie Rick, a pediatrician and clinical researcher at Childrens Hospital of Pittsburgh, told me: With both shots in widespread use, the risks of winter illness could forever look different for the youngest Americans.

But some experts worry that these powerful shots are being squandered. The CDCs seasonal recommendations governing their use may simply be too strict, Permar told me. In keeping with those guidelines, many practices stopped giving the maternal vaccine at the end of January; the main window for administering the monoclonal antibody is expected to close at the end of this week. The next eligibility windows wont open for months. The U.S has two brand-new shots that protect extraordinarily well against a deadly respiratory virusand that people actually want to takeand it is holding them back.

The guiding principle behind the CDCs recommendations has logic to it. RSV is a seasonal virus, and both injections are thought to offer protection for about six months. For the maternal vaccine, which is administered between 32 and 36 weeks of pregnancy, the clock on the babys protection starts after birth. So if a pregnant person gets the vaccine in Juneoutside of the CDCs recommended windowand has their baby in July, their child may be vulnerable again come February, before RSV season typically ends. In theory, spring and summer infants might be better protected by getting nirsevimab starting in October, when RSV usually arrives. Current guidelines also require a choice between the two options: Most infants that benefit from maternal vaccination are not eligible to also receive nirsevimab.

Read: The worst pediatric-care crisis in decades

This past season, though, nirsevimab was in severely short supplyin large part because drug companies seem to have underestimated demand, William J. Muller, a pediatric-infectious-disease expert at Northwestern who helped trial the monoclonal antibody, told me. Many hospital systems also balked at the cost of the new drug, which is pricier than the maternal vaccine, wasnt yet bundled into the expense of delivering infants, and wasnt consistently covered by insurance. The shortfalls became so dire that Sanofi, nirsevimabs manufacturer, stopped taking new orders for certain doses of the monoclonal antibody as early as October. The CDC issued a health alert, calling on providers to restrict administration of those doses to only the highest-risk infants. In our hospital system, we had some for the NICU babies, and that was literally it, Turner, of Lutheran Hospital, told me.

Nirsevimab should be more available this year: Spokespeople from AstraZeneca and Sanofi told me that the companies are confident we will meet the global demand for the antibody in 2024. But last year set quite a low bar. And when the window for administration opens in Octoberpotentially already coinciding with RSVs risesupplies could go fast, as parents who havent been able to get shots for themselves or their babies rush to catch up, Grace Lee, a pediatrician at Stanford, who advised the CDC on its RSV guidance, told me. (The CDC did not respond to a request for comment.) Opening the administration window earlier for either the vaccine or the monoclonal antibody could ease that burden: The U.S. starts immunizing people against the flu well ahead of the seasons start, Lee said, because its just not feasible to vaccinate the entire U.S. population in a week.

For several years, too, RSV has been on the move, Permar told me, thanks in large part to pandemic mitigations. The virus was virtually absent in 2020, only to come roaring back for a bizarrely early season that began during the summer of 2021 and had mostly concluded by the end of January 2022. In the past two seasons, the virus has also arrived somewhat early, starting with a September rise. If that pattern holds, waiting until September to vaccinate pregnant people or until October to immunize infants might leave many newborns more vulnerable than they need to be for weeks or months.

Many experts do anticipate that RSVs pattern will quickly settle back to its norm. Over the decades, its consistency has been remarkable, says Sarah Long, a pediatrician at Drexel University who advised the CDC on its guidelines for both new RSV interventions. But even in more predictable years, RSV transmission varies across regionssometimes kick-starting during the summer in the South and lingering until spring further north. The recommendations cant be a one-size-fits-all across the U.S., says Shabir Madhi, a vaccinologist at the University of the Witwatersrand, in South Africa, who helped lead clinical trials of the maternal vaccine. These are judgment calls: France opens its nirsevimab window earlier than the U.S.; Belgium will allow some pregnant people to receive a vaccine as early as the spring. The U.K. is weighing whether to offer both injections at any time of year.

One argument for the current seasonal window is that giving a vaccine or a monoclonal antibody injection too early might mean recipients miss out on protection at the end of the season, Karen Acker, a pediatrician at Weill Cornell, told me. But Permar and others are hopeful that the effects of the new RSV interventions might last longer than five or six months, which is about when clinical trials stopped directly testing their effects. Early data for nirsevimab, for instance, suggests that a little bit of protection may even trickle into subsequent seasons, Muller told me.

Read: Falls vaccination routine didnt have to be this hard

RSV is also of greatest threat to children within the first few months of life, when their respiratory tracts are still tiny and developing. Given the choice between offering the maternal vaccine a little earlywhich could leave an older infant a bit more vulnerable at the seasons endand waiting to administer nirsevimab to a young infant after RSV season has started, the former might actually be the safer strategy. Plus, summer babies who dont get nirsevimab at the hospital are less likely to get it later, especially if their parents arent regularly taking them to see a pediatrician. Giving a shot on the early side is better than never giving one all, Joshua Salomon, a health-policy researcher at Stanford, told me.

In theory, the CDCs guidelines do make room for adjustments in administration windows, in accordance with local RSV trends. But those decisions can be difficult to execute when providers have to place orders ahead of time and store vials in limited space. So far, many doctors offices and hospitals have stuck to the months outlined by the CDC guidance. The cutoff dates have been taken very dogmatically, Rick told me. At the start of the past season, infants just one day over the recommended dosing age of eight months or younger were denied nirsevimab, Turner told me. Then, a lot of providers simply stopped offering the maternal vaccine after January 31, or simply ran out.

When both the need and the enthusiasm for a vaccine or drug is strong, taking every opportunity for protection makes sense. Several experts I talked with supported wider windows; Permar thinks the U.S. should even consider offering the maternal vaccine year-round. To her mind, restrictions regarding both seasonality and gestational age too strongly limit the chances that a baby will be protected. Some providers also noted that, given all the uncertainties, they would recommend the maternal vaccine as primary defense, leaving nirsevimab as the backupsimply because the vaccine can be delivered first. A maternal shot can set babies up with protection from the moment of birth, a sort of insurance policy that can guard against nirsevimab supply or delivery issues. A wider window of vaccine eligibility might not be a perfect solution. But it could get more infants protected when they most need itputting to best use a shot that people are actually willing to get.

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Protecting Babies Against RSV Is Still Too Hard - The Atlantic

Opinion | 10 common concerns about vaccines and how to respond to them – The Washington Post

March 31, 2024

Youre reading The Checkup With Dr. Wen, a newsletter on how to navigate covid-19 and other public health challenges. Click here to get the full newsletter in your inbox, including answers to reader questions and a summary of new scientific research.

This week, I wrote about anti-vaccine messages in political discourse, prompting many readers to ask how they should respond if a family member or friend expresses skepticism toward routine childhood immunizations.

I spoke with Sean OLeary, a specialist of pediatric infectious diseases and a professor at the University of Colorado, whose expertise is vaccines and vaccine communication. He told me that when he has conversations with parents who are hesitant about immunizations, he keeps in mind that they are just trying to figure out what is best for their kids.

A similar approach could help people who arent medical professionals who want to help loved ones. Heres how to respond to 10 common vaccine concerns.

I dont need to vaccinate my kids because the chance of contracting the disease is so low.

As OLeary explained, The chance of getting the disease is so low because we vaccinate. Many diseases have been eliminated because of vaccinations, but this wont last if population immunity goes down. Not vaccinating could put your child and others around them at risk.

Natural immunity is better than immunity from vaccination.

This is just simply incorrect, OLeary said, because the diseases themselves are so severe and the vaccines are incredibly safe.

He shares with parents that when he began training in the late 90s, he treated many kids who had to be hospitalized for rotavirus, a then-common gastrointestinal ailment. Most were fine after hydration, but some children died from it. Since the rotavirus vaccine was widely adopted, he hardly ever sees kids hospitalized with this disease. Another vaccine introduced in recent decades is the pneumococcal conjugate vaccine, which has substantially decreased rates of pneumonia and meningitis in kids.

Vaccines dont go through the rigorous testing of other medicines.

This is wrong. In fact, vaccines are held to a much higher safety standard than other medicines because they are used to prevent rather than treat disease.

When we treat diseases, well tolerate some side effects, OLeary told me. Someone who has heart disease or diabetes will accept some side effects if it helps control their illness. But with vaccines, because they are used in healthy people who do not have the illness, there are even more stringent safety standards.

Vaccines must go through multiple levels of approval by the Food and Drug Administration and Centers for Disease Control and Prevention, and they are also subject to a robust safety surveillance system to detect rare side effects. Routine childhood immunizations have been around for decades, and millions of children in the United States and globally have safely received them.

I dont trust the FDA or CDC.

OLeary, of course, trusts federal health officials, but he recognizes that some people might not. In those cases, he advises them to consult resources such as their local childrens hospital and university or to speak with their pediatrician or family doctor.

I dont trust science.

This is tough, OLeary concedes. One possible approach he suggests is to ask whether they take any medicine or use electronics such as a smartphone.

The phone in your hand is built on decades of science, he said. It doesnt make a lot of sense to treat vaccines differently from other scientific developments.

Vaccines could cause autism.

Thats a very unfortunate example of something that has no basis in science, OLeary told me. That myth has been disproven many, many times, yet it still persists.

With some families, OLeary finds it helpful to go into the details of how the myth started a 1998 paper spearheaded by a man named Andrew Wakefield. But that study was retracted because of serious scientific flaws. Wakefield was subsequently exposed for deliberately perpetuating disinformation for financial gain. Crucially, many other studies have since proved that there is no association between immunizations and autism.

Someone I know has a child who developed [negative consequence].

A personal anecdote that elicits an emotional response can be hard to respond to. The thing we try to point out is that association does not equal causation, OLeary said. Just because something happened after something else doesnt mean it was causative. It can help to bring up again the safety surveillance systems that rigorously evaluates reports of possible associations.

My child had a bad reaction with another vaccine, so Im holding off on more.

Just because your child had a reaction to one vaccine doesnt mean they will have the same to another. OLeary also assures parents that more pronounced side effects such as fever or soreness at the injection site are signs that the immune system is responding appropriately. That means if their child encounters the disease in the future, they will have immunity to it.

Im not saying no to vaccines forever, just delaying them until my child is older and more robust.

Most diseases that we vaccinate for are most severe for the youngest children. Thats why the vaccine schedule starts in infancy. By waiting, OLeary tells parents, you are leaving your children at risk for infections at the time of their highest risk.

Vaccines are against my religion.

There really arent organized religions of any size that object to vaccination, OLeary explained. In fact, many urge vaccinations as part of adherents duties to safeguard those around them, especially the most vulnerable.

As loud as some anti-vaccine voices can be, they are a tiny minority. Less than 1 percent of kids in the United States are completely unvaccinated, OLeary said. Of these, a substantial proportion come from families that havent eschewed immunizations but lack access to medical care.

That means the vast majority of parents are choosing to vaccinate their children. Many of those folks feel pretty strongly, and we dont hear from them enough, he said.

OLeary urges those who feel passionate about vaccines to get involved with their local immunization coalition. Other advocacy venues include Voices for Vaccines and Immunize.org. Its not only health-care providers who can share their expertise; everyone can explain why they decided to vaccinate their kids and why vaccines protect us and everyone around us.

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Opinion | 10 common concerns about vaccines and how to respond to them - The Washington Post

Enhanced Melanoma Vaccine Offers Improved Survival for Men – UVA Health Newsroom

March 31, 2024

Craig L. Slingluff Jr., MD, and his team have developed a second-generation melanoma vaccine to treat the dangerous skin cancer.

A second-generation melanoma vaccine developed at UVA Cancer Center improves long-term survival for melanoma patients compared with the first-generation vaccine, new research shows. Interestingly, the benefit of the second-generation vaccine was greater for male patients than female patients. That finding could have important implications for other cancer vaccines, the researchers say.

The vaccine developers, led byCraig L. Slingluff Jr., MD, found that they could enhance the effectiveness of their melanoma vaccine by simultaneously stimulating important immune cells known as helper T cells to recognize melanoma proteins, in addition to stimulating killer T cells against melanoma. This boosted patient survival and helped prevent reoccurrences of the cancer.

The researchers are not sure why the approach was more effective in men, but biologic sex is emerging as an important factor in outcomes of patients with melanoma, in particular with immune therapies. The findings support the importance of understanding how best to benefit women and well as men with effective immunotherapies.

These findings support the promise of this second-generation melanoma vaccine for prolonging survival of patients after surgery for high-risk melanoma, said Slingluff, a surgical oncologist and translational immunologist at UVA Health and the University of Virginia School of Medicine. We hope that we can make this available to patients in addition to other effective immune therapies so that they may have even greater benefit than either treatment alone.

People commonly think of vaccines as something you take to avoid getting sick from viruses. Most cancers do not have a known viral cause, but melanoma vaccines can induce immune responses against human melanoma cells, and Slingluff and others have been working to make them effective for treatment of melanoma. (There are cancers that are caused by viruses, and some vaccines against those viruses have been very effective at preventing cancers they cause for example, there are vaccines against human papillomavirus and hepatitis B).

Slingluffs melanoma vaccine targets a form of skin cancer that kills thousands of Americans every year. In seeking to make the vaccine more effective, he and his team tested two different approaches to stimulating both CD4+ helper T cells and CD8+ killer T cells in patients with high-risk melanoma. More than 160 clinical trial volunteers were given, at random, one of two vaccine preparations of purified peptides to stimulate their helper T cells.

Fifteen years after the last participant was enrolled in the trial, overall survival rates were encouraging with both vaccine approaches, but overall survival was better for those with the second-generation vaccine. Those who benefitted most appeared to be younger men with earlier-stage melanoma. The researchers characterize the benefit as meaningful and durable in a new scientific paper outlining their findings.

We were very excited by these findings and for the promise to improve survival with these vaccines, Slingluff said. Combination of the second-generation vaccine with other immune therapies may further increase the benefit for patients.

The multicenter trials findings suggest that both age and sex may play important roles in determining immune therapy outcomes. That is important information for doctors and researchers developing these treatments, Slingluff says.

The differences in benefit based on age and biologic sex highlight the need to understand reasons for those differences so that we can provide the same benefit for all patients, Slingluff said. We are excited to build on these exciting findings.

Slingluffs pioneering research is part of UVA Cancer Centers ongoing mission to develop new ways to treat cancer and improve patients cancer treatment options. In recognition of those efforts, the National Cancer Center has named UVA Cancer Center one of only 56 comprehensive cancer centers in the country.The designationrecognizes elite cancer centers with the most outstanding patient care and research programs in the nation.

Advancing the field of immunotherapy is also a key pillar of UVAs upcomingPaul and Diane Manning Institute of Biotechnology, now under construction at Fontaine Research Park. The institute is poised to fast track the development of new treatments and cures and transform how healthcare is delivered across the state and beyond.

Slingluff and his team havepublished their findings in the scientific journal Nature Communications. In addition to Slingluff, the multi-institutional team included Emily K. Ninmer, Hong Zhu, Kimberly A. Chianese-Bullock, Margaret von Mehren, Naomi B. Haas, Merrick I. Ross and Lynn T. Dengel.

The research was supported by theNational Cancer Institute, grants R01CA118386 and P30CA044579; gifts from Alice and Bill Goodwin; and the Commonwealth Foundation for Cancer Research.

Slingluff disclosed that he receives licensing fees for patents for peptides used in cancer vaccines; his work has been supported by Celldex, Glaxo-Smith Kline, Merck, 3M and other companies. A full list of the authors disclosures is included in the paper.

To keep up with the latest medical research news from UVA, subscribe to theMaking of Medicineblog.

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Enhanced Melanoma Vaccine Offers Improved Survival for Men - UVA Health Newsroom

Muddy Paws offers free vaccinations, cheap microchips during monthly clinic – KETV Omaha

March 31, 2024

Muddy Paws Second Chance Rescue sponsored a vaccine clinic for dogs and all the shots were free.The rescue offered dog owners free distemper parvo vaccines and free will donation Bordetella shots.It also offered people the chance to get their dogs micro-chipped for only $15, including the registration of the chip for life.Muddy Paws said it provides the records and if you come to the clinic, it's no questions asked."We're really trying to get it out there, especially for the people who can't afford it or if it's the choice of vaccinating their dog or paying their light bill. We want to be here to help them. Giving up your dogs when they're sick is probably the most heartbreaking thing you can do. And if we can help prevent that, to help prevent the spread in the community. Well, absolutely. Keep doing this and running our tushies off," said Heather Reese of Muddy Paws.Muddy Paws said they typically average about 100 dogs every clinic and plan on hosting a clinic every month.Click here for the latest headlines from KETV NewsWatch 7

Muddy Paws Second Chance Rescue sponsored a vaccine clinic for dogs and all the shots were free.

The rescue offered dog owners free distemper parvo vaccines and free will donation Bordetella shots.

It also offered people the chance to get their dogs micro-chipped for only $15, including the registration of the chip for life.

Muddy Paws said it provides the records and if you come to the clinic, it's no questions asked.

"We're really trying to get it out there, especially for the people who can't afford it or if it's the choice of vaccinating their dog or paying their light bill. We want to be here to help them. Giving up your dogs when they're sick is probably the most heartbreaking thing you can do. And if we can help prevent that, to help prevent the spread in the community. Well, absolutely. Keep doing this and running our tushies off," said Heather Reese of Muddy Paws.

Muddy Paws said they typically average about 100 dogs every clinic and plan on hosting a clinic every month.

Click here for the latest headlines from KETV NewsWatch 7

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Muddy Paws offers free vaccinations, cheap microchips during monthly clinic - KETV Omaha

How Close Are Scientists To A New Anti-Tick Vaccine In Uganda? – Forbes

March 31, 2024

Stall experiments at COVAB in 2017.

COVAB/Makerere University

In Uganda, researchers are working towards field trials of a vaccine that aims to use proteins from disease-bearing ticks to protect cattle and reduce pesticide use.

Uganda is estimated to suffer an direct and indirect costs of over$1 billion a year from the impacts of ticks and tick-borne diseases, according to a 2021 review, threatening the countrys dairy sector, the second biggest foreign exchange earner after coffee.

Margaret Saimo-Kahwa, senior Lecturer at the College of Veterinary Medicine, Animal Resources and Biosecurity at Uganda's Makerere University says that diseases from ticks, such as East Coast Fever, Babesiosis, Anaplasmosis and Heartwater cause of high death rates in cattle, leading to higher food insecurity in Africa.

"Im researching the use of recombinant tick gut proteins identified from local ticks in Uganda, as a way of creating an anti-tick vaccine," she says adding that the hope is to protect cattle while reducing the use of acaricides (pesticides).

"The vaccine couldnt have come at a better time, when Uganda is grappling with acaricide resistant ticks, exacerbating tick-borne diseases," Saimo-Kahwa says, adding that today, the only practical preventative solution to East Coast Fever, has been the unconventional "infection and treatment method" developed in the 1970s.

Although anti-tick vaccines have been produced at scale in Australia, Cuba, Mexico, and Latin America for the past two decades, roll-out in sub-Saharan Africa has been hindered by their lack of efficacy against tick strains native to the region.

She explains that the genetic sequences of the tick gut protein variants (Ra92A and Ra85A) were synthesized into a yeast host: Pichia pastoris and the team has already built the technological capacity to produce these proteins and formulate them into a patent-pending candidate vaccine at a newly upgraded production facility.

"Once we mass produce these batches from our specialized vaccine line, we aim to test them in the field to access their immunogenicity, safety and efficacy in large numbers of cattle against all important tick species from the different geographical regions of Uganda," Saimo-Kahwa says, "Once we have achieved this, we will have developed locally in Uganda a conventional anti-tick vaccine ready not just for commercial up-scaling, but one which has cross-species protection against other tick infestations, on top of developing cGMP compliant vaccine production capacity, a first in Uganda and Africa."

R. appendiculatus ticks which are found in Uganda

getty

Saimo-Kahwa grew up in the small Budaka district in eastern Uganda,

After going through the Ugandan school system, she graduated with a bachelor of Veterinary Medicine at Makerere University in Kampala, Uganda and a master's degree in Applied Immunology at Brunel University in London, UK.

"It wasnt until 2005 when I received funding for a sandwich program at Makerere University and Wageningen University, the Netherlands, that I embarked on a PhD at Makerere University with interest in tick proteins with potential for candidate vaccines took shape," Saimo-Kahwa says, adding that during her PhD work, she investigated the potential of tick gut and salivary gland proteins for use in an anti-tick vaccine; and realized that Uganda might be in urgent need of an anti-tick vaccine.

Saimo-Kahwa explains that scientists from the Global South bring knowledge of the local conditions, problems, and solutions to solving a problem inherent to sub-Saharan African landscapes.

"I believe the need for Global South scientists who can solve the regions own health issues has never been more pressing, a fact never more evident than during the COVID-19 pandemic," she says, "I believe many African countries, including Uganda learnt the lessons from that period; Uganda is for instance doubling down on building domestic capacity not just in vaccine development and production, but in science-led national transformation."

Lab-growing culture in 2019.

COVAB, Makerere University

Meanwhile, the hunt for vaccines to a different disease spread by beasts of burden in the Global South is underway.

Amanda Elyssa Ruiz, a PhD student at Brown University in the United States and a Howard Hughes Medical Institute (HHMI) Gilliam Fellow, is looking for potential vaccines to protect against schistosomiasis, a disease that impacts over 250 million people every year, making it the second most socio-economically devastating parasitic disease after malaria.

In countries where schistosomiasis is found, water buffalo are the key labor force for wetland rice agriculture, as well as the main way that humans get infected, so finding a vaccine that protects both would be a big step forward.

"My main project is to identify novel vaccine candidates for schistosomiasis using epidemiologic data alongside immunologic and biochemical approaches," she says, "The Kurtis lab has developed a screening strategy for vaccine candidates which identifies the antigens on the parasite, Schistosoma japonicum."

I'm an Australian science journalist based in Cali, Colombia covering STEM in The Global South. I'm the current Vice-President of the Colombian Association of Science Journalism (ACPC) and helped organize the 12th World Conference of Science Journalists, with 600+ attendees in Medellin, Colombia.

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How Close Are Scientists To A New Anti-Tick Vaccine In Uganda? - Forbes

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