Health
UK starts mass COVID vaccination programme today
Britain on Tuesday recorded a turning point in the fight against the coronavirus pandemic, as it began the biggest vaccination programme in the country’s history with a new COVID-19 jab.
The first patients in line on what has been dubbed “V-Day” — the over-80s, care home workers and at-risk frontline health and social care staff — will roll up their sleeves for an initial dose from early morning.
They will then require a second jab in 21 days’ time.
Last week Britain became the first country to approve the Pfizer-BioNTech vaccine, raising hopes of a breakthrough in the pandemic, which has killed more than 1.5 million worldwide.
Britain has been one of the worst-affected countries in the world, with more than 61,000 deaths in the outbreak from 1.6 million cases.
Prime Minister Boris Johnson, who spent days in intensive care with Covid-19 earlier this year, called it a “huge step forward in the UK’s fight against coronavirus”.
UK Health Secretary Matt Hancock, who has offered to have the jab on live television to allay public fears, said the roll-out was a “key moment” that would protect the most vulnerable.
The head of the state-run National Health Service in England, Simon Stevens, said it was a “decisive turning point” against the “greatest health challenge” since the NHS was founded in 1948.
Regulatory approval for the vaccine was given last Wednesday, sparking a race against time to prepare scores of vaccination centres across the country.
The UK has ordered 40 million doses of the jab — enough to vaccinate 20 million people — with 800,000 in the first batch.
Up to four million doses are expected by the end of December.
Queen could lead way
The mass vaccination drive is a coordinated response by all four nations of the UK — England, Scotland, Wales and Northern Ireland — which normally set their own health policies.
The public has been largely favourable to the rapid approval of the vaccine, but ministers and health professionals are aware they still need to combat mistrust.
The independent Medicines and Healthcare products Regulatory Agency maintains that no corners were cut and its assessment and approval procedures met stringent international norms.
NHS England said thousands had already been given the jab during trials with no serious side effects.
Nevertheless, it has been reported Queen Elizabeth II, who at 94 is among those first in the line for the vaccination because of her age, could front a public awareness campaign urging compliance.
The government said it will hand out vaccine cards to remind people to get the booster after three weeks, but insisted it was not introducing immunity certificates.
The chief medical officers of England, Scotland, Wales and Northern Ireland said the vaccine will as a result only have a “marginal impact” on hospital numbers over the winter months.
Johnson called for patience and urged the public to stick to strict social distancing guidelines to prevent a spike in cases, particular as rules are relaxed over Christmas.
Health officials have already run into a logistical headache about how to administer the vaccine to elderly or infirm care home residents.
The vaccine needs to be stored at -70 degrees Celsius (-94 Fahrenheit), leaving hospitals and other medical hubs as the only places able to deal with such ultra-low temperatures.
With the Pfizer-BioNTech drug made in Belgium, concerns have also been raised about potential disruption to supply when Britain leaves the European Union’s single market and customs union.
But the UK government said the military is on stand-by to air-lift the vaccine if there is any border disruption from January 1.
The bulk of Britain’s vaccine requirements are expected to be met by a jab developed by AstraZeneca and the University of Oxford, which is awaiting regulatory approval.
The government has ordered an initial 100 million doses of the drug, which is cheaper to manufacture, and easier to store and transport using conventional fridges.
-AFP
Health
Studies show menopause can reduce women’s memory, concentration by 40%
Studies show menopause can reduce women’s memory, concentration by 40%
Women going through the menopause may experience a significant decline in memory, concentration, and the ability to carry out daily tasks, with research suggesting a drop of up to 40 per cent in cognitive performance. This revelation was highlighted at a recent international conference on women’s health.
Experts warn that as many as four in ten women could be affected, making it increasingly difficult to manage work responsibilities or daily routines. Researchers also note that younger women may experience temporary concentration difficulties at certain points in the menstrual cycle due to hormonal changes, performing better when oestrogen levels peak just before ovulation.
Professor Martha Hickey, an obstetrics and gynaecology expert at Melbourne University, told the American Society for Reproductive Medicine in Boston that compelling evidence now links menopause with declines in attention span, learning ability, and memory function. She identified possible causes, including a drop in oestrogen levels and sleep disruption from night sweats and hot flushes.
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“Oestrogen decline during the menopause may affect key areas of the brain responsible for memory and concentration, including the hippocampus, midbrain, and prefrontal cortex,” Professor Hickey said. Brain scans have shown changes in these regions in menopausal women, though she noted that previous research likely underestimated the effects due to less sensitive testing methods.
Professor Hickey is currently studying 105 women in the US undergoing oophorectomy (surgical removal of ovaries), which induces menopause, to further explore cognitive effects. Earlier studies, including a 2001 survey of 12,450 US women, found that post-menopausal women were 40% more likely to report forgetfulness. Another US study involving 16,000 women found that four in ten admitted to experiencing memory problems.
The average age of menopause is 52, although it can occur in the 30s or 40s. The condition is marked by the cessation of ovarian oestrogen production, which also leads to mood swings, hot flushes, and night sweats.
Studies show menopause can reduce women’s memory, concentration by 40%
Health
Scientists Identify Key Immune “Exhaustion Switch,” Opening New Path for Powerful Cancer Treatments
Scientists Identify Key Immune “Exhaustion Switch,” Opening New Path for Powerful Cancer Treatments
In a major scientific breakthrough that could transform cancer care, researchers at Weill Cornell Medicine have uncovered how tumours weaken the body’s immune defences—and how blocking that process can supercharge treatment. The findings, published in Nature Immunology, reveal a critical pathway that drives T cell exhaustion, a major obstacle in modern cancer immunotherapy.
According to the study, cancer cells exploit a molecular signal to drain T cells of their strength, reducing their ability to attack tumours. By blocking this signal, scientists were able to keep T cells active and dramatically enhance their tumour-fighting capacity.
“Our dream is to revive exhausted T cells so the immune system itself can defeat cancer. This discovery brings that future closer,” said co-senior author Dr. Taha Merghoub, noting that T cell exhaustion limits the long-term success of immunotherapies even in patients who initially respond well.
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The researchers focused on CD47, a protein known as the immune-evading “don’t eat me” signal used by cancer cells. Unexpectedly, the team discovered that T cells also produce CD47—and its levels surge when T cells become exhausted. Tests in mice revealed that animals lacking CD47 developed slower-growing tumours, showing the protein plays a powerful internal role in immune suppression.
Tumours appear to worsen this phenomenon by releasing thrombospondin-1, a protein that binds to CD47 and further weakens T cells. “Remove CD47 or thrombospondin-1, and T cells stay strong,” Merghoub said.
To counter this mechanism, researchers tested TAX2, a peptide that prevents CD47 and thrombospondin-1 from interacting. Mice treated with TAX2 displayed slower growth of melanoma and colorectal tumours, more active T cells, and stronger immune responses. TAX2 also significantly enhanced the effectiveness of PD1 immunotherapy, one of the most widely used cancer treatments.
Lead author Dr. Chien-Huan Weng described TAX2 as a “proof-of-concept,” adding that further work is underway to create safe and targeted ways to block this newly identified exhaustion pathway in human patients.
Scientists say the approach could form a powerful standalone therapy or boost existing immunotherapies, marking one of the most promising advances yet in the fight against cancer.
Scientists Identify Key Immune “Exhaustion Switch,” Opening New Path for Powerful Cancer Treatments
Health
Nigeria joins global ICH elite as NAFDAC achieves full international regulatory Status
Nigeria joins global ICH elite as NAFDAC achieves full international regulatory Status
Nigeria has recorded a major milestone in global health regulation as the National Agency for Food and Drug Administration and Control (NAFDAC) has secured full membership of the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH). The achievement positions Nigeria among the world’s most advanced national regulatory authorities and marks a transformative step for the country’s pharmaceutical sector.
The announcement was made during the ICH Assembly held in Singapore, where Nigeria was confirmed as the 24th out of only 25 national regulatory authorities (NRAs) globally recognised for their commitment to harmonised international pharmaceutical standards.
NAFDAC Director General, Prof. Moji Adeyeye, described the development as a “historic breakthrough for Nigeria and the African continent,” noting that full membership would significantly boost the availability of high-quality, safe, and effective medicines for Nigerians.
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She said:
“Full ICH membership means Nigerians will have better access to high-quality medicines. It confirms that our regulatory scientists can stand shoulder-to-shoulder with the best in the world.”
Nigeria’s journey to full ICH status began in 2022 after the agency secured Observer status and later participated in the 2023 ICH meeting in Vancouver, Canada, where NAFDAC made a formal presentation as part of the evaluation process.
Over the last two years, NAFDAC underwent extensive capacity-building, including training on multiple ICH guidelines, membership in expert working groups, and the hosting of a major international workshop in Lagos in April 2025 on the ICH M13A Bioequivalence Guideline.
Adeyeye credited the agency’s success to a “methodical and structured approach,” supported by Northeastern University, Boston, and the Bill & Melinda Gates Foundation.
Nigeria’s Ambassador to Singapore, H.E. Omayuli Francisca Kemi, praised NAFDAC for demonstrating “leadership, resilience, and expertise” in earning a place on the global regulatory stage.
Full ICH membership grants NAFDAC authority to contribute directly to the formulation of international pharmaceutical standards, while enhancing Nigeria’s capacity to regulate medicines, accelerate access to innovative therapies, and improve confidence in local pharmaceutical manufacturing.
Adeyeye also acknowledged the Federal Government for extending her tenure, saying the continuity was crucial to achieving this milestone.
“We will continue to safeguard the health of the nation—now with the full strength of the ICH global community behind us,” she declared.
NAFDAC expressed appreciation to President Bola Ahmed Tinubu, the Minister of Health and Social Welfare, and its international partners for their support. The agency reaffirmed its commitment to full implementation of ICH standards, strengthening Nigeria’s regulatory system, and advancing pharmaceutical innovation and production.
Nigeria Joins Global ICH Elite as NAFDAC Achieves Full International Regulatory Status
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