Britain and other nations are considering ways to stretch scarce supplies of Covid-19 vaccines, including by delaying second doses, reducing dose sizes and switching vaccine types between the first and second shots. The proposals have generated fierce debate among scientists. Here is the rationale behind, and criticism of, these alternative strategies: WHY DELAY THE SECOND DOSE? In clinical trials, companies tested specific doses of their vaccines at precise time intervals to generate evidence showing how well they work. All Covid-19 vaccines approved, so far, are designed to teach the immune system to recognise and defend against the virus with a first dose, and then provide a second booster dose to reinforce that lesson. Faced with a fast-spreading pandemic and new, more transmissible coronavirus variants, some countries are hoping to widen immunisation by giving some protection to as many people as possible with a first dose, and delaying second doses. Maximising the number of people who have partial immunity “should reduce the number of severe Covid-19 cases and thus alleviate the burden on hospitals”, said Michael Head, a global health expert at Britain’s University of Southampton. WHAT ABOUT SWITCHING BETWEEN COVID VACCINES? Mixing or switching between Covid-19 vaccines is largely driven by the same aim – vaccinating as many people as possible as the pandemic still rages. Giving a priming dose of one vaccine and a booster dose of another offers flexibility to offer whichever shots are available, rather than holding shots back so individuals always get both doses of the same vaccine. HAVE THESE STRATEGIES BEEN TESTED IN RIGOROUS TRIALS? No. None of the late-stage Covid-19 vaccine trials compared these dose-sparing strategies or the effects of mixing vaccine types, said Stephen Evans, a professor of pharmacoepidemiology at the London School of Hygiene & Tropical Medicine (LSHTM). Officials have cited limited evidence from trials that the Pfizer/BioNTech, the Oxford University/AstraZeneca and the Moderna vaccines all confer some protection against Covid-19 after the first dose. Britain’s MHRA health regulator said on Dec. 30 it had found an 80% success rate for the Oxford/AstraZeneca vaccine when two full doses are administered, three months apart, higher than the average that the developers themselves had found. The UK government’s vaccine advisory committee said on Dec. 31 that the Pfizer/BioNTech vaccine conferred 89% protection from two weeks after the first dose, and that for the Oxford/AstraZeneca vaccine “the evidence shows that the initial dose … offers as much as 70% protection against the effects of the virus”. It did not give detailed data. Moderna reported its vaccine was 80% protective after one dose, with efficacy peaking two weeks after the first shot. But there is no long-term evidence that any of these vaccines will offer lasting immunity based on just one dose, or how effective they will be if the second dose is delayed. BioNTech and Pfizer warned on Monday they had no evidence their vaccine would continue to be protective if the second dose was given more than 21 days after the first. Evans said that ideally “it is safest and most cautious” to use vaccines in conditions exactly matching those of their trials, but added: “In the real world, this is never so.” Anthony Fauci, director of the US National Institute of Allergy and Infectious Diseases, told CNN on Friday the United States was unlikely to delay giving second doses. “We’re going to keep doing what we’re doing,” he said. Likewise, scientists have raised concerns over the idea of mixing two different types of vaccines. Some experts speculate that, because all of the vaccines target the same outer “spike” protein of the virus, they could work together to train the body to fight off the virus. But there is no evidence this approach will work. “There is literally zero data. It has not been tested, or if it has been tested, the data have not been made available,” said John Moore, a professor of microbiology and immunology at Weill Cornell Medical College in New York. WHAT ABOUT REDUCING THE AMOUNT OF VACCINE IN EACH DOSE? In the United States, some health officials are considering offering half doses of Moderna’s vaccine to individuals aged 18 to 55. There is some clinical trial data backing this strategy. Moncef Slaoui, chief adviser to the US vaccine programme Operation Warp Speed, told CBS on Sunday that evidence from a Moderna trial showed the half dose induced an “identical immune response” to the higher 100 microgram dose in adults aged 55 and under. He said the US government was discussing the issue with Moderna and regulators. Slaoui said he believed injecting half of the volume of vaccine was “a more responsible approach that would be based on facts and data”. Several US scientists agreed, but noted the data was not publicly available. “It’s very fuzzy. I want to see that data,” said Eric Topol, a genomics expert and director of the Scripps Research Translational Institute in La Jolla, California. SO ARE THESE STRATEGIES SAFE? AND WILL THEY WORK? It’s not clear. While there is no scientific evidence on the impact of delaying Covid-19 vaccine doses, some experts believe it could be safe to wait and the potential payoff in protecting a larger swath of the population may be worth it. Others aren’t so sure. “There’s just no data,” said Ian Jones, a professor of virology at Britain’s Reading University. The British Society of Immunology said in a statement on Monday that delaying a second dose by eight weeks “would be unlikely to have a negative effect on the overall immune response”. It added that it would not expect any extra safety risks from the delay beyond the potential increased risk of disease during the interim between doses.