Hartford Courant (Sunday)

Vaccines are not making new COVID-19 variants worse

- By Faye Flam

A new COVID-19 variant called XBB.1.5 is driving a new wave of infections. But susceptibi­lity to it is not, as some contend, being fueled by vaccines. Still, the surges of ever more immune-evasive variants raise questions about whether vaccines and boosters are still protecting us from infection, or should only be recommende­d for their ability to prevent severe disease and death.

Jeremy Luban, a virologist at the University of Massachuse­tts, compares other currently circulatin­g variants to athletes slowly shaving off a hundredth of a second on the 100-meter dash. But XBB.1.5 is like Usain Bolt.

That’s one reason XBB.1.5 infection rates are shooting up fast. The other is timing: Winter is when past waves have surged, driven by weather and holiday gatherings.

How are vaccines affecting this trajectory? A Wall Street Journal column under the headline “Are Vaccines Fueling New Covid Variants?” makes the argument that XBB.1.5 started in one of the most heavily vaccinated parts of the world — the northeaste­rn U.S.

But the headline is misleading, because XBB.1.5 didn’t acquire its immune-evasive power in the U.S. Rather, XBB.1.5 is the offspring of two previously circulatin­g variants, called XBB and XBB.1, which probably arose somewhere in Asia, said Jesse Bloom, an evolutiona­ry biologist at the Fred Hutchinson Cancer Center in Seattle. The original XBB was the first variant known to have emerged through a process called recombinat­ion. Two versions of the omicron variant BA.2 must have infected the same person at the same time and swapped genetic material to produce something new.

XBB was better at evading immunity from past infections or vaccines than any previous variant, according to several published studies. XBB.1.5 is not more immune-evasive than XBB, said Bloom, but developed a mutation that makes it more transmissi­ble by better attaching to the ACE2 receptor on cells.

So, yes, vaccines do put evolutiona­ry pressure on the virus and in that way steer its evolution. But it’s misleading to suggest that vaccines are making our situation worse — without them, we’d still see immune-evading variants, and those infections would be causing more deaths.

Roby Bhattachar­yya, an assistant professor of medicine at Massachuse­tts General Hospital, told me that despite being dubbed a “super variant” on Twitter, XBB.1.5 is unlikely to cause the sort of massive spike in cases, hospitaliz­ations and deaths that the original omicron variant brought last winter.

He sees no reason to doubt that vaccineor infection-induced immunity will help to some degree — and we have a lot more of it in our population than we did a year ago, as most of the unvaccinat­ed among us have now been infected.

He’s also skeptical of an alarming, unpublishe­d study out of the Cleveland Clinic which has been making the rounds on Twitter and was cited in the WSJ piece, concluding that each booster actually increased the odds of getting infected.

That study followed 51,011 health care workers. Getting tested for COVID-19 was up to them, so the result might be explained by the fact that conscienti­ous rule-following people are both more likely to get all their boosters and more likely to test frequently — and pick up mild or asymptomat­ic infections. Moreover, the study was done before XBB.1.5 entered the scene.

The main author of the study didn’t respond to an interview request, but if there’s a take-home message in it, it’s that we really don’t know how boosters are affecting the odds of getting a mild or asymptomat­ic illness and transmitti­ng it.

It’s highly unlikely vaccines are making people more susceptibl­e to COVID-19. Bhattachar­yya pointed to a study he led last year showing that vaccinatio­n probably didn’t accelerate the initial omicron wave — omicron spread equally fast in highly vaccinated states as in poorly vaccinated states.

What we need are randomized, controlled trials of the benefits and risks of booster shots — studies that pit boosters against placebos and ask participan­ts to be regularly tested. Bhattachar­yya said he agrees that it’s ethical to do this using volunteers at low risk of severe disease.

If we want policies that follow the science, then we need the right kinds of scientific studies.

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