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Two years into the coronavirus pandemic, Americans can be forgiven if they’ve lost track of the latest variants circulating nationally and around the world. We’ve heard of the alpha, beta, gamma, delta, amoxil tab a500 and omicron variants, but a new Greek-letter variant hasn’t come onto the scene in almost half a year.

Instead, a seemingly endless stream of “subvariants” of omicron, the most recent Greek-letter variant, has emerged in the past few months.

How different are these subvariants from one another? Can infection by one subvariant protect someone from infection by another subvariant? And how well are the existing coronavirus vaccines — which were developed before omicron’s emergence — doing against the subvariants?

We asked medical and epidemiological experts these and other questions. Here’s a rundown.

Q: What are the subvariants? How much do they differ from one another?

The omicron subvariants seem like an alphabet soup of letters and numbers. The original omicron variant was called B.1.1.529. The initial omicron variant begat such subvariants as BA.1; BA.1.1; BA.2; BA.2.12.1; BA.3; and the most recent, BA.4 and BA.5.

“They all differ from each other by having different mutations in the spike protein,” which is the part of the virus that penetrates host cells and causes infection, said Dr. Monica Gandhi, a professor of medicine at the University of California-San Francisco.

The minor-to-modest mutations in these subvariants can make them marginally more transmissible from person to person. Generally, the higher the number following “BA” in the subvariant’s name, the more transmissible that subvariant is. For instance, BA.2 is thought to be about 30% to 60% more transmissible than previous subvariants.

These mutations have enabled subvariants to spread widely, only to be overtaken by a slightly more transmissible subvariant within a few weeks. Then the process repeats.

In the United States, for instance, BA.1.1 was dominant in late January, having overtaken the initial variant, B.1.1.529. But by mid-March, BA.1.1 began losing ground to BA.2, which became dominant by early April. By late April, another subvariant — BA.2.12.1 — was gaining steam, accounting for almost 29% of infections, according to data from the Centers for Disease Control and Prevention. (The delta wave of late 2021 has been a non-factor during this time frame.)

Q: What about the severity of illness?

Fortunately, the illnesses caused by omicron have typically been less severe than those caused by previous variants — a pattern that seems to hold for all the subvariants studied so far. One analysis from Denmark showed that BA.2 doesn’t cause more hospitalizations than the BA.1 subvariant, Gandhi said.

Even the most recent subvariants that have been discovered, BA.4 and BA.5, show “no evidence to suggest that it is more worrisome than the original omicron, other than a potentially slight increase in transmissibility,” said Brooke Nichols, an infectious-disease mathematical modeler at Boston University.

Dennis Cunningham, the system medical director of infection control and prevention at Henry Ford Health in Detroit, told NBC News that the symptoms from the omicron subvariants “have been pretty consistent. There’s less incidence of people losing their sense of taste and smell. In a lot of ways, it’s a bad cold, a lot of respiratory symptoms, stuffy nose, coughing, body aches, and fatigue.”

Q: If you get infected by one subvariant, will you be protected against others?

So far, in all variants to date, the ability of the virus to evade existing immune protection “is only partial, much like it is for the seasonal flu,” said Colin Russell, a professor of applied evolutionary biology at the University of Amsterdam’s medical center.

While some people who had BA.1 have also gotten BA.2, the initial research suggests that infection with BA. 1 “provides strong protection against reinfection with BA.2,” the World Health Organization has said.

“This may explain why our BA.2 surge in the U.S. was not that large as the very large BA.1 surge over the winter,” Gandhi said.

The level of protection can vary depending on how sick you were, with mild cases boosting immunity for perhaps a month or two and recovery from a severe illness granting up to a year.

Q: How do existing covid-19 vaccines stack up against these subvariants?

Although the current vaccines and boosters aren’t quite as successful in protecting against omicron as they are against earlier variants, they will generally protect people from severe disease if they are infected by one of the new subvariants.

“We’re steady as she goes with the vaccines we’re using,” said Dr. William Schaffner, a professor of preventive medicine and health policy at Vanderbilt University. “I have not seen a single study from the field that shows a substantial distinction between the vaccine responses to omicron subvariants.”

The vaccines generate cells known as “memory B cells” and have been shown to recognize different variants as they emerge, Gandhi said. The vaccines also trigger the production of T cells, which protect against severe disease, she said.

“While B cells serve as memory banks to produce antibodies when needed, T cells amplify the body’s response to a virus and help recruit cells to attack the pathogen directly,” Gandhi said.

The end result is that a breakthrough infection for a vaccinated individual “should remain mild with the subvariants,” she said.

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