Skip to content

It appears the feared double-whammy of simultaneous COVID-19 and influenza peaks won't happen. The CDC influenza data are a little harder to interpret because of the omicron peak affecting counts of influenza-like illness (ILI); ILI is high, though coming down, but likely most of the numbers are omicron, not influenza. Most of the influenza that is being identified is influenza A H3 which could contain a clade that has a bit of a mismatch with this year's vaccines. CDC's influenza web site is always informative.

More on Vaccine Myocarditis in Adolescents

The New England Journal published brief correspondence from Israel updating Pfizer vaccine-associated myocarditis in teenagers. The latest numbers, looking just at ages 12-15 years, are 1 case per 12,361 second vaccine doses in males and 1 per 144,439 in females. These numbers are in the same ballpark as previously reported in US and Israel. The current data are based on hospitalizations for myocarditis. Note that the illness still looks to be very mild so the Israeli data could be missing cases managed as outpatients.

UK.gov

My new BFF in the world of COVID-19 listservs is from the United Kingdom. I signed up for daily alerts a while back. They come through at around 3 or 4 AM Eastern time and range from 1 to many different updates. All have summaries and links to raw data. Some days I'm almost overwhelmed with new reports. The graphics aren't as attractive as CDC's web site, but in general I think the UK does a better job than CDC in explaining nuances to the general public. I'll highlight 2 reports from this past week. Browse through if you are interested, but it's a definite rabbit hole for COVID nerds.

First is a January 26 report with some interesting mathematical modeling that attempted to determine the numbers of adults who would have tested positive for SARS-CoV-2 antibodies from either vaccination or infection. Not surprisingly, the older age groups with positive testing likely would have been due to vaccination. Another portion of the report looked at children 8 - 15 years of age where of course relatively little of the antibody positivity would have been due to vaccination. This type of analysis is important in understanding new methods to track pandemic/endemic activity.

Friday's report, which generally includes the big picture infection survey for the week, also had a nice report on the BA.2 variant risk assessment; this is the omicron variant getting a fair amount of media attention now. They have a lot of background data elsewhere, but their one-pager is a nice overview comparing the BA.2 variant to BA.1, the original omicron variant. They expressed moderate confidence that there is evidence of community growth advantage for BA.2 in more than one country (Denmark seems to be the country with a lot of BA.2 at the moment). However, they felt only low confidence that increased transmissibility of BA.2 explains this growth advantage. Also with low confidence, they saw no evidence that BA.2 was more able to evade the immune system (i.e. vaccines or monoclonal antibody treatments less effective) compared to BA.1. They had insufficient data to comment on whether infection severity is different. For now, BA.2 is yet another variant to keep an eye on.

No point in sugar-coating, things are likely to get worse before they get better. The news is disappointing, but we can at least hope that omicron and influenza will crest quickly and recede somewhat.

Omicron is Different

Yes, you already knew that. We certainly know it is (much) more highly transmissible but we still don't have enough data to know if severity is different. Full vaccination (primary series plus booster) is likely to be helpful against severe illness though much less so against infection itself.

Our most commonly available monoclonal antibody regimens are unlikely to be effective against omicron; at Children's National we have paused offering both the bamlanivimab/etesevimab and casinivimab/imdevimab monoclonal cocktails given the high rate of omicron in our region. Sotrovimab should be effective against omicron, but currently we don't have this agent on hand and availability is likely to be limited for the next few weeks. Note that use is limited to outpatients 12 years of age and older and weight 40 kg and greater with positive SARS-CoV-2 testing and high risk for hospitalization or death.

We now have emergency use authorization for 2 oral medications, molnupiravir and nirmatrelvir/ritonavir (Paxlovid), for treatment of mild-to-moderate COVID-19 illness. Paxlovid, consisting of 2 viral protease inhibitors, is authorized down to the 12 years of age/40 kg weight category with high risk for disease progression. Note that Paxlovid is a CYP3A inhibitor, so beware of drug interactions. Molnupiravir is less effective but can be used in adults at high risk for progression who cannot access or receive other treatment options. In the coming weeks molnupiravir is likely to be more available than Paxlovid, but note that it should not be given to children - concerns for joint problems in juvenile animals likely will delay pediatric trials. Because it is a mutagenic agent, use in pregnancy is an unknown risk and patients of reproductive age should use methods to prevent pregnancy while taking the medication and for either 4 days after (females) or 3 months after (males) the 5-day treatment course.

Another difference for omicron is that some SARS-CoV-2 tests may show false negative results. It is a little tough to keep track of new information about this, but the FDA has a great resource.

Influenza on the Rise

Influenza has been creeping up nationally and also at Children's National Hospital, though at the hospital it has not yet reached numbers that we associate with the official start of flu season. Now a preprint study suggests that the 2021-22 influenza vaccine has reduced ability to inhibit replication of the H3N2 clade most likely to be circulating this year. That could mean an antigenic mismatch for this flu season, but we won't have an estimate of that for at least a few months. Even if this is true, influenza vaccination is still very important and I would encourage everyone to be immunized - it's not too late.

Somebody pushed the reset button this past week. Although we don't yet have the weekly variant reports from CDC (they are published on Tuesdays) it is very clear from just my small world at Children's National Hospital that omicron has hit with a vengeance. I was speaking in the hallway on Friday with my longtime friend and esteemed colleague Dr. Larry D'Angelo who likened what we are seeing to the early situation in South Africa where omicron increased exponentially even while delta was still very much present. An important caveat, however: it's risky to make too much out of day-to-day data, many factors affect case rates and sometimes we can be misled by "hot off the presses" numbers.

A Triple Whammy Ahead?

Most winters in pre-pandemic times I kept my fingers crossed that we would not have our RSV and influenza seasons occur concurrently; the few years we had a double whammy like that it really strained our resources. This winter could be worse. The good news is that although RSV is still around it seems to be on a downward trend. However, influenza A numbers have been increasing both at Children's National and nationally, suggesting we will hit full-blown flu season soon. The second and third components of the trifecta are delta and omicron. If we see all 3 of these viruses causing infections in large numbers at the same time it will be very tough. One silver lining of the omicron era is that it may stimulate more individuals to seek out primary series and booster vaccinations. Also, with school winter break and perhaps a bit more caution on the part of the public, we might have less viral circulation the next couple of weeks. We'll see.

For now clinicians should remember we have two effective influenza antiviral medications, oseltamivir (Tamiflu) and baloxivir marboxil (Xofluza), available. From a treatment perspective we don't have a lot of choices for outpatient therapy for pediatric SARS-CoV-2 infections, and the monoclonal antibody combination bamlanivimab and etesivimab just authorized for use down to newborn ages but isn't likely to be effective against omicron. (Note that currently Children's National is not using age under 1 year as an independent risk factor for use of this combination.) NIH has a nice web site to check the latest on effects of different therapeutics for SARS-CoV2 variants, much based on in vitro data rather than solid efficacy studies because it's just too soon in the omicron wave for reliable analysis.

Setback and Hope for Pediatric COVID-19 Management

On December 17 we all learned via a press release that the Pfizer vaccine trial failed to reach the pre-established noninferiority margin for children 2 - 4 years of age, although that goal was reached in the 6 - 23 month old age group. As you know I am an investigator in that trial, at the time of this writing still waiting to hear specific plans for modification of the trial presumably to administer third doses to those children.

Also on December 17, CDC released reports of 2 studies of the "Test to Stay" (TTS) strategy for managing school attendance with positive covid cases, one from Los Angeles County, CA, and the other from Lake County, IL. A lot of us have been waiting for high-quality published data on this approach. The basic approach to TTS is described on the CDC web site, suffice to say ready access to testing must be available as well as compliance with masking and other prevention methods. We of course do not have data available for TTS efficacy in the omicron era but at the moment this seems to be a reasonable approach.

Bottom line for all of this, we are entering another worrisome time for COVID-19, no reason to panic but be careful and stay abreast of new developments. Please encourage everyone to get their influenza and COVID-19 vaccinations, including boosters for the latter.

We are now seeing the predicted post-holiday surge of COVID-19 disease in many parts of the country, driven not by the new omicron variant but by our old friend delta and fueled by high rates of unvaccinated individuals. Of course even the vaccinated and boosted are not immune from infection and, rarely, hospitalization. Expect this surge to persist for several weeks now with more holiday and indoor gatherings serving as incubators.

What Do We Really Know About Omicron?

Still relatively little, though evidence is accumulating that it is highly transmissible and possibly not highly virulent. We still don't have a lot of data on the other important trait of how well it can evade host immunity from prior natural infections or vaccination. Preliminary data strongly suggest it will to some extent, but we need more than in vitro preprint data to support that view.

I wanted to alert readers to a site I haven't mentioned before that I think gives a good graphical view of how many more mutations omicron carries, compared to our current scourge delta. A quick glance shows you the rather remarkable increase in numbers of mutations, especially in the spike protein region designated by the green band.

In the next few weeks we'll see increasingly more information about omicron that likely will allow us to chart a more informed plan of action for the coming months.

Should 16 and 17 Year-Olds Get a Booster?

As most of you are aware, the FDA authorized the Pfizer vaccine for booster doses in this age group, and the CDC stated that these individuals "can" (rather than should) get boosted. It boils down to a risk/benefit consideration, particularly since this may be the prime age group for development of the rare (and generally mild) complication of post-vaccine myocarditis. It doesn't appear that the FDA had any new data, other than Pfizer's request, to make this authorization. So, it may be useful to look back at the myocarditis risks presented previously by CDC colleagues. At the November 19 ACIP meeting, CDC presented data on myocarditis rates based on VAERs data through August 18. At that time, the highest post-vaccine myocarditis risk was in males in the 18-29 year-old age group, with a rate of 13 cases per million vaccine doses. Obviously this is extremely low, and in fact a booster (assuming that vaccine efficacy declines from the primary series) would prevent 114 million hospitalizations per million doses in this same age group, counting both sexes. So, those data still pretty clearly favor boosting but does not give us anything more specific for 16-17 year-olds. However, I doubt the numbers would be terribly different.

Trying to transform these rare risk event numbers into something understandable for most people is tough, plus we have no idea how the omicron variant and potential need for vaccines modified for omicron will figure in. I think probably the best plan for healthcare providers is to mention the "can" versus "should" CDC statement as an indication that the data aren't as solid as for older individuals, but I wouldn't necessarily wait on an omicron vaccine to appear - it isn't even clear that we will need it, plus it will take a least a few months to become available. In the meantime, we can expect the holiday delta surge to continue.

2

Around the middle of this past week I was having trouble finding some interesting news to include for this week's blog. At the same time, scientists in South Africa were first confirming the alarming facts about what is now known as the omicron variant, and as a result I ended up with too much to cover this week. I hope I can help cut through some questions and inaccuracies circulating about this newest variant of concern.

I'll devote all of today's blog to omicron, it's that important, but I want to stress one point first. The government of South Africa has one of the premier pandemic monitoring systems in the world that has given the rest of the world a bit of a lead time to prepare in case omicron turns out to be the next game-changer in the pandemic. We'll probably never know the origins of this variant, but we already know a lot about it thanks to South Africa. Furthermore, much of what I'll be relaying below comes from a press conference in South Africa! Our sound-bite specialists in the US should take a page out of their book: let the actual scientists tell the story with their own words and graphs.

The Beginning of Omicron

As part of South Africa's surveillance system (set up in February 2020, by the way), epidemiologists noted a sharp increase in COVID-19 cases from districts in the province of Guateng. When samples taken November 12-20 were analyzed it became clear that this was a different variant containing many mutations in the spike protein genome. Some were well-known, others had not been described previously, but the main concern was the sheer number affecting a region of the genome that could dramatically change the behavior of the virus.

Looking at the gene diagrams from the press conference, I count 35 separate mutations in the spike protein gene of omicron. Scarier still is the fact that 10 of those are in the receptor binding domain (RBD), a key portion of the genome with regard to many phenotypic properties of SARS-CoV-2. By comparison, the delta variant has 2 mutations in the RBD. So, we need to look very carefully for evidence of how omicron behaves with regard to transmissibility, detectability, immune escape (evading immunity from natural infection and vaccines, poor response to monoclonal antibody or convalescent plasma therapy), and disease severity.

With respect to transmissibility, it is very likely that omicron has heightened ability to spread within a population. Preliminary data from Gauteng suggest a reproductive number of 1.93, not off the charts but pretty healthy. Note this estimate could change significantly because it is based on so few cases in just one country. More concerning is that in just a couple weeks it appears that omicron is replacing delta as the predominant strain in Gauteng and possibly in other provinces as well. The latter information comes from an interesting property of the variant that can be detected by PCR testing rather than waiting for the more technically-difficult and time-consuming method of whole genome sequencing (WGS). A new variant with increased transmissibility and multiple mutations that could affect other viral behavior makes omicron a great concern.

Omicron displays what is called "S gene dropout" where the S gene is so different that it tests negative for that gene in conventional PCR testing. Most PCR tests look at more than one gene, usually the nucleoprotein (N) and open reading frame (ORF) genes in addition to S. So, a specimen that is strongly positive for N or ORF but negative for S could very likely be omicron. As you might surmise, any PCR test that looks only at S gene will likely miss omicron altogether. Still, this property of omicron has allowed South African scientists to hypothesize that this new variant isn't just a fluke in one province but likely has extended across South Africa. What they are now seeing is this same S gene dropout in their newer cases elsewhere. WGS studies now in progress are needed to confirm this, and we should have those answers in the next several days.

Immune escape is a feared property of any variant. Delta expressed this to some degree; in general our vaccines and immune-based therapies don't work quite as well for delta as for the original SARS-CoV-2 strain, but they still provide decent protection from severe disease. At this point we just don't know if this is happening with omicron. We will know, likely within 1-2 weeks, how individual sera from people previously infected or vaccinated can neutralize omicron. It will take much longer to understand how innate immunity and the rest of the immune system behaves with this new variant. Every vaccine manufacturer is now scurrying to look at this and prepare new prototype vaccines in case they are needed for protection from omicron.

Does omicron cause more severe disease? That also will take a bit of time to know. In general, new outbreaks tend to affect younger and healthier populations; they are the ones more out and about to be exposed. So, we can be misled early on into thinking that this new variant is associated with milder disease. If it does spread more extensively we'll end up with a broader population infected and will have the answer to the question of disease severity. Unfortunately there isn't a reliable method to determine this in the laboratory.

What to Do Now?

In the US we may have a little lead time, although I'd be very surprised if we don't eventually learn that omicron is already here. First and foremost, we need to vaccinate the unvaccinated. Yes, it may be that the current vaccines turn out to be less effective against omicron, but based on everything we know about this virus it is clear that partial protection is far better than no protection. Second, everyone who is eligible for a booster should get one now. We do know that neutralizing antibody titers measured one month after a booster dose are very high; this can help overcome some slight decrease in effectiveness against omicron. Don't wait for a new vaccine tailored to omicron; this will take at least three months to see the light of day.

Third, we need to go back to those non-pharmaceutical interventions (NPIs) that have proved so successful in the past: masking especially for indoor activities, social distancing, good hand hygiene, and avoiding large gatherings. We already likely will have a spike in cases from Thanksgiving holiday activities; let's not aggravate an already problematic situation by ignoring NPIs.

Notice that I didn't mention travel bans among the NPIs. That's because they likely aren't effective in the long run. I guess one could argue that this ban on travel from 8 countries in southern Africa gives us another week or two to prepare for omicron.

I'll be watching immunization rates very closely the next couple of weeks; maybe we've learned our lesson and those who have been hesitant will come forward in larger numbers to start their vaccine series.

No One is Safe Until We All are Safe

The Johns Hopkins Coronavirus Resource Center tracks, among other topics, vaccination coverage across the world. It's very clear where the haves and have-nots reside. In Africa only one country, the small island nation of Mauritius, has a fully vaccinated rate of 72% that is above the world average. South Africa's rate is listed as 24% (compare to US of 60% which is pretty dismal itself), but South Africa actually has more vaccine doses available than it does residents seeking vaccine. However, many African countries are in the single digits and do not have access to vaccines. I reiterate that we need to remove all barriers to COVID-19 vaccination across the world. We are running out of Greek letters, but more importantly we are losing lives needlessly.