Michael Mina Profile picture
Sep 30, 2020 11 tweets 4 min read Read on X
To detect #COVID19 before it spreads to others, we need frequent accessible testing.

We cannot detect pre/asymptomatic people before they spread if we do not test frequently.

A new article in @NEJM by ⁦@DanLarremore⁩, Roy Parker and Me

1/x nejm.org/doi/full/10.10…
An ideal screening test is one with high sensitivity.

During a pandemic of a fast moving virus that transmits asymptomatically, it is difficult to detect people before they transmit to others.

2/x
This far we have focused almost all of our screening efforts on the use of the very sensitive (and specific - a good thing) qPCR.

The qPCR meets the molecular needs of detecting this virus. It has an extraordinary sensitivity.

But it is extremely limited

3/x
Focusing on PCR as a screening method today necessarily equates to low frequency screening.

With a virus that transmits before people feels symptoms, low frequency testing equates to missing the infectious stage of most people’s infections. Catching them too late, or never.

4/x
So in the @NEJM piece, we suggest that the goal should shift away from the sensitivity of the test to detect molecules and towards the sensitivity of the testing program to find infectious people and filter them out before infecting others.

5/x
In other words, we want to focus on the *sensitivity of the testing regime* to detect and stop transmission, rather than focus on the analytical sensitivity of the test to find molecules in the relatively small number of samples that can be reasonably tested.

6/x
The PCR test is wonderful and has a terrific sensitivity. But it comes at the expense of being very limited.

In short, the best test in the world with the highest molecular sensitivity has a near zero % sensitivity to detect infectious people if it can barely be used.

7/x
If the world can create cheaper faster tests that can be produced and distributed to millions of people and used frequently, then the greater frequency more than makes up for the potentially lower molecular sensitivity of the frequent and accessible tests.

8/x
Ultimately this means that a low molecular sensitivity test that is used very frequently by many people will have a MUCH greater *sensitivity to catch infectious people* before they have a chance to spread virus to others.

To put this in perspective...

9/x
Collectively, in US, our screening programs based on high molecular sensitivity PCR likely catch less than <5% of infectious people in time to act and prevent them from spreading.

Thus, our PCR based testing has a <5% sensitivity to detect #COVID19 before it spreads.

10/x
This is why we must rethink the meaning of sensitivity of #COVID19 tests. We must move away from thinking just about the ability to detect molecules and towards the ability to detect infectious people.

The sensitivity of the testing program must be high - not the test.

@US_FDA

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More from @michaelmina_lab

Jan 16
A lot of questions still on:

How long should I isolate?

Do I need to isolate?

When can I go back to work?

Is 5 days enough?

What if I’m still positive?

Why am I not positive when I first get symptoms?

This thread below (and the embedded thread) goes through many of these questions
Now that symptoms start earlier w COVID (bc immunity activates symptoms fast after exposure)

A frequent ? that comes up is what this means for Paxlovid

Often ppl think it means you have to start Paxlovid earlier

Nope - Opposite! You have more time

2/
Bc symptoms start faster but the growth of the virus still takes about the same time as it used to…

Symptom onset today is ~2d post exposure where before it was ~5d

So, as far as virus growth is concerned, day 5 post symptoms (when the trials took place) is day ~8 today

3/
Read 6 tweets
Jan 8
A heartbreaking consequence of lapses in vaccination!

A measles outbreak is spreadinf in Philadelphia.

MEASLES! It sends kids to the hospital, erases existing immune memory (creating long term risks) and kills 1 in 1000

It was eliminated in the US, but we seem hell bent on reversing that

inquirer.com/health/measles…
A particularly deadly consequence of measles is its erasure of previously acquired immune memory - setting kids and adults up for infections that they shouldn’t be at risk from!

We found for example that measles can eliminate as much as 80% of someone’s previously acquired immunity to other pathogens!
science.org/doi/full/10.11…
Image
Read 6 tweets
Jan 3
This paper from Kaiser on new XBB1.5 vax formulation is misleading

NO, it does NOT say that prior vaccination w non updated XBB1.5 vaccines offer no protection

No, it doesn’t even say the XBB1.5 updates to the vaccine formulation are important

🧵
1/
medrxiv.org/content/10.110…
Here are the key conclusions.
They are WAY misleading

The major issue is w the timing

The comparison is

A) a VERY recent XBB1.5 vaccine given in last 30 days,

Vs…

B) A vaccine received ~1 year or more ago!

Any effect is first and foremost owing to recency of vax

2/ Image
Given everything we know about major short term (weeks - few months) immune responses after vax or infections

The comparison is NOT able to say anything about the importance of updating the vaccine formulation for variants

It simply says what any Immunology 101
Text says..

3/
Read 15 tweets
Dec 24, 2023
Tip on pooling home tests

I’m gathering w family. Had one @Pfizer Lucira multiplex COVID-Flu home molecular test

Had 6 people and 6 swabs

Everyone used one swab. Dunked all 6 into one Pfizer Lucira test

Neg.

Tested everyone for price of one!

Pooling at home works!
Pooling can work w home tests including rapid antigen and rapid molecular tests

However for antigen id be a bit more cautious and not put more than 3 swabs in the buffer

With molecular, particularly Pfizer Lucira bc it has a large volume buffer, 6 is no problem.
Here’s a nasal swab that would work. Don’t use it as a nasopharyngeal swab at home - just use it like any home self swab and swab the anterior nares

a.co/d/iCO1nsI
Read 4 tweets
Dec 15, 2023
Please note - If you use expired rapid antigen tests - here's how I think about interpreting them

1) If Negative - do not trust it - especially if control line is faint / absent

BUT

2) If Positive - trust it - *very likely* true positive.

(short thread)
1/
An expired test will Not aberrantly turn positive just because it's old

Expiry makes lines not show up. Does make them become dark.

So, if using an expired test:

Do Trust a Positive.
Do Not Trust a Negative.

*And note that many tests have had extended expiry dates...

2/
Here is a thread about the extensions to the expiration dates.

Not all tests are extended but many of them have and that means that the dates on the box may be different from the actual expiration date. I write about it here and how to find out

3/

Read 4 tweets
Nov 28, 2023
Does halving a vax booster dose make a difference to protection?

It shouldn’t

But could lower adverse effects

New @TheLancet paper is a great reminder that the immune system works on exponential scales

Halving the dose has min impact

Compare blue vs orange (half) per group https://www.thelancet.com/journals/lanwpc/article/PIIS2666-6065(23)00271-7/fulltext#secsectitle0010  No impact between a full dose (in blue) compared to a half dose (orange) in various prime boost groupings.
The paper is a great demonstration of the studies to perform in order to enhance vaccine distribution & access globally

If in emergencies we halve doses could we drive costs down and massively increase access??

Immune kinetics suggests so.

thelancet.com/journals/lanwp…
This is a bit like Ct values on a PCR test.

You can perform two swabs. One can be only half as effective as the first - and it only amounts to a single Ct difference.

One could be a full 90% less efficient and it’s still only 3Cts different!

We often gloss over exponential
Read 4 tweets

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