Tony Breu Profile picture
13 Mar, 18 tweets, 8 min read
1/14
How does fever help us fight infections?

For millennia, fever has been recognized as a beneficial response to invading pathogens.

If this is so, why don't we have a resting temperature of 102°F (38.9°C)? Wouldn't that protect us even better?

Let's have a look.
2/
Fever emerged approximately 600 million years ago and is conserved in vertebrates. This suggests its benefit.

As you'll see in the next tweet, even ectothermic (cold-blooded) vertebrates demonstrate a "febrile" response.

pubmed.ncbi.nlm.nih.gov/24692136/
3/
In a 1975 study, ectothermic lizards were infected with A. hydrophila and placed in environments at varying temperatures.

😀75% survived at 42°C (107.6°F)
😕25% survived at 38°C (100.4°F)
🥴0% survived at 34°C (93.2°F)

🔑↑temperatures = ↑survival

pubmed.ncbi.nlm.nih.gov/1114347/
4/
There is even evidence that PLANTS experience fever when infected.

In one experiment, the temperature of the leaves from a bean plant rose by ~2°C after infection with a fungus.

How cool is that!

pubmed.ncbi.nlm.nih.gov/25976513/
content.time.com/time/subscribe…
5/
There are some human correlative data suggesting that fever is beneficial.

A 2017 meta-analysis showed that fever is associated with lower mortality in sepsis:

🔹Fever: 22% mortality
🔹Normal temperature: 31% mortality
🔹Hypothermia: 47% mortality

pubmed.ncbi.nlm.nih.gov/28081244/
6/
Fever has even used to treat infections.

The most famous example was malariotherapy for syphilis. For more on this, listen to an amazing episode of @AdamRodmanMD's Bedside Rounds.

7/
We can now address the original question: how does fever help us fight infections. There are a few potential answers. Fever might:

🔹Have direct anti-pathogen effects
🔹Help activate the immune response

Which is it?
8/
Fever likely hinders the growth of some pathogens.

One study from 1932 examined testicular extracts containing T. pallidum. In vitro growth of the spirochete was greatly reduced at higher temperatures.

This suggests a direct anti-pathogen mechanism.

pubmed.ncbi.nlm.nih.gov/19870097/
9/
Still, there are a few problems with the direct anti-pathogen explanation.

🔹Temperatures required are often higher than seen in most fevers
🔹If this were the only mechanism, one might expect pathogens to have evolved a defense...

...particularly after 600 million years!
10/
The key effect of fever is the activation of immune and active immunity. For example, fever leads to:

🔹Release of neutrophils from bone marrow
🔹Enhanced lymphocyte trafficking across high endothelial venules

And a lot more!

pubmed.ncbi.nlm.nih.gov/25976513/
pubmed.ncbi.nlm.nih.gov/8698984/
11/
If fever protects us against pathogens, why haven't we gotten continuously warmer over time?

Among other things, there is a metabolic cost: for every 1°C increase in temperature, metabolic rate increases ~13%. This would require more caloric intake.

dx.doi.org/10.1001/jama.1…
12/
There are other reasons to keep our resting temperature below febrile-range.

🔹Having the immune system active at all times isn't ideal!
🔹A change in temperature may be necessary to activate immunity, possibly via the heat shock system

pubmed.ncbi.nlm.nih.gov/8698984/
13a/
Before closing, one final question: If fever is beneficial does this mean that antipyretics should be avoided?

This topic has been covered well by others so I'll defer its discussion here. I will highlight a few. There are surely others I have forgotten!
13e/
YouTube video by Paul Offit (@DrPaulOffit)

I also highly recommend his book Overkill: When Medicine Goes Too Far - amazon.com/Overkill-When-…

14/14
🌡️Fever is preserved evolutionarily, suggesting benefit
🌡️The benefit relates to its direct anti-pathogen effects and its ability to augment innate and adaptive immunity
🌡️There is a metabolic cost to fever which may partly explain why we're not just evolving to be hotter

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More from @tony_breu

27 Jan
1/14
Why is cerebrospinal fluid (CSF) glucose low in bacterial meningitis?

Before we review potential mechanisms, I'm interested in the explanation you've heard/used.

What do you think causes low CSF glucose (hypoglycorrhachia)?
2/
First, let's examine the most common causes of hypoglycorrhachia.

☞ While bacterial meningitis is the single most common cause, it accounts for fewer than a quarter of cases.

We'll come back to this.

pubmed.ncbi.nlm.nih.gov/24326618/
pubmed.ncbi.nlm.nih.gov/26299186/ Image
3/
Now to the potential mechanisms. A number of hypotheses have been offered to explain hypoglycorrhachia.

🔹Bacterial consumption of glucose
🔹WBC consumption
🔹Brain consumption
🔹Decreased entry into CSF

...and others

Let's examine these.
Read 14 tweets
30 Dec 20
1/16
Why do B12 and folate deficiencies lead to HUGE red blood cells?

And, if the issue is DNA synthesis, why are red blood cells (which don't have DNA) the key cell line affected?

For answers, we'll have to go back a few billion years.
2/
RNA came first. Then, ~3-4 billion years ago, DNA emerged.

Among their differences:
🔹RNA contains uracil
🔹DNA contains thymine

But why does DNA contains thymine (T) instead of uracil (U)?

pubmed.ncbi.nlm.nih.gov/12110897/
3/
🔑Cytosine (C) can undergo spontaneous deamination to uracil (U).

In the RNA world, this meant that U could appear intensionally or unintentionally. This is clearly problematic. How can you repair RNA when you can't tell if something is an error?

pubmed.ncbi.nlm.nih.gov/18837522/
Read 16 tweets
28 Nov 20
1/17
How does calcium "stabilize the cardiac membrane" in hyperkalemia?

I learned early in my intern year to use calcium in the setting of severe hyperkalemia.

I never really learned how it works. The answer requires some history. And uncovers a forgotten alternative treatment.
2/
First, some history.

While Sidney Ringer was developing his eponymous fluid, he observed that increasing potassium content led to progressively weaker ventricular contractions.

He reported these findings in 1883.

pubmed.ncbi.nlm.nih.gov/16991336/
3/
How does hyperkalemia affect the heart? To understand the answer, recall that the generation of an action potential is dependent on the:

(1) resting membrane potential (−90mV for myocytes)
(2) threshold potential (-70mV)
(3) activation state of membrane sodium channels
Read 17 tweets
25 Oct 20
1/14
Why is secondary dengue infection more likely to cause hemorrhagic fever than primary infection?

Not all infections confer immunity, but why would prior exposure lead to WORSE outcomes?

To answer these questions, we'll need to discuss "Original Antigenic Sin".

Let's go!
2/
Dengue is caused by any of the four dengue virus serotypes (DENV 1-4).

Dengue hemorrhagic fever (DHF) is a severe form of dengue characterized by vascular leakage, hemorrhage, and thrombocytopenia.

This can lead to organ failure and death.

apps.who.int/iris/bitstream…
3/
The biggest risk factor for DHF is secondary infection (i.e. patients with DHF have been infected with dengue once before).

Multiple cohorts have shown that DHF is rare the first time someone is infected.

pubmed.ncbi.nlm.nih.gov/23471635/
Read 14 tweets
20 Sep 20
1/5
Why is meperidine (Demerol) particularly good at treating rigors?

This is another association I learned early in training without hearing a potential mechanism.

For the second installment in my fevers, chills, and rigors tweetorial follow-up, let's have a brief look.
2/
The ability of meperidine to treat fevers and rigors associated with amphotericin B was demonstrated in 1980 in a SMALL randomized, placebo-controlled trial.

Percent with cessation of side effects with 30 minutes:
☞ Meperidine: 100%
☞ Placebo: 30%

pubmed.ncbi.nlm.nih.gov/7362377/ Image
3/
Meperidine is able to treat rigors (and post-anesthesia shivering) by lowering the shivering threshold.

The same temperature that would typically result in rigors isn't low enough after the use of meperidine.

pubmed.ncbi.nlm.nih.gov/9158353/ Image
Read 7 tweets
17 Sep 20
1/4
Why does amphotericin B lead to rigors and fever?

I learned about his side effect by the moniker "shake and bake" (thank you First Aid).

Let's have a brief look at this commonly tested side-effect.
2/
Amphotericin B was introduced in the 1950s.

It was clear early on that fevers and chills were common side effects.

More contemporary data show lower - though still relevant - rates of both side effects.

pubmed.ncbi.nlm.nih.gov/13749466/ - 1960
pubmed.ncbi.nlm.nih.gov/10072411/ - 1999
3/
When thinking back to the mechanism of fever, recall that PGE₂ is a key mediator.

Amphotericin B leads to an increase in PGE₂. This is likely the mechanism of chills and fever.

As this study shows, amphotericin B acts in a similar way to LPS!

pubmed.ncbi.nlm.nih.gov/3309074/
Read 5 tweets

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