Paul Sax Profile picture
Nov 21, 2021 21 tweets 8 min read Read on X
Yesterday I posted a long thread on the extraordinary progress we’ve made in HIV care and research since report of the first cases 40 years ago. Now for Part 2!

(I stopped at around year 20. Here’s the link to Part 1, in case you want to catch up )
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When we left off, we'd experienced the thrill of effective combination ART. Our 2 major news magazines featured advances in HIV on their covers! One of these guys was a basketball star, the other an HIV researcher -- see if you can guess which one is which

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But the excitement of having effective ART was tempered by the realization that these treatments had major issues, including side effects, high pill burdens, and low resistance barriers. The "when to start?" question became a central part of HIV care

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How did we move forward? First, the limitations of early ART stimulated drug development, with substantial improvements that made older treatments mostly obsolete

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Second, the AIDS Conference in Durban in 2000 was a wake-up call to the world that HIV treatment was *desperately* needed around the globe -- where ART worked just as well as it did in richer countries, despite ill-informed skepticism or irrational fears

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Further progress: Carefully done large research studies on both intermittent Rx (SMART) or early Rx (START) clearly established that suppressive ART -- before immunosuppression -- was key to improving clinical outcomes, outweighing toxicity and resistance concerns

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Results from the SMART and START studies, and better drugs, meant that virologic suppression became the norm, not the exception. Here's one of many cohort studies showing this wonderful trend

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Remember that discouraging study from Hopkins with only 37% suppression in 1998? They repeated their analysis in 2011, and rate was now up to 87% -- especially notable in this challenging patient population
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doi.org/10.1093/cid/ci…
In response, I wrote an editorial highlighting the timelines for various advances in ART.

TL/DR: *Lots* to celebrate here

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One of the most important advances was the introduction of the first INSTI (raltegravir) in 2007, which meant that even people with multi-drug resistance HIV could achieve viral suppression. Many experienced "undetectable" for the 1st time in the late 2000s -- so great

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Of course this integrase inhibitor drug class was just getting started. Look at on-treatment responses today using dolutegravir and bictegravir-containing regimens. And this with no treatment-emergent resistance

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The apotheosis of the high resistance barrier concept is demonstrated in the recently published NADIA trial, demonstrating that both DTG and DRV/r achieve high rates of viral suppression even with no predicted activity from TDF/3TC or ZDV/3TC. Still amazed by these results!

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And it's not just treatment of HIV that has had extraordinary advances. Let me shift now to prevention, which has been equally miraculous

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We can start with the fact that we've had *amazingly* accurate diagnostic test for HIV almost as long as we've known about the virus. This rapidly made the blood supply so much safer. Risk for transfusion-related HIV now one in approximately 1.5 to 2 million units

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Next up is 076, which demonstrated that maternal zidovudine markedly reduced the risk of mother-to-child transmission of HIV. This came in the early 1990s, when we really needed a win for HIV research, and was so welcome

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It took some time for the next great advance in HIV prevention, but wow it was a big one -- HPTN 052 conclusively showed that treatment of HIV reduced the risk of sexual transmission of the virus. Such a motivator for PWH to start and stay on ART

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Follow-up observational studies in serodiscordant couples choosing not to use condoms have confirmed that U most definitely equals U! ART as prevention has a staggeringly powerful effect

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The next advance in prevention was PrEP. It's a strategy that once would have been unfathomable due to drug toxicity -- but with TDF/FTC, TAF/FTC, and soon cabotegravir, it can be widely and safely deployed

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Are we done yet? Of course not -- still plenty to accomplish if we want to end the HIV epidemic. The scientific challenges of an HIV cure and effective vaccine remain formidable, and sadly there are still residual inequities in access to diagnosis and treatment

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But challenges notwithstanding, it has been a privilege to watch (and be a small part) of this extraordinary progress. As we approach #WorldAIDSDay and Thanksgiving, I am so grateful for it, and hope we can apply what we've learned from HIV to our current pandemic

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Here's a link to the full slide set. Thanks to all for the feedback, and to Fundacion Fernandez-Cruz for inviting me to give this talk -- it was a joy to put together
(Woof.)
dropbox.com/s/zgihz3p3431m…
fin.

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More from @PaulSaxMD

Feb 8, 2023
Ever submit a paper to a high-quality, high-impact factor journal and have it rejected, even though the reviews are mostly good and eminently addressable?

Certainly I have. 🙋‍♂️
1/x
Wouldn't it be awesome if those reviews could be used by another journal?

Peer review, after all, is a limited but critical resource in academic medicine.

Why should these reviews go to waste? And getting good peer review takes time!
2/x
That's why I'm delighted to announce that @CIDJournal -- and soon *all* the @IDSA journals -- will accept outside reviews from other high-impact journals. Some details in screen captures below.
3/x academic.oup.com/cid/pages/Manu…
Read 4 tweets
Nov 29, 2022
Way back in April of this year, I received a kind invitation from @PaulPottingerMD to speak about Twitter at this year’s IDWeek.
1/x Image
Sounded like fun--plus I could learn from @KrutikaKuppalli and @Payal_Patel, so I readily accepted ...

... little imagining that shortly after IDWeek, this site would be embroiled in various controversies -- about which many others have already weighed in wisely!
2/x
But here's a condensed version of the talk, which explains why I'm sticking around (at least for now).

Let’s start with the (dreaded) “Learning Objectives”, which I’ve tried to enliven with pic of my pup.
3/x Image
Read 25 tweets
Feb 5, 2022
Since talks on Covid get out of date as soon as you click "save", might as well post the talk given this week at @harvardmed Medical Grand Rounds, along with by @k_stephensonMD @SanjatKanjilal and Dr. Ruanne Barnabas
Here's the topic:
1/x
Let’s start with the controversy over disease severity, subject that appears both to excite and annoy people (for reasons that I hope to explain)

Also, a reminder that Omicron was a (very unwelcome) 2022 holiday "gift" -- will always link it to Thanksgiving!

2/X
These early anecdotal reports came from South Africa that the disease was milder with Omicron.
True? Or just wishful thinking?
3/X
Read 32 tweets
Dec 31, 2021
We HIV/ID clinicians have been dealing with these for years.

Yes it's a long list, but five days will seem relatively manageable compared with chronic ritonavir administration, especially since the effect is quick on/quick off.

1/x
... or should I say *relatively* quick on/off, right @ErinMcCreary? doi.org/10.1093/jac/dk…

2/x Image
Some drugs on this list (e.g. statins) can be held for 5 days. Others (calcineurin inhibitors) dose-reduced and monitored. Some aren't used very often any more. There are alternatives that can be temporarily substituted in some pts (e.g. lorazepam for clonazepam).

3/x
Read 5 tweets
Nov 20, 2021
The "History of HIV" talk I gave last week actually has this title, which I don't think is an overstatement. Posting it now with gratitude, just in time for Thanksgiving (my favorite holiday -- the gratitude and family part).

(Part 1 thread)
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Must start with this 1981 @CDCMMWR report of 5 cases of PCP in Los Angeles. Have already commented on the surprising page 2 placement. There's a story behind it, right @deborahcottonmd? (Later moved to Page 1 on reprints.) Note “blue diazo” slide style

2/x
During my first year of med school, we had one lecture on AIDS, with putative causes. Not an auspicious start.
(Yes, 1983. I'm old.)

3/x
Read 15 tweets

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