Today we will review some of the common types of #HIVDrugResistance tests.
2/ I first break down testing into 2 broad categories of resistance tests:
3/ There are 2 major types of genotype tests that we use to detect #HIVDrugResistance
4/ In a standard genotype test, a patient’s circulating HIV is isolated, amplified by PCR, and reverse transcribed in vitro to DNA. The polymerase (RT), protease, and integrase genes can then be sequenced and compared to wildtype (more on this in 10-12).
-pts have to be viremic (doesn’t work for patients who are suppressed)
-not all standard genotypes include integrase (may need order separately)
-only mutations present in ~80% are typically detected.
6/ In archived genotypes, cell-associated proviral HIV DNA is isolated from whole blood, amplified, sequenced, and compared to wildtype (more on this in 10-12).
7/ Studies are mixed on how well standard and archived genotypes correlate. Standard HIV genotypes are still the preferred tests. Archived genotypes are specific but sometimes lack sensitivity.
8/ If you see a resistance mutation in an archived geno, you can be sure it’s real. If you don’t see a mutation you are expecting based on pt hx, you might want to work under the assumption that it’s there even if not detected by the archived geno.
9/ The major advantage of an archived genotype is that you can do it when a patient is suppressed.
10/ Whether you do a standard or an archived genotype, you will get a sequence that can be compared to wildtype sequence. Recall that the DNA sequence predicts an RNA sequence which predicts an amino acid sequence.
11/ There are well-defined amino acid substitutions that we know, when present, will render specific ARVs resistant. Ex: A mutation that leads to a substitution of lysine (K) for asparagine (N) at position 103 in the RT gene results in resistance to nevirapine and efavirenz.
12/ This graphic emphasizes the nomenclature we use for describing genotype resistance mutations.
13/ Let's move on to phenotypes.
HIV phenotype testing is not done as often as genotype testing because it is expensive and time-consuming. The concept of this test is analogous to determining MICs in vitro for antibiotics against bacterial pathogens.
14/ In phenotype testing, virus from a patient is isolated and the viral genes (RT, protease) are amplified and then inserted into a lab strain of HIV without these genes. These recombinant clones are then tested for drug susceptibility in vitro.
15/ The phenotype test measures and reports the IC50 or the drug concentration required to inhibit replication of the patient’s HIV by 50%. This is then compared to wildtype strains. The further the patient’s curve is shifted to the right, the higher degree of resistance.
16/ We will talk about indications for resistance testing and when you might choose on over another next time.
17/ For now, remember that like any test, an #HIVDrugResistance test can never be interpreted in isolation. A patient’s ART history, adherence history, and prior resistance tests are all essential in helping interpret resistance tests and making management decisions.
• • •
Missing some Tweet in this thread? You can try to
force a refresh
Great conversation with @IAS_USA panelists on the new guidelines!
For those with tuberculous meningitis, high-dose steroids should be initiated along with tuberculosis treatment and ART should be initiated within 2 weeks after starting tuberculosis treatment and steroids
✅TAF and rifampin OK
✅Do DTG bid if using rifampin
✅DTG daily OK if using rifabutin
🚫BIC with rifamycins
💥Also new: earlier ART start in crypto meningitis recommended if access to LP & monitoring
"For individuals with cryptococcal meningitis with access to close monitoring and supportive care for adverse events, ART should be initiated 2-4 weeks after starting antifungal therapy"
2/
Curiosity is an itchy state of mind
Lying West of wonder and East of ecstacy
Not well localized in a brain bound by murmuring limbics
Not with its own bump in the phrenology of CT and PET
A defiantly defining feature of being human and alive
3/
Compassion is a practice, of the brain not defined by it
I aspire to compassion as I once yearned to be cool
Seems some people just are; for me empathy takes time
For me, curiosity is the hook, line and sinker
Caught my attention to compassion’s lifetime work.
When CrCl <30, technically should stop TAF and FTC/3TC. TAF can be used down to CrCl 15 not on dialysis (think HBV monoinfection tx data) BUT technically FTC or 3TC should be renally-dosed at these lower CrCl.
I've seen FTC and/or 3TC continued at these lower CrCl levels since risk of lactic acidosis and/or other AE is still low but technically would not be "appropriate"
To keep the momentum going, let’s move on to transmitted drug resistance. For those just joining, we previously discussed that #HIVDrugResistance is important yet challenging for learners.
2/ We also reviewed the basic principle that HIV resistance develops when HIV replicates in the setting of subtherapeutic drug levels. Virions containing resistance mutations are selected for in this case.
3/ Today we’ll define transmitted drug resistance (TDR) (vs acquired drug resistance). TDR = acquisition of drug-resistant HIV at the time of new HIV infection. We identify TDR when we do a baseline HIV genotype (recommended for all patients who are newly diagnosed with HIV).