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CROI 2016: VRC01 Antibody Delays But Does Not Prevent HIV Rebound After ART Interruption

VRC01, a broadly neutralizing antibody targeting HIV's CD4 binding site, was able to modestly delay the return of viral replication following interruption of antiviral therapy (ART), according to a study presented at the Conference on Retroviruses and Opportunistic Infections (CROI 2016)last month in Boston. VRC01 did not maintain viral suppression on its own, but it may play a role in combination therapy for HIV treatment or a functional cure.

Studies of antibodies for HIV prevention and treatment have mostly been disappointing because the virus is highly variable. The recent discovery of a number of broadly neutralizing monoclonal antibodies, or bNAbs, that can target multiple HIV strains has given new impetus to this line of research. Antibodies for HIV prevention or treatment was the topic of a plenary lecture by John Mascola from the U.S. National Institute of Allergy and Infectious Diseases Vaccine Research Center as well as a talk at the Community HIV Cure Research Workshop preceding CROI. (See this overview of those presentations.)

Katharine Bar from the University of Pennsylvania and fellow investigators with the AIDS Clinical Trials Group A5340 team evaluated whether one of the most promising bNAbs, known as VRC01, could delay or prevent the return of HIV viremia after ART interruption.

VRC01 attaches to the CD4 binding site of HIV's envelope protein, preventing the virus from binding to the CD4 receptor on the surface of T-cells that it uses to gain entry. The CD4 binding site is conserved, or consistent across HIV strains, and VRC01 neutralizes around 90% of diverse viral isolates from multiple clades in the laboratory.

Thisopen-label study looked at the safety, tolerability, pharmacokinetics, and antiviral activity of VRC01 in HIV-positive people with suppressed viral load (<50 copies/mL) for more than 6 months on an ART regimen containing a protease inhibitor or integrase inhibitor.

The study enrolled 14 participants. All were men, half were African
American, and the median age was 38 years. They had well-preserved immune function with a median CD4 count of approximately 900 cells/mm³ and a CD nadir (lowest-ever level) above 200. They had been on ART for a median of 4.7 years.

Participants received intravenous (IV) infusions of 40 mg/kg VRC01 every 3 weeks for 3 doses. They started a carefully monitored analytical treatment interruption 1 week after the first infusion. ART was restarted if they had a viral load >1000 copies/mL or their CD4 count fell below 350 cells/mm³. One patient stopped ART before the first VRC01 dose and was excluded from the efficacy analysis.

Results

• VRC01 was generally safe and well-tolerated, with no grade 3 or 4 (severe) adverse events, nor any grade 2 (moderate) events considered related to VRC01.
• VRC01 remained at adequate concentrations (>50
mcg/mL) for 8 weeks after stopping ART.
• Despite high antibody levels, a majority of participants experienced viral
rebound by week 5 of the treatment interruption.
• The remaining 2 participants maintained viral suppression for 8 and 11 weeks off ART before rebounding.
• However, viral rebound was delayed compared to the time it took for virus to return in people who stopped non-NNRTI ART regimens in prior ACTG studies:

o   At 4 weeks after the interruption, 38% of VRC01 recipients maintained viral suppression compared to 13% of historical control subjects, a significant difference.

o   At 8 weeks, 8% of VRC01 recipients still maintained viral suppression compared to 3% of historical controls, which was no longer significant.

• Time to viral rebound was not associated with VRC01 level, age, baseline or nadir CD4 count, or duration of ART.
• Participants re-established viral suppression after restarting ART.
• Genetic sequencing of rebounding virus suggested that in some cases VRC01 restricted clonality (number of different strains) and in other cases it selected for pre-existing VRC01-resistant variants in the viral reservoir.

"The passive immunization of VRC01 is safe and well tolerated, modestly delays the return of viremia when compared to historical controls, but does not maintain viral suppression in the majority of patients," the researchers concluded.

Multiple VRC01 Doses

Tae-Wook Chun and colleagues from NIAID conducted a similar exploratory trial looking at the effect of VRC01 on plasma viral rebound following discontinuation of ART in people who started treatment during chronic HIV infection and had viral suppression for more than 3 years.

The 10 participants in this open-label study had been on ART for an average of 10.6 years and had mean CD4 and CD8 counts of 796 and 768 cells/mm³, respectively. They received infusions of 40mg/kg VRC01 at 3 days prior to ART interruption, again at 14 and 28 days following interruption, and monthly thereafter for up to 6 months.

Multiple infusions of VRC01 were safe and well-tolerated. All 10 participants experienced viral rebound between 11 and 86 days (media 39 days) following ART interruption, and 9 restarted treatment. VRC01 levels were high (142-583 mcg/mL) at the time of viral rebound. Several patients had evidence of VRC01-resistent virus prior to antibody infusion.

"While multiple infusions of VRC01 were safe and well-tolerated, the majority of patients experienced plasma viral rebound despite adequate levels of antibody in plasma," the researchers concluded. "Therefore, therapeutic strategies involving passive transfer of bNAbs may require a combination(s) of antibodies and/or resistance pre-screening in order to achieve sustained virologic control in HIV-infected individuals upon withdrawal of ART."

3/31/16

References

KJ Bar, LJ Harrison, ET Overton, et al. ACTG 5340: The Effect of VRC01 on Viral Kinetics After Analytic Treatment Interruption. Conference on Retroviruses and Opportunistic Infections. Boston, February 22-25, 2016. Abstract 32LB.

T-W Chun, M Sneller, C Seamon, K Clarridge, A Fauci, et al. Effect of Infusion of Broadly Neutralizing Antibody VRC01 on HIV Plasma Rebound. Conference on Retroviruses and Opportunistic Infections. Boston, February 22-25, 2016. Abstract 311LB.