Cerebrospinal fluid HIV escape associated with progressive neurologic dysfunction in patients on antiretroviral therapy with well controlled plasma viral load

MJ Peluso, F Ferretti, J Peterson, E Lee, D Fuchs… - Aids, 2012 - journals.lww.com
MJ Peluso, F Ferretti, J Peterson, E Lee, D Fuchs, A Boschini, M Gisslén, N Angoff, RW Price…
Aids, 2012journals.lww.com
Objective: To characterize HIV-infected patients with neurosymptomatic cerebrospinal fluid
(CSF)'escape', defined as detectable CSF HIV RNA in the setting of treatment-suppressed
plasma levels or CSF RNA more than 1-log higher than plasma RNA. Design: Retrospective
case series. Setting: Four urban medical centers in the United States and Europe.
Participants: Virologically controlled HIV-infected patients on antiretroviral therapy (ART)
with progressive neurologic abnormalities who were determined to have CSF 'escape' …
Abstract
Objective:
To characterize HIV-infected patients with neurosymptomatic cerebrospinal fluid (CSF)‘escape’, defined as detectable CSF HIV RNA in the setting of treatment-suppressed plasma levels or CSF RNA more than 1-log higher than plasma RNA.
Design:
Retrospective case series.
Setting:
Four urban medical centers in the United States and Europe.
Participants:
Virologically controlled HIV-infected patients on antiretroviral therapy (ART) with progressive neurologic abnormalities who were determined to have CSF ‘escape’.
Intervention:
Optimization of ART based upon drug susceptibility and presumed central nervous system exposure.
Main outcome measures:
Levels of CSF HIV RNA and inflammatory markers, clinical signs and symptoms, and MRI findings.
Results:
Ten patients presented with new neurologic abnormalities, which included sensory, motor, and cognitive manifestations. Median CSF HIV RNA was 3900 copies/ml (range 134–9056), whereas median plasma HIV RNA was 62 copies/ml (range< 50 to 380). Median CD4+ T-cell count was 482 cells/μl (range 290–660). All patients had been controlled to less than 500 copies/ml for median 27.5 months (range 2–96) and five of 10 had been suppressed to less than 50 copies/ml for median 19.5 months (range 2–96). Patients had documentation of a stable ART regimen for median 21 months (range 9–60). All had CSF pleocytosis or elevated CSF protein; seven of eight had abnormalities on MRI; and six of seven harbored CSF resistance mutations. Following optimization of ART, eight of nine patients improved clinically.
Conclusion:
The development of neurologic symptoms in patients on ART with low or undetectable plasma HIV levels may be an indication of CSF ‘escape’. This study adds to a growing body of literature regarding this rare condition in well controlled HIV infection.
Lippincott Williams & Wilkins