No difference in HIV-1 integrase inhibitor resistance between CSF and blood compartments

Basma Abdi1, Mouna Chebbi1, Marc Wirden1

  • 1Sorbonne Université, INSERM, Institut Pierre Louis d'Epidémiologie et de Santé Publique, AP-HP, Hôpitaux Universitaires Pitié-Salpêtrière-Charles Foix, Laboratoire de Virologie, F75013, Paris, France.

Insights

HIV-1 integrase inhibitor resistance in the central nervous system (CNS) is poorly understood. This study found similar resistance profiles in cerebrospinal fluid (CSF) and plasma, suggesting CSF can serve as a marker for CNS resistance.

Area of Science:

  • Virology
  • Infectious Diseases
  • Pharmacology

Background:

  • Limited knowledge exists regarding human immunodeficiency virus type 1 (HIV-1) integrase inhibitor resistance within the central nervous system (CNS).
  • Understanding resistance patterns in the CNS is crucial for effective HIV-1 treatment strategies.

Purpose of the Study:

  • To assess integrase inhibitor resistance in cerebrospinal fluid (CSF) as a surrogate marker for CNS resistance.
  • To compare HIV-1 integrase inhibitor resistance in CSF with that observed in plasma.

Main Methods:

  • Sequencing of HIV-1 integrase from both plasma and CSF samples of 59 HIV-1 patients.
  • Collection of clinical and biological data from routine patient care.
  • Analysis of resistance mutations in relation to antiretroviral (ARV) treatment status and HIV-1 subtypes.

Main Results:

  • HIV-1 integrase sequences from CSF showed resistance mutations in 33.3% of ARV-naive and 25.0% of ARV-treated patients.
  • Common resistance mutations included L74I, T97A, and E157Q.
  • Integrase inhibitor resistance patterns in CSF were largely consistent with those found in plasma, with one exception.

Conclusions:

  • The study demonstrates comparable integrase inhibitor resistance profiles between the CNS (as indicated by CSF) and plasma in HIV-1 viraemic patients.
  • Cerebrospinal fluid can be utilized as a reliable indicator of integrase inhibitor resistance within the CNS.
Abstract