Shedding light on IRIS: from Pathophysiology to Treatment of Cryptococcal Meningitis and Immune Reconstitution Inflammatory Syndrome in HIV-Infected Individuals

HIV Med. 2019 Jan;20(1):1-10. doi: 10.1111/hiv.12676. Epub 2018 Oct 25.

Abstract

Objectives: The aim of this work was to review current treatment options and propose alternatives for immune reconstitution inflammatory syndrome (IRIS) in HIV-infected individuals with cryptococcal meningitis (CM) (termed 'HIV-CM IRIS'). As a consequence of the immunocompromised state of these individuals, the initial immune response to CM is predominantly type 2 T helper (Th2) /Th17 rather than Th1, leading to inefficient fungal clearance at the time of antiretroviral initiation, and a subsequent overexaggeration of the Th1 response and life-threatening IRIS development.

Methods: An article-based and clinical trial-based search was conducted to investigate HIV-CM IRIS pathophysiology and current treatment practices.

Results: Guidelines for CM treatment, based on the Cryptococcal Optimal Antiretroviral Timing (COAT) trial, recommend delayed antiretroviral therapy (ART) following antifungal treatment. The approach aims to decrease fungal burden and allow immune balance restoration prior to ART initiation. If the initial immune balance is not restored, the fungal burden is not sufficiently reduced and there is a risk of developing IRIS post-ART, highlighted by a Th1 immune overcompensation, leading to increased mortality. The mainstay treatment for Th1-biased IRIS is corticosteroids; however, this treatment has been shown to correlate with increased mortality and significant associated adverse events. We emphasize targeting a more specific Th1 mechanism via the tumour necrosis factor (TNF)-α cytokine antagonist thalidomide, as it is the only TNF-α antagonist currently approved for use in infectious disease settings and has been shown to decrease Th1 overreaction, restoring immune balance in HIV-CM IRIS.

Conclusions: Although the side effects and limitations of thalidomide must be considered, it is currently being successfully used in infectious disease settings and warrants mainstream application as a therapeutic option for treatment of IRIS in HIV-infected patients with CM.

Keywords: COAT trial; HIV/AIDS; Th1/Th2 balance; cryptococcal meningitis; immune reconstitution inflammatory syndrome; immune restoration; thalidomide; tumour necrosis factor-α antagonist.

Publication types

  • Review

MeSH terms

  • AIDS-Related Opportunistic Infections / drug therapy
  • AIDS-Related Opportunistic Infections / immunology*
  • Adrenal Cortex Hormones / therapeutic use
  • Anti-Retroviral Agents / therapeutic use
  • Clinical Trials as Topic
  • HIV Infections / drug therapy*
  • HIV Infections / immunology
  • HIV Infections / microbiology
  • Humans
  • Immune Reconstitution Inflammatory Syndrome / drug therapy
  • Immune Reconstitution Inflammatory Syndrome / immunology*
  • Meningitis, Cryptococcal / drug therapy
  • Meningitis, Cryptococcal / immunology*
  • Th1 Cells / metabolism
  • Th17 Cells / metabolism
  • Th2 Cells / metabolism
  • Thalidomide / therapeutic use

Substances

  • Adrenal Cortex Hormones
  • Anti-Retroviral Agents
  • Thalidomide