Publications & Reports

Immune restoration diseases reflect diverse immunopathological mechanisms.

Price P, Murdoch DM, Agarwal U, Lewin SR, Elliott JH, French MA
School of Pathology and Laboratory Medicine, University of Western Australia, Rear 50 Murray Street, Perth 6000, Western Australia, Australia. patricia.price@uwa.edu.au

Abstract

Up to one in four patients infected with human immunodeficiency virus type 1 and given antiretroviral therapy (ART) experiences inflammatory or cellular proliferative disease associated with a preexisting opportunistic infection, which may be subclinical.

These immune restoration diseases (IRD) appear to result from the restoration of immunocompetence. IRD associated with intracellular pathogens are characterized by cellular immune responses and/or granulomatous inflammation.

Mycobacterial and cryptococcal IRD are attributed to a pathological overproduction of Th1 cytokines. Clinicopathological characteristics of IRD associated with viral infections suggest different pathogenic mechanisms.

For example, IRD associated with varicella-zoster virus or JC polyomavirus infection correlate with a CD8 T-cell response in the central nervous system.

Exacerbations or de novo presentations of hepatitis associated with hepatitis C virus (HCV) infection following ART may also reflect restoration of pathogen-specific immune responses as titers of HCV-reactive antibodies rise in parallel with liver enzymes and plasma markers of T-cell activation.

Correlations between immunological parameters assessed in longitudinal sample sets and clinical presentations are required to illuminate the diverse immunological scenarios described collectively as IRD.

Here we present salient clinical features and review progress toward understanding their pathogeneses.

Publication

  • Journal: Clinical Microbiology Reviews
  • Published: 01/10/2009
  • Volume: 22
  • Issue: 4
  • Pagination: 651-663

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