Cryptococcal Immune Reconstitution Inflammatory Syndrome

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Cryptococcal Immune Reconstitution Inflammatory Syndrome
 
Dr. Tihana Bicanic
Reader and Consultant in Infectious Diseases
Centre for Global Health, Institute of Infection and Immunity,
St. George’s, University of London; St George's Hospital NHS Foundation Trust
 
 
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To understand what immune reconstitution inflammatory syndrome is
To be aware of the predictors for C-IRIS
To be aware of the different manifestations of C-IRIS
To understand the management and prevention of C-IRIS
 
Immune Reconstitution Inflammatory Syndrome
 
Rapid reversal of immunodeficiency 
leads to 
restoration of T-cell mediated 
Cryptococcus
-
specific immune responses, promoting an (exaggerated) inflammatory reaction to antigens
(dead or alive)
Two clinical scenarios:
 
1. “
Unmasking
” IRIS: 
NEW
 presentation of subclinical/ latent OI
 
2. “
Paradoxical
” IRIS: symptom recurrence in previously treated OI (clinical/ microbiologic response)
Incidence: Paradoxical: 6-45% in HIV+ (usually 1-2 months post start of ART), 5-11% solid
organ transplant recipients)
Acute mortality 0-36%: lower if recognised early and managed appropriately
 
Haddow 
et al. Lancet Infect Dis 
2010; 10:791-802
Longley 
et al
. 
Curr Opin Infect Dis. 
2013;26(1) : 26–34
 
Immune Reconstitution Inflammatory Syndrome
 
CNS presentation most common
: headache, meningism,
seizures
Lumbar Puncture: CSF    WBC,  protein,  glucose;
   fungal cultures sterile (paradoxical) or positive (unmasking)
 
Non CNS
Pneumonitis
Lymphadenitis (including mediastinal)
Rarely: skin, 
soft tissue, bone and joint lesions
 
Immune Reconstitution Inflammatory Syndrome
 
Diagnostic criteria
New appearance or worsening of the following
:
I.
Clinical or radiographic manifestations consistent with an inflammatory
process
II.
Histopathology showing granulomatous lesions
III.
Symptoms occurring during receipt of appropriate antifungal therapy with no
alternative cause identified on investigation
IV.
Negative results of cultures, or stable or reduced biomarkers for the initial
fungal pathogen during the diagnostic workup for the inflammatory process
(Unmasking= NEW presentation with cultures positive)
 
Haddow 
et al. Lancet Infect Dis. 
2010; 10:791-802
Maziarz & Perfect: 
Infect Dis Clin N Am .
 2016;30:179-206
 
Immune Reconstitution Inflammatory Syndrome
 
Predictors:
1.
High fungal burden at diagnosis and at start of ART: baseline CrAg titre >1:1024,
fungaemia + poor fungal clearance 
 
positive CSF cultures prior to ART start
2.
Host immune factors: rapid immune reconstitution (decline in HIV viral load , increasing
CD4 count); poor CNS inflammatory responses (CSF WBC and cytokine responses pre-ART
including TNF alpha and IFN gamma)
 
 
 
Longley 
et al
. 
Curr Opin Infect Dis
. 2013; 26(1): 26–34
 
Immune Reconstitution Inflammatory Syndrome
 
Management of C-IRIS
No trials: based on expert opinion
Check adherence to fluconazole/ ART
Do LP / investigate to seek alternative explanations
Modification of antifungals not indicated; Continue ART
Minor cases improve without specific treatment
Corticosteroid therapy if persistent/ severe CNS manifestations:
0.5–1.0 mg/kg per day of prednisolone or dexamethasone: 2-6 weeks reducing
Anti-TNF-
α
/ thalidomide case reports
Therapeutic LPs if raised CSF OP
 
Longley 
et al
. 
Curr Opin Infect Dis
. 2013; 26(1): 26–34
Maziarz & Perfect
: Infect Dis Clin N Am. 
2016;30:179-206
 
Prevention of IRIS
 
Paradoxical:
Use 
best available 
initial induction CM treatment regimen to sterilise the CSF (AmB 1mg/kg/d+5FC
100mg/kg/d OR Fluconazole 1200mg/d+5FC)
Perform LP at 2 weeks to assess CSF culture status
Prompt ART initiation: aim to start at 4-6 weeks from CM diagnosis: when CNS symptoms (incl raised
ICP) resolved and CSF cultures sterile
Unmasking
Screen for serum CrAg in patients with CD4<100/uL: if positive, LP if symptoms; treat pre-emptively
with fluconazole
 
Summary
 
C-IRIS is due to exaggerated immune responses to Cryptococcus after immune
restoration
Can be both unmasking and paradoxical: diagnosis challenging (case
definition)
CNS manifestation most common (raised ICP, seizures)
Corticosteroids for refractory symptoms; mortality low if recognised early and
managed
Can be prevented by good induction CM treatment, appropriate ART timing
and CRAG screening programmes
undefined
 
END
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Cryptococcal Immune Reconstitution Inflammatory Syndrome (C-IRIS) is a condition where rapid reversal of immunodeficiency triggers exaggerated inflammatory reactions in response to Cryptococcus antigens. It can manifest as either Unmasking IRIS or Paradoxical IRIS, with common CNS presentations including headache, meningism, and seizures. Diagnostic criteria involve new or worsening clinical, radiographic, or histopathological manifestations during antifungal therapy. Predictors include high fungal burden and host immune factors. Management and prevention strategies are crucial to reduce mortality rates associated with C-IRIS.

  • C-IRIS
  • Cryptococcus
  • Inflammatory Syndrome
  • Immune Reconstitution
  • Infectious Diseases

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  1. Cryptococcal Immune Reconstitution Inflammatory Syndrome Dr. Tihana Bicanic Reader and Consultant in Infectious Diseases Centre for Global Health, Institute of Infection and Immunity, St. George s, University of London; St George's Hospital NHS Foundation Trust

  2. Intended Learning Outcomes To understand what immune reconstitution inflammatory syndrome is To be aware of the predictors for C-IRIS To be aware of the different manifestations of C-IRIS To understand the management and prevention of C-IRIS

  3. Immune Reconstitution Inflammatory Syndrome Rapid reversal of immunodeficiency leads to restoration of T-cell mediated Cryptococcus- specific immune responses, promoting an (exaggerated) inflammatory reaction to antigens (dead or alive) Two clinical scenarios: 1. Unmasking IRIS: NEW presentation of subclinical/ latent OI 2. Paradoxical IRIS: symptom recurrence in previously treated OI (clinical/ microbiologic response) Incidence: Paradoxical: 6-45% in HIV+ (usually 1-2 months post start of ART), 5-11% solid organ transplant recipients) Acute mortality 0-36%: lower if recognised early and managed appropriately Haddow et al. Lancet Infect Dis 2010; 10:791-802 Longley et al. Curr Opin Infect Dis. 2013;26(1) : 26 34

  4. Immune Reconstitution Inflammatory Syndrome CNS presentation most common: headache, meningism, seizures Lumbar Puncture: CSF WBC, protein, glucose; fungal cultures sterile (paradoxical) or positive (unmasking) Non CNS Pneumonitis Lymphadenitis (including mediastinal) Rarely: skin, soft tissue, bone and joint lesions

  5. Immune Reconstitution Inflammatory Syndrome Diagnostic criteria New appearance or worsening of the following: I. Clinical or radiographic manifestations consistent with an inflammatory process II. Histopathology showing granulomatous lesions III. Symptoms occurring during receipt of appropriate antifungal therapy with no alternative cause identified on investigation IV. Negative results of cultures, or stable or reduced biomarkers for the initial fungal pathogen during the diagnostic workup for the inflammatory process (Unmasking= NEW presentation with cultures positive) Haddow et al. Lancet Infect Dis. 2010; 10:791-802 Maziarz & Perfect: Infect Dis Clin N Am . 2016;30:179-206

  6. Immune Reconstitution Inflammatory Syndrome Predictors: 1. High fungal burden at diagnosis and at start of ART: baseline CrAg titre >1:1024, fungaemia + poor fungal clearance positive CSF cultures prior to ART start 2. Host immune factors: rapid immune reconstitution (decline in HIV viral load , increasing CD4 count); poor CNS inflammatory responses (CSF WBC and cytokine responses pre-ART including TNF alpha and IFN gamma) Longley et al. Curr Opin Infect Dis. 2013; 26(1): 26 34

  7. Immune Reconstitution Inflammatory Syndrome Management of C-IRIS No trials: based on expert opinion Check adherence to fluconazole/ ART Do LP / investigate to seek alternative explanations Modification of antifungals not indicated; Continue ART Minor cases improve without specific treatment Corticosteroid therapy if persistent/ severe CNS manifestations: 0.5 1.0 mg/kg per day of prednisolone or dexamethasone: 2-6 weeks reducing Anti-TNF- / thalidomide case reports Longley et al. Curr Opin Infect Dis. 2013; 26(1): 26 34 Maziarz & Perfect: Infect Dis Clin N Am. 2016;30:179-206 Therapeutic LPs if raised CSF OP

  8. Prevention of IRIS Paradoxical: Use best available initial induction CM treatment regimen to sterilise the CSF (AmB 1mg/kg/d+5FC 100mg/kg/d OR Fluconazole 1200mg/d+5FC) Perform LP at 2 weeks to assess CSF culture status Prompt ART initiation: aim to start at 4-6 weeks from CM diagnosis: when CNS symptoms (incl raised ICP) resolved and CSF cultures sterile Unmasking Screen for serum CrAg in patients with CD4<100/uL: if positive, LP if symptoms; treat pre-emptively with fluconazole

  9. Summary C-IRIS is due to exaggerated immune responses to Cryptococcus after immune restoration Can be both unmasking and paradoxical: diagnosis challenging (case definition) CNS manifestation most common (raised ICP, seizures) Corticosteroids for refractory symptoms; mortality low if recognised early and managed Can be prevented by good induction CM treatment, appropriate ART timing and CRAG screening programmes

  10. END

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