Cryptococcal Meningitis Treatment Beyond HIV: Recognizing the Need for Individualized Immune-Based Strategies

The promising results of the AMBITION-cm trial in persons with HIV have sparked interest in treating non-HIV-associated cryptococcal meningitis with single 10-mg/kg liposomal amphotericin B, combined with oral flucytosine and fluconazole. However, caution is warranted when applying this approach to non-HIV organ transplant recipients, whose immune status may vary due to the effects of immunosuppressive drugs. In these patients, cryptococcal disease, which generally occurs after initial immunosuppressant doses are reduced, may be driven by fungal growth, an immune response to cryptococcal antigens, or both. The latter is particularly relevant as potent antimicrobial therapy can lyse Cryptococcus, releasing antigens that trigger inflammation and cause host-mediated damage. Reducing iatrogenic immunosuppression may enhance host immune responses, which, in the context of neurological infections, may be fatal. This highlights the importance of understanding the immune status of non-HIV organ transplant recipients within the context of the Damage-Response Framework to guide personalized treatment strategies.

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Publication Details

Journal
Clinical Infectious Diseases
Published
2025-04-24
DOI
https://doi.org/10.1093/cid/ciaf218
Citations
4
Primary Topic
Fungal Infections and Studies
Type
article
Field-Weighted Citation Impact
5.42
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article

Cryptococcal Meningitis Treatment Beyond HIV: Recognizing the Need for Individualized Immune-Based Strategies

David R. Boulware, Hyunah Yoon, Liise-anne Pirofski
4 citations
Clinical Infectious Diseases
Fungal Infections and Studies
5.42
article

Cryptococcal Meningitis Treatment Beyond HIV: Recognizing the Need for Individualized Immune-Based Strategies

David R. Boulware, Hyunah Yoon, Liise-anne Pirofski
article en
4 citations

Abstract

The promising results of the AMBITION-cm trial in persons with HIV have sparked interest in treating non-HIV-associated cryptococcal meningitis with single 10-mg/kg liposomal amphotericin B, combined with oral flucytosine and fluconazole. However, caution is warranted when applying this approach to non-HIV organ transplant recipients, whose immune status may vary due to the effects of immunosuppressive drugs. In these patients, cryptococcal disease, which generally occurs after initial immunosuppressant doses are reduced, may be driven by fungal growth, an immune response to cryptococcal antigens, or both. The latter is particularly relevant as potent antimicrobial therapy can lyse Cryptococcus, releasing antigens that trigger inflammation and cause host-mediated damage. Reducing iatrogenic immunosuppression may enhance host immune responses, which, in the context of neurological infections, may be fatal. This highlights the importance of understanding the immune status of non-HIV organ transplant recipients within the context of the Damage-Response Framework to guide personalized treatment strategies.

Clinical Infectious DiseasesVol. 81(5)
Albert Einstein College of Medicine (US), University of Minnesota (US), Montefiore Medical Center (US)
Good health and well-being
Openalex Percentile: Top 4%
Fungal Infections and Studies
5.42
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Cryptococcal Meningitis Treatment Beyond HIV: Recognizing the Need for Individualized Immune-Based Strategies — David R. Boulware, Hyunah Yoon, et al. · Clinical Infectious Diseases (2025) | TGRS Research Map | TGRS