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Relative Contribution of Pharmacokinetics and Immune Signatures to Clinical Outcomes in Patients With HIV-associated Cryptococcal Meningitis

Stott, KE; Tembo, D; Kajanga, C; Ahmadu, A; Namakhwa, D; Kolamunnage-Dona, R; Sarker, C; Moyo, M; Gondwe, E; Chimang'anga, W; et al. Stott, KE; Tembo, D; Kajanga, C; Ahmadu, A; Namakhwa, D; Kolamunnage-Dona, R; Sarker, C; Moyo, M; Gondwe, E; Chimang'anga, W; Chasweka, M; Shah, RV; Lawrence, DS; Harrison, TS; Jarvis, JN; Lalloo, DG; Hope, W; Mwandumba, HC (2025) Relative Contribution of Pharmacokinetics and Immune Signatures to Clinical Outcomes in Patients With HIV-associated Cryptococcal Meningitis. OPEN FORUM INFECTIOUS DISEASES, 12 (4). ISSN 2328-8957 https://doi.org/10.1093/ofid/ofaf190
SGUL Authors: Harrison, Thomas Stephen

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Abstract

Background Host immune responses to HIV-associated cryptococcal meningitis are critical in disease outcome. Their interaction with antifungal drug exposure is poorly understood. This study explored associations between immune biomarkers, antifungal drug exposure, and clinical outcomes in HIV-associated cryptococcal meningitis. Methods We analyzed serial plasma and cerebrospinal fluid immune biomarkers from 64 participants recruited from the AMBITION-cm trial. We estimated individual-level exposure to amphotericin B, flucytosine, and fluconazole. Associations between immune biomarkers, pharmacokinetic parameters, and clinical outcomes were evaluated. Results An inflammatory cerebrospinal fluid response, characterized by coordination between tumor necrosis factor-α, granulocyte colony-stimulating factor, and interleukin-7 signaling, was linked to low fungal burden, low intracranial pressure, and survival. However, the value of specific immune biomarkers did not predict EFA or mortality. Exposure to amphotericin B was significantly associated with EFA. Conclusions Favorable clinical outcomes from HIV-associated cryptococcal meningitis are associated with coordinated inflammatory and cytotoxic responses in the central nervous system. Antifungal drug exposure was the dominant predictor of EFA.

Item Type: Article
Additional Information: © The Author(s) 2025. Published by Oxford University Press on behalf of Infectious Diseases Society of America. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
Keywords: amphotericin B, cryptococcal meningitis, immunomodulation, pharmacodynamics, pharmacokinetics
SGUL Research Institute / Research Centre: Academic Structure > Infection and Immunity Research Institute (INII)
Journal or Publication Title: OPEN FORUM INFECTIOUS DISEASES
ISSN: 2328-8957
Language: en
Publisher License: Creative Commons: Attribution 4.0
Projects:
Project IDFunderFunder ID
203919/Z/16/ZWellcome Trusthttp://dx.doi.org/10.13039/100004440
NIHR134342National Institute for Health Researchhttp://dx.doi.org/10.13039/501100000272
TRIA2015-1092European and Developing Countries Clinical Trials Partnershiphttp://dx.doi.org/10.13039/501100001713
MR/P006922/1Joint Global Health Trials SchemeUNSPECIFIED
RP-2017-08-ST2-012National Institute for Health Researchhttp://dx.doi.org/10.13039/501100000272
NIHR134342National Institute for Health Researchhttp://dx.doi.org/10.13039/501100000272
URI: https://openaccess.sgul.ac.uk/id/eprint/117535
Publisher's version: https://doi.org/10.1093/ofid/ofaf190

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