Evidence map›Paper›PMID 40271162›Full record

ArticleOpen forum infectious diseases2025

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

Katharine E Stott, Dumizulu Tembo, Cheusisime Kajanga, Ajisa Ahmadu, Dumisan Namakhwa, Ruwanthi Kolamunnage-Dona, Chandni Sarker, Melanie Moyo, Ebbie Gondwe, Wezi Chimang'anga and 9 more

Abstract read
In one paragraph

Article in Open forum infectious diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

19 authors.

Katharine E StottAntimicrobial Pharmacodynamics and Therapeutics group, Department of Pharmacology and Therapeutics, University of Liverpool, Liverpool, UK.
Dumizulu TemboMucosal and Vascular Immunology Group, Malawi Liverpool Wellcome Programme, Blantyre, Malawi.
Cheusisime KajangaMucosal and Vascular Immunology Group, Malawi Liverpool Wellcome Programme, Blantyre, Malawi.
Ajisa AhmaduMucosal and Vascular Immunology Group, Malawi Liverpool Wellcome Programme, Blantyre, Malawi.
Dumisan NamakhwaMucosal and Vascular Immunology Group, Malawi Liverpool Wellcome Programme, Blantyre, Malawi.
Ruwanthi Kolamunnage-DonaDepartment of Health Data Science, University of Liverpool, Liverpool, UK.
Chandni SarkerDepartment of Health Data Science, University of Liverpool, Liverpool, UK.ORCID https://orcid.org/0009-0007-0786-3422
Melanie MoyoMucosal and Vascular Immunology Group, Malawi Liverpool Wellcome Programme, Blantyre, Malawi.ORCID https://orcid.org/0000-0002-0483-4817
Ebbie GondweMucosal and Vascular Immunology Group, Malawi Liverpool Wellcome Programme, Blantyre, Malawi.
Wezi Chimang'angaMucosal and Vascular Immunology Group, Malawi Liverpool Wellcome Programme, Blantyre, Malawi.
Madalitso ChaswekaMucosal and Vascular Immunology Group, Malawi Liverpool Wellcome Programme, Blantyre, Malawi.
Reya V ShahInstitute of Infection and Immunity, City St George's University London, London, UK.ORCID https://orcid.org/0009-0003-6678-2885
David S LawrenceDepartment of Clinical Research, Faculty of Infectious and Tropical Diseases, London School of Tropical Medicine, London, UK.ORCID https://orcid.org/0000-0002-5439-4039
Thomas S HarrisonInstitute of Infection and Immunity, City St George's University London, London, UK.
Joseph N JarvisDepartment of Clinical Research, Faculty of Infectious and Tropical Diseases, London School of Tropical Medicine, London, UK.
David G LallooLiverpool School of Tropical Medicine, Liverpool, UK.ORCID https://orcid.org/0000-0001-7680-2200
William HopeAntimicrobial Pharmacodynamics and Therapeutics group, Department of Pharmacology and Therapeutics, University of Liverpool, Liverpool, UK.ORCID https://orcid.org/0000-0001-6187-878X
Henry C MwandumbaMucosal and Vascular Immunology Group, Malawi Liverpool Wellcome Programme, Blantyre, Malawi.ORCID https://orcid.org/0000-0003-4470-3608
AMBITION Study Group

Funding

Wellcome Trust
6 · The paper itself

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.

Indexed as

amphotericin Bcryptococcal meningitisimmunomodulationpharmacodynamicspharmacokinetics

Identifiers

PMID40271162
PMCPMC12015468

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.