Evidence map›Paper›PMID 42381185›Full record

ArticleTransplant infectious disease : an official journal of the Transplantation Society

Toxoplasmosis Beyond Transplantation: Diagnostic and Prevention Challenges in a Patient Receiving Targeted Immunomodulators.

Joy Mouanes-Abelin, Christelle Pomares, José G Montoya, Morgane Pondrom, Lucille DE Maria, Andrea J Zimmer, Carlos A Gomez

Abstract readCase Reports
In one paragraph

Article in Transplant infectious disease : an official journal of the Transplantation Society. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

7 authors.

Joy Mouanes-AbelinLaboratory of Hematology, Hôpital de l'ARCHET, Nice, France.ORCID https://orcid.org/0009-0004-6461-7488
Christelle PomaresLaboratoire De Parasitologie-Mycologie, Centre Hospitalier Universitaire De Nice, Inserm U 1065, Hôpital de l'ARCHET, Université De La Côte d'Azur, Nice, France.ORCID https://orcid.org/0000-0002-6192-3293
José G MontoyaDr. Jack S. Remington Laboratory for Specialty Diagnostics, Sutter Health, Palo Alto Medical Foundation, Palo Alto, California, USA.ORCID https://orcid.org/0000-0002-3378-8071
Morgane PondromPediatric Onco-Hematology Department, Hôpital de l'ARCHET, Nice, France.
Lucille DE MariaLaboratory of Hematology, Hôpital de l'ARCHET, Nice, France.ORCID https://orcid.org/0009-0002-5573-7926
Andrea J ZimmerDivision of Infectious Diseases, Department of Internal Medicine, University of Nebraska Medical Center, Omaha, Nebraska, USA.ORCID https://orcid.org/0000-0002-1460-0774
Carlos A GomezDivision of Infectious Diseases, Department of Internal Medicine, University of Nebraska Medical Center, Omaha, Nebraska, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Toxoplasmosis has long been recognized as a serious complication in immunocompromised host, particularly those with advanced HIV/AIDS, hematopoietic stem-cell transplantation (HSCT), solid-organ transplant (SOT), and hematological malignancies. The rapid expansion of targeted immunomodulators, including chimeric antigen receptor T-cell (CAR-T) therapies, monoclonal antibodies, and small-molecule inhibitors, is creating new at-risk populations beyond traditional transplant settings. We present a 9-year-old boy with high-risk B-cell acute lymphoblastic leukemia (B-ALL), who developed prolonged fever and macrophage activation syndrome (MAS). After an extensive unrevealing workup, disseminated acute toxoplasmosis was identified incidentally on bone marrow aspirate via morphologic identification of tachyzoites and confirmed by Toxoplasma gondii PCR. This case exemplifies the emerging threat of toxoplasmosis in non-transplant immunomodulated hosts and supports three core mitigation strategies. First, baseline Toxoplasma IgG and IgM serology should be obtained in all patients initiating targeted immunotherapy, recognizing that B-cell depletion or hypogammaglobulinemia may render IgG unreliable, and that IgM may be falsely negative, delayed, or persistently positive in immunocompromised individuals. Second, targeted PCR from clinically relevant compartments or metagenomic next-generation sequencing when conventional diagnostics is unrevealing should be applied early. Third, prevention requires a bundled approach: baseline screening, patient education for seronegative individuals, and trimethoprim-sulfamethoxazole prophylaxis with or without serial qPCR monitoring for seropositive patients. Toxoplasmosis is no longer a transplant-exclusive concern. As targeted immunomodulators reshape practice across rheumatology, oncology, neurology, and autoimmune disease, infectious diseases specialists must lead efforts to raise cross-specialty awareness, establish guidelines, and build registries to define the true burden of toxoplasmosis in these growing populations.

Indexed as

Immunocompromised HostImmunologic FactorsImmunomodulating AgentsToxoplasmosisAntibodies, ProtozoanChildHumansImmunoglobulin GImmunoglobulin MMacrophage Activation SyndromeMaleToxoplasmaAntibodies, ProtozoanImmunoglobulin GImmunoglobulin MImmunologic FactorsImmunomodulating AgentsbiologicsCAR T‐cell therapydisseminated toxoplasmosishematologic malignancymacrophage activation syndromePCRtargeted immunotherapyToxoplasma gondiitoxoplasmosis

Identifiers

PMID42381185
PMCPMC13450287

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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.