Evidence map›Paper›PMID 42853462›Full record

ArticleJournal of hematopathology2026

EBV-positive Hodgkin lymphoma with an immunosuppressive microenvironment during guselkumab (interleukin-23 inhibitor) therapy for chronic plaque psoriasis.

Bhaumik Shah, Janusz Franco-Barraza, Kathy Q Cai, Mariia Dmitrieva, Marcus Messmer, Yibin Yang, Mariusz Wasik, Edna Cukierman, Reza Nejati

Abstract readCase Reports
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In one paragraph

Article in Journal of hematopathology, 2026. 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
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1 · What the graph read from it

What it found

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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

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5 · Who and what money

Authors and funding

9 authors.

Bhaumik ShahDepartment of Pathology, Fox Chase Cancer Center, Temple Health, Philadelphia, PA, USA.
Janusz Franco-BarrazaCancer Signaling & Microenvironment Program, Fox Chase Cancer Center, Temple Health, 333 Cottman Avenue, Philadelphia, PA, 19111, USA.
Kathy Q CaiCancer Signaling & Microenvironment Program, Fox Chase Cancer Center, Temple Health, 333 Cottman Avenue, Philadelphia, PA, 19111, USA.
Mariia DmitrievaCancer Signaling & Microenvironment Program, Fox Chase Cancer Center, Temple Health, 333 Cottman Avenue, Philadelphia, PA, 19111, USA.
Marcus MessmerCancer Signaling & Microenvironment Program, Fox Chase Cancer Center, Temple Health, 333 Cottman Avenue, Philadelphia, PA, 19111, USA.
Yibin YangCancer Signaling & Microenvironment Program, Fox Chase Cancer Center, Temple Health, 333 Cottman Avenue, Philadelphia, PA, 19111, USA.
Mariusz WasikDepartment of Pathology, Fox Chase Cancer Center, Temple Health, Philadelphia, PA, USA.
Edna CukiermanCancer Signaling & Microenvironment Program, Fox Chase Cancer Center, Temple Health, 333 Cottman Avenue, Philadelphia, PA, 19111, USA.
Reza NejatiDepartment of Pathology, Fox Chase Cancer Center, Temple Health, Philadelphia, PA, USA. Reza.Nejati@fccc.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPsoriasis is an independent risk factor for classic Hodgkin lymphoma (cHL). Guselkumab has a favorable malignancy safety profile in clinical trials. PURPOSE: To report the first documented Epstein-Barr virus (EBV)-positive cHL arising in a biologic-naive patient with psoriatic arthritis during guselkumab therapy for chronic plaque psoriasis, and to describe its tumor microenvironment.

methodsExcisional biopsy with immunohistochemistry, EBER in situ hybridization, and targeted sequencing, plus spatial single-cell proteomics (9-plex sequential immunofluorescence) of the diagnostic lymph node.

resultsA man in his early 40s developed night sweats, syncope, and bulky right cervical lymphadenopathy 7 months after starting guselkumab. Biopsy showed mixed-cellularity EBV-positive cHL (latency IIa: EBER+, LMP1+, EBNA-2-). HRS cells were weak PAX5+, CD20 negative, CD15+, strong CD30+, OCT2 negative/weak, BOB1 negative/weak, and strong CD200+. The microenvironment contained CTLA4+ immunosuppressive T cells (10.15%), M2 macrophages (10.35%), modest Th2 cells (0.38%), a low Th1/Th2 ratio (~0.39), and Th17 cells (~13%). GATA3 and CCR4 immunohistochemistry confirmed modest Th2 skewing. After guselkumab was stopped, he achieved a complete metabolic response with ABVD and involved-site radiotherapy and remains in remission on apremilast.

conclusionsThe short latency and atypical Th2-skewed, myeloid-enriched microenvironment, in contrast to the typical Th1-dominant profile of EBV-positive cHL, raise the possibility of immune-milieu alteration under IL-23 inhibition. This case supports continued pharmacovigilance for rare lymphomas in patients receiving IL-23 inhibitors and the need for larger studies to clarify potential class effects.

Indexed as

Antibodies, Monoclonal, HumanizedEpstein-Barr Virus InfectionsHerpesvirus 4, HumanHodgkin DiseasePsoriasisTumor MicroenvironmentChronic DiseaseHumansInterleukin-23MaleAntibodies, Monoclonal, HumanizedguselkumabInterleukin-23Classic Hodgkin lymphomaEpstein-Barr virusGuselkumabIL-23 inhibitorPsoriatic arthritisTh2 cellsTumor microenvironment

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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.