Evidence map›Paper›PMID 41884120›Full record

ArticleFrontiers in medicine2026

Reed-Sternberg cells express CD161 and lectin-like transcript 1 in Hodgkin lymphoma.

Anwar Rjoop, Rania Al-Samama'h, Laith Al-Eitan

Abstract read
In one paragraph

Article in Frontiers in medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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

1 citing paper in PubMed.

  1. Article
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

3 authors.

Anwar RjoopDepartment of Pathology and Microbiology, Faculty of Medicine, Jordan University of Science and Technology, Irbid, Jordan.
Rania Al-Samama'hDepartment of Medical Laboratory Science, Faculty of Applied Medical Science, Jordan University of Science and Technology, Irbid, Jordan.
Laith Al-EitanDepartment of Biotechnology and Genetic Engineering, Jordan University of Science and Technology, Irbid, Jordan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Hodgkin lymphoma (HL) is a B-cell lymphoma, and it is diagnosed by the presence of Reed-Sternberg (RS) cells surrounded by heavy immune cell infiltration in a tissue biopsy. CD161 (Cluster of differentiation 161) and its ligand Lectin-like transcript 1 (LLT1) have recently emerged as a novel immune-regulatory axis that modulates natural killer (NK) and T cell-mediated function in cancer and inflammatory conditions, but their expression in RS cells and association with HL patients' clinical-pathological features remain poorly defined. Methods: In this study, 60 formalin-fixed paraffin-embedded (FFPE) tissue samples were collected from patients in Northern Jordan. In addition to 60 FFPE samples of positive control from benign reactive lymph node tissues and tonsils. Immunohistochemistry (IHC) was performed to assess the expression levels and patterns (cytoplasmic, membranous, or both) of CD161 and LLT1 in RS cells and then correlated with EBV status and clinical-pathological features such as subtype and disease stages. Results: LLT1 expression in RS cells was predominantly cytoplasmic, with occasional dual cytoplasmic and membranous expressions. This is the first study in the literature to detect CD161 expression in RS cells as neoplastic cells at protein level. Statistical analyses showed no significant association between LLT1 or CD161 expression in RS cells and HL subtype, stage or EBV status. Discussion: These findings provide the first characterization of LLT1 and CD161 expression in RS cells and suggest their potential use as a target in immunotherapy approaches in HL.

Indexed as

CD161FFPEHodgkin lymphomaImmune RegulationimmunohistochemistryImmunotherapy TargetsLLT1Reed-Sternberg cells

Identifiers

PMID41884120
PMCPMC13008727

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