Evidence map›Paper›PMID 40991376›Full record

Trial reportBlood advances2025

Outcomes with third-party virus-specific T cells after the use of single-antigen cell lines to predict HLA restriction.

Jeremy D Rubinstein, Giang Pham, Anusha Sridharan, Ruby Khoury, YunZu M Wang, Zahra Hudda, Jamie Wilhelm, Daniel A Lichtenstein, Daria Heyenbruch, Jose A Cancelas and 3 more

Registry-linked trialAbstract readClinical Trial, Phase IIMulticenter Study
In one paragraph

Trial report in Blood advances, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02532452 (Third Party Viral Specific T-cells), which is not on this 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

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.

NCT02532452 phase2recruitingnot on this map

Third Party Viral Specific T-cells (VSTs) for Treatment of Viral Infections in Immunocompromised Patients

TypeinterventionalSponsorChildren's Hospital Medical Center, CincinnatiRan2015 to 2027Enrolled750ConditionsViral Infection, Viral Reactivation, Infection in an Immunocompromised HostArmsViral Specific VST Infusion
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

13 authors.

Jeremy D RubinsteinDepartment of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH.ORCID 0000-0002-1934-2954
Giang PhamDivision of Experimental Hematology, Cancer and Blood Diseases Institute, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
Anusha SridharanDivision of Experimental Hematology, Cancer and Blood Diseases Institute, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.ORCID 0000-0003-0552-0956
Ruby KhouryDepartment of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH.
YunZu M WangDepartment of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH.ORCID 0000-0002-7362-8267
Zahra HuddaDepartment of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH.
Jamie WilhelmDivision of Bone Marrow Transplantation and Immune Deficiency, Cancer and Blood Diseases Institute, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
Daniel A LichtensteinDepartment of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH.ORCID 0000-0002-4883-6240
Daria HeyenbruchHoxworth Blood Center, University of Cincinnati, Cincinnati, OH.
Jose A CancelasDepartment of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH.ORCID 0000-0002-1291-7233
Stella M DaviesDepartment of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH.
Carolyn LutzkoDepartment of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH.
Michael S GrimleyDepartment of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH.ORCID 0000-0003-2056-5167

Funding

Allogeneic virus-specific T-cell therapy after hematopoietic stem cell transplant: determinants of treatment success and failureR01HL169242 · NHLBI · CINCINNATI CHILDRENS HOSP MED CTR · PI Jeremy D Rubinstein · 2024 to 2026
$2.0M
NHLBI NIH HHS R01 HL169242
6 · The paper itself

Abstract

abstractPatients with significant T-cell dysfunction from chemotherapy or hematopoietic stem cell transplant are at significant risk for complications of viral infections. Off-the-shelf third-party virus-specific T cells (TP VSTs) are an effective and well-tolerated treatment for the management of infection with adenovirus, BK polyomavirus, cytomegalovirus, and Epstein-Barr virus. TP VST product selection for any particular patient incorporates maximizing the number of HLA matches between the product and the patient, along with consideration of the antiviral activity of the product. We have previously shown that single-antigen cell lines (SALs), cell lines expressing a single HLA molecule, can be used in a flow cytometric-based assay to determine sites of HLA restriction for TP VST products. We hypothesized that incorporating match at sites of HLA restriction into TP VST product selection would improve response rates. Here we report on 25 patients who received TP VSTs for the treatment of 26 viral infections with at least 1 match at an HLA-restricted site. In this cohort, the overall response rate was 96.2%, with a complete response rate of 69.2%. These data suggest the annotation of VST banks to include SAL-derived HLA restriction could lead to improved product selection and efficacy. This trial was registered at www.clinicaltrials.gov as #NCT02532452.

Indexed as

HLA AntigensImmunotherapy, AdoptiveT-LymphocytesVirus DiseasesAdultCell LineFemaleHistocompatibility TestingHumansMaleMiddle AgedTreatment OutcomeHLA Antigens

Identifiers

PMID40991376
PMCPMC12744286

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Registered trials

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.