Evidence map›Paper›PMID 31258526›Full record

ArticleFrontiers in immunology2019

Dissecting Allo-Sensitization After Local Administration of Human Allogeneic Adipose Mesenchymal Stem Cells in Perianal Fistulas of Crohn's Disease Patients.

Alvaro Avivar-Valderas, Cristina Martín-Martín, Cristina Ramírez, Borja Del Río, Ramón Menta, Pablo Mancheño-Corvo, Maitane Ortiz-Virumbrales, Ángel Herrero-Méndez, Julián Panés, Damián García-Olmo and 5 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 2 pooled it
7.1field-weighted citation impact, top 2% of its field
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

24 citing papers in PubMed, 2 syntheses or guidelines pooled it, 50 citations in OpenAlex.

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  20. Human leukocyte antigen selected allogeneic mesenchymal stromal cell therapy in renal transplantation: The Neptune study, a phase I single-center study.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2020
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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

15 authors at 3 institutions in 1 country.

Alvaro Avivar-ValderasTakeda Madrid, Cell Therapy Technology Center-Cell Therapies, Madrid, Spain.
Cristina Martín-MartínDepartment of Immunology, University Hospital Ramon y Cajal, Madrid, Spain.
Cristina RamírezTakeda Madrid, Cell Therapy Technology Center-Cell Therapies, Madrid, Spain.
Borja Del RíoTakeda Madrid, Cell Therapy Technology Center-Cell Therapies, Madrid, Spain.
Ramón MentaTakeda Madrid, Cell Therapy Technology Center-Cell Therapies, Madrid, Spain.
Pablo Mancheño-CorvoTakeda Madrid, Cell Therapy Technology Center-Cell Therapies, Madrid, Spain.
Maitane Ortiz-VirumbralesTakeda Madrid, Cell Therapy Technology Center-Cell Therapies, Madrid, Spain.
Ángel Herrero-MéndezTakeda Madrid, Cell Therapy Technology Center-Cell Therapies, Madrid, Spain.
Julián PanésDepartment of Gastroenterology, Hospital Clínic, IDIBAPS, CIBERehd, Barcelona, Spain.
Damián García-OlmoDepartment of Surgery, Hospital U. Fundación Jiménez Díaz, Madrid, Spain.
José Luís CastañerDepartment of Immunology, University Hospital Ramon y Cajal, Madrid, Spain.
Itziar PalaciosTakeda Madrid, Cell Therapy Technology Center-Cell Therapies, Madrid, Spain.
Eleuterio LombardoTakeda Madrid, Cell Therapy Technology Center-Cell Therapies, Madrid, Spain.
Wilfried DalemansTiGenix NV, Leuven, Belgium.
Olga DelaRosaTakeda Madrid, Cell Therapy Technology Center-Cell Therapies, Madrid, Spain.
Hospital Universitario Ramón y Cajal · ESConsorci Institut D'Investigacions Biomediques August Pi I Sunyer · ESHospital Universitario Fundación Jiménez Díaz · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Adipose mesenchymal stem cells (ASC) are considered minimally immunogenic. This is due to the low expression of human leukocyte antigens I (HLA-I), lack of HLA-II expression and low expression of co-stimulatory molecules such as CD40 and CD80. The low rate of observed immunological rejection as well as the immunomodulatory qualities, position ASC as a promising cell-based therapy for the treatment of a variety of inflammatory indications. Yet, few studies have addressed relevant aspects of immunogenicity such as ASC donor-to-patient HLA histocompatibility or assessment of immune response triggered by ASC administration, particularly in the cases of presensitization. The present study aims to assess allo-immune responses in a cohort of Crohn's disease patients administered with allogeneic ASC (darvadstrocel formerly Cx601) for the treatment of complex perianal fistulas. We identified donor-specific antibodies (DSA) generation in a proportion of patients and observed that patients showing preexisting immunity were prone to generating DSA after allogeneic therapy. Noteworthy, naïve patients generating DSA at week 12 (W12) showed a significant reduction in DSA titer at week 52 (W52), whereas DSA titer was reduced in pre-sensitized patients only with no specificities against the donor administered. Remarkably, we did not observe any correlation of DSA generation with ASC therapeutic efficacy.

Indexed as

Mesenchymal Stem Cell TransplantationAdipose TissueAdultAnimalsCells, CulturedCohort StudiesComplement ActivationCrohn DiseaseFemaleFistulaGraft RejectionHLA AntigensHumansImmunity, HumoralImmunizationIsoantigensHLA AntigensIsoantigensMembrane Cofactor Proteinallogeneicallo-sensitizationASCCD46cell therapy and immunotherapycomplement dependent cytotoxicity (CDC)crispr gene editingHLA class 1

Identifiers

PMID31258526
PMCPMC6587893
OpenAlexW2950422746

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.