Evidence map›Paper›PMID 29702606›Full record

Trial reportInternational journal of molecular sciences2018

Safety and Feasibility of Lin- Cells Administration to ALS Patients: A Novel View on Humoral Factors and miRNA Profiles.

Anna Sobuś, Bartłomiej Baumert, Zofia Litwińska, Monika Gołąb-Janowska, Jacek Stępniewski, Maciej Kotowski, Ewa Pius-Sadowska, Miłosz P Kawa, Dorota Gródecka-Szwajkiewicz, Jarosław Peregud-Pogorzelski and 3 more

Open access · goldAbstract readClinical Trial
In one paragraph

Trial report in International journal of molecular sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
3.7field-weighted citation impact, top 7% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 28 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Review
  19. Article
  20. 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 at 1 institution in 1 country.

Anna SobuśDepartment of General Pathology, Pomeranian Medical University, 70-111 Szczecin, Poland. ania.sobus@gmail.com.
Bartłomiej BaumertDepartment of General Pathology, Pomeranian Medical University, 70-111 Szczecin, Poland. baumertbartlomiej@gmail.com.
Zofia LitwińskaDepartment of General Pathology, Pomeranian Medical University, 70-111 Szczecin, Poland. z.litwinska@gmail.com.ORCID 0000-0003-0451-8723
Monika Gołąb-JanowskaDepartment of Neurology, Pomeranian Medical University, 71-252 Szczecin, Poland. monikagj@op.pl.
Jacek StępniewskiDepartment of Medical Biotechnology, Faculty of Biochemistry, Biophysics and Biotechnology, 30-387 Krakow, Poland. jacek.stepniewski@uj.edu.pl.
Maciej KotowskiDepartment of General Pathology, Pomeranian Medical University, 70-111 Szczecin, Poland. maciej.j.kotowski@gmail.com.
Ewa Pius-SadowskaDepartment of General Pathology, Pomeranian Medical University, 70-111 Szczecin, Poland. ewapius@wp.pl.
Miłosz P KawaDepartment of General Pathology, Pomeranian Medical University, 70-111 Szczecin, Poland. kawamilosz@gmail.com.
Dorota Gródecka-SzwajkiewiczDepartment of General Pathology, Pomeranian Medical University, 70-111 Szczecin, Poland. d.szwajkiewicz@op.pl.
Jarosław Peregud-PogorzelskiDepartment of Paediatric Oncology, Pomeranian Medical University, 71-252 Szczecin, Poland. peregud@tstd.pl.
Józef DulakDepartment of Medical Biotechnology, Faculty of Biochemistry, Biophysics and Biotechnology, 30-387 Krakow, Poland. jozef.dulak@uj.edu.pl.
Przemysław NowackiDepartment of Neurology, Pomeranian Medical University, 71-252 Szczecin, Poland. kneurolo@pum.edu.pl.
Bogusław MachalińskiDepartment of General Pathology, Pomeranian Medical University, 70-111 Szczecin, Poland. machalin@pum.edu.pl.
Pomeranian Medical University · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Therapeutic options for amyotrophic lateral sclerosis (ALS) are still limited. Great hopes, however, are placed in growth factors that show neuroprotective abilities (e.g., nerve growth factor (NGF), brain-derived neurotrophic factor (BDNF), and vascular endothelial growth factor (VEGF)) and in the immune modulating features, in particular, the anti-inflammatory effects. In our study we aimed to investigate whether a bone marrow-derived lineage-negative (Lin-) cells population, after autologous application into cerebrospinal fluid (CSF), is able to produce noticeable concentrations of trophic factors and inflammatory-related proteins and thus influence the clinical course of ALS. To our knowledge, the evaluation of Lin- cells transplantation for ALS treatment has not been previously reported. Early hematopoietic Lin- cells were isolated from twelve ALS patients’ bone marrow, and later, the suspension of cells was administered into the subarachnoid space by lumbar puncture. Concentrations of selected proteins in the CSF and plasma were quantified by multiplex fluorescent bead-based immunoassays at different timepoints post-transplantation. We also chose microRNAs (miRNAs) related to muscle biology (miRNA-1, miRNA-133a, and miRNA-206) and angiogenesis and inflammation (miRNA-155 and miRNA-378) and tested, for the first time, their expression profiles in the CSF and plasma of ALS patients after Lin- cells transplantation. The injection of bone marrow cells resulted in decreased concentration of selected inflammatory proteins (C3) after Lin- cells injection, particularly in patients who had a better clinical outcome. Moreover, several analyzed miRNAs have changed expression levels in the CSF and plasma of ALS patients subsequent to Lin- cells administration. Interestingly, the expression of miR-206 increased in ALS patients, while miR-378 decreased both in the CSF and plasma one month after the cells’ injection. We propose that autologous lineage-negative early hematopoietic cells injected intrathecally may be a safe and feasible source of material for transplantations to the central nervous system (CNS) environment aimed at anti-inflammatory support provision for ALS adjuvant treatment strategies. Further research is needed to evaluate whether the observed effects could significantly influence the ALS progression.

Indexed as

Hematopoietic Stem Cell TransplantationAdultAmyotrophic Lateral SclerosisCerebrospinal FluidFemaleHematopoietic Stem CellsHumansImmunity, HumoralMaleMicroRNAsMiddle AgedProspective StudiesSpinal PunctureSubarachnoid SpaceTranscriptomeTransplantation, AutologousMicroRNAsamyotrophic lateral sclerosis (ALS)complementLin- cellsmicroRNAneurotrophinstrophic effects of stem cell-based therapy

Identifiers

PMID29702606
PMCPMC5983708
OpenAlexW2800010511

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.