Evidence map›Paper›PMID 28835507›Full record

ArticleEMBO molecular medicine2017

Genome editing for scalable production of alloantigen-free lentiviral vectors for

Michela Milani, Andrea Annoni, Sara Bartolaccini, Mauro Biffi, Fabio Russo, Tiziano Di Tomaso, Andrea Raimondi, Johannes Lengler, Michael C Holmes, Friedrich Scheiflinger and 3 more

Open access · goldAbstract read
In one paragraph

Article in EMBO molecular medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

52 citing papers in PubMed, 63 citations in OpenAlex.

  1. Article
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  7. Article
  8. In Vivo CAR-T Therapies-A New Era of Programmable Immunity.International journal of molecular sciences · 2026
    Review
  9. FromImmune network · 2026
    Review
  10. Frontiers in immunology · 2026
    Review
  11. Article
  12. In vivo CAR cell therapy: from bench to bedside.Journal of hematology & oncology · 2025
    Review
  13. Article
  14. In vivo CAR engineering for immunotherapy.Nature reviews. Immunology · 2025
    Review
  15. Review
  16. The deLIVERed promises of gene therapy: Past, present, and future of liver-directed gene therapy.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Review
  17. Article
  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 4 institutions in 3 countries.

Michela MilaniSan Raffaele Telethon Institute for Gene Therapy, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Andrea AnnoniSan Raffaele Telethon Institute for Gene Therapy, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Sara BartolacciniSan Raffaele Telethon Institute for Gene Therapy, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Mauro BiffiSan Raffaele Telethon Institute for Gene Therapy, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Fabio RussoSan Raffaele Telethon Institute for Gene Therapy, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Tiziano Di TomasoSan Raffaele Telethon Institute for Gene Therapy, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Andrea RaimondiIRCCS San Raffaele Scientific Institute, Milan, Italy.
Johannes LenglerBaxalta (former Baxter) Innovation GmbH, Vienna, Austria.
Michael C HolmesSangamo Therapeutics, Inc., Richmond, CA, USA.
Friedrich ScheiflingerBaxalta (former Baxter) Innovation GmbH, Vienna, Austria.
Angelo LombardoSan Raffaele Telethon Institute for Gene Therapy, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Alessio CantoreSan Raffaele Telethon Institute for Gene Therapy, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Luigi NaldiniSan Raffaele Telethon Institute for Gene Therapy, IRCCS San Raffaele Scientific Institute, Milan, Italy luigi.naldini@hsr.it.ORCID 0000-0002-7835-527X
The San Raffaele Telethon Institute for Gene Therapy · ITVita-Salute San Raffaele University · ITBaxter (Austria) · ATSangamo BioSciences (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lentiviral vectors (LV) are powerful and versatile vehicles for gene therapy. However, their complex biological composition challenges large-scale manufacturing and raises concerns for

Indexed as

AnimalsCD55 AntigensCell LineFactor IXGene EditingGenetic TherapyGenetic VectorsHEK293 CellsHemophilia BHumansIsoantigensLentivirusMembrane Cofactor ProteinMiceMice, Inbred C57BLMice, KnockoutCD55 AntigensFactor IXIsoantigensMembrane Cofactor ProteinReceptors, Complement 3bgene therapyhemophilialentiviral vectorsMHC‐Istable producer cell line

Identifiers

PMID28835507
PMCPMC5666310
OpenAlexW2745793084

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.