Evidence map›Paper›PMID 38483362›Full record

ReviewCytotherapy2024

Strategic infection prevention after genetically modified hematopoietic stem cell therapies: recommendations from the International Society for Cell & Gene Therapy Stem Cell Engineering Committee.

Tami D John, Gabriela Maron, Allistair Abraham, Alice Bertaina, Senthil Velan Bhoopalan, Alan Bidgoli, Carmem Bonfim, Zane Coleman, Amy DeZern, Jingjing Li and 10 more

Abstract readReview
In one paragraph

Review in Cytotherapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
–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.

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

5 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Guideline
  2. Review
  3. Review
  4. Clinical hematopoietic stem cell-based gene therapy.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Review
  5. 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

20 authors.

Tami D JohnDivision of Hematology, Oncology, Stem Cell Transplantation and Regenerative Medicine, Department of Pediatrics, Stanford University, Stanford, California, USA.
Gabriela MaronDepartment of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
Allistair AbrahamCenter for Cancer and Immunology Research, CETI, Children's National Hospital, Washington, District of Columbia, USA.
Alice BertainaDivision of Hematology, Oncology, Stem Cell Transplantation and Regenerative Medicine, Department of Pediatrics, Stanford University, Stanford, California, USA.
Senthil Velan BhoopalanDepartment of Bone Marrow Transplantation and Cellular Therapy, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
Alan BidgoliDivision of Blood and Marrow Transplantation, Children's Healthcare of Atlanta, Aflac Blood and Cancer Disorders Center, Emory University, Atlanta, Georgia, USA.
Carmem BonfimPediatric Blood and Marrow Transplantation Division and Pelé Pequeno Príncipe Research Institute, Hospital Pequeno Príncipe, Curitiba, Brazil.
Zane ColemanDepartment of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
Amy DeZernBone Marrow Failure and MDS Program, John Hopkins Medicine, Baltimore, Maryland, USA.
Jingjing LiGraduate School of Biomedical Engineering, University of New South Wales, Sydney, New South Wales, Australia.
Chrystal LouisZentalis Pharmaceuticals, New York, New York, USA.
Joseph OvedStem Cell Transplantation and Cellular Therapies Service, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Mara Pavel-DinuDivision of Hematology, Oncology, Stem Cell Transplantation and Regenerative Medicine, Department of Pediatrics, Stanford University, Stanford, California, USA.
Duncan PurtillDepartment of Haematology, Fiona Stanley Hospital, Perth, Western Australia, Australia.
Annalisa RuggeriIRCCS Ospedale San Raffaele, Segrate, Milan, Italy.
Athena RussellCenter for Cellular Immunotherapies, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Robert WynnFaculty of Biology, Medicine and Health, The University of Manchester, Manchester, UK.
Jaap Jan BoelensStem Cell Transplantation and Cellular Therapies Service, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Susan ProckopDana-Farber/Boston Children's Cancer and Blood Disorders Center, Boston, Massachusetts, USA.
Akshay SharmaDepartment of Bone Marrow Transplantation and Cellular Therapy, St. Jude Children's Research Hospital, Memphis, Tennessee, USA. Electronic address: akshay.sharma@stjude.org.

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
Viral Vector Technology (VVTSR)P30CA021765 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI CHARLES ROBERTS · 1985 to 2026
$166.9M
Novel therapeutic gene editing to induce fetal hemoglobin for sickle cell diseaseU01HL163983 · NHLBI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI Akshay Sharma, Shengdar Tsai · 2023 to 2026
$4.9M
Hematopoietic stem cell defects in Diamond-Blackfan AnemiaK99DK134844 · NIDDK · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI BHOOPALAN, SENTHIL VELAN · 2024 to 2025
$180k
NCI NIH HHS P30 CA008748NCI NIH HHS P30 CA021765NHLBI NIH HHS U01 HL163983NIDDK NIH HHS K99 DK134844
6 · The paper itself

Abstract

There is lack of guidance for immune monitoring and infection prevention after administration of ex vivo genetically modified hematopoietic stem cell therapies (GMHSCT). We reviewed current infection prevention practices as reported by providers experienced with GMHSCTs across North America and Europe, and assessed potential immunologic compromise associated with the therapeutic process of GMHSCTs described to date. Based on these assessments, and with consensus from members of the International Society for Cell & Gene Therapy (ISCT) Stem Cell Engineering Committee, we propose risk-adapted recommendations for immune monitoring, infection surveillance and prophylaxis, and revaccination after receipt of GMHSCTs. Disease-specific and GMHSCT-specific considerations should guide decision making for each therapy.

Indexed as

Genetic TherapyHematopoietic Stem Cell TransplantationCell- and Tissue-Based TherapyHematopoietic Stem CellsHumansInfectionsgenetically modified hematopoietic stem cell therapiesimmune reconstitutionprophylaxisvaccination

Identifiers

PMID38483362
PMCPMC11213676

What OpenQuestion holds

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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.