Evidence map›Paper›PMID 8877390›Full record

ReviewImmunobiology1996

Cyclophosphamide-induced immunological tolerance: an overview.

H Mayumi, M Umesue, K Nomoto

4 registry-linked trialsAbstract readReview
PubMed Publisher
In one paragraph

Review in Immunobiology, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 4 registered trials, which are not on this map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
0.6field-weighted citation impact, top 31% 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.

NCT02169791 phase2completednot on this mapstarted 2014, after this paper: background citation

A Phase II Trial of Nonmyeloablative Haploidentical Peripheral Blood Stem Cell Transplantation Followed By Maintenance Therapy With the Novel Oral Proteasome Inhibitor, MLN9708, in Patients With High-risk Hematologic Malignancies

TypeinterventionalSponsorNorthside Hospital, Inc.Ran2014 to 2020Enrolled29ConditionsAcute Leukemia, Chronic Leukemia, Myelodysplastic Syndrome, LymphomasArmsMLN9708
NCT02193880 nacompletednot on this mapstarted 2014, after this paper: background citation

Safety of Post-transplant Alpha-beta Depleted T-cell Infusion Following Haploidentical Stem Cell Transplant (Haplo SCT)

TypeinterventionalSponsorAyman SaadRan2014 to 2018Enrolled7ConditionsHematologic Neoplasms, Graft-Versus-Host DiseaseArmsAlpha-beta depleted T-cell infusion after post-transplant cyclophosphamide.
NCT06828796 phase2recruitingnot on this mapstarted 2025, after this paper: background citation

Early Use of Tacrolimus in HLA-Mismatched Haploidentical Allogeneic Hematopoietic Transplantation With Post-Transplant Cyclophosphamide

TypeinterventionalSponsorNorthside Hospital, Inc.Ran2025 to 2028Enrolled20ConditionsHematologic Disease and Disorders, Hematopoietic Cell TransplantArmsTacrolimus, Cyclophosphamide, Mycofenolate mofetil
NCT07719946 phase2recruitingnot on this mapstarted 2025, after this paper: background citation

Phase II Trial of Reduced Dose Post Transplant Cyclophosphamide After Haploidentical Hematopoietic Stem Cell Transplant in Hematological Malignancies

TypeinterventionalSponsorTata Memorial CentreRan2025 to 2028Enrolled20ConditionsHaploidentical Hematopoietic Stem Cell Transplant, Hematological MalignanciesArmsCyclophosphamide
3 · Its place in the literature

Who cites it

63 citing papers in PubMed, 135 citations in OpenAlex.

  1. Trial
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  6. HLA-haploidentical bone marrow transplantation for hematologic malignancies using nonmyeloablative conditioning and high-dose, posttransplantation cyclophosphamide.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2008
    Trial
  7. Article
  8. Article
  9. Review
  10. Article
  11. Haploidentical HSCT in the Treatment of Pediatric Hematological Disorders.International journal of molecular sciences · 2024
    Review
  12. Allogeneic bone marrow transplantation for aplastic anemia.International journal of hematology · 2024
    Review
  13. Review
  14. Review
  15. Article
  16. New strategies for mismatched unrelated donor (MMUD) hematopoietic cell transplant (HCT).Hematology. American Society of Hematology. Education Program · 2022
    Article
  17. Article
  18. Article
  19. Review
  20. Proliferation kinetics of immune cells during early phase of bone marrow transplantation in mouse model based on chemotherapy conditioning.Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2021
    Article

3 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

H MayumiDepartment of Cardiovascular Surgery, National Kyushu Medical Center Hospital, Japan.
M Umesue
K Nomoto
Kyushu University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A cyclophosphamide (CP)-induced tolerance system in mice that primarily consists of donor cell injection followed by CP-treatment was found useful for inducing a long-lasting allo- or xeno-tolerance to various solid organs. In the cells-followed-by-CP system, the sequential mechanisms of tolerance were clarified using the specific correlation between superantigens and certain T cell receptor (TCR) V beta segments. Those include the clonal destruction of antigen-stimulated mature T cells, the peripheral clonal deletion associated with peripheral chimerism, the intrathymic clonal deletion associated with intrathymic chimerism, and the clonal anergy. The generation of suppressor T cells was another important mechanism of tolerance in the late stage. Special care was taken to overcome the " hard" barriers of allo- or xeno-combinations by reducing the "split tolerance" produced through the clonal destruction mechanism. For this purpose, the tolerogen, antimitotic drugs, their doses, timing, route of administration, combined immunosuppressants, and supportive treatment were all crucial for successful induction of a long-lasting skin tolerance. This system may be applicable to human transplantation.

Indexed as

AnimalsCyclophosphamideHumansImmune ToleranceCyclophosphamide

Identifiers

PMID8877390
OpenAlexW2134077221

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.