Evidence map›Paper›PMID 17690955›Full record

ArticleJournal of clinical immunology2007

Resetting the adaptive immune system after autologous stem cell transplantation: lessons from responses to vaccines.

D M C Brinkman, C M Jol-van der Zijde, M M ten Dam, P A W te Boekhorst, R ten Cate, N M Wulffraat, R Q Hintzen, J M Vossen, M J D van Tol

Open access · hybridAbstract readComparative Study
In one paragraph

Article in Journal of clinical immunology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

11 citing papers in PubMed, 32 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. [Still's disease in children and adults].Zeitschrift fur Rheumatologie · 2017
    Review
  5. National Institutes of Health Hematopoietic Cell Transplantation Late Effects Initiative: The Immune Dysregulation and Pathobiology Working Group Report.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2017
    Review
  6. [Still's disease in children and adults].Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete · 2017
    Review
  7. Article
  8. Article
  9. Hematopoietic cell transplantation for autoimmune disease: updates from Europe and the United States.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2010
    Review
  10. Article
  11. Review
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

9 authors at 3 institutions in 1 country.

D M C BrinkmanDepartment of Pediatrics, Leiden University Medical Center, 2300 RC, Leiden, The Netherlands. d.m.c.brinkman@lumc.nl
C M Jol-van der Zijde
M M ten Dam
P A W te Boekhorst
R ten Cate
N M Wulffraat
R Q Hintzen
J M Vossen
M J D van Tol
Leiden University Medical Center · NLErasmus MC · NLUniversity Medical Center Utrecht · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autologous stem cell transplantation (ASCT) to treat autoimmune diseases (AID) is thought to reset immunological memory directed against autoantigens. This hypothesis can only be studied indirectly because the exact nature of the pathogenetic autoantigens is unknown in most AID. Therefore, 19 children with juvenile idiopathic arthritis (JIA) or systemic lupus erythematodes (SLE) and 10 adults with multiple sclerosis (MS) were vaccinated with the T-cell-dependent neoantigen rabies and the recall antigen tetanus toxoid after, respectively before, bone marrow harvest. Both vaccinations were repeated after ASCT. All except two of the responders mounted a primary antibody response to rabies after revaccination, and 44% of the responders mounted a primary antibody response to tetanus boost after ASCT. These data show that immunological memory to a neoantigen is lost in most patients with AID after immunoablative pretreatment; however, memory to a recall antigen boosted before bone marrow harvest is only lost in part of the patients. Disease progression was arrested in all patients with JIA/SLE except one, but only in a minority of MS patients. Clinical outcome on a per case basis was not associated with the profile of the immune response toward the vaccination antigens after ASCT.

Indexed as

Hematopoietic Stem Cell TransplantationImmunity, InnateAdolescentAdultAutoimmune DiseasesChildChild, PreschoolFemaleHumansImmunologic MemoryMaleMiddle AgedProspective StudiesRabies VaccinesTetanus ToxoidTransplantation, AutologousRabies VaccinesTetanus Toxoid

Identifiers

PMID17690955
PMCPMC2075528
OpenAlexW2028678802

What OpenQuestion holds

Textmetadata
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.