Evidence map›Paper›PMID 21927032›Full record

ArticleBone marrow transplantation2012

Immunohistochemistry of affected tissue may guide cGVHD treatment decisions.

K M Williams, L W Ostrow, D M Loeb, T Chung, R D Cohn, A M Corse, A L Mammen, A R Chen

Abstract readCase Reports
In one paragraph

Article in Bone marrow transplantation, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. 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

8 authors.

K M WilliamsDepartment of Pediatric Hematology-Oncology, Experimental Transplantation and Immunology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA. williaki@mail.nih.gov
L W Ostrow
D M Loeb
T Chung
R D Cohn
A M Corse
A L Mammen
A R Chen

Funding

Translational Research Central ServicesP30CA006973 · NCI · JOHNS HOPKINS UNIVERSITY · PI Rosalie Wollett · 1985 to 2026
$208.6M
The Pathogenesis and Treatment of chronic GVHDZIABC011370 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI WILLIAMS, KIRSTEN · 2011 to 2012
$139k
NCI NIH HHS P30 CA006973
6 · The paper itself

Abstract

Chronic graft-vs-host disease (cGVHD) myositis is a rare complication of hematopoietic SCT, for which the pathogenesis and optimal therapy are unclear. We performed immunohistochemistry on muscle biopsies from pediatric cGVHD myositis and typical cases of autoimmune dermatomyositis and polymyositis. The immunostaining pattern of cGVHD myositis was distinct from that of typical cases of autoimmunity. There was a high proportion of CD20+ and CD68+ cells, and the best therapeutic response was achieved with rituximab (anti-CD20). These results suggest that cGVHD myositis may be mediated by different leukocytes than similar autoimmune diseases and that treatment may be optimized by targeting the specific cellular infiltrates identified in affected tissue.

Indexed as

Antibodies, Monoclonal, Murine-DerivedAntigens, CDAntigens, CD20Antigens, Differentiation, MyelomonocyticAutoimmune DiseasesB-LymphocytesCD68 MoleculeChildDermatomyositisGraft vs Host DiseaseHematopoietic Stem Cell TransplantationHumansImmunohistochemistryPolymyositisRituximabAntibodies, Monoclonal, Murine-DerivedAntigens, CDAntigens, CD20Antigens, Differentiation, MyelomonocyticCD68 antigen, humanCD68 MoleculeRituximab

Identifiers

PMID21927032
PMCPMC4251459

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.