Evidence map›Paper›PMID 18174545›Full record

ArticleAmerican journal of respiratory and critical care medicine2008

Th-17, monokines, collagen type V, and primary graft dysfunction in lung transplantation.

Joseph L Bobadilla, Robert B Love, Ewa Jankowska-Gan, Qingyong Xu, Lynn D Haynes, Ruedi K Braun, Mary S Hayney, Alejandro Munoz del Rio, Keith Meyer, Daniel S Greenspan and 8 more

3 registry-linked trialsOpen access · greenAbstract read
In one paragraph

Article in American journal of respiratory and critical care medicine, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 3 registered trials, which are not on this map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
6.8field-weighted citation impact, top 3% 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.

NCT01163799 phase1terminatednot on this mapstarted 2010, after this paper: background citation

A Pilot Study to Assess the Safety and Efficacy of Alefacept in de Novo Kidney Transplant Recipients

TypeinterventionalSponsorNorthwestern UniversityRan2010 to 2012Enrolled9ConditionsTransplant, Failure, KidneyArmsAlefacept (ASP0485)
NCT01199887 phase1completednot on this mapstarted 2010, after this paper: background citation

A Phase One, Open Label, Multi-Dose Study to Evaluate the Safety, Tolerability, and Biologic Effects of Three Doses of IW001 in Patients With Idiopathic Pulmonary Fibrosis (IPF)

TypeinterventionalSponsorImmuneWorksRan2010 to 2012Enrolled30ConditionsIdiopathic Pulmonary FibrosisArmsIW001
NCT01715883 phase2terminatednot on this mapstarted 2011, after this paper: background citation

Sodium Nitrite Administration at the Time of Lung Organ Procurement and Transplantation to Minimize the Risk of Pulmonary Graft Dysfunction

TypeinterventionalSponsorGladwin, Mark, MDRan2011 to 2017Enrolled3ConditionsPrimary Graft DysfunctionArmsSodium Nitrite
3 · Its place in the literature

Who cites it

54 citing papers in PubMed, 93 citations in OpenAlex.

  1. Trial
  2. Genetic variation in the prostaglandin E2 pathway is associated with primary graft dysfunction.American journal of respiratory and critical care medicine · 2014
    Trial
  3. Trial
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Autoantibodies in lung transplantation.Transplant international : official journal of the European Society for Organ Transplantation · 2020
    Review
  13. Idiopathic Pulmonary Fibrosis (IPF): An Overview.Journal of clinical medicine · 2018
    Review
  14. Article
  15. IL-17 in the lung: the good, the bad, and the ugly.American journal of physiology. Lung cellular and molecular physiology · 2018
    Review
  16. Review
  17. Report of the ISHLT Working Group on Primary Lung Graft Dysfunction Part III: Mechanisms: A 2016 Consensus Group Statement of the International Society for Heart and Lung Transplantation.The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation · 2017
    Review
  18. Th17 Responses to Collagen Type V, kα1-Tubulin, and Vimentin Are Present Early in Human Development and Persist Throughout Life.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2017
    Article
  19. Protein biomarkers associated with primary graft dysfunction following lung transplantation.American journal of physiology. Lung cellular and molecular physiology · 2017
    Review
  20. 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

18 authors at 6 institutions in 2 countries.

Joseph L BobadillaMicrobiology and Immunology, Director, Center for Immunobiology, Indiana University School of Medicine, Van Nuys Medical Sciences Building MS224, 635 Barnhill Drive, Indianapolis, IN 46202-5120, USA.
Robert B Love
Ewa Jankowska-Gan
Qingyong Xu
Lynn D Haynes
Ruedi K Braun
Mary S Hayney
Alejandro Munoz del Rio
Keith Meyer
Daniel S Greenspan
Jose Torrealba
Kathleen M Heidler
Oscar W Cummings
Takekazu Iwata
David Brand
Robert Presson
William J Burlingham
David S Wilkes
University of Wisconsin–Madison · USLoyola University Chicago · USIndiana University School of MedicineChiba University · JPIndiana University – Purdue University Indianapolis · USUniversity of Tennessee Health Science Center · US

Funding

Type V Collagen Prevents Lung Allograft RejectionR01HL067177 · NHLBI · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI WILKES, DAVID S · 2001 to 2011
$3.7M
Molecular Biology Of Collagen Type VR01AR047746 · NIAMS · UNIVERSITY OF WISCONSIN-MADISON · PI GREENSPAN, DANIEL S · 2001 to 2013
$3.0M
IMMUNE RESPONSES IN LUNG ALLOGRAFT REJECTIONR01HL060797 · NHLBI · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI WILKES, DAVID S · 1999 to 2006
$2.2M
MMPs in Alloimmune and Autoimmune Lung DiseaseR01HL081350 · NHLBI · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI WILKES, DAVID S · 2005 to 2008
$1.6M
IMMUNE REGULATION IN LUNG TRANSPLANTATIONR01AI048624 · NIAID · UNIVERSITY OF WISCONSIN MADISON · PI BURLINGHAM, WILLIAM J · 2000 to 2003
$1.1M
Innovative Methods for Immune Tolerance in Lung Transpl*R21HL069727 · NHLBI · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI WILKES, DAVID S · 2001 to 2003
$662k
NHLBI NIH HHS HL081350NHLBI NIH HHS HL/AL67177NHLBI NIH HHS R01 HL60797NHLBI NIH HHS R21 HL069727NIAID NIH HHS R01 AI48624NIAID NIH HHS R01 HL/AI67177NIAMS NIH HHS R01 AR47746PHS HHS R21 A1049900
6 · The paper itself

Abstract

rationaleThe pathogenesis of primary graft dysfunction (PGD), a serious complication of lung transplantation, is poorly understood. Human studies and rodent models have shown that collagen type V (col[V]), stimulates IL-17-dependent cellular immunity after lung transplantation.

objectivesTo determine whether patients with end-stage lung disease develop pretransplant col(V)-specific cellular immunity, and if so, the impact of this response on PGD.

methodsTrans-vivo delayed-type hypersensitivity (TV-DTH) assays were used to evaluate memory T-cell responses to col(V) in 55 patients awaiting lung transplantation. Pa(O(2))/Fi(O(2)) index data were used to assess PGD. Univariate risk factor analysis was performed to identify variables associated with PGD. Rats immunized with col(V) or irrelevant antigen underwent lung isografting to determine if prior anti-col(V) immunity triggers PGD in the absence of alloreactivity. MEASUREMENTS AND MAIN

resultsWe found that 58.8% (10/17) of patients with idiopathic pulmonary fibrosis, and 15.8% (6/38) of patients without idiopathic pulmonary fibrosis tested while on the wait list for a lung transplant were col(V) DTH positive. Col(V) reactivity was CD4(+) T-cell and monocyte mediated, and dependent on IL-17, IL-1beta, and tumor necrosis factor (TNF)-alpha. Pa(O(2))/Fi(O(2)) indices were impaired significantly 6-72 hours after transplantation in col(V)-reactive versus nonreactive patients. Univariate risk factor analysis identified only preoperative TV-DTH to col(V) and ischemic time as predictors of PGD. Finally, in a rat lung isograft model, col(V) sensitization resulted in significantly lower Pa(O(2))/Fi(O(2)), increased local TNF-alpha and IL-1beta production, and a moderate-to-severe bronchiolitis/vasculitis when compared with control isografts.

conclusionsThe data suggest that activation of innate immunity by col(V)-specific Th-17 memory cells represents a novel pathway to PGD after lung transplantation.

Indexed as

T-Lymphocytes, Helper-InducerAdultAnimalsCollagen Type VDelayed Graft FunctionFemaleHumansHypersensitivity, DelayedImmunity, CellularInterleukin-17Lung TransplantationMaleMiddle AgedRatsRats, Inbred WKYT-Lymphocyte SubsetsCollagen Type VInterleukin-17

Identifiers

PMID18174545
PMCPMC2267340
OpenAlexW2032360822

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.