Evidence map›Paper›PMID 21649795›Full record

ReviewHaemophilia : the official journal of the World Federation of Hemophilia2011

Haemophilia management: time to get personal?

T E Howard, C Yanover, J Mahlangu, A Krause, K R Viel, C K Kasper, K P Pratt

Registry-linked trialAbstract readReview
In one paragraph

Review in Haemophilia : the official journal of the World Federation of Hemophilia, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01626105 (Study of Severe Hemophilia A Patients Who Have Only Received a Single Recombinant FVIII Therapeutic for the Purpose of Identifying the Pharmacogenetic Determinants of Tolerance and Immunogenicity), which is not on this map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.2field-weighted citation impact, top 23% 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.

NCT01626105 unknown statusnot on this mapstarted 2012, after this paper: background citation

Study of Severe Hemophilia A Patients Who Have Only Received a Single Recombinant FVIII Therapeutic for the Purpose of Identifying the Pharmacogenetic Determinants of Tolerance and Immunogenicity

TypeobservationalSponsorVictor J Marder, M.D.Ran2012 to 2014Enrolled55ConditionsHemophilia A
3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Factor VIII inhibitor and source of replacement therapy.Blood transfusion = Trasfusione del sangue · 2012
    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

7 authors at 6 institutions in 3 countries.

T E HowardDepartment of Pathology and Laboratory Medicine, Veterans Affairs Greater Los Angeles Healthcare System, Los Angeles, CA, USA. tom.howard@va.gov
C Yanover
J Mahlangu
A Krause
K R Viel
C K Kasper
K P Pratt
University of the Witwatersrand · ZABloodworks Northwest · USFred Hutch Cancer Center · USTranslational Research Institute · AUUniversity of Southern California · USVA Greater Los Angeles Healthcare System · US

Funding

Mechanisms of Race-Based Differences in Factor VIII Immunogenicity in HemophiliaRC2HL101851 · NHLBI · SEPULVEDA RESEARCH CORPORATION · PI HOWARD, TOM EUGENE, PRATT, KATHLEEN PALMER · 2009 to 2010
$6.5M
Genetic Variation in Factor IX and Thrombosis RiskR01HL072533 · NHLBI · TEXAS BIOMEDICAL RESEARCH INSTITUTE · PI ALMASY, LAURA A. · 2003 to 2006
$1.5M
Genetic Variation in Factor IX and Thrombosis RiskK08HL071130 · NHLBI · TEXAS BIOMEDICAL RESEARCH INSTITUTE · PI HOWARD, TOM E. · 2002 to 2006
$634k
NHLBI NIH HHS 1 RC2-HL10185NHLBI NIH HHS 1RC2-HL101851NHLBI NIH HHS HL-71130NHLBI NIH HHS HL-72533NHLBI NIH HHS RC2 HL101851
6 · The paper itself

Abstract

The possibility of alloimmunization in patients receiving protein replacement therapy depends on (at least) three risk factors, which are necessary concomitantly but insufficient alone. The first is the degree of structural difference between the therapeutic protein and the patient's own endogenous protein, if expressed. Such differences depend on the nature of the disease mutation and the pre-mutation endogenous protein structure as well as on post-translational changes and sequence-engineered alterations in the therapeutic protein. Genetic variations in the recipients' immune systems comprise the second set of risk determinants for deleterious immune responses. For example, the limited repertoire of MHC class II isomers encoded by a given person's collection of HLA genes may or may not be able to present a 'foreign' peptide(s) produced from the therapeutic protein - following its internalization and proteolytic processing - on the surface of their antigen-presenting cells (APCs). The third (and least characterized) variable is the presence or absence of immunologic 'danger signals' during the display of foreign-peptide/MHC-complexes on APCs. A choice between existing therapeutic products or the manufacture of new proteins, which may be less immunogenic in some patients or patient populations, may require prior definition of the first two of these variables. This leads then to the possibility of developing personalized therapies for disorders due to genetic deficiencies in endogenous proteins, such as haemophilia A and B. [Correction made after online publication 11 July 2011: several critical corrections have been made to the abstract].

Indexed as

Factor VIIIHemophilia AEconomics, PharmaceuticalGenetic Predisposition to DiseaseHistocompatibility Antigens Class IIHumansImmune ToleranceIsoantibodiesRisk FactorsFactor VIIIHistocompatibility Antigens Class IIIsoantibodies

Identifiers

PMID21649795
PMCPMC5319386
OpenAlexW1534426876

What OpenQuestion holds

Textmetadata
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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.