Evidence map›Paper›PMID 18773308›Full record

ReviewImmunologic research2008

Translational applications of antibody phage display.

Don L Siegel

Abstract readReview
PubMed Publisher
In one paragraph

Review in Immunologic research, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.7field-weighted citation impact, top 25% 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

8 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Systems approaches to design of targeted therapeutic delivery.Wiley interdisciplinary reviews. Systems biology and medicine
    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

1 author at 1 institution in 1 country.

Don L SiegelDivision of Transfusion Medicine, Department of Pathology & Laboratory Medicine, University of Pennsylvania School of Medicine, 510 Stellar-Chance Laboratories, 422 Curie Blvd., Philadelphia, PA, 19104, USA. siegeld@mail.med.upenn.edu
University of Pennsylvania · US

Funding

STRUCTURAL STUDIES OF PLATELET GPIIB/IIIA ACTIVATIONP50HL054500 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI BRASS, LAWRENCE F · 1996 to 2005
$13.1M
THE ROLE OF SEMA4D/CD100 AND ITS RECEPTORS IN PLATELET BIOLOGY AND THROMBOSISP50HL081012 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI PRICE, THOMAS · 2006 to 2010
$11.9M
Penn Dermatology Research Training ProgramT32AR007465 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI Elizabeth Anne Grice, David Joel Margolis · 1986 to 2026
$9.0M
Cloning and genetics of human pemphigus autoantibodiesR01AR052672 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI STANLEY, JOHN R · 2006 to 2015
$3.7M
TRANSFUSION MEDICINE RESEARCH TRAINING PROGRAMT32HL007775 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI SIEGEL, DONALD LAWRENCE · 1993 to 2023
$2.8M
RED BLOOD CELL AUTOANTIBODIES-- B CELL ORIGIN AND ANTIGENIC TARGETSP50HL054516 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI EMERSON, STEVEN · 1996 to 2000
$2.0M
Mechanisms of Blister Formation by Staphylococcal ToxinsR01AR048223 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI STANLEY, JOHN R · 2002 to 2006
$1.9M
Phage Display Tools for Automated Blood TypingR42HL073533 · NHLBI · PHENOTECH, INC. · PI SIEGEL, DONALD LAWRENCE · 2006 to 2007
$1.0M
MONOCLONAL ITP AUTOANTIBODIES--PARADIGM FOR AUTOIMMUNITYR01HL061844 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI SIEGEL, DONALD L · 1998 to 2002
$835k
Phage Display Tools for Automated Blood TypingR41HL073533 · NHLBI · INTEGRAL MOLECULAR · PI SIEGEL, DONALD LAWRENCE · 2003 to 2004
$240k
BIOLOGY OF HUMAN WARM AUTOIMMUNE HEMOLYTIC ANEMIAK08HL002621 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI SIEGEL, DONALD L · 1991 to 1993
–
NHLBI NIH HHS K08-HL02621NHLBI NIH HHS P50-HL54500NHLBI NIH HHS P50-HL54516NHLBI NIH HHS P50-HL81012NHLBI NIH HHS R01-HL61844NHLBI NIH HHS R41-HL73533NHLBI NIH HHS R42-HL73533NHLBI NIH HHS T32-HL07775NIAMS NIH HHS R01-AR052672NIAMS NIH HHS R01-AR48223NIAMS NIH HHS T32-AR07465
6 · The paper itself

Abstract

Recent developments in molecular immunology have facilitated the expression of immune repertoires in the form of immunoglobulin fragments on the surface of filamentous bacteriophage. Such approaches, known as "phage display", have provided powerful tools for producing monoclonal antibodies for research, clinical, and therapeutic applications. Our laboratory has combined these techniques with novel selection methods to isolate extraordinarily large arrays of human antibodies that can be used for developing new diagnostic reagents and methods for their use, as well as reagents that may serve as leads for the design of novel therapeutic molecules. In particular, application of phage display to the study of antibody-mediated autoimmune disease, notably idiopathic thrombocytopenic purpura, thrombotic thrombocytopenic purpura, and pemphigus have facilitated comprehensive genetic and serologic analyses of pathogenic autoantibodies thereby offering new insights into disease pathophysiology and approaches for their treatment.

Indexed as

Peptide LibraryAnimalsAntibodies, MonoclonalAutoantibodiesAutoimmune DiseasesHumansImmunoglobulin FragmentsImmunotherapyPemphigusPurpura, ThrombocytopenicAntibodies, MonoclonalAutoantibodiesImmunoglobulin FragmentsPeptide Library

Identifiers

PMID18773308
OpenAlexW2041609579

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.