Evidence map›Paper›PMID 17395779›Full record

ArticleBlood2007

Bovine apolipoprotein B-100 is a dominant immunogen in therapeutic cell populations cultured in fetal calf serum in mice and humans.

Norihisa Sakamoto, Kazuhide Tsuji, Linda M Muul, Ann M Lawler, Emanuel F Petricoin, Fabio Candotti, Julia A Metcalf, Jorge A Tavel, H Clifford Lane, Walter J Urba and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

23 citing papers in PubMed, 55 citations in OpenAlex.

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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

14 authors at 11 institutions in 2 countries.

Norihisa SakamotoDivision of Therapeutic Proteins, Center for Drug Evaluation and Research, U.S. Food and Drug Administration, Bethesda, MD 20892, USA.
Kazuhide Tsuji
Linda M Muul
Ann M Lawler
Emanuel F Petricoin
Fabio Candotti
Julia A Metcalf
Jorge A Tavel
H Clifford Lane
Walter J Urba
Bernard A Fox
Ajit Varki
Joan K Lunney
Amy S Rosenberg
Center for Drug Evaluation and Research · USNational Human Genome Research Institute · USNational Institutes of Health · USAgricultural Research Service · USCancer Research Center · USGeorge Mason University · USJohns Hopkins University · USNational Institute of Allergy and Infectious Diseases · USProvidence Portland Medical Center · USUnited States Food and Drug Administration · USUniversity of California, San Diego · US

Funding

Pathogenesis and Treatment of HIV InfectionZIAAI000585 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI LANE, CLIFFORD · 2009 to 2025
$26.8M
Gene Therapy Approaches for Primary ImmunodeficienciesZIAHG000122 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI CANDOTTI, FABIO · 2009 to 2014
$6.5M
Molecular and Clinical Studies of Primary ImmunodeficienciesZIAHG000121 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI CANDOTTI, FABIO · 2009 to 2014
$6.2M
PATHOGENIC MECHANISMS IN HUMAN IMMUNODEFICIENCY VIRUS INFECTIONSZ01AI000585 · NIAID · NIAID EXTRAMURAL ACTIVITIES · PI LANE, HENRY C · 1990 to 2008
$4.5M
GENE THERAPY APPROACHES FOR PRIMARY IMMUNODEFICIENCIESZ01HG000122 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI CANDOTTI, FABIO · 1998 to 2008
$3.2M
GENE TRANSFER INTO HEMATOPOIETIC STEM CELLSZ01HG000121 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI CANDOTTI, FABIO · 1998 to 2008
$2.1M
Intramural NIH HHS
6 · The paper itself

Abstract

Recent studies have demonstrated that cell populations intended for therapeutic purposes that are cultured in heterologous animal products can acquire xenoantigens, potentially limiting their utility. In investigations of the immune response to murine embryonic stem cells, we found that a strong antibody response was generated after the second infusion. Both polyclonal and monoclonal antibody responses, derived from immunized mice, were found to be specific for bovine apolipoprotein B-100, which binds to abundant low-density lipoprotein receptors on the cell surface and is internalized. Here we show that in the majority of patients administered 3 different types of cell-based therapies using cells grown in fetal calf serum-containing media, an antibody response to bovine apolipoprotein B-100 develops after the second infusion and is the dominant specificity. The known and potential clinical effects of such antibodies are discussed.

Indexed as

VaccinesAnimalsAntibody FormationAntigens, HeterophileApolipoprotein B-100Blood BanksCattleEmbryonic Stem CellsFemaleFetal BloodHumansMiceMice, Inbred C57BLMice, Inbred StrainsMice, TransgenicNational Institutes of Health (U.S.)Antigens, HeterophileApolipoprotein B-100Vaccines

Identifiers

PMID17395779
PMCPMC1924480
OpenAlexW2121247045

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.