Evidence map›Paper›PMID 19056129›Full record

ReviewVeterinary immunology and immunopathology2009

The piglet as a model for B cell and immune system development.

J E Butler, K M Lager, I Splichal, D Francis, I Kacskovics, M Sinkora, N Wertz, J Sun, Y Zhao, W R Brown and 11 more

Abstract readReview
In one paragraph

Review in Veterinary immunology and immunopathology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
13.0field-weighted citation impact, top 1% 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

51 citing papers in PubMed, 134 citations in OpenAlex.

  1. Review
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  5. Immunoglobulin M-degrading enzyme ofFrontiers in immunology · 2023
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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

21 authors at 12 institutions in 7 countries.

J E ButlerDepartment of Microbiology, University of Iowa, Iowa City, IA, United States. john-butler@uiowa.edu
K M Lager
I Splichal
D Francis
I Kacskovics
M Sinkora
N Wertz
J Sun
Y Zhao
W R Brown
R DeWald
S Dierks
S Muyldermans
J K Lunney
P B McCray
C S Rogers
M J Welsh
P Navarro
F Klobasa
F Habe
J Ramsoondar
Czech Academy of Sciences · CZAbbott (United Kingdom) · GBAbbott (United States) · USChina Agricultural University · CNEötvös Loránd University · HULohmann Tierzucht (Germany) · DENational Animal Disease Center · USPioneer (United States) · USSouth Dakota State University · USUniversity of Iowa · USUniversity of Ljubljana · SIWake Forest University · US

Funding

Vector CoreP01HL051670 · NHLBI · UNIVERSITY OF IOWA · PI MCCRAY, PAUL B · 1993 to 2019
$36.5M
Respiratory virus infection in early cystic fibrosis lung diseaseP01HL091842 · NHLBI · UNIVERSITY OF IOWA · PI STOLTZ, DAVID A · 2008 to 2022
$34.2M
Howard Hughes Medical InstituteNHLBI NIH HHS P01 HL051670NHLBI NIH HHS P01 HL091842
6 · The paper itself

Abstract

The ability to identify factors responsible for disease in all species depends on the ability to separate those factors which are environmental from those that are intrinsic. This is particularly important for studies on the development of the adaptive immune response of neonates. Studies on laboratory rodents or primates have been ambiguous because neither the effect of environmental nor maternal factors on the newborn can be controlled in mammals that: (i) transmit potential maternal immunoregulatory factors in utero and (ii) are altricial and cannot be reared after birth without their mothers. Employing the newborn piglet model can address each of these concerns. However, it comes at the price of having first to characterize the immune system of swine and its development. This review focuses on the porcine B cell system, especially on the methods used for its characterization in fetal studies and neonatal piglets. Understanding these procedures is important in the interpretation of the data obtained. Studies on neonatal piglets have (a) provided valuable information on the development of the adaptive immune system, (b) lead to important advances in evolutionary biology, (c) aided our understanding of passive immunity and (d) provided opportunities to use swine to address specific issues in veterinary and biomedical research and immunotherapy. This review summarizes the history of the development of the piglet as a model for antibody repertoire development, thus providing a framework to guide future investigators.

Indexed as

Models, AnimalAnimalsAnimals, NewbornB-LymphocytesGerm-Free LifeHumansImmune SystemSwine

Identifiers

PMID19056129
PMCPMC2828348
OpenAlexW2047851930

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.