Evidence map›Paper›PMID 30154800›Full record

ArticleFrontiers in immunology2018

Bovine Neonatal Pancytopenia-Associated Alloantibodies Recognize Individual Bovine Leukocyte Antigen 1 Alleles.

Rahel Kasonta, Jacqueline Mauritz, Christina Spohr, Carola Sauter-Louis, Karin Duchow, Klaus Cussler, Mark Holsteg, Max Bastian

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.3field-weighted citation impact, top 18% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. 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

8 authors at 3 institutions in 1 country.

Rahel KasontaPaul-Ehrlich-Institut, Langen, Germany.
Jacqueline MauritzPaul-Ehrlich-Institut, Langen, Germany.
Christina SpohrPaul-Ehrlich-Institut, Langen, Germany.
Carola Sauter-LouisFriedrich-Loeffler-Institut, Greifswald-Insel Riems, Germany.
Karin DuchowPaul-Ehrlich-Institut, Langen, Germany.
Klaus CusslerPaul-Ehrlich-Institut, Langen, Germany.
Mark HolstegLandwirtschaftskammer Nordrhein-Westfalen, Bonn, Germany.
Max BastianPaul-Ehrlich-Institut, Langen, Germany.
Paul Ehrlich Institut · DEFriedrich-Loeffler-Institut · DELandwirtschaftskammer Nordrhein-Westfalen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bovine neonatal pancytopenia (BNP) was a vaccine-induced alloimmune disease observed in young calves and characterized by hemorrhages, pancytopenia, and severe destruction of the hematopoietic tissues. BNP was induced by alloreactive maternal antibodies present in the colostrum of certain cows vaccinated with a highly adjuvanted vaccine against bovine viral diarrhea. Bioprocess impurities, originating from the production cell line of the vaccine, are likely to have induced these alloreactive antibodies. One prominent alloantigen recognized by vaccine-induced alloantibodies is highly polymorphic bovine major histocompatibility complex class I antigen (bovine leukocyte antigen 1-BoLA I). Aim of this study was to define the fine specificity of BNP-associated anti-BoLA I alloantibodies. In total, eight different BoLA I alleles from the production cell line were identified. All genes were cloned and recombinantly expressed in murine cell lines. Using these cells in a flow cytometric assay, the presence of BoLA I specific alloantibodies in BNP dam sera was proven. Three BoLA I variants were identified that accounted for the majority of vaccine-induced BoLA I reactivity. By comparing the sequence of immunogenic to non-immunogenic BoLA I variants probable minimal epitopes on BoLA I were identified. In general, dams of BNP calves displayed high levels of BoLA I reactive alloantibodies, while vaccinated cows delivering healthy calves had significantly lower alloantibody titers. We identified a subgroup of vaccinated cows with healthy calves displaying very high alloantibody titers. Between these cows and BNP dams no principle difference in the BoLA I reactivity pattern was observed. However, with a limited set of dam-calf pairs it could be demonstrated that serum from these cows did not bind to BoLA I expressing leukocytes of their offspring. By contrast, when testing cells from surviving BNP calves with the corresponding dam's serum there was significant binding. We therefore conclude that predominantly highly alloreactive cows are at risk to induce BNP and it depends on the paternally inherited BoLA I whether or not the calf develops BNP.

Indexed as

AllelesAmino Acid SequenceAnimalsAnimals, NewbornCattleCattle DiseasesCell LineGene ExpressionHistocompatibility Antigens Class IImmunizationIsoantibodiesModels, MolecularPancytopeniaProtein ConformationHistocompatibility Antigens Class IIsoantibodiesalloantibodiesalloimmunitybovine leukocyte antigen Ibovine neonatal pancytopeniaveterinary vaccines

Identifiers

PMID30154800
PMCPMC6102493
OpenAlexW2886737275

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.