Evidence map›Paper›PMID 25142581›Full record

ArticleJournal of virology2014

Immunogenicity studies of proteins forming the T4 phage head surface.

Krystyna Dąbrowska, Paulina Miernikiewicz, Agnieszka Piotrowicz, Katarzyna Hodyra, Barbara Owczarek, Dorota Lecion, Zuzanna Kaźmierczak, Andrey Letarov, Andrzej Górski

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 104 papers.

0numbers the graph read from it
0cells of the map it votes in
104citing papers in PubMed
6.8field-weighted citation impact, top 3% 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

104 citing papers in PubMed, 173 citations in OpenAlex.

  1. Article
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  4. Immune Responses to Phage Therapy in Humans: A Review.The Journal of infectious diseases · 2026
    Review
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  12. Observational
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44 more citing papers are in PubMed but not listed here.

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

9 authors at 1 institution in 1 country.

Krystyna DąbrowskaInstitute of Immunology and Experimental Therapy, Polish Academy of Sciences, Wrocław, Poland dabrok@iitd.pan.wroc.pl.
Paulina MiernikiewiczInstitute of Immunology and Experimental Therapy, Polish Academy of Sciences, Wrocław, Poland.
Agnieszka PiotrowiczInstitute of Immunology and Experimental Therapy, Polish Academy of Sciences, Wrocław, Poland.
Katarzyna HodyraInstitute of Immunology and Experimental Therapy, Polish Academy of Sciences, Wrocław, Poland.
Barbara OwczarekInstitute of Immunology and Experimental Therapy, Polish Academy of Sciences, Wrocław, Poland.
Dorota LecionInstitute of Immunology and Experimental Therapy, Polish Academy of Sciences, Wrocław, Poland.
Zuzanna KaźmierczakInstitute of Immunology and Experimental Therapy, Polish Academy of Sciences, Wrocław, Poland.
Andrey LetarovWinogradsky Institute of Microbiology, RAS, Moscow, Russia.
Andrzej GórskiInstitute of Immunology and Experimental Therapy, Polish Academy of Sciences, Wrocław, Poland Institute of Transplantology, Medical University of Warsaw, Warsaw, Poland.
Polish Academy of Sciences · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

unlabelledAdvances in phage therapy and novel applications of phages in biotechnology encourage interest in phage impact on human and animal immunity. Here we present comparative studies of immunogenic properties of T4 phage head surface proteins gp23*, gp24*, Hoc, and Soc, both as elements of the phage capsid and as isolated agents. Studies comprise evaluation of specific antibodies in the human population, analysis of the proteins' impact on the primary and secondary responses in mice, and the effect of specific antibodies on phage antibacterial activity in vitro and in vivo in mice. In humans, natural antibodies specific to T4-like phages were abundant (81% of investigated sera). Among those, significantly elevated levels of IgG antibodies only against major head protein (gp23*) were found, which probably reflected cross-reactions of T4 with antibodies induced by other T4-like phages. Both IgM and IgG antibodies were induced mostly by gp23* and Hoc, while weak (gp24*) and very weak (Soc) reactivities of other head proteins were noticed. Thus, T4 head proteins that markedly contribute to immunological memory to the phage are highly antigenic outer capsid protein (Hoc) and major capsid protein (gp23*). Specific anti-gp23* and anti-Hoc antibodies substantially decreased T4 phage activity in vitro and to some extent in vivo. Cooperating with antibodies, the immune complement system also contributed to annihilating phages. IMPORTANCE: Current descriptions of phage immunogenicity and its biological consequences are still vague and incomplete; thus, the central problem of this work is timely and may have strong practical implications. Here is presented the very first description of the contribution of bacteriophage proteins to immunological memory of the phage. Understanding of interactions between phages and mammalian immunology may help in biotechnological adaptations of phages for therapeutic requirements as well as for better appreciation of phage ecology and their role in the biosphere.

Indexed as

AdolescentAdultAnimalsAntibodies, ViralBacteriophage T4Complement System ProteinsFemaleHumansImmunoglobulin GImmunoglobulin MMaleMiceMice, Inbred C57BLViral ProteinsYoung AdultAntibodies, ViralComplement System ProteinsImmunoglobulin GImmunoglobulin MViral Proteins

Identifiers

PMID25142581
PMCPMC4248953
OpenAlexW2139150373

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.