Evidence map›Paper›PMID 11157050›Full record

ArticleThe Journal of experimental medicine2001

Impairment of CD4(+) T cell responses during chronic virus infection prevents neutralizing antibody responses against virus escape mutants.

A Ciurea, L Hunziker, P Klenerman, H Hengartner, R M Zinkernagel

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
8.4field-weighted citation impact, top 2% 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

37 citing papers in PubMed, 89 citations in OpenAlex.

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  10. Modeling the adaptive immune response in HBV infection.Journal of mathematical biology · 2011
    Article
  11. Article
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  15. Article
  16. CD4+ T cell responses in hepatitis C virus infection.World journal of gastroenterology · 2007
    Review
  17. Article
  18. Article
  19. Article
  20. 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

5 authors at 1 institution in 1 country.

A CiureaInstitute for Experimental Immunology, University Hospital, CH-8091 Zürich, Switzerland. adrian.ciurea@dim.usz.ch
L Hunziker
P Klenerman
H Hengartner
R M Zinkernagel
University Hospital of Zurich · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We have shown previously that neutralizing antibodies (nAbs) are important contributors to the long-term immune control of lymphocytic choriomeningitis virus infection, particularly if cytotoxic T cell responses are low or absent. Nevertheless, virus escape from the nAb response due to mutations within the surface glycoprotein gene may subsequently allow the virus to persist. Here we show that most of the antibody-escape viral mutants retain their immunogenicity. We present evidence that the failure of the infected host to mount effective humoral responses against emerging neutralization-escape mutants correlates with the rapid loss of CD4(+) T cell responsiveness during the establishment of viral persistence. Similar mechanisms may contribute to the persistence of some human pathogens such as hepatitis B and C viruses, and human immunodeficiency virus.

Indexed as

Antigens, ViralPoint MutationViral ProteinsAnimalsAntibodies, ViralCD4-Positive T-LymphocytesCell LineChronic DiseaseCricetinaeGenetic VariationGlycoproteinsHumansLymphocytic ChoriomeningitisLymphocytic choriomeningitis virusMiceMice, KnockoutAntibodies, ViralAntigens, Viralglycoprotein peptide, Lymphocytic choriomeningitis virusGlycoproteinsViral Proteins

Identifiers

PMID11157050
PMCPMC2195917
OpenAlexW2128417270

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.