Evidence map›Paper›PMID 18182457›Full record

Trial reportJournal of leukocyte biology2008

Stimulation of the primary anti-HIV antibody response by IFN-alpha in patients with acute HIV-1 infection.

Laura Adalid-Peralta, Véronique Godot, Céline Colin, Roman Krzysiek, Thi Tran, Pascal Poignard, Alain Venet, Anne Hosmalin, Pierre Lebon, Christine Rouzioux and 3 more

Abstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Journal of leukocyte biology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

24 citing papers in PubMed, 39 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Metabolic engineering ofApplied and environmental microbiology · 2026
    Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Serum levels of B-cell activating factor in chronic hepatitis B virus infection: association with clinical diseases.Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research · 2014
    Article
  12. Review
  13. Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Immune reconstitution of acquired immune deficiency syndrome.Chinese journal of integrative medicine · 2010
    Article
  19. Innate immune activation in primary HIV-1 infection.The Journal of infectious diseases · 2010
    Review
  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

13 authors at 6 institutions in 1 country.

Laura Adalid-PeraltaINSERM U764, Clamart, France.
Véronique Godot
Céline Colin
Roman Krzysiek
Thi Tran
Pascal Poignard
Alain Venet
Anne Hosmalin
Pierre Lebon
Christine Rouzioux
Genevieve Chene
Dominique Emilie
Interprim ANRS 112 Study Group
Inserm · FRAssistance Publique – Hôpitaux de Paris · FRBordeaux Population Health · FRHôpital Antoine-Béclère · FRInstitut Cochin · FRUniversité Paris Cité · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Type I IFNs are needed for the production of antiviral antibodies in mice; whether they also stimulate primary antibody responses in vivo during human viral infections is unknown. This was assessed in patients acutely infected with HIV-1 and treated with IFN-alpha2b. Patients with acute HIV-1 infection were randomized to receive antiretroviral therapy alone (Group A, n=60) or combined for 14 weeks with pegylated-IFN-alpha2b (Group B, n=30). Emergence of anti-HIV antibodies was monitored during 32 weeks by Western blot (WB) analyses of serum samples. IFN-alpha2b treatment stimulated the production of anti-HIV antibodies. On Week 32, 19 weeks after the last IFN-alpha2b administration, there were 8.5 (6.5-10.0) HIV WB bands (median, interquartile range) in Group B and 7.0 (5.0-10.0) bands in Group A (P=0.054), and band intensities were stronger in Group B (P<0.05 for p18, p24, p34, p40, and p55 HIV antigens). IFN-alpha2b treatment also increased circulating concentrations of the B cell-activating factor of the TNF family (P<0.001) and ex vivo production of IL-12 (P<0.05), reflecting its effect on innate immune cells. Withdrawal of antiretroviral treatment on Week 36 resulted in a lower rebound of HIV replication in Group B than in Group A (P<0.05). Therefore, type I IFNs stimulate the emerging anti-HIV immune response in patients with acute HIV-1 infection, resulting in an improved control of HIV replication. Type I IFNs are thus critical in the development of efficient antiviral immune responses in humans, including the production of antiviral antibodies.

Indexed as

Antibody FormationAcquired Immunodeficiency SyndromeAcute DiseaseAnti-HIV AgentsAntiretroviral Therapy, Highly ActiveFranceHIV-1HIV AntibodiesHIV InfectionsHumansImmunoglobulin GInterferon-alphaInterferon alpha-2Polyethylene GlycolsRecombinant ProteinsViral LoadAnti-HIV AgentsHIV AntibodiesImmunoglobulin GInterferon-alphaInterferon alpha-2peginterferon alfa-2bPolyethylene GlycolsRecombinant Proteins

Identifiers

PMID18182457
PMCPMC4749666
OpenAlexW2133540759

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.