Evidence map›Paper›PMID 26501424›Full record

ArticlePloS one2015

HIV-Infected Spleens Present Altered Follicular Helper T Cell (Tfh) Subsets and Skewed B Cell Maturation.

Lucie Colineau, Angeline Rouers, Takuya Yamamoto, Yin Xu, Alejandra Urrutia, Hang-Phuong Pham, Sylvain Cardinaud, Assia Samri, Karim Dorgham, Pierre-Grégoire Coulon and 10 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
4.2field-weighted citation impact, top 5% 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

40 citing papers in PubMed, 62 citations in OpenAlex.

  1. Protein-dependent CD4iScience · 2026
    Article
  2. Article
  3. Review
  4. The immune response to SARS-CoV-2 in people with HIV.Cellular & molecular immunology · 2024
    Review
  5. Review
  6. Article
  7. Article
  8. Naive and memory CD4iScience · 2022
    Article
  9. Interleukin-21 in Viral Infections.International journal of molecular sciences · 2021
    Review
  10. Article
  11. Review
  12. Gene Expression: the Key to Understanding HIV-1 Infection?Microbiology and molecular biology reviews : MMBR · 2020
    Review
  13. Follicular regulatory T cells: a novel target for immunotherapy?Clinical & translational immunology · 2020
    Review
  14. Review
  15. Article
  16. Review
  17. Review
  18. Article
  19. Review
  20. Review
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

20 authors at 7 institutions in 3 countries.

Lucie ColineauSorbonne Universités, UPMC Université Paris 06, Center for Immunology and Microbial Infections-CIMI-Paris, Paris, France; INSERM, U1135, Center for Immunology and Microbial Infections-CIMI-Paris, Paris, France; CNRS, ERL 8255, Center for Immunology and Microbial Infections-CIMI-Paris, Paris, France.
Angeline RouersSorbonne Universités, UPMC Université Paris 06, Center for Immunology and Microbial Infections-CIMI-Paris, Paris, France; INSERM, U1135, Center for Immunology and Microbial Infections-CIMI-Paris, Paris, France; CNRS, ERL 8255, Center for Immunology and Microbial Infections-CIMI-Paris, Paris, France.
Takuya YamamotoImmunology Laboratory, Vaccine research center, National Institute of Allergy and Infectious Diseases (NIAID), NIH, Bethesda, Maryland, United States of America.
Yin XuThe Kirby Institute for Infection and Immunity in Society, University of New South Wales, Sydney, Australia.
Alejandra UrrutiaSorbonne Universités, UPMC Université Paris 06, Center for Immunology and Microbial Infections-CIMI-Paris, Paris, France; INSERM, U1135, Center for Immunology and Microbial Infections-CIMI-Paris, Paris, France; CNRS, ERL 8255, Center for Immunology and Microbial Infections-CIMI-Paris, Paris, France.
Hang-Phuong PhamSorbonne Universités UPMC Université Paris 06, UMRS 959, Immunology-Immunopathology-Immunotherapy (I3), Paris, France; INSERM, UMRS 959, Immunology-Immunopathology-Immunotherapy (I3), Paris, France; CNRS, FRE3632, Immunology-Immunopathology-Immunotherapy (I3), Paris, France.
Sylvain CardinaudSorbonne Universités, UPMC Université Paris 06, Center for Immunology and Microbial Infections-CIMI-Paris, Paris, France; INSERM, U1135, Center for Immunology and Microbial Infections-CIMI-Paris, Paris, France; CNRS, ERL 8255, Center for Immunology and Microbial Infections-CIMI-Paris, Paris, France.
Assia SamriSorbonne Universités, UPMC Université Paris 06, Center for Immunology and Microbial Infections-CIMI-Paris, Paris, France; INSERM, U1135, Center for Immunology and Microbial Infections-CIMI-Paris, Paris, France; AP-HP, Hôpital Pitié-Salpêtière, Department of Immunology, Paris, France.
Karim DorghamSorbonne Universités, UPMC Université Paris 06, Center for Immunology and Microbial Infections-CIMI-Paris, Paris, France; INSERM, U1135, Center for Immunology and Microbial Infections-CIMI-Paris, Paris, France; AP-HP, Hôpital Pitié-Salpêtière, Department of Immunology, Paris, France.
Pierre-Grégoire CoulonSorbonne Universités, UPMC Université Paris 06, Center for Immunology and Microbial Infections-CIMI-Paris, Paris, France; INSERM, U1135, Center for Immunology and Microbial Infections-CIMI-Paris, Paris, France; CNRS, ERL 8255, Center for Immunology and Microbial Infections-CIMI-Paris, Paris, France.
Rémi CheynierINSERM, U1016, Institut Cochin, Paris, France; CNRS, UMR8104, Paris, France; Université Paris Descartes, Sorbonne Paris Cité, Paris, France.
Anne HosmalinINSERM, U1016, Institut Cochin, Paris, France; CNRS, UMR8104, Paris, France; Université Paris Descartes, Sorbonne Paris Cité, Paris, France; AP-HP, Hôpital Cochin, Paris, France.
Eric OksenhendlerUniversité Paris Diderot, Assistance Publique-Hôpitaux de Paris, Département d'Immunologie Clinique, Hôpital Saint-Louis, Paris, France.
Adrien SixSorbonne Universités UPMC Université Paris 06, UMRS 959, Immunology-Immunopathology-Immunotherapy (I3), Paris, France; INSERM, UMRS 959, Immunology-Immunopathology-Immunotherapy (I3), Paris, France; CNRS, FRE3632, Immunology-Immunopathology-Immunotherapy (I3), Paris, France.
Anthony D KelleherThe Kirby Institute for Infection and Immunity in Society, University of New South Wales, Sydney, Australia.
John ZaundersSt. Vincent's Centre for Applied Medical Research, St. Vincent's Hospital, Sydney, Australia.
Richard A KoupImmunology Laboratory, Vaccine research center, National Institute of Allergy and Infectious Diseases (NIAID), NIH, Bethesda, Maryland, United States of America.
Brigitte AutranSorbonne Universités, UPMC Université Paris 06, Center for Immunology and Microbial Infections-CIMI-Paris, Paris, France; INSERM, U1135, Center for Immunology and Microbial Infections-CIMI-Paris, Paris, France; AP-HP, Hôpital Pitié-Salpêtière, Department of Immunology, Paris, France.
Arnaud MorisSorbonne Universités, UPMC Université Paris 06, Center for Immunology and Microbial Infections-CIMI-Paris, Paris, France; INSERM, U1135, Center for Immunology and Microbial Infections-CIMI-Paris, Paris, France; CNRS, ERL 8255, Center for Immunology and Microbial Infections-CIMI-Paris, Paris, France; AP-HP, Hôpital Pitié-Salpêtière, Department of Immunology, Paris, France.
Stéphanie Graff-DuboisSorbonne Universités, UPMC Université Paris 06, Center for Immunology and Microbial Infections-CIMI-Paris, Paris, France; INSERM, U1135, Center for Immunology and Microbial Infections-CIMI-Paris, Paris, France; CNRS, ERL 8255, Center for Immunology and Microbial Infections-CIMI-Paris, Paris, France.
Centre National de la Recherche Scientifique · FRInserm · FRDélégation Paris 5 · FRNational Institute of Allergy and Infectious Diseases · USUNSW Sydney · AUSt Vincent's Hospital Sydney · AUUniversité Paris Cité · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Follicular helper T (Tfh) cells within secondary lymphoid organs control multiple steps of B cell maturation and antibody (Ab) production. HIV-1 infection is associated with an altered B cell differentiation and Tfh isolated from lymph nodes of HIV-infected (HIV+) individuals provide inadequate B cell help in vitro. However, the mechanisms underlying this impairment of Tfh function are not fully defined. Using a unique collection of splenocytes, we compared the frequency, phenotype and transcriptome of Tfh subsets in spleens from HIV negative (HIV-) and HIV+ subjects. We observed an increase of CXCR5+PD-1highCD57-Tfh and germinal center (GC) CD57+ Tfh in HIV+ spleens. Both subsets showed a reduced mRNA expression of the transcription factor STAT-3, co-stimulatory, regulatory and signal transduction molecules as compared to HIV- spleens. Similarly, Foxp3 expressing follicular regulatory T (Tfr) cells were increased, suggesting sustained GC reactions in chronically HIV+ spleens. As a consequence, GC B cell populations were expanded, however, complete maturation into memory B cells was reduced in HIV+ spleens where we evidenced a compromised production of B cell-activating cytokines such as IL-4 and IL-10. Collectively our data indicate that, although Tfh proliferation and GC reactions seem to be ongoing in HIV-infected spleens, Tfh "differentiation" and expression of costimulatory molecules is skewed with a profound effect on B cell maturation.

Indexed as

B-LymphocytesCell DifferentiationCytokinesDNA, ViralFlow CytometryGene Expression ProfilingHIV InfectionsHumansReal-Time Polymerase Chain ReactionSpleenSTAT3 Transcription FactorT-Lymphocytes, Helper-InducerVirus IntegrationCytokinesDNA, ViralSTAT3 protein, humanSTAT3 Transcription Factor

Identifiers

PMID26501424
PMCPMC4621058
OpenAlexW1846295020

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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.