Evidence map›Paper›PMID 26829983›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2016

LLT1 and CD161 Expression in Human Germinal Centers Promotes B Cell Activation and CXCR4 Downregulation.

Alba Llibre, Constantino López-Macías, Teresa Marafioti, Hema Mehta, Amy Partridge, Carina Kanzig, Felice Rivellese, Jacob D Galson, Lucy J Walker, Paul Milne and 6 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 13% 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

31 citing papers in PubMed, 1 synthesis or guideline pooled it, 40 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. MAIT cells modulating the oral lichen planus immune microenvironment: a cellular crosstalk perspective.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2025
    Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. B cells in human lymphoid structures.Clinical and experimental immunology · 2022
    Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. 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

16 authors at 7 institutions in 3 countries.

Alba LlibrePeter Medawar Building for Pathogen Research, University of Oxford, Oxford OX1 3SY, United Kindgom;
Constantino López-MacíasMedical Research Unit on Immunochemistry, Specialties Hospital, National Medical Centre "Siglo XXI," Mexican Institute for Social Security, 06720 Mexico City, Mexico;
Teresa MarafiotiDepartment of Histopathology, University College London, London WC1E 6JJ, United Kingdom;
Hema MehtaPeter Medawar Building for Pathogen Research, University of Oxford, Oxford OX1 3SY, United Kindgom;
Amy PartridgePeter Medawar Building for Pathogen Research, University of Oxford, Oxford OX1 3SY, United Kindgom;
Carina KanzigPeter Medawar Building for Pathogen Research, University of Oxford, Oxford OX1 3SY, United Kindgom;ORCID http://orcid.org/0000-0003-3315-9424
Felice RivelleseCentre for Experimental Medicine and Rheumatology, William Harvey Research Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London EC1M 6BQ, United Kingdom;
Jacob D GalsonOxford Vaccine Group, Department of Paediatrics, National Institute for Health Research, Oxford Biomedical Research Centre, University of Oxford, Oxford OX3 7LJ, United Kingdom;ORCID http://orcid.org/0000-0003-4916-800X
Lucy J WalkerNewcastle University, Newcastle upon Tyne NE1 7RU, United Kingdom;
Paul MilneNewcastle University, Newcastle upon Tyne NE1 7RU, United Kingdom;
Rodney E PhillipsPeter Medawar Building for Pathogen Research, University of Oxford, Oxford OX1 3SY, United Kindgom;
Dominic F KellyOxford Vaccine Group, Department of Paediatrics, National Institute for Health Research, Oxford Biomedical Research Centre, University of Oxford, Oxford OX3 7LJ, United Kingdom;
Gordon J FreemanDepartment of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA 02215; and.
Mohey Eldin El ShikhCentre for Experimental Medicine and Rheumatology, William Harvey Research Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London EC1M 6BQ, United Kingdom; chris.willberg@ndm.ox.ac.uk m.elshikh@qmul.ac.uk.
Paul KlenermanPeter Medawar Building for Pathogen Research, University of Oxford, Oxford OX1 3SY, United Kindgom; Oxford National Institute for Health Research Biomedical Research Centre, Oxford OX3 9DU, United Kingdom.
Christian B WillbergPeter Medawar Building for Pathogen Research, University of Oxford, Oxford OX1 3SY, United Kindgom; Oxford National Institute for Health Research Biomedical Research Centre, Oxford OX3 9DU, United Kingdom chris.willberg@ndm.ox.ac.uk m.elshikh@qmul.ac.uk.ORCID http://orcid.org/0000-0001-5299-9344
University of Oxford · GBNational Institute for Health Research · GBNewcastle University · GBQueen Mary University of London · GBHarvard University · USMexican Social Security Institute · MXUniversity College London · GB

Funding

Virology CoreU19AI082630 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI RAYMOND T CHUNG, GEORG Michael LAUER · 2009 to 2026
$48.1M
NIAID NIH HHS 1U19AI082630-01NIAID NIH HHS U19 AI082630Wellcome Trust 091663Wellcome Trust 109965/Z/15/ZWellcome Trust WT091663MA
6 · The paper itself

Abstract

Germinal centers (GCs) are microanatomical structures critical for the development of high-affinity Abs and B cell memory. They are organized into two zones, light and dark, with coordinated roles, controlled by local signaling. The innate lectin-like transcript 1 (LLT1) is known to be expressed on B cells, but its functional role in the GC reaction has not been explored. In this study, we report high expression of LLT1 on GC-associated B cells, early plasmablasts, and GC-derived lymphomas. LLT1 expression was readily induced via BCR, CD40, and CpG stimulation on B cells. Unexpectedly, we found high expression of the LLT1 ligand, CD161, on follicular dendritic cells. Triggering of LLT1 supported B cell activation, CD83 upregulation, and CXCR4 downregulation. Overall, these data suggest that LLT1-CD161 interactions play a novel and important role in B cell maturation within the GC in humans.

Indexed as

B-LymphocytesCell SeparationDown-RegulationFlow CytometryGerminal CenterHumansImmunohistochemistryLectins, C-TypeLymphocyte ActivationNK Cell Lectin-Like Receptor Subfamily BReal-Time Polymerase Chain ReactionReceptors, Cell SurfaceReceptors, CXCR4CLEC2D protein, humanCXCR4 protein, humanKLRB1 protein, humanLectins, C-TypeNK Cell Lectin-Like Receptor Subfamily BReceptors, Cell SurfaceReceptors, CXCR4

Identifiers

PMID26829983
PMCPMC4760235
OpenAlexW2253832057

What OpenQuestion holds

Textmetadata
LicenceTDM
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.