Evidence map›Paper›PMID 26400081›Full record

ArticleThe Journal of biological chemistry2015

Antigen-B Cell Receptor Complexes Associate with Intracellular major histocompatibility complex (MHC) Class II Molecules.

Margarida Barroso, Heidi Tucker, Lisa Drake, Kathleen Nichol, James R Drake

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 15% 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

28 citing papers in PubMed, 1 synthesis or guideline pooled it, 42 citations in OpenAlex.

  1. Pooled it
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  6. Review
  7. Article
  8. Article
  9. Updates of the role of B-cells in ischemic stroke.Frontiers in cellular neuroscience · 2024
    Review
  10. Article
  11. Review
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  17. Article
  18. The Plasticity of Newly Formed B Cells.Journal of immunology (Baltimore, Md. : 1950) · 2019
    Review
  19. Article
  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

5 authors at 1 institution in 1 country.

Margarida BarrosoCenter for Cardiovascular Sciences, Albany Medical College, Albany, New York 12208.
Heidi TuckerCenter for Immunology and Microbial Disease, Albany Medical College, Albany, New York 12208.
Lisa DrakeCenter for Immunology and Microbial Disease, Albany Medical College, Albany, New York 12208.
Kathleen NicholCenter for Immunology and Microbial Disease, Albany Medical College, Albany, New York 12208.
James R DrakeCenter for Immunology and Microbial Disease, Albany Medical College, Albany, New York 12208. Electronic address: drakej@mail.amc.edu.
Albany Medical Center Hospital · US

Funding

Characterization of the MHC Class II Peptide Loading ComplexR21AI097673 · NIAID · ALBANY MEDICAL COLLEGE · PI DRAKE, JAMES R · 2012 to 2013
$423k
The 3D whole Body Distribution of NIR transferrin using FRET tomography imagingR21CA161782 · NCI · ALBANY MEDICAL COLLEGE · PI BARROSO, MARGARIDA · 2011 to 2012
$379k
NCI NIH HHS CA-161782NCI NIH HHS R21 CA161782NIAID NIH HHS AI-097673NIAID NIH HHS R21 AI097673
6 · The paper itself

Abstract

Antigen processing and MHC class II-restricted antigen presentation by antigen-presenting cells such as dendritic cells and B cells allows the activation of naïve CD4+ T cells and cognate interactions between B cells and effector CD4+ T cells, respectively. B cells are unique among class II-restricted antigen-presenting cells in that they have a clonally restricted antigen-specific receptor, the B cell receptor (BCR), which allows the cell to recognize and respond to trace amounts of foreign antigen present in a sea of self-antigens. Moreover, engagement of peptide-class II complexes formed via BCR-mediated processing of cognate antigen has been shown to result in a unique pattern of B cell activation. Using a combined biochemical and imaging/FRET approach, we establish that internalized antigen-BCR complexes associate with intracellular class II molecules. We demonstrate that the M1-paired MHC class II conformer, shown previously to be critical for CD4 T cell activation, is incorporated selectively into these complexes and loaded selectively with peptide derived from BCR-internalized cognate antigen. These results demonstrate that, in B cells, internalized antigen-BCR complexes associate with intracellular MHC class II molecules, potentially defining a site of class II peptide acquisition, and reveal a selective role for the M1-paired class II conformer in the presentation of cognate antigen. These findings provide key insights into the molecular mechanisms used by B cells to control the source of peptides charged onto class II molecules, allowing the immune system to mount an antibody response focused on BCR-reactive cognate antigen.

Indexed as

AnimalsAntigen PresentationB-LymphocytesCell LineFluorescence Resonance Energy TransferHistocompatibility Antigens Class IIHumansMiceMultiprotein ComplexesProtein BindingReceptors, Antigen, B-CellRecombinant ProteinsHistocompatibility Antigens Class IIMultiprotein ComplexesReceptors, Antigen, B-CellRecombinant Proteinsantigen presentationantigen-presenting cell (APC)antigen processingB cell receptor (BCR)FRETimaginglymphocyteMHC

Identifiers

PMID26400081
PMCPMC4646406
OpenAlexW2262313435

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.