Evidence map›Paper›PMID 7664491›Full record

ArticleClinical and experimental immunology1995

Increased dimeric IgA-producing B cells in tonsils in IgA nephropathy determined by in situ hybridization for J chain mRNA.

S J Harper, A C Allen, M C Béné, J H Pringle, G Faure, I Lauder, J Feehally

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Article in Clinical and experimental immunology, 1995. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.9field-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

14 citing papers in PubMed, 56 citations in OpenAlex.

  1. IgA class-switched CD27-CD21+ B cells in IgA nephropathy.Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2025
    Article
  2. Review
  3. Review
  4. Article
  5. A New Vision of IgA Nephropathy: The Missing Link.International journal of molecular sciences · 2019
    Review
  6. Review
  7. Article
  8. New Insights into the Pathogenesis of IgA Nephropathy.Kidney diseases (Basel, Switzerland) · 2015
    Article
  9. Genetics and immunopathogenesis of IgA nephropathy.Clinical reviews in allergy & immunology · 2011
    Review
  10. Immunopathogenesis of IgAN.Seminars in immunopathology · 2007
    Review
  11. Article
  12. Article
  13. Article
  14. 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

7 authors at 3 institutions in 2 countries.

S J HarperDepartment of Nephrology, Leicester General Hospital, UK
A C Allen
M C Béné
J H Pringle
G Faure
I Lauder
J Feehally
Leicester General Hospital · GBCentre Hospitalier Régional et Universitaire de Nancy · FRUniversity of Leicester · GB

Funding

Wellcome Trust
6 · The paper itself

Abstract

The origin of mesangial IgA deposits in IgA nephropathy (IgAN) remains obscure. A significant proportion of deposited immunoglobulin is dimeric (J chain-positive). Previous studies of J chain expression within lymphoid tissue in IgAN have utilized antibodies which other investigators have found to be non-specific. To address this problem, we have developed and in situ hybridization (ISH) method for the detection of J chain mRNA within IgA plasma cells. Tonsils from 12 patients with IgAN and 12 controls were studied using (i) non-isotopic ISH for J chain mRNA, and (ii) combined immunofluorescence (IF) and fluorescent ISH. J chain mRNA-positive cells were identified in germinal centres, and within the subepithelial and interfollicular zones. A greater number of J chain mRNA-positive cells were found in the germinal centres of patients (mean 57.7 +/- 4.6 cells/10(5) micron2) compared with controls (mean 36.9 +/- 3.5 cells/10(5) micron2) (P < 0.001). Combined IF and fluorescent ISH showed a greater proportion of J chain mRNA-positive interfollicular IgA cells in patient tonsils (32 +/- 3.4%) compared with controls (21 +/- 2.3%; P < 0.02). These results indicate a shift towards dimeric IgA production in the tonsils in IgAN. In addition, the finding of excess numbers of J chain-positive Iga-negative cells within germinal centres suggests that an abnormality may be present at the B cell differentiation stage before IgA switching. These results further highlight immune abnormalities within the tonsil as a central feature of abnormal polymeric IgA biology in this common form of glomerulonephritis.

Indexed as

AdolescentAdultB-LymphocytesChildFemaleGlomerulonephritis, IGAHumansImmunoglobulin AImmunoglobulin J-ChainsIn Situ HybridizationMaleMiddle AgedPalatine TonsilRNA, MessengerImmunoglobulin AImmunoglobulin J-ChainsRNA, Messenger

Identifiers

PMID7664491
PMCPMC1553245
OpenAlexW2159033284

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Registered trials

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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.