Evidence map›Paper›PMID 1334971›Full record

ArticleThe Journal of clinical investigation1992

Sequence analyses of three immunoglobulin G anti-virus antibodies reveal their utilization of autoantibody-related immunoglobulin Vh genes, but not V lambda genes.

D F Huang, T Olee, Y Masuho, Y Matsumoto, D A Carson, P P Chen

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in The Journal of clinical investigation, 1992. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.2field-weighted citation impact, top 11% 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

12 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
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  4. A monoclonal IgG anticardiolipin antibody from a patient with the antiphospholipid syndrome is thrombogenic in mice.Proceedings of the National Academy of Sciences of the United States of America · 1996
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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

6 authors at 2 institutions in 3 countries.

D F HuangDepartment of Medicine, University of California, San Diego, La Jolla 92093-0663.
T Olee
Y Masuho
Y Matsumoto
D A Carson
P P Chen
Scripps Research Institute · USUniversity of California San Diego · US

Funding

VALIDATION OF SELF ADMINISTERED QUALITY OF WELL BEING SCALE IN ARTHRITISP60AR040770 · NIAMS · UNIVERSITY OF CALIFORNIA SAN DIEGO · PI SILVERMAN, GREGG JOSHUA · 1991 to 2000
$787k
MOLECULAR GENETICS OF AUTOANTIBODIES IN HUMANSR01AI032243 · NIAID · UNIVERSITY OF CALIFORNIA SAN DIEGO · PI CHEN, POJEN P · 1991 to 2000
$275k
RHEUMATOID FACTOR: GENETICS, PATHOGENESIS, &MODULATIONR01AR025443 · NIAMS · SCRIPPS CLINIC AND RESEARCH FOUNDATION · PI CARSON, DENNIS A · 1986 to 1988
–
RHEUMATOID FACTOR: GENETICS, PATHOGENESIS AND MODULATIONR37AR025443 · NIAMS · UNIVERSITY OF CALIFORNIA SAN DIEGO · PI CARSON, DENNIS A · 1989 to 1998
–
NIAID NIH HHS AI-32243NIAMS NIH HHS AR-25443NIAMS NIH HHS AR-40770
6 · The paper itself

Abstract

Accumulated sequence analyses of the antibody repertoire have revealed that most autoantibodies and developmentally regulated antibodies share a small set of germline Ig-variable region (V) genes. The findings have prompted speculation that certain autoantibodies are of developmental importance and may be instrumental in maintaining homeostasis of the adult antibody repertoire. In order to evaluate this hypothesis critically, it is first necessary to determine the V gene usage in human antibodies against foreign substances. Unfortunately, only a few such antibodies have had their heavy and light chains characterized. To rectify the situation, we adapted the anchored polymerase chain reaction to clone and analyze rapidly the expressed V genes for three anti-virus IgG antibodies. The results show that all three heavy chain V (Vh) genes are highly homologous to the known autoantibody-related Vh genes. In contrast, two light chain V (VL) genes of the V lambda 1 subgroup are similar to a non-autoantibody-related germline V lambda 1 gene. Taken together with the reported Vh and VL sequences of several antibodies against viruses and bacteria, the data show that many antipathogen antibodies may use the same small set of Vh genes that encode autoantibodies, but diverse VL genes that are distinct from autoantibody-related VL genes. Thus, only a small portion of the potentially functional germline Vh genes are used recurrently to generate most antibodies in a normal antibody repertoire, regardless of their reactivities with either self or non-self.

Indexed as

Genes, ImmunoglobulinAmino Acid SequenceAntibodies, ViralAutoantibodiesBase SequenceCloning, MolecularHerpesvirus 3, HumanHumansImmunoglobulin GImmunoglobulin Heavy ChainsImmunoglobulin lambda-ChainsImmunoglobulin Variable RegionMolecular Sequence DataOligodeoxyribonucleotidesPolymerase Chain ReactionSequence AlignmentAntibodies, ViralAutoantibodiesImmunoglobulin GImmunoglobulin Heavy ChainsImmunoglobulin lambda-ChainsImmunoglobulin Variable RegionOligodeoxyribonucleotides

Identifiers

PMID1334971
PMCPMC443370
OpenAlexW2020082741

What OpenQuestion holds

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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.