Evidence map›Paper›PMID 1541667›Full record

ArticleThe Journal of clinical investigation1992

Immunoglobulin light chain variable region gene sequences for human antibodies to Haemophilus influenzae type b capsular polysaccharide are dominated by a limited number of V kappa and V lambda segments and VJ combinations.

E E Adderson, P G Shackelford, R A Insel, A Quinn, P M Wilson, W L Carroll

Open access · bronzeAbstract read
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 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
7.4field-weighted citation impact, top 2% 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, 67 citations in OpenAlex.

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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 1 country.

E E AddersonDivision of Infectious Diseases, Washington University School of Medicine, St. Louis Children's Hospital, Missouri 63110.
P G Shackelford
R A Insel
A Quinn
P M Wilson
W L Carroll
University of Rochester · USMallinckrodt (United States) · US

Funding

ANTIBODY TO H. INFLUENZAE CAPSULAR POLYSACCHARIDER01AI017217 · NIAID · UNIVERSITY OF ROCHESTER · PI INSEL, RICHARD A. · 1985 to 1989
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SUBCLASS RESPONSE TO POLYSACCHARIDE ANTIGENS IN CHILDRENR01AI019350 · NIAID · WASHINGTON UNIVERSITY · PI SHACKELFORD, PENELOPE G · 1985 to 1995
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NCRR NIH HHS RR-36NIAID NIH HHS AI17217NIAID NIH HHS R01 AI19350
6 · The paper itself

Abstract

The immune repertoire to Haemophilus influenzae type b capsular polysaccharide (Hib PS) appears to be dominated by certain light chain variable region genes (IgVL). In order to examine the molecular basis underlying light chain bias, IgVL genes have been cloned from a panel of heterohybridomas secreting human anti-Hib PS (antibody) (anti-Hib PS Ab). One hybridoma, representative of the predominant serum clonotype of anti-Hib PS Ab in older children and adults following immunization or Hib infection, uses a V kappa II segment identical to the germline gene A2, and a JK3 segment. A second kappa hybridoma uses a member of the V kappa I family and a JK4 segment. Four lambda antibodies, all cross-reactive with the structurally related antigen Escherichia coli K100 PS, use V lambda VII segments which are 96-98% homologous to one another, and may originate from a single germline gene. Two additional lambda antibodies, not K100-cross-reactive, are encoded by members of the V lambda II family. All lambda antibodies use highly homologous J lambda 2 or J lambda 3 segments. The VJ joints of all lambda antibodies and the V kappa II-encoded antibody are notable for the presence of an arginine codon, suggesting an important role in antigen binding. Although more complex than heavy chain variable region gene usage, a significant portion of serum anti-Hib PS Ab is likely to be encoded by a limited number of V kappa and V lambda segments and VJ combinations, which may be selectively expressed during development, or following antigen exposure.

Indexed as

Genes, ImmunoglobulinHaemophilus VaccinesAdultAge FactorsAmino Acid SequenceAntibodies, BacterialBacterial CapsulesBacterial VaccinesBase SequenceBlotting, SouthernChildChild, PreschoolHaemophilus influenzaeHumansHybridomasImmunoglobulin kappa-ChainsAntibodies, BacterialBacterial VaccinesHaemophilus influenzae type b polysaccharide vaccineHaemophilus VaccinesImmunoglobulin kappa-ChainsImmunoglobulin lambda-ChainsImmunoglobulin Variable RegionPolysaccharides, Bacterial

Identifiers

PMID1541667
PMCPMC442915
OpenAlexW2020166995

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.