Evidence map›Paper›PMID 7607710›Full record

ArticleImmunogenetics1995

Idiotypic diversity and variable region gene usage by mouse anti-HLA-DQ3 mAb.

Y Iwasaki, H Takabatake, M Monestier, S Ferrone

Abstract read
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In one paragraph

Article in Immunogenetics, 1995. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 93% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

4 authors at 2 institutions in 1 country.

Y IwasakiDepartment of Microbiology and Immunology, New York Medical College, Valhalla 10595, USA.
H Takabatake
M Monestier
S Ferrone
New York Medical College · USTemple University · US

Funding

MONOCLONAL ANTIBODIES TO HUMAN MELANOMA ANTIGENSR01CA037959 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI FERRONE, SOLDANO · 1985 to 2001
$518k
NCI NIH HHS CA37959
6 · The paper itself

Abstract

The anti-HLA-DQ3 monoclonal antibodies (mAb) KS13, SO1, SO2, SO3, SO4, and SO5 recognize spatially close but distinct antigenic determinants, since they crossinhibit each other in their binding to HLA-DQ3 antigens, but do not share idiotopes recognized in their antigen combining site by syngeneic and anti-id antisera and mAb. Furthermore, mAb SO1, SO3, SO4, and SO5 react also with HLA-DQ allospecificities other than HLA-DQ3. Sequence analysis of the heavy (VH) and light (VL) chain variable region of the six mAb revealed preferential usage of VH 36-60 and VK 12/13 gene families. However, the individual VH and VL germline gene usage by the six mAb is diverse and the utilization of D, JH, and JL gene segments is heterogeneous. The diverse usage of VH and VL gene segments and heterogeneous amino acid sequences of VH and VL CDR, together with the heterogeneous idiotypic profile, may reflect the complexity of the determinants recognized by the six mAb on HLA-DQ3 antigens. The results we have presented provide for the first time information about the structural basis of the diversity of antibodies recognizing human histocompatibility antigens.

Indexed as

Amino Acid SequenceAnimalsAntibodies, Anti-IdiotypicAntibodies, MonoclonalAntibody SpecificityBase SequenceCells, CulturedDNAHLA-DQ AntigensHumansImmunoglobulin Variable RegionMaleMiceMice, Inbred BALB CMolecular Sequence DataAntibodies, Anti-IdiotypicAntibodies, MonoclonalDNAHLA-DQ3 antigenHLA-DQ AntigensImmunoglobulin Variable Region

Identifiers

PMID7607710
OpenAlexW1977806238

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.