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PMID: 6173362 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Further characterization of two "DR supertypic" specificities. Additional evidence that they reside on molecules different from those carrying HLA-DR locus specificities.

Human immunology ·Vol. 3 ·No. 2 ·1981-10-00 ·Pages 93-108

Tanigaki N, Tosi R, Centis D, Ferrara GB, Pressman D

Abstract

Peripheral lymphocytes from a panel of individuals who had been assayed for DR specificities by the conventional cytotoxicity assay were typed for DR "supertypic" specificities, DC1 and BR4 x 7, by the radioimmunoassay. A positive and a negative population were clearly distinguished for both specificities and the strong association of the DC1 specificity with DR1, 2, and w6 was confirmed as well as the BR4 x 7 specificity with DR4 and 7. Family study also supported this strong association. Appropriate papain digestion separated molecules carrying DC1 determinant from those carrying DR2 as well as from those carrying DRw6, and separated molecules carrying BR4 x 7 from those carrying DR4. Specificity analysis of the 8th Workshop antisera by use of these separated antigen preparations showed that some anti-DC1 antisera do not possess appreciable anti-DR1, 2, or w6 activity and vice versa. The same was found for DR4 x 7 in its relationship with DR4 and 7. The existing evidence could be explained most economically by assuming a genetic model of two loci in linkage disequilibrium each coding for analogous but distinct forms of the small (beta) subunits of Ia molecules.

MeSH Terms
Epitopes Female HLA-DR Antigens Histocompatibility Antigens Class II/genetics,immunology Humans Male Radioimmunoassay
Chemicals
Epitopes HLA-DR Antigens Histocompatibility Antigens Class II
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Tanigaki N
Tosi R
Centis D
Ferrara G B
Pressman D
Article Info
Journal
Human immunology
Abbr.
Hum Immunol
ISSN
0198-8859
Published
1981-10-00
Pages
93-108
Language
English
Region
United States
NLM ID
8010936
Subset
IM
Grants
NIAID NIH HHS · AI08899 · United States
NCI NIH HHS · CA17276 · United States
NCI NIH HHS · CA17609 · United States
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