Literature DB >> 6180011

Two subgroups of HLA Bw44 defined by cell-mediated lympholysis that differ in Bw44 expression on platelets and in patterns of genetic linkage disequilibrium.

W A Tekolf, W E Biddison, R D Aster, S Shaw.   

Abstract

Possible immunogenic heterogeneity of the HLA-Bw44 antigen was investigated using cytotoxic T lymphocytes (CTL) generated between donors identical for HLA-A2,3,-B7,w44. Highly discriminatory CTL combinations were identified that defined two subgroups of Bw44, designated 44.1 and 44.2. Out of 47 Bw44-positive donors tested in a population study, 30 were lysed by the CTL defining 44.1, and 19 were lysed by the CTL defining 44.2. All Bw44 cells could be typed as either 44.1 or 44.2, except two Bw44-positive cells that were phenotypically homozygous for the serologically defined Bw44 antigen and were lysed by both CTL. No Bw44-negative donors (zero out of 37) expressed either 44.1 or 44.2, although cold target blocking was required to eliminate a contaminating reactivity of one CTL population on Bw35 and some Bw45 cells. CTL were also raised between responder/stimulator combinations mismatched for Bw44. These CTL lysed all Bw44-positive target cells, indicating a CML antigen shared by all Bw44 cells. But clear discrimination of the 44.1 and 44.2 subgroups was obtained when appropriate cold target blocking cells were added. All donors with 44.2 expressed high levels of serologically detectable Bw44 on their platelets, and all with 44.1 expressed low levels (p less than 0.005). Furthermore, population studies indicate that 44.1 is in positive linkage disequilibrium with HLA-A2 and possibly DR4, whereas 44.2 is in positive linkage disequilibrium with HLA-DR7 and possibly HLA-A23, -A26, and -A29. These data suggest the existence of two genetically and functionally different subgroups of Bw44 antigens.

Entities:  

Mesh:

Substances:

Year:  1982        PMID: 6180011

Source DB:  PubMed          Journal:  J Immunol        ISSN: 0022-1767            Impact factor:   5.422


  7 in total

1.  Structural analysis of an HLA-B27 functional variant: identification of residues that contribute to the specificity of recognition by cytolytic T lymphocytes.

Authors:  M A Vega; A Ezquerra; S Rojo; P Aparicio; R Bragado; J A López de Castro
Journal:  Proc Natl Acad Sci U S A       Date:  1985-11       Impact factor: 11.205

2.  IEF patterns of HLA-B13 antigens from Orientals and Caucasians.

Authors:  S Y Yang; A Chang; R Olivero; V Relias; E J Yunis
Journal:  Immunogenetics       Date:  1985       Impact factor: 2.846

3.  Identification of HLA-B44 subtypes associated with extended MHC haplotypes.

Authors:  M S Kruskall; E E Eynon; Z Awdeh; C A Alper; E J Yunis
Journal:  Immunogenetics       Date:  1987       Impact factor: 2.846

4.  Identification of several functional subgroups of HLA-B27 by restriction of the activity of antiviral T killer lymphocytes.

Authors:  A Toubert; E Gomard; F C Grumet; B Amor; J Y Muller; J P Levy
Journal:  Immunogenetics       Date:  1984       Impact factor: 2.846

5.  Comparison of one-dimensional IEF patterns for serologically detectable HLA-A and B allotypes.

Authors:  S Y Yang; Y Morishima; N H Collins; T Alton; M S Pollack; E J Yunis; B Dupont
Journal:  Immunogenetics       Date:  1984       Impact factor: 2.846

6.  Cross-reactivity of self-HLA-restricted Epstein-Barr virus-specific cytotoxic T lymphocytes for allo-HLA determinants.

Authors:  J S Gaston; A B Rickinson; M A Epstein
Journal:  J Exp Med       Date:  1983-12-01       Impact factor: 14.307

7.  In vitro generation of cytotoxic cells specific for human minor histocompatibility antigens by lymphocytes from a normal donor potentially primed during pregnancy.

Authors:  W A Tekolf; S Shaw
Journal:  J Exp Med       Date:  1983-06-01       Impact factor: 14.307

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.