𝔖 Bobbio Scriptorium
✦   LIBER   ✦

The pathogenetic role of HLA-B27 in chronic arthritis

✍ Scribed by JoséA López de Castro


Publisher
Elsevier Science
Year
1998
Tongue
English
Weight
912 KB
Volume
10
Category
Article
ISSN
0952-7915

No coin nor oath required. For personal study only.

✦ Synopsis


Population and peptide specificity analyses and studies in transgenic rodents support a role of HLA-B27 as an antigen-presenting molecule in spondyloarthropathy. The interplay between HLA-B27 and arthritogenic bacteria on infected cells suggests that HLA-B27 might also influence disease by other mechanisms. Recent genetic advances promise the identification of additional susceptibility genes.


📜 SIMILAR VOLUMES


The pathogenetic role of HLA-B27
✍ T.E.W. Feltkamp; Muhammad A. Khan; JoséA.Lopez de Castro 📂 Article 📅 1996 🏛 Elsevier Science 🌐 English ⚖ 187 KB
The pathogenetic aspects of spondyloarth
✍ H. Kellner; D. Yu 📂 Article 📅 1992 🏛 Springer 🌐 English ⚖ 871 KB

The association of HLA-B27 and seronegative spondyloarthropathies, especially ankylosing spondylitis has been known for almost two decades. The spontaneous development of spondyloarthropathy like joint disease in HLA-B27 transgenic rats verifies the suspicion that the HLA-B27 antigens are directly r

A comparative study of HLA genes in HLA–
✍ Pia Westman; Marjatta Leirisalo-Repo; Jukka Partanen; Saija Koskimies 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 722 KB

## Objective: To determine whether hla-b27 positive patients with ankylosing spondylitis (as) and reactive arthritis (rea) share additional hla factors that confer disease susceptibility. ## Methods: Hla class i antigens were typed serologically, and class ii antigens molecularly, in samples take

A model for the role of HLA-DQ molecules
✍ J. P. Haas; A. Andreas; B. Rutkowski; H. Brunner; E. Keller; J. Hoza; S. Havelka 📂 Article 📅 1991 🏛 Springer 🌐 English ⚖ 741 KB

Restriction fragment length polymorphism (RFLP) typing of MHC-class II loci DRB, DQA1, DQB1, DQA2 and DPB1 was performed in 94 patients with seronegative juvenile chronic arthritis (JCA) and 184 random controls. Analysis of allele frequencies and MHC-class II 4-loci haplotypes indicate: (1) Suscepti