Emerging biochemical, microbial and immunological evidence in the search for why HLA-B∗27 confers risk for spondyloarthritis

Eric M Brown; Phuong N U Nguyen; Ramnik J Xavier

doi:10.1016/j.chembiol.2024.07.012

Emerging biochemical, microbial and immunological evidence in the search for why HLA-B^∗27 confers risk for spondyloarthritis

Cell Chem Biol. 2024 Aug 20:S2451-9456(24)00314-3. doi: 10.1016/j.chembiol.2024.07.012. Online ahead of print.

Authors

Eric M Brown¹, Phuong N U Nguyen², Ramnik J Xavier³

Affiliations

¹ Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA; Center for Computational and Integrative Biology, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114, USA.
² Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.
³ Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA; Center for Computational and Integrative Biology, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114, USA; Department of Molecular Biology, Massachusetts General Hospital, Boston, MA 02114, USA. Electronic address: [email protected].

PMID: 39168118
DOI: 10.1016/j.chembiol.2024.07.012

Abstract

The strong association of the human leukocyte antigen B^∗27 alleles (HLA-B^∗27) with spondyloarthritis and related rheumatic conditions has long fascinated researchers, yet the precise mechanisms underlying its pathogenicity remain elusive. Here, we review how interplay between the microbiome, the immune system, and the enigmatic HLA-B^∗27 could trigger spondyloarthritis, with a focus on whether HLA-B^∗27 presents an arthritogenic peptide. We propose mechanisms by which the unique biochemical characteristics of the HLA-B^∗27 protein structure, particularly its peptide binding groove, could dictate its propensity to induce pathological T cell responses. We further provide new insights into how TRBV9⁺ CD8⁺ T cells are implicated in the disease process, as well as how the immunometabolism of T cells modulates tissue-specific inflammatory responses in spondyloarthritis. Finally, we present testable models and suggest approaches to this problem in future studies given recent advances in computational biology, chemical biology, structural biology, and small-molecule therapeutics.

Publication types

Review