Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

MHC class I (MHC-I) molecules undergo an intricate folding process in order to pick up antigenic peptide to present to the immune system. In recent years, the discovery of a new peptide editor for MHC-I has added an extra level of complexity in our understanding of how peptide presentation is regulated. On top of this, the incredible diversity in MHC-I molecules leads to significant variation in the interaction between MHC-I and components of the antigen processing and presentation pathway. Here, we review our current understanding regarding how polymorphisms in human leukocyte antigen class I molecules influence their interactions with key components of the antigen processing and presentation pathway. A deeper understanding of this may offer new insights regarding how apparently subtle variation in MHC-I can have a significant impact on susceptibility to disease.

More information Original publication

DOI

10.1111/iji.12546

Type

Journal article

Publication Date

2021-08-01T00:00:00+00:00

Volume

48

Pages

317 - 325

Total pages

8

Addresses

D, e, p, a, r, t, m, e, n, t, , o, f, , P, a, t, h, o, l, o, g, y, ,, , U, n, i, v, e, r, s, i, t, y, , o, f, , C, a, m, b, r, i, d, g, e, ,, , C, a, m, b, r, i, d, g, e, ,, , U, K, .

Keywords

Humans, Peptides, Antigens, Histocompatibility Antigens Class I, Histocompatibility Antigens Class II, Antigen Presentation, Polymorphism, Genetic