Cultural advice

The Australian National University acknowledges, celebrates and pays our respects to the Ngunnawal and Ngambri people of the Canberra region and to all First Nations Australians on whose traditional lands we meet and work, and whose cultures are among the oldest continuing cultures in human history.

Aboriginal and Torres Strait Islander peoples are advised that ANU Library collections may include images, names, voices, and other representations of deceased persons.

Material in the collection may contain terms, language or views that reflect the period in which the item was created and may be considered inappropriate today.

Absence of mucosal-associated invariant T cells in a person with a homozygous point mutation in MR1

Loading...
Thumbnail Image

Date

Authors

Howson, Lauren J.
Awad, Wael
von Borstel, Anouk
Lim, Hui Jing
McWilliam, Hamish E. G.
Sandoval-Romero, Maria L.
Majumdar, Shamuk
Hamzeh, Abdul Rezzak
Andrews, Dan
McDermott, David H.

Journal Title

Journal ISSN

Volume Title

Publisher

American Association for the Advancement of Science

Abstract

The role unconventional T cells play in protective immunity in humans is unclear. Mucosal-associated invariant T (MAIT) cells are an unconventional T cell subset restricted to the antigen-presenting molecule MR1. Here, we report the discovery of a patient homozygous for a rare Arg31His (R9H in the mature protein) mutation in MR1 who has a history of difficult-to-treat viral and bacterial infections. MR1R9H was unable to present the potent microbially derived MAIT cell stimulatory ligand. The MR1R9H crystal structure revealed that the stimulatory ligand cannot bind due to the mutation lying within, and causing structural perturbation to, the ligand-binding domain of MR1. While MR1R9H could bind and be up-regulated by a MAIT cell inhibitory ligand, the patient lacked circulating MAIT cells. This shows the importance of the stimulatory ligand for MAIT cell selection in humans. The patient had an expanded γδ T cell population, indicating a compensatory interplay between these unconventional T cell subsets.

Description

Keywords

Citation

Source

Science Immunology

Book Title

Entity type

Access Statement

License Rights

Restricted until

2099-12-31

Downloads

abcd