Publication highlights

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Explore a selection of research case studies from the past five years.

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Intro

Researchers at the Crick are tackling the big questions about human health and disease, and new findings are published every week.

Our faculty have picked some of the most significant papers published by Crick scientists, all of which are freely available thanks to our open science policy.

Highlights

Bowel cancer tumour

Protein level predicts immunotherapy response in bowel cancer

Researchers at the Crick and Barts Cancer Institute, Queen Mary University of London, have shown that the amount of a protein called CD74 can indicate which people with bowel cancer may respond best to immunotherapy. Bowel cancer falls into two categories: a deficient subtype and proficient subtype, and immunotherapy isn't yet used to treat both subtypes. The team found that three types of immune cells needed to be present for the tumour to respond to treatment: T cells, NK cells and macrophages. When all three were present and near to cancer cells, the T cells produced interferons, triggering a signal in macrophages and tumour cells. The researchers then found that a measurable component of this signal was a protein called CD74. This finding was mirrored in clinical trial data, showing that people who responded to immunotherapy had significantly higher levels of CD74. Therefore measuring CD74 levels could predict whether someone will respond to immunotherapy regardless of subtype.

A constitutive interferon-high immunophenotype defines response to immunotherapy in colorectal cancer

Published in Cancer Cell

Published

CD1d-mediated lipid presentation by CD11c+ cells regulates intestinal homeostasis

Intestinal homeostasis requires a continuous dialogue between commensal bacteria and intestinal immune cells. Natural Killer T (NKT) cells are a population of CD1d-restricted lipid-reactive lymphocytes contributing to the regulation of mucosal immunity, but the mechanisms underlying this are poorly understood. Here we show that lipid presentation by CD1d+ intestinal dendritic cells and macrophages controls NKT cell function and activation which in turn regulates commensal bacteria and immune cell populations in the gut. These results reveal an NKT cell-dendritic cell crosstalk as a key mechanism for the regulation of intestinal homeostasis.

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Published in EMBO Journal

Published