by Wellcome Trust Sanger Institute

The first detailed cell atlas of the immune cells and gut bacteria within the human colon has been created by researchers. The study from the Wellcome Sanger Institute and collaborators revealed different immune niches, showing changes in the bacterial microbiome and immune cells throughout the colon. As part of the Human Cell Atlas initiative to map every human cell type, these results will enable new studies into diseases which affect specific regions of the colon, such as ulcerative colitis and colorectal cancer.

Published in Nature Immunology, this study revealed the interaction between the microbiomeand our immune cells. These results form an important resource, which will help scientists to understand how these microbial cells are tolerated by the immune system in health.

The gut microbiome is a complex ecosystem composed of millions of microbes, and these bacteria are thought to play important roles in digestion, in regulating the immune system and in protecting against disease. They are essential to human health, and imbalances in our gut microbiome can contribute to autoimmune diseases such as inflammatory bowel diseases and asthma.

The gut also has a rich community of immune cells, which help to repair tissues and defend against infection. However, there is little detailed information on how the microbiome interacts with the gut resident immune cells, which immune cells co-exist with bacteria in different locations, and why different diseases affect distinct areas of the gut.

To shed light on this, researchers studied three different parts of the healthy colon from organ donors, simultaneously analyzing the immune cells and the bacterial microbiome from each area. By sequencing the active genes of 41,000 individual immune cells, they were able to identify cell type specific genes that were switched on in different immune cell populations in each location. They also identified the bacteria present in the same colon region, to reveal how the immune system and bacteria interact.

Dr. Kylie James, a first author on the study from the Wellcome Sanger Institute, said: “The gut microbiome plays a major role in health and disease, and understanding how this interacts with the immune system is vital. Our unique approach allowed us to create the first in-depth map of immune cells and their neighboring bacteria in the healthy human colon, and revealed that surprisingly, there are distinct immune niches across the colon, with different cell activation states in different areas.”

The study revealed that not only were there differences between the immune cells in different parts of the colon, but that the microbiome also subtly changed, with a broader range of bacteria further down the colon.

Dr. Trevor Lawley, an author on the paper from the Wellcome Sanger Institute, said: “We are made up of as many bacteria as human cells and there is a symbiotic relationship between humans and their microbiome. We know this is linked to many aspects of health, with imbalances in gut bacteria associated with immune diseases ranging from Inflammatory Bowel Disease to asthma. By revealing the diversity of the microbiome in specific locations in the colon, and the interactions with immune cells, we can start to understand the biology behind this, and inform future research on site-specific gut bacteria.”

Previous work on mice had shown that immune cells in lymph nodes could be targeted to particular destinations—like an immune satnav. For the first time, this study showed that regulatory immune cells, which dampen down an immune response, moved from lymph nodes to the colon. This could be one way the intestine tolerates or even welcomes the microbiome.

Dr. Sarah Teichmann, the senior author on the paper from the Wellcome Sanger Institute, and co-chair of the Human Cell Atlas Organising Committee, said: “This study is part of the global Human Cell Atlas initiative to map every cell type in the human body. It gives a new understanding of the relationship between immune cells and the microbiome in healthy colon tissue and by allowing us to hone in on cells in particular areas, it will be a critical reference for ongoing work into diseases that affect specific regions of the colon.”