The immune system performs a difficult balancing act. It must respond rapidly to dangerous microorganisms that threaten the host, yet also coexist peacefully with the large array of microorganisms that colonize barrier surfaces such as those of the skin and gut. Writing in Cell, Linehan et al.1 examine the interactions between immune cells and a bacterium that normally resides on the skin, and identify a signalling pathway that governs the immune response to such microbes.
Most immunological research has focused on how immune cells recognize and eliminate viral and bacterial pathogens, and the insights obtained have led to the development of many immune-based therapies. However, attention has also turned to microbial communities at barrier surfaces and the long-term influence they exert on host immune responses. Accordingly, Linehan and colleagues studied the skin-dwelling bacterium Staphylococcus epidermidis in mice and rhesus monkeys, as well as analysing human-tissue samples from the clinic.
Staphylococcus epidermidis belongs to a group of microorganisms termed commensals, and usually colonizes human skin without causing disease. However, in premature newborns and people who are in an immunosuppressed state or who have received artificial joints, S. epidermidis can cause severe disease or chronic infection2. Furthermore, even though the bacterium is normally harmless, it is not ignored by the immune system. In mouse skin, the response3 to an initial encounter with certain strains of S. epidermidis is dominated by a type of immune cell called a cytotoxic CD8+ T cell, also known as a killer T cell. Linehan and colleagues asked two key questions about this response, and the answers they obtained are illuminating.
The first question was, how do T cells recognize S. epidermidis? A response to bacteria is thought to occur when a T cell recognizes a bacterial peptide fragment bound to the ‘classical’ class Ia protein component of the major histocompatibility complex (MHC), which presents such fragments to immune cells. However, using a mouse model system, Linehan and colleagues found that a ‘non-classical’ protein, H2-M3, which belongs to the MHC class Ib family, was instead involved in MHC presentation in the response to S. epidermidis. H2-M3 can present4 bacterial peptides in which the amino-acid residue methionine has been modified by addition of an N-formyl group.
The other question Linehan and colleagues sought to answer was whether this non-classical immune-recognition pathway might also be coupled to ‘unconventional’ T-cell behaviour. The team investigated this by comparing gene-expression patterns of CD8+ T cells responding to S. epidermidis with those of other types of T-cell population in the mouse skin that did not respond to the bacterium. The authors found that the responsive CD8+ T cells expressed genes associated with wound healing and tissue repair (Fig. 1). This was surprising because responding CD8+ T cells would be expected to express genes associated with activation of the pathways involved in killing unwanted cells or in the release of pro-inflammatory signalling molecules.
Using an in vivo mouse model of skin-wound healing in association with S. epidermidis colonization, the authors demonstrated that the tissue-repair gene-expression signature in responding T cells was linked to promotion of a healing response. Thus, immune recognition of bacterial residents of the skin can induce a form of immunity that does not directly retaliate against the bacterium, but instead aids tissue repair.
The authors’ finding adds to a growing recognition of the diverse functions of other unconventional T cells that are found at barrier sites and that can recognize evolutionarily conserved microbial molecules. These cells include, for example, mucosal-associated invariant T cells, which are abundant in humans and induced by commensals, and which share several features5 of the T-cell population studied by Linehan and colleagues — such as the production of the signalling molecule interleukin-17A. These and other T-cell populations in humans and mice, such as invariant natural killer T cells and germline-encoded mycolyl-reactive T cells, also act in response to MHC class Ib-mediated bacterial-peptide recognition6,7. A human equivalent to mouse H2-M3 has not been identified so far. It is possible that, if such an equivalent is found, a human T-cell population might fulfil a similar role to that of the CD8+ T cells observed by Linehan and colleagues.
As the authors note, many of the day-to-day interactions between immune-system cells and microbes are probably with the commensals in the skin, gut and airways. Therefore, an immune response that maintains the status quo, rather than driving bacterial elimination, which is usually accompanied by inflammation and tissue damage, could be beneficial. But should such a response really be considered unconventional? Although the roles of classical MHC molecules and responding immune cells were identified first, non-classical MHC and MHC-like proteins are evolutionarily older8,9 than MHC class Ia molecules. Linehan and colleagues reveal a direct link between the role of MHC class Ib molecules and tissue homeostasis. Therefore, these functions might have evolved in parallel and represent the broadly ‘conventional’ functions of the immune system, with additional immune-system specializations evolving over time.
The authors’ study hints at the potential broad, long-term effects of microbial residents on the immune system. If future studies mechanistically link individual microorganisms to specific types of immune response, it might be possible not only to understand the roles of some abundant and relatively unexplored immune-cell populations, but also to determine how resident microbes affect health and disease in a way that might lead to new treatment approaches.
Nature 555, 594-595 (2018)
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