I m m u n e A c t i v a t i o n in

Sepsis
Andrew Conway-Morris, MB ChB, PhD, FFICMa,b,*, Julie Wilson, MB ChB
c,d
,
Manu Shankar-Hari, MSc, MD, PhD, MB BS, FRCA, FFICMc,d

KEYWORDS
 Sepsis  Inflammation  Immunosuppression

KEY POINTS
 Sepsis is a dysregulated multisystem response to infection.
 The immune responses begin as compartmentalized, progressive processes of microbial
recognition, followed by triggering and amplification of inflammation and homeostatic
regulation.
 How these immune responses become dysregulated and maladaptive remains a key
conundrum.

INTRODUCTION

Sepsis is defined as life-threatening organ dysfunction caused by a dysregulated host

response to infection.1 These dysregulated host responses underpin the clinical phe-
notypes that range from a mild, self-limiting illness to a severe progressive illness
resulting in multiorgan failure and death. A complex, interlinked system of cells, recep-
tors, secreted proteins, enzymes, and structural and chemical defense elements such
as epithelium and associated antimicrobial proteins, together referred to as the im-
mune system, protect the human body from infection. This protection involves four
interlinked tasks: danger signal surveillance and recognition from nonself, effector
functions in response to sensing danger signals, homeostatic regulation, and genera-
tion of immunologic memory in certain situations. Functionally distinct innate and
adaptive immune systems work in synergy to perform these tasks. In this article, a sim-
ple conceptual overview is provided of the current understanding of these dysregu-
lated immune responses in sepsis.

All authors declare that they have no conflicts of interest.

a
Division of Anaesthesia, Department of Medicine, Addenbrooke’s Hospital, University of
Cambridge, Hills Road, Box 93, Cambridge CB2 0QQ, UK; b John V Farman Intensive Care
Unit, Addenbrooke’s Hospital, Hills Road, Cambridge, CB2 0QQ, UK; c Intensive Care Unit,
Guy’s and St Thomas’ NHS Foundation Trust, ICU Support Offices, St Thomas’ Hospital, 1st
Floor, East Wing, London SE1 7EH, UK; d Division of Infection, Inflammation and Immunity,
King’s College London, Guy’s Hospital, 3rd Floor, Borough Wing, Great Maze Pond, London
SE1 9RT, UK
* Corresponding author.
E-mail address: [email protected]

Crit Care Clin 34 (2018) 29–42

http://dx.doi.org/10.1016/j.ccc.2017.08.002 criticalcare.theclinics.com
0749-0704/18/ª 2017 Elsevier Inc. All rights reserved.
30 Conway-Morris et al

Overview of Innate and Adaptive Immune System Response to Pathogens

Pathogens access a normally sterile area following breach of either epithelial or
mucosal barriers (infection). The innate immune system is the first line of defense
against infections (surveillance and recognition of nonself). The innate immune system
consists of cells of myeloid lineage with the ability to clear and kill pathogens by
phagocytosis (such as granulocytes, monocytes/macrophages, and dendritic cells)
and the complement system of proteins, aside from epithelial- and mucosa-
associated structural and chemical defense mechanisms.
Innate immunity to infection can be broadly categorized into two categories:
An immediate response (0–4 hours), where the infection is recognized by preformed,
nonspecific, and broadly specific effectors such as the complement system
An early induced immune response (beyond 4 hours) with recruitment and activation
of effector cells that rely on evolutionarily conserved pattern recognition receptors
(PRRs) of danger signals for infection clearance
Innate immune cells with the ability to process and present antigens (antigen-pre-
senting cells; APCs), in particular dendritic cells, form a link to the adaptive immune
system. These inform the adaptive immune cells of danger, on the need to generate
a specific immune response against the inciting pathogen, and also provide essential
initiating signals for these responses. This occurs in secondary lymphoid organs such
as spleen, lymph nodes, and mucosal-associated lymphoid tissues (MALT). The adap-
tive immune system consists of 2 major cell types: B and T lymphocytes. These cells
express specific antigen-detecting receptors on the cell surface: B cell receptors
(BCRs) and T cell receptors (TCRs). In contrast to the innate immune cell PRRs, the
adaptive immune cell receptors have antigen specificity, (ie, the ability to individually
identify different antigens as opposed to common patterns on antigens). This speci-
ficity is a product of creation of a diverse repertoire of receptors, plus selection and
clonal expansion of the adaptive immune cells.

Complement and Coagulation Cascades in Sepsis

On breaching the epithelial surface barrier, the pathogen encounters complement
system proteins (C), a group of soluble proteins produced by the liver that circulate nor-
mally in an inactive form. The complement system can be activated by antibody-
coated pathogens (classical pathway), by the pathogen alone (alternative pathway),
and by carbohydrate-binding proteins (eg, mannose-binding lectin, ficolins) that coat
the pathogens (lectin pathway). All three pathways converge on generating a C3
convertase enzyme that cleaves the complement protein C3 into C3a and C3b. C3b re-
mains on the pathogen surface as a potent opsonin that is recognized by phagocytes.
C3a is released into the circulation, acting as a potent proinflammatory molecule that
recruits more phagocytes to the site of infection. In sepsis, the complement system un-
dergoes massive activation with deleterious effects. This is predominantly mediated by
the activated complement molecules C3a and C5a, the anaphylatoxins.2 The systemic
activation of the coagulation and fibrinolytic systems results in deposition of fibrin and
formation of microthrombi in the microcirculation; this may contribute to the impaired
microcirculation seen in sepsis.3 Activated complement products, C5a in particular,
activate the coagulation system via tissue factor,4 while thrombin from the activated
coagulation cascade cleaves C5 into C5a and C5b independent of its upstream path-
ways.5 This illustrates the positive feedback loop seen in sepsis between the dysregu-
lated, systemic activation of the complement, coagulation, and fibrinolytic cascades,
exacerbating tissue damage and organ dysfunction.6,7
 Immune Activation 31

Danger Signals and Sepsis

The first step in the pathobiology of sepsis is detection of the presence of pathogens
within a normally sterile tissue or body cavity. This is achieved by leukocyte recogni-
tion of pathogen-associated molecular patterns (PAMPs). Microorganisms express a
range of molecules that are structurally or metabolically critical, such as lipopolysac-
charide (LPS), peptidoglycan, flagellin, and double-stranded RNA. The tissue damage
that occurs with established infection also generates danger signals. These danger-
associated molecular patterns (DAMPs) or alarmins include, among others, heat
shock proteins (HSPs),8 cathelicidins,9 uric acid,10 fibrinogen, free cellular and mito-
chondrial DNA, and high-mobility group box-1 (HMGB-1). DAMPs activate a variety
of receptors including RAGE, Toll-like receptors (TLRs) and specific receptors such
as IL (interleukin)-1R.11 As these DAMPs are related to illness severity, it is likely
that the dysregulated host response in sepsis is influenced by these DAMPs.12,13

Danger Signal Sensors

Unifying characteristics of these danger signals (DAMPs and PAMPs) are conserved
molecular patterns that can be easily sensed by pattern recognition receptors
(PRRs) on leukocytes. These PRRs are germline-encoded receptors present on
both the cell surface and intracellularly. Five subclasses of PRRs have been described
thus far: TLRs, nucleotide oligomerization domain-like receptors (NODs or NLRs), ret-
inoic acid-inducible gene (RIG-1)-like receptors, C-type lectin receptors, and
absence-in-melanoma 2 (AIM-2)-like receptors.14 The sensing of PAMPs or DAMPs
by PRRs upregulates the transcription of genes involved in inflammation. PRRs can
recognize a wide range of microbial membrane components from gram-positive bac-
teria, gram-negative bacteria, atypical organisms, parasites, viral nucleic acids, and
yeasts.

Transduction of Danger Signals by Pattern Recognition Receptors

Ligation of PRRs triggers intracellular signaling pathways that depend on MyD88 or
TRIF.15 These pathways transduce PRR signals into an inflammatory response via
activation of inflammasome protein complexes16 and by induction of inflammatory
gene transcription via nuclear factor kappa-B (NF-KappaB).17 The inflammasome is
a multimeric protein complex that assembles in the cytosol following PRR signaling,
cleaving precursor proteins (eg, pro- IL-1beta) into active cytokines (eg, IL-1beta).18
These usually assist in eliminating the pathogen, resulting in resolution of the infection.
However, excessive systemic activation of inflammatory pathways outside the normal
homeostatic regulations may drive the host toward organ dysfunction (ie, sepsis).19

Amplification
The process whereby signals from pattern recognition receptors are transduced into
inflammatory cytokine release results in an exponential amplification of multiple im-
mune responses through feedback loops. A key molecule that provides exponential
amplification is nuclear factor kappa B (NF-kappaB). This increases transcription of
precursor proteins (eg, pro-IL-1beta), so providing further substrate for the inflamma-
some. The products of inflammasome activation can in turn induce further NF-kappaB
activation in neighboring cells,20 leading to a self-sustaining and amplifying inflamma-
tory response. Conversely, a recently identified negative feedback loop involving
NF-KappaB-mediated elimination of damaged mitochondria will constrain inflamma-
some activation.21 A greater understanding of how these positive and negative feed-
back loops interact will bring crucial new insights into the processes by which
32 Conway-Morris et al

inflammation spreads from the site of primary infection to the systemic manifestations
that characterize sepsis.

Host Response Patterns in Sepsis

The plethora of immune responses in sepsis, mostly characterized using whole blood
leukocyte transcriptome profiles, will generate two distinct immune response pat-
terns. In pattern 1, both pro- and anti-inflammatory responses generated by innate
and adaptive immune cells are present at the onset of the sepsis illness. Early deaths
are thought to occur from excessive innate immune system-driven inflammation. Re-
covery is characterized by restoration of homeostasis in both adaptive and innate im-
mune systems, with resolution of inflammation and recovery of immune cell paresis. In
this pattern, late deaths are caused by a progressive and adaptive immune system
impairment resulting in immunosuppression. This pattern of immune response in
sepsis is conventional wisdom and is supported by identification of immunosuppres-
sion phenotypes in immune cells observed from the spleen and lung in patients who
die from protracted sepsis. Indirect evidence supporting this hypothesis is the lack
of response to anti-inflammatory therapies in all sepsis trials to date. Pattern-2 is
similar to pattern-1, where both pro- and anti-inflammatory responses are activated
at the onset of sepsis illness, and early deaths are also caused by an excessive, innate
immune system-driven inflammation. Likewise, recovery of illness is characterized by
restoration of homeostasis in both adaptive and innate immune systems, with resolu-
tion of inflammation and recovery of immune cell paresis. However, in this pattern, the
late deaths are caused by intractable inflammation-induced organ injury, although
immunosuppression does occur during the late phase. This pattern of immune re-
sponses is supported by observations from young patients suffering from trauma
and in endotoxin-related effects in volunteers. Indirect evidence to support this pattern
of response comes from pneumonia cohorts who have subclinical inflammation well
beyond the acute phase assessed using IL-6 and IL-10 profiling, associated with
worse survival characteristics.22

Cytokines and Other Mediators in Sepsis

Following detection of PAMPs from infecting pathogens and DAMPs generated sec-
ondary to tissue injury associated with the infection, the innate immune cells and
the adaptive immune cells generate a plethora of pro- and anti-inflammatory cytokines
that mediate the systemic responses seen in sepsis. Cytokines are small proteins
(<25 kDa) released by immune cells that act in an autocrine, paracrine, and endocrine
manner. Proinflammatory cytokines that are well characterized in sepsis include inter-
leukin (IL)-1, -6, -8, and -12; tumor necrosis factor (TNF); macrophage inhibitory factor
(MIF); and the interferons. Cytokines with anti-inflammatory effects include IL-4, -6
and -10, and TGF-b. Chemoattractant cytokines (chemokines) promote leukocyte
migration. These have a prefix CC or CXC depending on whether there are 2 cysteine
residues adjacent to each other (CC) or separated by another amino acid (CXC); they
act via the receptors CCR1-9 or CXCR1-6, respectively. A summary of the likely sour-
ces and roles of cytokines and other mediators in sepsis is shown in Table 1.

Compartmentalization of Host Responses

The presence of systemic inflammation is pathognomonic of sepsis, yet the presence
and manifestations of immune activation are not uniform across the body spaces
and organs. In human sepsis, the ready accessibility to blood makes this the best
understood compartment. It is also the likely conduit by which a focus of infection
at one site can produce organ damage at a distant site.70 However, the apparently
Table 1
Summary of the sources, usual function and identified roles in sepsis pathophysiology of cytokines and soluble immune mediators

Cytokine Main Source Normal Physiologic Role Evidence in Sepsis

Proinflammatory
IL-1b Monocytes, macrophages Immune cell proliferation YSerum levels23 and Ymonocyte mRNA Levels in septic shock24
and differentiation [serum levels in non-survivors25
Levels frequently raised at tissue site of infection26
IL-6 T cells, macrophages Stimulates B and T [Serum levels vs controls25,27
lymphocytes; has both Serum levels correlate with septic shock28 and disease severity29
pro- and anti- Persistently [serum levels associated with increased risk of death30
inflammatory actions Decreasing trend in serum levels associated with better prognosis31
IL-8 Macrophages, Endothelial Promotes Granulocyte [Serum27 and tissue26 Levels vs controls
cells chemotaxis, induces [serum levels associated with increased risk of sepsis in burns32
phagocytosis, stimulates Persistently higher serum levels seen in patients with sepsis compared with
angiogenesis uncomplicated infection33
Predictor of 28-d mortality34
IL-12 Dendritic cells, Induces differentiation of [serum levels vs controls25
macrophages, Th1 cells from naı̈ve T Serial increase in serum levels noted in survivors vs non-survivors35
lymphoblastoid cells cells Impaired monocyte IL-12 production associated with increased risk of sepsis
post-operatively36

Immune Activation
(continued on next page)

33
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Conway-Morris et al
Table 1
(continued )
Cytokine Main Source Normal Physiologic Role Evidence in Sepsis
IL-17 Th17 cells Induces synthesis of a wide [percentage of IL-17-producing T cells vs controls37
variety of cytokines and May have a role in development of renal failure in septic shock38
chemokines Animal models suggest that neutralisation of IL-17 may improves outcomes39
IL-18 Macrophages, monocytes Induces production of a [serum levels vs controls27,29
wide variety of cytokines Increased plasma levels associated with poor outcome40
and chemokines May be able to distinguish between Gram-positive and -negative
infections41
IL-33 Macrophages, mast cells, Induces production of [serum levels vs controls42
dendritic cells, cytokines by eosinophils, May contribute to sepsis-induced immunosuppression through promoting
endothelial cells, mast cells and Th2 cells expansion of regulatory T cells43
fibroblasts
TNF-a Activated macrophages, Activates inflammatory [serum levels vs controls27
CD4+ T cells, NK cells, cascade Associated with development of renal failure44
neutrophils, eosinophils Potential as therapeutic target45
and mast cells
IFN-b Monocytes, fibroblasts Stimulates chemokine and Evidence of contribution to both hyperinflammatory and
cytokine production, immunosuppressed states46
activates adaptive Inhibits secretion of pro-inflammatory cytokines47
immunity; also has some
anti-inflammatory
effects
IFN-g CD4 and CD8 T cells, NK Activator of macrophages [serum levels but Y in septic shock48
cells Important in anti-viral Yproduction by NK cells49
immunity
GM-CSF T cells, macrophages, mast Stimulates neutrophil, Yserum levels in non-survivors50
cells monocyte and Potential therapeutic agent51
macrophage
development from stem
cells
Macrophage Monocytes, macrophages; Recruitment of leukocytes [serum levels vs controls52
migration endothelial/epithelial to sites of inflammation Levels correlate with mortality53
inhibitory cells Inhibits immune cell
factor (MIF) apoptosis
Counter-acts
glucocorticoid-induced
suppression of
inflammatory response
Monocyte Macrophages, monocytes, Recruits CD4 T cells, [serum levels in non-survivors27
chemotactic dendritic cells monocytes, and May play a role in the development of liver and lung injury in sepsis54
protein (MCP)-1 dendritic cells to site of
inflammation
Leukotrienes Leukocytes, mast cells, Regulation of [serum levels vs controls, but Yproduction in non-survivors55
neutrophils inflammatory mediators, Potential role for leukotriene inhibitors suggested by animal studies56
neutrophil chemotaxis

(continued on next page)

Immune Activation
35
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Conway-Morris et al
Table 1
(continued )
Cytokine Main Source Normal Physiologic Role Evidence in Sepsis
Anaphylotoxins Plasmalytic cascade, Recruits and activates Direct role in vasodilatation and capillary leak, and recruitment of immune
(C3a, C5a) multiple mechanisms of neutrophils, monocytes cells to sites of organ damage2
activation and macrophages Excessive levels can impair neutrophil antimicrobial responses57
Anti-inflammatory
IL-1ra Monocytes, macrophages, Anti-inflammatory; binds [serum levels vs controls58
neutrophils, fibroblasts IL-1 receptor and so [serum levels in septic shock compared with uncomplicated sepsis59
prevents IL-1 binding
IL-4 Activated T cells, mast cells, Promotes proliferation of B IL-4 mRNA expression higher in sepsis survivors60
basophils, eosinophils and T cells. In mouse studies blockade of IL-4 prevents shift toward Th-2 profile, and
Promotes differentiation improves survival61
of CD4 T cells into Th2
cells.
Induces release of IL-13
from macrophages.
IL-10 B cells, CD4+ Th2 cells, Inhibits synthesis of pro- [serum levels in sepsis vs controls,27 and in septic shock compared with
monocytes inflammatory cytokines uncomplicated sepsis62
by macrophages and Sustained upregulation associated with worse prognosis27
helper T cells Mediator of monocyte endotoxin tolerance63
IL-11 Epithelial cells, fibroblasts Induces expression of IL-4; Uncertain role in human sepsis, animal studies suggest increased mRNA
inhibits production of levels64
IFN-g and IL-2
IL-13 Th2 cells Inhibits pro-inflammatory [serum levels in non-survivors65
cytokine production [serum levels in septic shock.62 Mouse studies suggest a protective role in a
Associated with prolonged model of fecal peritonitis through suppression of inflammatory cytokines
monocyte survival in tissues66
IL-35 Regulatory T cells Converts naı̈ve T cells into [serum levels vs controls, with levels correlating with severity67
regulatory T cells
Stimulates proliferation of
regulatory T cells
TGF-b Macrophages, smooth Inhibits B cell proliferation Negative effects on T cell and NK cell function suggested by animal models68
muscle cells Promotes development of
CD4 T cells into Th17 cells
Inhibits activated
macrophages
Prostaglandin E2 Macrophages, antigen- Inhibition of B and T cell Some evidence from animal studies of a role in sepsis-induced
presenting cells proliferation immunosuppression69
Promotion of T cell
apoptosis

Immune Activation
37
38 Conway-Morris et al

hyperinflammatory cytokine levels and recruitment of immune cells at the site of infec-
tion may not be reflected in the blood compartment,71 and septic plasma may have a
net immunosuppressive effect.63 In conditions such as pneumonia26 and abscess for-
mation,72 immune cell function is frequently as (if not more) impaired in cells taken
from the site of infection as in cells taken from the blood compartment.
Gene transcription responses to an infective insult also vary markedly from organ to
organ.73 This is particularly the case in the lung, which is among the most common
sites of secondary organ damage. In contrast to other phagocytes resident in other
tissues, alveolar macrophages do not demonstrate tolerance to lipopolysaccharide.74
Indeed, they may demonstrate enhanced TNF-alpha release following a prior insult
such as trauma-haemorrhage.75 These differential and compartmentalized responses
may explain the typical patterns of infection focus and organ damage commonly seen
in patients with sepsis.

How Immune Responses Become Dysregulated Remains Unclear

Identifying the mediators involved in sepsis, the sequence of events, and the points at
which adaptive inflammatory responses descend into maladaptive processes is
extremely challenging. Patients usually present after the septic insult is apparent.
The lag time between onset and presentation is often not objectively quantifiable.
As noted, blood is the most commonly studied body fluid but seldom reflects the
compartmentalization and differences in regional immune responses.26,72 Investiga-
tors are therefore obliged to rely in part on data acquired from animal models, which
are imperfect guides to human disease.76,77 It seems likely that differential regulation
of the host response, by a combination of genetic, physiologic, and microbiological
factors, interacts with the initial insult to trigger the systemic activation of inflammation
that characterizes the early phases of sepsis. Animal models and human studies sug-
gest an early rise in proinflammatory molecules such as IL-1 and TNF-alpha, which, in
blood at least, tend to peak early (within minutes) before declining.18 Slightly later re-
sponses involve molecules such as IL-6,78 monocyte chemotactic proteins 1 and 2
(MCP-1 and 2),79 and IL-8,80 as well as anti-inflammatory molecules such as IL-10
and the soluble TNF and IL-1 receptors.18 Later mediators include HMGB-1.81 Inter-
estingly, as predictors of outcome in sepsis, the magnitude of the anti-inflammatory
response (as gauged by IL-10 concentrations) performs better than the proinflamma-
tory response (as gauged by TNF-alpha, IL-1, IL-6, and IL-8).82
In summary, sepsis remains a clinical and biological challenge. The immune system
has provided therapeutic targets and will continue to do so. Understanding how these
immune response modulators will alter the amplified feedback host response loops in
sepsis is necessary to inform future therapy.

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