Regulatory T-cells (Treg) have emerged as a crucial cellular checkpoint acting to
prevent potentially harmful immune responses. Due to its highly diverse activities,
regulating the immune system requires more than general suppression. Particularly,
during the developing immune response to infection, Treg need to balance the host
reaction to achieve both an effective response against the invading pathogen as well
as to prevent immunopathology from excessive or inappropriate activity. In this opinion
article we discuss the dual roles of IL-2 as both a key inducer of Treg activity and
also a target of Treg control during the acute phase of infection. We propose a model
in which Foxp3+ regulatory T-cells dynamically “measure” IL-2 availability and restrict
its access to effector T-cells, thereby controlling differentiation of these useful
but potentially harmful cells.
CD4+ T-lymphocytes play a central role in orchestrating immune responses by modifying
the functionality of other immune cells and guiding the qualitative features of a
response to one optimal for resisting a particular microorganism. Besides augmenting
both innate and adaptive immune responses, CD4+ T-cells limit excessive immune activation
and immunopathology during infections. Among CD4+ T-cells, Foxp3+ regulatory T-cells
(Treg) are essential for the maintenance of peripheral tolerance (Kim et al., 2007;
Lahl et al., 2007). These cells also modulate the responses to pathogens (Belkaid
and Tarbell, 2009). A plethora of mechanisms for how Treg exert their function have
been suggested (Shevach, 2009; Josefowicz et al., 2012). However, there is still an
ongoing debate as to which functions of Treg are essential under which circumstances.
Likely, Treg function can be attuned to specific conditions and distinct “rules” govern
Treg behavior in the steady-state versus inflammatory environments, secondary lymphoid
(SLO) versus peripheral organs, developing versus ongoing immune responses, or acute
versus chronic infections, for example. In this article we focus on the function of
Treg in the SLO during a developing acute infection and, although several cytokines
are relevant, we concentrate on IL-2 as a central platform that enables effective
immune control, as it (1) links activation of effector and regulatory responses, (2)
establishes a feed-back loop for T-cell expansion, and (3) allows control over T-cell
differentiation and fate decisions, preserving memory formation.
IL-2 is a Central Cytokine for T-Cell Activation
IL-2, originally discovered as a mitogenic factor for T-cells, is bound as a quaternary
complex with CD25 (IL2Rα-chain), CD122 (IL2Rβ-chain), and CD132 (common γ-chain).
The α/β-heterodimer facilitates IL-2 capture with high affinity and, further stabilized
by the γ-chain, forms a very stable complex which is terminated via receptor internalization
rather than ligand dissociation (Smith, 2006). Upon activation by TCR interactions
and additional co-stimulation via CD80/CD86, conventional T-cells (Tconv) produce
IL-2 and upregulate CD25 expression, which enhances IL-2 capture and consequently
IL-2 signaling, further promoting CD25 expression, T-cell activation, and proliferation.
This feed-forward loop can lead to activation-induced cell death, but highly activated,
proliferating T-cells also undergo apoptosis when acutely deprived of IL-2 signals.
Therefore, IL-2 is a master regulator of T-cell activation, proliferation, and death,
excellently reviewed in Malek and Castro (2010), Boyman and Sprent (2012).
Activation of Treg Through IL-2: Anticipation and Sensing of Effector Responses
In contrast to conventional T-cells (Tconv), Treg constitutively express CD25 (Sakaguchi
et al., 1995) and have STAT5 phosphorylation in the steady-state, arguing for continuous
or high frequency intermittent IL-2 signaling in the absence of infection. Indeed,
IL-2 signals seem to be pivotal for Treg survival because animals that lack IL-2,
CD25, or CD122 are largely devoid of peripheral Treg and suffer from severe autoimmunity
(Sadlack et al., 1993; Suzuki et al., 1995; Willerford et al., 1995; Fontenot et al.,
2005). Treg do not produce IL-2 themselves when stimulated through the TCR and therefore
rely on paracrine IL-2 for their maintenance. Tconv produce IL-2 upon activation and
then gradually upregulate CD25. Since Treg constitutively express CD25, they can sense
and signal via IL-2 as soon as it is produced, assuming that these Treg are within
suitable proximity to the cytokine secreting cells. Because IL-2 signaling further
upregulates CD25, Treg can even increase their ability to capture IL-2 as compared
to Tconv which need to initiate CD25 expression post TCR-mediated activation (Feinerman
et al., 2010). Indeed, it has been shown in vivo that Treg are the first cells to
respond to IL-2 upon antigenic challenge of Tconv (O’Gorman et al., 2009). As the
amount of IL-2 produced by T-cells correlates with the extent of co-stimulation from
DC in vitro (Shahinian et al., 1993) and in vivo (Kastenmuller et al., 2011), it might
reflect the magnitude of pathogen burden and the extent of innate stimulation. Therefore,
Treg “sense” the initiation of an adaptive immune response in a qualitative and potentially
quantitative manner when responding to IL-2 signals derived from adaptive effectors.
Treg Control the Availability of IL-2
Given the relative abundance of Treg in SLO, where adaptive responses are initiated
and IL-2 is being produced, it seems likely that the “sensing” of IL-2 by Treg consumes
a significant amount of the totally available IL-2. In this scenario, the mere presence
of Treg could reduce IL-2 availability and limit Teff responses, without a need for
active regulation (cytokine-sink model). Indeed, the presence of Treg leads to substantial
competition for IL-2, resulting in impaired proliferation of Teff cells in vitro.
Competition was further demonstrated in vivo, with a primary effect on the survival
of Teff and not on their proliferation (Pandiyan et al., 2007; Kastenmuller et al.,
2011). Treg also control IL-2 production (Thornton and Shevach, 1998), either by directly
acting on T-cells (Bodor et al., 2007; Vaeth et al., 2011) or indirectly, through
DC (Onishi et al., 2008). The latter concept is based on in vitro evidence of a positive
correlation between IL-2 production by Teff, the strength of ConA stimulation, and
the amount of CD28 expression (Shahinian et al., 1993). Treg express significant levels
of surface CTLA-4 on their surface and this molecule can directly block co-stimulatory
molecules and CD28-CD80/86-interactions, or, via trans endocytosis, modulate the amount
of CD80/86 that is displayed by DC (Wing et al., 2008; Qureshi et al., 2011). Importantly,
the amount of CTLA-4 expressed on Treg is again regulated by IL-2 signals. Consequently,
Treg control the level of co-stimulation through CD80/CD86 surface expression not
only during steady-state (Schildknecht et al., 2010), but, importantly, also during
highly inflammatory processes such as viral infection (Kastenmuller et al., 2011).
Therefore, DC appear to constitute a platform on which both stimulation and regulation
of conventional T-cells is executed, with IL-2 being a central mediator that activates
both Teff and Treg. Feed-back loops involving the constitutive high levels of CD25
on Tregs and the IL-2-promoted upregulation of CTLA-4 on these cells operate in concert
to restrict IL-2 availability to activated Teff, controlling their expansion, differentiation,
and survival (Figure 1).
Figure 1
Treg sense IL-2 early during immune responses and restrict cytokine availability to
control T-cell fates. Left panel: TCR signals (not depicted) and co-stimulatory signals
via CD80/86 activate naïve T-cells to upregulate CD25 and produce IL-2. Treg have
constitutive expression of CD25, which enables them to “sense” early (d0) production
of IL-2 and become activated. Right panel: Once activated T-cells divide, they become
heterogeneous for CD25 expression (d2–4): a fraction of cells downregulates CD25,
avoiding further IL-2 signals – and potentially regulation through Treg – in order
to differentiate into long-lived memory cells (MPEC or TH-1CM), follicular helper
cells or TH-17 cells, or they maintain CD25 expression for prolonged IL-2 signals
to undergo terminal effector differentiation. Treg can balance this differentiation
processes by regulating the availability of IL-2 via multiple mechanisms, among them
(1) the blocking and reduction of CD80/86 via CTLA-4, (2) the direct inhibition of
IL-2 production by T-cells, (3) the competition for IL-2, and (4) the consumption
and degradation of IL-2.
Treg Selectively Regulate Effector T-Cell Responses but Preserve Memory Development
Recently, the effects of IL-2 during acute infection have been further refined through
analysis of the role of this cytokine in the various stages of CD8+ T-cell differentiation.
After their initial activation and induction of CD25 expression, a subpopulation of
CD8+ T-cells decrease CD25 levels and become unresponsive to further IL-2 signals,
and, at the same time, upregulate the IL-7Rα-chain and develop into long-lived memory
cells. This is in contrast to T-cells that are exposed to IL-2 for a prolonged period
and maintain CD25 expression, undergo enhanced expansion, but differentiate into short-lived
effector cells (SLEC) that are prone to apoptosis and severe population contraction
after the peak of the response (Kalia et al., 2010; Obar et al., 2010; Pipkin et al.,
2010). The recent development of genetic models allowing the specific depletion of
Foxp3+ Treg (Kim et al., 2007; Lahl et al., 2007) without blocking IL-2/CD25 interactions
(Murakami et al., 2002; Suvas et al., 2003; Toka et al., 2004; Heit et al., 2008)
enabled asking whether Treg differentially affect these CD8+ T-cell subpopulations.
Indeed, manipulating the numbers of activated Treg
in vivo impacted CD25 expression on activated CD8+ T-cells, indicative of altered
IL-2 availability. This resulted in specific changes in numbers of SLEC while leaving
the memory CD8+ T-cell compartment largely unaltered (Kastenmuller et al., 2011; McNally
et al., 2011). Interestingly, the “window of opportunity” for the regulation of CD8+
T-cell responses by Treg overlapped with the time of CD25 expression on CD8+ T-cells:
depletion of Treg cells as late as d2–3 post infection enhanced antigen-specific T-cell
numbers in a viral infection model, but depletion later than d5 (when CD8+ T-cells
do not express CD25) failed to do so (Kastenmuller et al., 2011). In addition, enhanced
expansion of SLEC in the absence of Treg was abrogated through the neutralization
of IL-2 (McNally et al., 2011). Therefore, by controlling the availability of IL-2,
Treg cells can act as rheostats that balance the differentiation and expansion of
pathogen-specific CD8+ effector T-cells. Importantly, by selectively regulating SLEC
over memory precursor T-cells, which rapidly seem to become independent of IL-2 signals
(d2–3), Treg can limit the extent of acute effector responses without blunting the
development of long-lived memory (Kastenmuller et al., 2011). However, once memory
is formed and the host is re-challenged with a pathogen, Treg can again control the
expansion of secondary effector cells adapted to the extent and requirements of the
current infection.
Treg Mediated Restriction of IL-2 as a General Mechanism to Regulate Fate Decisions
in T-Cells
Beyond CD8+ T-cells, IL-2 likely serves as a central element that allows Treg to regulate
population size and differentiation of T-cells in general. A series of recent studies
have established the role of IL-2 in CD4+ T-cell differentiation into TH1, TH2, TH17,
and TFH cells (Liao et al., 2011; Boyman and Sprent, 2012). As with CD8+ T-cells discussed
above, CD4+ T-cells segregate into CD25high and CD25low cells within the first days
of a response to an acute infection, and prolonged IL-2 signals in CD25high cells
leads to terminal differentiation and Blimp1 and T-bet upregulation in CD4+ effector
cells. In contrast, CD25low cells gave rise to long-lived CXCR5highCCR7highT-betlow
precursors of central memory cells, as well as CXCR5highBcl6high follicular T-helper
cells (TFH; Choi et al., 2011; Pepper et al., 2011). In line with this, Treg limit
the expansion of antiviral CD4+ during acute infection, yet do not influence the generation
of neutralizing antibodies (Kastenmuller et al., 2011).
Therefore, by limiting excessive IL-2, Treg might not only blunt Teff response but
also ensure the generation of TFH cells and consequently the development of appropriate
humoral immunity early during acute infection, as IL-2 signals negatively regulate
TFH differentiation (Ballesteros-Tato et al., 2012; Johnston et al., 2012). By restricting
IL-2 during acute infection, Treg might additionally enhance mucosal immunity and
regeneration (potentially preventing superinfection) through promotion of TH17 generation,
because production of this class of effector cells is inhibited by IL-2 (Chen et al.,
2011; Pandiyan et al., 2011).
Summary and Perspective
In summary, we propose a model in which IL-2 availability is a central factor that
controls the magnitude and shapes the character of adaptive immune responses. Treg
control access of other T-cells to this crucial cytokine by limiting its production
through interference with co-stimulatory molecule availability on DC, as well as by
reducing its abundance through consumption. Importantly, this does not act to simply
blunt the overall immune response but selectively impacts on T-cell fates that require
larger amounts of IL-2. In contrast, other T-cell subpopulations, such as memory-precursors
or TFH, are not suppressed, allowing for the generation of cellular and humoral immunological
memory to protect the host from future pathogen encounters (Figure 1). Treg are therefore
not merely immunosuppressive, they actively participate in guiding the differentiation
and fate decisions of other T-cells by regulating the availability of IL-2 in SLO.
In this regard, Treg controlling IL-2 availability remind us of the three Moirai (the
incarnation of destiny in greek mythology) who controlled the thread of life and thereby
directed the fate of individuals.
In addition to this early regulation of effector responses through IL-2, Treg can
undergo functional specialization that parallels the differentiation of conventional
CD4+ T-cells in terms of transcription factor usage and expression of chemokine receptors
important for homing to peripheral sites (Chaudhry et al., 2009; Koch et al., 2009;
Zheng et al., 2009; Chung et al., 2011; Linterman et al., 2011). This differentiation
might facilitate Treg control of fully differentiated effector cells in infected tissues,
which is likely to involve mechanisms distinct from regulating or competing for IL-2
(Soper et al., 2007), such as the production of immunosuppressive cytokines (Rubtsov
et al., 2008) or cytotoxic molecules (Cao et al., 2007; Loebbermann et al., 2012).
Based on the emerging picture of selective control of effector T-cell fates, we speculate
that interfering with Treg function will help to optimize short-term immunotherapeutic
approaches, but might be less promising to increase the efficacy of prophylactic vaccines
aiming at the induction of long-term memory through T- and B-cells.