Stockinger B, Veldhoen MDifferentiation and function of Th17 T cells. Curr Opin Immunol 19: 281-286

Division of Molecular Immunology, The MRC National Institute for Medical Research, The Ridgeway, Mill Hill, London, UK. .
Current Opinion in Immunology (Impact Factor: 7.48). 07/2007; 19(3):281-6. DOI: 10.1016/j.coi.2007.04.005
Source: PubMed


IL-17-producing T cells have recently been classified as a new effector T-cell subset, termed Th17, which is distinct from Th1, Th2 and Treg subsets. There has been much progress in the past year, leading to identification of the molecular mechanisms that drive differentiation of Th17 T cells. This has helped to clarify many aspects of their role in host defense as well as in autoimmunity. Nevertheless, many intriguing questions remain to be answered regarding the regulation of Th17-mediated responses as well as their interactions with the other T-cell subsets. Furthermore, the role of pathogens and pathogen-derived molecules in influencing effector T-cell polarization needs to be re-evaluated in the light of the differentiation conditions that favor Th17 T-cell responses.


Available from: Marc Veldhoen, Sep 01, 2015
Differentiation and function of Th17 T cells
Brigitta Stockinger and Marc Veldhoen
IL-17-producing T cells have recently been classified as a new
effector T-cell subset, termed Th17, which is distinct from Th1,
Th2 and Treg subsets. There has been much progress in the
past year, leading to identification of the molecular
mechanisms that drive differentiation of Th17 T cells. This has
helped to clarify many aspects of their role in host defense as
well as in autoimmunity. Nevertheless, many intriguing
questions remain to be answered regarding the regulation of
Th17-mediated responses as well as their interactions with the
other T-cell subsets. Furthermore, the role of pathogens and
pathogen-derived molecules in influencing effector T-cell
polarization needs to be re-evaluated in the light of the
differentiation conditions that favor Th17 T-cell responses.
Division of Molecular Immunology, The MRC National Institute for
Medical Research, The Ridgeway, Mill Hill, London NW7 1AA,
United Kingdom
Corresponding author: Stockinger, Brigitta (
Current Opinion in Immunology 2007, 19:281–286
This review comes from a themed issue on
Lymphocyte activation
Edited by Ulrich von Andrian and Federica Sallusto
Available online 12th April 2007
0952-7915/$ see front matter
# 2007 Elsevier Ltd. All rights reserved.
DOI 10.1016/j.coi.2007.04.005
Although the importance of the IL-17 cytokine family
and in part icular of IL-17A and IL-17F has been known
for several years [1], it was only recently that it became
clear that IL-17-producing T cells constitute a separate
T-cell subset, termed Th17, distinct from Th1 and Th2
cells [2,3]. Th17 T cells had been linked with the pro-
inflammatory cytokine IL-23, because IL-23-deficient
) mice contain very few Th17 cells and are pro-
tected from autoi mmune diseases such as experime ntal
autoimmune encephalomyelitis (EAE) and collagen-
induced arthritis [4]. However, although IL-23 seems
to be involved in Th17-mediated immune pathology, it
is not required for the differentiation of Th17 from naı
CD4 T cells. A breakthrough for the field came with the
description of transforming growth factor b (TGF-b) and
interleukin-6 (IL-6) as the factors responsible for differ-
entiation of this subset from naı
ve T cells [5
]. Two
further reports confirmed these findings and suggested an
intriguing link to regulatory T cells (Treg) that can be
generated in vitro by stimulation with TGF-b in the
absence of IL-6 [6
]. The characterization of Th17
as a fourth major CD4 T-cell subset and the elucidation of
the crucial factors involved in its differentiation offer a
host of new insights into the differentiation and func-
tional activities of this important new T-cell subset.
In this review, we discuss the conditions that lead to
differentiation of Th17 T cells, their relationship to Treg,
and their probable physiological role in autoimmunity and
host defense.
Differentiation of Th17 T cells
IL-17-producing T cells entered the limelight with the
description of their involvement in autoimmune inflam-
mation [4]. The pro-inflammatory cytokine IL-23
appeared to take a prominent role in this process, as
IL-23-deficient p19
mice were reported to be resistant
to induction of EAE and to lack IL-17-producing T cells.
However, IL-23 did not seem sufficient to generate Th17
from naı
ve T-cell precursors, and the number of IL-17-
producing T cells detected following stimulation of T
cells in vitro with IL-23 remained very low with the few
cells detected having arisen from pre-existing activated T
cells [8,9]. In fact, once the crucial factors required for the
de novo differentiation of Th17 T cells were known, it
became clear that IL-23 is entirely dispensable for this
process and that Th17 will develop unperturbed in the
presence of IL-23-blocking anti-p40 antibodies on
the condition that the essential factors IL-6 and TGF-b
are present [5
]. Th17 T cells do not express the Th1 or
Th2 lineage-defining transcription factors Tbet or
GATA3, respectively [2,3,5
], which further underlines
their separate origin. The recent identification of the
orphan nuclear receptor RORgt as the key transcription
factor that specifies the Th17 lineage [10
] was the final
step in establishing this T-cell population as a unique and
distinct CD4 T-cell subpopulation (Figure 1).
Despite the description of the differentiation pathway of
Th17 cells, there is still considerable confus ion in the
literature regarding experimental protocols. One note of
caution concerns the interpretation of experimental find-
ings from incompletely purified T-cell populatio ns. Thus,
it is often stated that Th17 can be generated using either
IL-23 or TGF-b and IL-6. This is incorrect, as IL-23 will
only allow the outgrowth of already differentiated Th17
[8]. Such cells will contaminate T-cell populations that
are not rigorously sorted on the basis of markers for naı
T cells. Naı
ve T cells, by contrast, will only differentiate
to Th17 in the presence of TGF-b and IL-6. A similar
misinterpretation concerns the secretion of IL-6 by Th17. Current Opinion in Immunology 2007, 19:281–286
Page 1
The only T-cell subset capable of producing IL-6 is Th2.
Th17 make no IL-6, but this cytokine can be mistakenly
attributed to Th17, again because of insufficient purifi-
cation. Magnetic cell sorting (MACS) purification leaves
behind a proportion of dendritic cells; although difficult to
see by fluorescence activated cell sorter (FACS) analysis,
this nevertheless represents a substantial contamination
with IL-6 because dendritic cells produce high levels of
this cytokine, and the presence of IL-17 further increases
IL-6 production [1].
IL-1 and TNF were ascribed supporting roles in promot-
ing Th17 differentiation, but neither of these cytokines,
alone or in combination, was sufficient for this differen-
tiation step. Because activation of dendritic cells will
elicit IL-6, IL-1 and TNF simult aneously, the presence
of dendritic cells is sufficient to guarantee optimal sup-
port for Th17 differentiation in vitro; however, optimal
Th17 differentiation in a stringently dendritic cell free
culture system (using FACS sorted cells) depends on the
addition of all three cytokines together with TGF-b [5
This seems in contrast with a recent report that showed
abrogation of Th17 induction and EAE in mice deficient
for IL-1 receptor [11]. However, absence of IL-1 receptor
might affect IL-6 responses by antigen-presenting cells
[12] and furthermore skews T-cell responses towards Th2
[13], both of which are expected to compromise Th17
Socs3 was found to be a negative regulator of Th17
generation affecting Stat3 phosphorylation (probably in
response to IL-6 rather than to IL-23), and Soc3-deficient
mice show enhanced Th17 generation [14]. More
recently, IL-27, a cytokine that belongs to the IL-6
family, was shown to antagonize Th17 development in
a signal transducers and activators of transcription 1
(Stat1)-dependent manner [15
The Treg/Th17 dichotomy
Foxp3-expressing CD25
Treg that have suppres-
sive function can be generated by culture of naı
ve T cells
with TGF-b [17–19], although TGF-b is not required for
intrathymic development of Treg [20]. Differentiation of
Treg from naı
ve precursors is strongly inhibited by Toll-
like receptor (TLR) stimulation through IL-1 and IL-6,
and differentiation of Treg versus Th17 was found to be
282 Lymphocyte activation
Figure 1
Effector differentiation of CD4 T-cell subsets. Following activation, naı
ve CD4 T cells differentiate towards Th1 in the presence of IL-12, which
upregulates IFNg via Stat4, leading to IFNg-mediated Stat1 activation and induction of the Th1 lineage determining transcription factor Tbet.
Th2 by contrast differentiates in response to IL-4, which activates Stat6, resulting in induction of GATA3. The Th17 T-cell subset develops in
response to IL-6 and TGFb, and this differentiation step is strongly inhibited by Th1 or Th2 cytokines. Signaling via IL-6 activates Stat3 and the
lineage-determining transcription factor RORgt. Signaling through TGFb receptor is also essential for Th17 development, as T cells defective in
TGFbRII signalling cannot differentiate to Th17. Additional cytokines modify the response of the three T-cell subsets. IL-18 strongly increases
IFNg secretion by Th1, IL-33 upregulates IL-5 and IL-13 in Th2, and IL-23 induces IL-22 secretion in Th17.
Current Opinion in Immunology 2007, 19:281–286
Page 2
mutually exclusive [6
]. Pasare and Medzhitov [21]
reported that the suppressive function of Treg is reversed
by TLR activation of dendritic cells, resulting in restor-
ation of proliferation in co-cultures of naı
ve T cells and
Treg. Upon a closer examination we found, however, that
suppression of IL-2 and interferon g (IFNg) production
remains unchanged in these cultures [5
]. Thus,
the increased proliferative response probably reflects
the differentiation of IL-17-producing T cells under
these conditions rather than alleviation of Treg suppres-
sor function. Although there are reports that TGF-b
administration or transgenic expres sion expands Foxp3-
expressing Treg in vivo [22,23], it is difficult to envisage
this pathway to operate with the exclusion of Th17
generation. Any T-cell activation in vivo is unlikely to
proceed in the absence of innate stimul i that would divert
Treg generati on to Th17 generation. In fact, mice over-
expressing TGF- b were used by Bettelli et al. [6
demonstrate increased Th17 generation and EAE path-
ology. By contrast, it cannot be ruled out that TGF-b-
driven Th17 differentiation and autoi mmune pathology
might cause even more damage if there was no expansion
of Treg by TGF-b in parallel. Thus, sharing one import-
ant factor involved in either differentiation or functional
activity does not make these two T-cell subpopulations
close relatives, but it remains to be seen whether their
joint usage of TGF-b has functional significance in vivo.
The role of IL-23 in Th17 development
Although IL-23 is not involved in Th17 differentiation, it
plays an important role in maintaining Th17 effector
function. Thus, infection with the intestinal pathogen
Citrobacter rodentium induced Th17 in both wi ld-type and
IL-23-deficient hosts, but IL-23-deficient hosts failed to
clear the infection [7
IL-1 receptor antagonist deficient (IL-1Ra
) mice spon-
taneously develop arthritis and have high numbers of
IL-17-expressing T cells in inflamed joints [24]; the aug-
mented joint pathology in these mice seems to correlate
with increased levels of IL-23 p19 mRNA [25]. Treatment
of mice with anti-p19 antibody effectively disrupts chronic
relapsing EAE [26], suggesting that interference with
chronic inflammation might ameliorate autoimmune
symptoms. In light of the new findings concerning Th17
differentiation, the phenotype of p19
mice might need
to be re-evaluated. It is unlikely that the absence of IL-23
in these mice would compromise Th17 generation, but
intriguing roles for IL-23 could be in the preservation of
effector function as well as recruitment of Th17 to sites of
inflammation. IL-17 is not the only cytokine released by
Th17 T cells, and it was recently described that IL-22,
which until recently had been considered a Th1-related
cytokine, is in fact produced in much higher levels by Th17
]. Interestingly, the presence of IL-23 upregulates
IL-22 production and enhances the expansion of IL-22-
producing cells. This highlights the fact that IL-23 might
modulate the effector function of Th17 cells. IL-22 is
crucial in the innate skin immunity and induces the
expression of antimicrobial peptides in keratinocytes [28].
Th17 and autoimmunity
The crucial role of TGF-b in the formation of Th17 T
cells was highlighted by the finding that mice overex-
pressing TGF-b under control of the IL-2 promoter
generated more Th17 cells and had exacerbated EAE
pathology [6
]. However, the final proof that TGF-b-
mediated signals are obligatory for the development of
EAE was obtained using mice that had defective TGF-b
signaling (CD4dnTGFbRII) in their T cells [29
]. These
data also provide unequivocal evidence that, in the
absence of Th17, no autoimmune pathology develops
despite the fact that mice expressing a dominant- negative
TGF-b receptor II are reported to have over-exuberant
Th1 responses caused by lack of TGF-b-mediated nega-
tive feedback mechanisms [30]. These features of auto-
immune-like activation are exacerbated in mice that
completely lack TGF-b RII in T cells [31,32], illustrating
that Th17 T cells, which are probably absent also from
these mice, are not responsible for all autoimmune syn-
dromes. The resistance of IL-6-deficient mice to EAE
and collagen-induced arthritis has been reported earlier
[33,34] and is in line with its essential function in Th17
differentiation. Treatment with neutralizing antibodies to
IL-17 after the onset of collagen-induced arthritis ame-
liorates joint damage [35], and more recently experimen-
tal vaccination strategies resulting in an auto-vaccine
against IL-17, were shown to protect mice against myo-
carditis, EAE and arthritis [36–38]. These data emphasize
the important effector function of IL-17.
IL-27, a negative regulator of Th17 differentiation, was
found to suppress severe inflammation in the nervous
system, as mice deficient in IL-27 were hyperresponsive
to myelin oligodendrocyte glycoprotein (MOG)-induced
EAE and developed severe symptoms of neuroinflamma-
tion following infection with Toxoplasma gondii [15
During the acute stage of EAE, about 50% of the Th17 T
cells found in the spinal cord co-express IL-17 and IFNg
]; BS and MV, unpublished) a remarkable feature,
because IFNg strongly inhibits de novo generation of Th17
T cells. This suggests that effector Th17 T cells might
respond to IL-12 at certain stages of their differentiation.
Another cytokine receptor traditionally linked with Th1 T
cells also plays a role in Th17 responses, as indicated by the
finding that IL-18Ra-deficient mice are protected from
EAE, in contrast to IL-18-deficient mice, which are
susceptible. In this case it was engagement of the
IL-18R on antigen-presenting cells by an alternative, to
date unidentified, ligand that was required for Th17 patho-
genicity a phenomenon that seemed to be linked to
the amounts of IL-23 secreted by antigen-presenting cells
[39]. Thus, it seems that the induction of Th17 responses
can be uncoupled from autoimmune pathogenesis. As we
Th17 functional differentiation Stockinger and Veldhoen 283 Current Opinion in Immunology 2007, 19:281–286
Page 3
reported recently, zymosan stimulation preferentially
drives Th17 differentiation, but although co-injection of
MOG peptide will induce EAE the disease is self-limiting
and reversal of disease parameters is correlated with
reduced IL-23 production [29
]. This suggests that down-
stream positive as well as negative regulation of proin-
flammatory cytokines determine whether an autoimmune
T-cell response becomes pathogenic. Targeting such regu-
latory events might be particularly promising for interven-
tion, even at later stages of autoimmune diseases such as in
multiple sclerosis or rheumatoid arthritis.
Th17 and host defense
Th17 T cells have become notorious for their involve-
ment in a range of autoimmune diseases, but an exclusive
role as mediators of pathology is unlikely to be their
primary function. IL-17 stimulates the mobilization
and de novo generation of neutrophils by granulocyte-
colony stimulating factor (G-CSF) [40], thereby bridging
innate and adaptive immunity. It has been suggested that
this might constitute an early defense mechanism agai nst
severe trauma that would result in tissue necrosis or sepsis
[41]. IL-17 is also important in the host defense against
extracellular bacteria such as Klebsiella pneumoniae [42]or
Bacteroides fragilis [43] and against fungi such as Candida
albicans [44]. The fact that other pathogens such as
Mycobacterium tuberculosis or Borrelia burgdorferi [45]as
well as the fungal cell wall component zymosan [29
stimulate IL-17 expression suggests an important role of
IL-17-producing T cells in a wide range of infections.
There is a clear link between immune responses to
certain pathogens and the development of autoimmunity.
Infection with B. burgdorferi , for instance, results in devel-
opment of arthritis an event that can be blocked by
inhibition of IL-17 [46]. Similarly, arthritis is induced in
genetically susceptible mice by exposure to zymosan or
purified b-glucans [47]. These data suggest that certain
pathogen-derived molecules have differential effects on
antigen-presenting cells, which is likely to shape T-cell
differentiation. Zymosan is an example for such modu-
lation as it has been shown that dendritic cells exposed to
zymosan secrete IL-10 [48] and reduced levels of IL-12
p35 [29
,49] and macrophages secrete TGF-b following
stimulation with zymosan [49]. It will be important
to study the effect of pathogens or pathogen-derived
molecules on activation and cytokine secretion by anti-
gen-presenting cells, as these events will shape the devel-
opmental program of effector T-cell differentiation.
The new CD4 T-cell subset of Th17 T cells is proving to
fill many gaps in our understanding of how immune
responses are regulated. Identification of the crucial differ-
entiation factors has highlighted an interesting collabor-
ation of pro-inflammatory mediators such as IL-6, TNF
and IL-1 with TGF-b that has contradictory pro- or anti-
inflammatory roles depending on the location and timing of
the immune response. The role of Th17 T cells in host
defense against pathogens is only beginning to emerge, as
emphasis has mainly concentrated on their destructive
potential in autoimmune diseases to date. Nevertheless,
the crucial role of interactions between antigen-presenting
cells and pathogen-derived molecules, not only for
initiation of Th17 T cells but also for their potentially
pathogenic role in many autoimmune diseases, warrants
further investigation and could represent a unique chance
of intervention even after onset of disease symptoms.
We would like to acknowledge our funding from the Medical Research
Council UK.
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286 Lymphocyte activation
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    • "e l s e v i e r . c o m / l o c a t e / t o x i c o l variety of autoimmune diseases, including psoriasis and rheumatoid arthritis (Harrington et al., 2005; Park et al., 2005; Weaver et al., 2007; Stockinger and Veldhoen, 2007), the identification of ligands that regulate the RORs has been the focus of significant interest due to their potential for clinical use (Huh and Littman, 2012; Solt and Burris, 2012). Unlike most members of the nuclear receptor superfamily, RORs bind as monomers to ROR response element (RORE), consisting of an AGGTCA element preceded by an AT-rich sequence, in the promoter regulatory region of the target genes. "
    [Show abstract] [Hide abstract] ABSTRACT: The retinoic acid receptor-related orphan receptors α and γ (RORα and RORγ), are key regulators of helper T (Th)17 cell differentiation, which is involved in the innate immune system and autoimmune disorders. In this study, we investigated the effects of isoflavones on RORα/γ activity and the gene expression of interleukin (IL)-17, which mediates the function of Th17 cells. In doxycycline-inducible CHO stable cell lines, we found that four isoflavones, biochanin A (BA), genistein, formononetin, and daidzein, enhanced RORα- or RORγ-mediated transcriptional activity in a dose-dependent manner. In an activation assay of the Il17a promoter using Jurkat cells, these compounds enhanced the RORα- or RORγ-mediated activation of the Il17a promoter at concentrations of 1×10(-6)M to 1×10(-5)M. In mammalian two-hybrid assays, the four isoflavones enhanced the interaction between the RORα- or RORγ-ligand binding domain and the co-activator LXXLL peptide in a dose-dependent manner. In addition, these isoflavones potently enhanced Il17a mRNA expression in mouse T lymphoma EL4 cells treated with phorbol myristate acetate and ionomycin, but showed slight enhancement of Il17a gene expression in RORα/γ-knockdown EL4 cells. Immunoprecipitation and immunoblotting assays also revealed that BA enhanced the interaction between RORγt and SRC-1, which is a co-activator for nuclear receptors. Taken together, these results suggest that the isoflavones have the ability to enhance IL-17 gene expression by stabilizing the interactions between RORα/γ and co-activators. This also provides the first evidence that dietary chemicals can enhance IL-17 gene expression in immune cells. Copyright © 2015. Published by Elsevier Ireland Ltd.
    Full-text · Article · Jan 2015 · Toxicology
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    • "Because dendritic cells (DCs) are the main cells involved in orchestrating immune responses during Leishmania sp. infection through the release of cytokines which might be involved in the differentiation of Th17 cells [33], we first evaluated, using flow cytometry analyses, the maturation profile of dendritic splenic cells of the WT and 5-LO −/− mice infected at 6th wpi by evaluating the costimulatory molecules in the CD11c high cells. In terms of percentage, the DC expressing CD86 (Figure 5(b)) or MHC- II (Figure 5(c)) is slightly reduced in the absence of 5-LO that was ∼20% less compared with WT. "
    [Show abstract] [Hide abstract] ABSTRACT: Visceral leishmaniasis (VL) is a chronic and fatal disease caused by Leishmania infantum in Brazil. Leukocyte recruitment to infected tissue is a crucial event for the control of infections such as VL. Leucotriens are lipid mediators synthesized by 5-lipoxygenase (5-LO) and they display a protective role against protozoan parasites by inducing several functions in leucocytes. We determined the role of 5-LO activity in parasite control, focusing on the inflammatory immune response against Leishmania infantum infection. LTB4 is released during in vitro infection. The genetic ablation of 5-LO promoted susceptibility in highly resistant mice strains, harboring more parasites into target organs. The susceptibility was related to the failure of neutrophil migration to the infectious foci. Investigating the neutrophil failure, there was a reduction of proinflammatory cytokines involved in the related Th17 axis released into the organs. Genetic ablation of 5-LO reduced the CD4(+)T cells producing IL-17, without interfering in Th1 subset. L. infantum failed to activate DC from 5-LO(-/-), showing reduced surface costimulatory molecule expression and proinflammatory cytokines involved in Th17 differentiation. BLT1 blockage with selective antagonist interferes with DC maturation and proinflammatory cytokines release. Thus, 5-LO activation coordinates the inflammatory immune response involved in the control of VL.
    Full-text · Article · Sep 2014 · BioMed Research International
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    • "IL-17 producing Th17 cells are represented in high numbers in the LP of the small intestine, where they play a role in protection against extracellular pathogens (103). The differentiation of Th17 cells is dependent on their expression of the transcription factor RORγt, and it is driven by signals from TGF-β and IL-21 or IL-6 (109). Additionally, Th17 cells require IL-23 for maturation and survival (110). "
    [Show abstract] [Hide abstract] ABSTRACT: Vertebrates have co-evolved with microorganisms resulting in a symbiotic relationship, which plays an important role in health and disease. Skin and mucosal surfaces are colonized with a diverse population of commensal microbiota, over 1000 species, outnumbering the host cells by 10-fold. In the past 40 years, studies have built on the idea that commensal microbiota is in constant contact with the host immune system and thus influence immune function. Recent studies, focusing on mutualism in the gut, have shown that commensal microbiota seems to play a critical role in the development and homeostasis of the host immune system. In particular, the gut microbiota appears to direct the organization and maturation of lymphoid tissues and acts both locally and systemically to regulate the recruitment, differentiation, and function of innate and adaptive immune cells. While the pace of research in the area of the mucosal-immune interface has certainly intensified over the last 10 years, we are still in the early days of this field. Illuminating the mechanisms of how gut microbes shape host immunity will enhance our understanding of the causes of immune-mediated pathologies and improve the design of next-generation vaccines. This review discusses the recent advances in this field, focusing on the close relationship between the adaptive immune system and commensal microbiota, a constant and abundant source of foreign antigens.
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