Aspects of Tryptophan and Nicotinamide Adenine Dinucleotide in Immunity: A New Twist in an Old Tale

Abstract

Increasing evidence underscores the interesting ability of tryptophan to regulate immune responses. However, the exact mechanisms of tryptophan’s immune regulation remain to be determined. Tryptophan catabolism via the kynurenine pathway is known to play an important role in tryptophan’s involvement in immune responses. Interestingly, quinolinic acid, which is a neurotoxic catabolite of the kynurenine pathway, is the major pathway for the de novo synthesis of nicotinamide adenine dinucleotide (NAD+). Recent studies have shown that NAD+, a natural coenzyme found in all living cells, regulates immune responses and creates homeostasis via a novel signaling pathway. More importantly, the immunoregulatory properties of NAD+ are strongly related to the overexpression of tryptophan hydroxylase 1 (Tph1). This review provides recent knowledge of tryptophan and NAD+ and their specific and intriguing roles in the immune system. Furthermore, it focuses on the mechanisms by which tryptophan regulates NAD+ synthesis as well as innate and adaptive immune responses.

Introduction

Tryptophan was initially discovered by Hopkins and Cole in 1901 after isolation from casein protein.¹ Tryptophan is 1 of the 8 essential amino acids that cannot be synthesized by the human body.² Although tryptophan has the lowest concentration in the body of all the essential amino acids, only very low concentrations are required for healthy nutrition.² Tryptophan has been extensively studied due to its important metabolic functions, which include the synthesis of hormones such as kynurenine, serotonin, tryptamine, melatonin, and essential coenzymes, particularly nicotinamide adenine dinucleotide (NAD⁺), that are known to play critical physiological functions.^2,3

Tryptophan has been associated with several clinical disorders. Historically, tryptophan was associated with pellagra, a dermatological condition associated with deficiency in tryptophan and niacin.^4,5 Most notably, tryptophan is involved in behavioral changes through synthesis of serotonin and tryptamine, 2 major players in neuropsychiatric disorders.^2,6 Tryptophan deprivation induces depression, separation anxiety,^7,8 chronic fatigue syndrome, and fibromyalgia. Furthermore, increasing evidence shows the role of tryptophan in brain tumor pathogenesis^9,10 and other cancer types, such as colorectal, breast, and bladder cancers.^7,11–13

Interestingly, tryptophan deprivation also sensitizes activated T-cells to apoptosis in novo¹⁴ and favors the induction of regulatory T-cells (Tregs) via dendritic cells.^15,16 Although the role of tryptophan in regulating the immune system has been previously described,¹⁷ research in this area has been scarce until recently. Several recent publications highlighted the involvement of tryptophan in inflammation, immune activation, and immune tolerance,^{11,13,18–20} raising awareness of tryptophan catabolism and its role in the immune system.

Kynurenine is an important biosynthetic pathway in tryptophan catabolism.²¹ Moreover, most of the immunologic function accredited to tryptophan was attributed to the kynurenine pathway.^3,18,22,23 More importantly, the kynurenine pathway is essential for the de novo synthesis of NAD⁺²⁴ and acts as a substrate for several other molecules.^25,26 Of note, the NAD⁺ levels have been described as very volatile; therefore, the de novo synthesis of NAD⁺ plays an important role in maintaining adequate NAD⁺ levels.²⁷ Quinolinic acid (QUIN), a product of tryptophan degradation, was found to be essential for de novo synthesis of NAD⁺ and may serve as a precursor of NAD⁺ in the tryptophan/kynurenine pathway. Although QUIN is neurotoxic,^9,22,28 recent publications have underscored the capacity of NAD⁺ to regulate T-cell fate and promote homeostasis^29–31 independent of the classical pathways that have considered cytokine environment and transcription factors as the major regulator of CD4⁺ T-cell differentiation and adaptive immune response.

The kynurenine pathway is initiated by 2 rate-limiting enzymes: indoleamine 2,3-dioxygenase (IDO) and tryptophan 2,3-dioxygenase (TDO), which are essential in tryptophan catabolism. Indoleamine 2,3-dioxygenase has been found in many immune cells, such as dendritic cells (DCs) and macrophages,^32,33 whereas TDO has been found in the liver and neurons.³² Moreover, both IDO³⁴ and TDO¹¹ are present in several malignancies such as prostate, colorectal, pancreatic, and breast cancers. Increasing evidence points toward an important role of IDO in the regulation of the immune system.^12,17,35 Interestingly, IDO is involved in the activation of the protein aryl hydrocarbon receptor (AhR),³² a ligand-activated transcription factor that regulates the immune system and inflammatory responses.^36–38 Indeed, on activation, AhR can promote the differentiation of type 1 regulatory cells (Tr1)^39,40 and control Treg/T_H17 differentiation,^37,41 critical CD4⁺ T-cell subsets involved in immunosuppression or pro-inflammatory responses. Furthermore, IDO promotes long-term tolerance by DCs through transforming growth factor β (TGF-β) in a noninflammatory context in novo.^42,43

Collectively, these findings indicate the existence of other pathways that regulate the immune system. These alternative pathways play key roles in a myriad of diseases and may serve as an alternative to develop novel therapeutic approaches. In this mini-review, we discuss the current knowledge of the increasing evidence of tryptophan and its role in immune regulation, with an overview of the kynurenine/QUIN/NAD⁺ pathway and emphasize missing links for which more research is needed. We also discuss possible models and key players in immune regulation via the kynurenine/QUIN/NAD⁺ pathway.

Tryptophan and Its Role in Immune Responses

Tryptophan has been implicated in many metabolic processes, including the metabolic synthesis of major proteins, such as kynurenine, serotonin, tryptamine, melatonin, and other coenzymes, particularly NAD/NADP (NAD phosphate).² Although these metabolic processes are critical, the role of tryptophan in the immune system is still poorly understood.

The kynurenine pathway is a major route for the catabolism of tryptophan and has an important role in the immune system.^17,21,32,44 The kynurenine pathway is initiated by cleavage of the indole ring, which is initiated by tryptophan 2,3-dioxygenase 2 (TDO-2), indoleamine 2,3-dioxygenase 1 (IDO-1), or IDO-2, which shares similarities with IDO-1 but has limited catabolic activity compared with TDO-2 and IDO-1.^22,45–47 TDO-2 has been found primarily in the liver and central nervous system (CNS), but recent publications have identified TDO-2 in different types of cancer.^10,23 TDO-2 suppresses antitumor immune responses and promotes tumor cell survival.⁴⁸ Furthermore, TDO-2 promotes metastasis in breast cancer^49,50 and the progression of lung cancer in vivo.⁵¹ Moreover, enzymatically active TDO-2 is overexpressed in a significant proportion of human tumors.¹⁰ TDO-2 overexpression has been correlated with poor prognosis in high-grade gliomas.⁴⁵ Current immunosuppressive therapies aim to inhibit TDO-2.¹¹ Pilotte et al¹⁰ were able to restore the ability to reject TDO-expressing tumors using a self-developed TDO-inhibitor (compound 680C91). Furthermore, Crosignani et al⁵² presented their preclinical assessment of a TDO-2-inhibitor (iTeos) in the 29th Annual Meeting of the Society for Immunotherapy Cancer, with similar results on a p815 mastocytoma tumor model overexpressing TDO-2.

Contrary to TDO-2, IDO-1 is found extrahepatically and is present in several immune cells.^35,53,54 Indeed, IDO-1 is present in human tumor cells and can prevent tumor cell rejection due to a lack of accumulation of specific T-cells.³⁴ Moreover, IDO-1 is upregulated by several pro-inflammatory molecules.^55,56 The interaction between IDO-1 and DCs has been the most studied to date. The rapid switch in function from immunogenic to tolerogenic activity is dependent on IFN-γ, whereas the tolerogenic phenotype is conferred by IDO-1. Indeed, IFN-γ is a potent activator of gene expression and enzymatic activity of IDO-1.^57,58 The tolerogenic phenotype induced by IDO-1 plays a double role in immune responses. Indoleamine 2,3-dioxygenase expands human CD4⁺CD25^highFoxp3⁺ Tregs by promoting maturation of DCs.⁵⁹ Second, IDO-expressing DCs suppressed allograft rejection by expansion of CD4⁺CD25^highFoxp3⁺ Tregs.³³ In contrast, IDO promotes tolerance toward tumor cells and can promote resistance toward immunotherapies.⁶⁰ More importantly, tumors expressing Foxp3⁺/IDO⁺ are associated with more advanced disease.⁴⁴ Interestingly, therapies targeting IDO have been shown to be effective against different types of cancer by measuring messenger RNA.^12,61,62 Similar interactions between IDO and other cells of the immune system have been described. Among these immune cells, we found interactions with macrophages,^54,63 mast cells,^32,42 and Tregs.^64,65

The initial activation models for the kynurenine pathway showed a redundant activation through TDO-2 and IDO-1.²² However, present evidence suggests specific roles for each of these enzymes in the tryptophan catabolic pathway. As Puccetti notes, in the early events of systemic inflammation, cortisol induces the release of acute phase proteins such as TDO-2. TDO-2 release activates the AhR, as explained below, transcribing interleukin (IL)-10 and IDO-1. Finally, the transcription of IL-10 and IDO-1 will create homeostasis.⁴⁷ This model indicates different gene activation processes and roles for TDO-2 and IDO-1.^47,66

Immune Implications of the AhR and Tryptophan Catabolic Enzymes

We have recently shown that kynurenine was able to promote mast cell activation by activating the AhR.³² As previously reported, activation of AhR has been linked to activation of Tr1 and to control of Tregs and T_H17 differentiation.^39–41 Interestingly, most immune cells—T-cells, B cells, macrophages, DCs, and natural killer cells—express AhR.⁶⁷ These findings suggest an important role of AhR in regulation of the immune system.

AhR is a transcription factor in the cytosol that is activated on ligand binding.^67,68 AhR is a key regulator of xenobiotic toxicity, such as 2,3,7,8,9-tetracholodibenzo-p-dioxin (TCDD) and dioxin, the most prominent member of the environmental pollutants.^36,67 However, AhR has also been identified as a key player in several signaling cascades and other cell biological events. Most likely, one of the most interesting and newly identified aspects of AhR is its involvement in immune regulation and tolerance.

AhR has been shown to regulate CD4⁺CD25⁺Foxp3⁺ Tregs as well as T_H17 cell fate, which are 2 major subsets of the adaptive immune system; extensive studies have underscored the importance of Tregs and T_H17 cell balance.^69–71 Indeed, Tregs are responsible for homeostasis and immune tolerance and are very robust immunosuppressive cells, whereas T_H17 cells are considered to be pro-inflammatory cells involved in a myriad of diseases including autoimmunity.^72,73 Interestingly, AhR has been found to control Tregs and T_H17 cell differentiation in experimental autoimmune encephalomyelitis (EAE),⁴¹ which are the most commonly used experimental model for multiple sclerosis. In this study, the authors found that AhR activation by TCDD controls Treg development in vivo, suppressing the severity of EAE. Furthermore, activation of AhR via another ligand, 6-formylindolo 3,2-b carbazole (FICZ), increased T_H17 differentiation, thereby increasing the severity of EAE.⁴¹ Interestingly, FICZ has been shown to control Tregs via the activation of epidermal DCs when keratinocytes were exposed to UV-B light.⁷⁴ Indeed, UV-B light activation of AhR is believed to generate FICZ in the skin.⁷⁵ FICZ and TCDD have shown exert different effects on T_H17/Treg development either in vitro or in vivo.⁷⁶ It is now clear that AhR modulates the immune system in response to ligands of diverse origin.³⁷ Furthermore, AhR ligands affect several pathways and responses depending on the tissue/cellular context.³⁶ There is a range of potential physiological ligands for AhR.⁷⁷ However, the exact molecular mechanisms remain elusive and are subject of current research.

The role of AhR as a mediator of homeostasis and immune tolerance is further supported by its involvement in the regulation of type 1 Tregs (Tr1). Tr1 cells have the capacity to coproduce IFN-γ and IL-10^30,78 and have emerged as an important immunosuppressive CD4⁺ T-cell subset that dampens inflammatory responses, promotes transplant tolerance, and prevents tissue damage.^29,79,80 Gandhi et al⁴⁰ observed induction of Tr1 cells by activation of AhR through TCDD in human cells. Interestingly, in the same study, they found that adding TGF-β1 to the activation of AhR through TCDD induced functional Tregs.⁴⁰ Independent of the type of regulatory cell that is activated, AhR activation through TCDD induces a significantly higher expression of IL-10 in human cells.⁴⁰ Simultaneously, Apetoh and Quintana³⁹ corroborated the findings from Gandhi. Furthermore, they showed that AhR interacts with c-Maf, a transcription factor shown to regulate synthesis of IL-10,⁸¹ to contribute to Tr1-cell differentiation.³⁹ The high expression of IL-10 could protect animals from EAE. Tullius et al²⁹ and Wang et al³¹ have also shown that IL-10 is capable of promoting homeostasis and protecting from EAE via the direct activation of Tr1 cells.

As previously mentioned, the metabolites generated from the tryptophan/IDO/TDO pathway act as ligands for AhR.⁶⁷ Indeed, the IDO-1/AhR interaction appears to be a more effective pathway for 2 main reasons: it is self-regulated because AhR presides over the regulatory proteolysis of IDO-1, and it acts in a feed-forward loop initiated by kynurenine, followed by AhR activation, promoting IDO-1 transcription.⁴⁷ Interestingly, the IDO-1/AhR axis is very dependent on the presence or absence IL-6, an essential pro-inflammatory cytokine for the induction of T_H17 cells, and it can be antagonized by IL-10.⁸²

The absence of IL-6 is paramount for the IDO-1/AhR axis to be effective in IL-10 production and to create homeostasis.³⁶ However, in the early phases of inflammation, IL-6 is required as an initial defense mechanism.^83,84 During the early phase of inflammation, the source of kynurenine must be from somewhere other than the IDO-1/AhR axis.⁴⁷ Once the IDO-1/AhR axis is started through an external kynurenine source, AhR can repress IL-6 via the transcription of IL-10.³⁶ An interesting model suggested by Puccetti indicates cortisol as an outsource for kynurenine through TDO-2.⁴⁷ Cortisol is released with pro-inflammatory cytokines in the early phases of inflammation and releases acute phase proteins by the liver, one of which is TDO-2.^47,48,85 Interestingly, clinical trials indicated that cortisol and IL-6 increased the percentages of Tregs.⁸⁴ Furthermore, both cortisol and IL-6 can produce high amounts of TDO-2 by the liver activating the kynurenine pathway.⁸⁶ Indeed, other sources for the activation of AhR might be involved in this process and warrant further investigation.

Immunoregulatory Properties of NAD⁺ and Tryptophan

The major catabolic pathway of tryptophan is the kynurenine pathway, which ultimately leads to biosynthesis of NAD⁺,¹⁸ a vital cofactor that can rewire metabolism, activate sirtuins, and maintain mitochondrial fitness.⁸⁷

Nicotinamide adenine dinucleotide was originally discovered by Sir Arthur Harden and his colleagues in 1906.⁸⁸ However, its key role in hydrogen transfer in biochemical reactions was not discovered until 1935.⁸⁷ Nicotinamide adenine dinucleotide plays an important role in energy metabolism, but the roles of NAD⁺ have expanded beyond its initial function as a coenzyme linking cellular metabolism to several signaling and transcriptional events.^{27,29,30,87,89,90}

One of the most interesting newly discovered roles of NAD⁺ is probably its involvement in homeostasis and immune responses. Data increasingly support the notion of NAD⁺-regulating immune responses. For example, NAD⁺ regulates cytokine production of peripheral blood lymphocytes and monocytes.^91,92 Based on these findings, we investigated the role of NAD⁺ and T-cells. We found that intraperitoneal injections of NAD⁺ protected mice against autoimmune diseases and prolonged allograft survival after skin transplantation.^29,30 In our studies, NAD⁺ induced a systemic increase in IL-10 despite the reduction in Tregs and increase in T_H17 cells. The increased IL-10 production was mediated via the immunosuppressive Tr1 cells. Moreover, NAD⁺ induced T-cell differentiation, despite the cytokine milieu and well-established transcription factors. Interestingly, a genome-wide gene expression profile assessed by microarray analysis showed tryptophan hydroxylase 1 (Tph1) to be upregulated under the influence of NAD⁺, mostly described on mast cells. Collectively, our data indicate NAD⁺ as a potent immune regulator through tryptophan catabolism.

Several publications have indicated a strong relation between NAD⁺ and tryptophan, particularly with the kynurenine pathway.^27,89,93,94 Furthermore, NAD⁺ is essential for cells under physiological stress to avoid cell damage.¹⁷ Nicotinamide adenine dinucleotide can be synthesized through niacin, which is typically present in an adequate diet^2,87,94 and is the main source of NAD⁺ synthesis or de novo through tryptophan and the kynurenine pathway.^27,95

De novo synthesis of NAD⁺ starts with the catalysis of tryptophan by either TDO-2 or IDO-1⁹⁵ into formylkynurenine followed by conversion into l-kynurenine. Three more enzymatic reactions described elsewhere⁹ lead to the conversion into 2-amino-3-carboxymuconate semialdehyde (ACMS). ACMS can go either through an enzymatic pathway leading to total oxidation or through a nonenzymatic cyclization to QUIN. QUIN is essential for de novo synthesis of NAD⁺.^17,87 Interestingly, QUIN has been shown to be neurotoxic.^28,96 Moreover, QUIN accumulates in human glioma cells and is associated with malignant phenotypes.⁹⁷ Furthermore, QUIN was found to confer resistance of gliomas to oxidative stress. The cytotoxic properties of QUIN in the brain have extensively been discussed in the literature, but very little is known about its role in immune responses. Nicotinamide adenine dinucleotide has been found to induce programmed cell death and hinder Tregs.^98,99 Although we were able to confirm that NAD⁺ induces apoptosis of naïve CD4⁺ T-cells and reduces the number of Tregs,²⁹ CD4⁺ T-cells that were differentiated into T_H1, T_H2, T_H17, and iTreg were protected against apoptosis by NAD⁺.

Our previous studies showed the importance of the tryptophan/NAD⁺ pathway in inflammation, including autoimmune diseases and transplantation. These studies were performed in the context of antigen and antigen presentation. Our unpublished data indicate that the NAD⁺/tryptophan signaling pathway can trigger innate and adaptive immune responses in the absence of antigen. This is consistent with previous studies reporting that tryptophan administration promotes wound healing.¹⁰⁰ However, the effects of exogenous tryptophan in immune responses have not been well studied. Interestingly, a previous study by Swanson et al¹⁰¹ showed that exogenous addition of tryptophan to recover lung interstitial antigen-presenting cells (APCs)–induced T-cell proliferation in mixed leukocyte reactions. Of note, the addition of exogenous tryptophan can restore pathogens and replication of some bacteria and viruses⁴³; thus, further studies are required to elucidate the role of exogenous tryptophan in immune responses.

Antigen-presenting cells play a unique role in the regulation of adaptive immune responses due to their ability to capture, process, and present antigens via their major histocompatibility complex (MHC) cell surface molecule to the T-cell receptor (TCR) to mount a restricted MHC immune response.^102–104 DCs are still considered the major APCs bridging innate and adaptive immune responses.^105,106 The mode of action of DCs is mediated through at least 3 signals: (1) TCR activation, (2) activation of co-stimulatory molecules, and (3) secretion of chemokines and pro-inflammatory cytokines.¹⁰⁵ In addition, DCs can regulate innate and adaptive immune responses by recognizing pathogen-associated molecular patterns, such as microbial nucleic acids, lipoproteins, and carbohydrates, or damage-associated molecular patterns that are released from injured cells via intracellular or surface-expressed pattern recognition receptors (PRRs).¹⁰⁷ Thus, our unpublished data, indicating that the tryptophan/NAD⁺ pathway can trigger the immune system in the absence of pathogen invasion or PRRs’ activation, suggest a novel cellular and molecular signaling pathway distinct from the classical ag-APCs (DCs)-MHCII-TCR signaling machinery. It would therefore be interesting to further investigate the path used by tryptophan/NAD⁺, particularly the cells and molecules involved.

Tryptophan and NAD⁺ in the CNS

Active interactions between the CNS and the immune system are essential to maintain CNS integrity and homeostasis. The intact blood-brain barrier allows traffic of peripheral immune cells, CNS neurons and glia regulate macrophage and lymphocyte responses, and microglia play key roles in both innate and adaptive immune responses, providing the CNS with the strategic means to respond to pathogens. Thus, the past 30 years have seen significant changes in notions of CNS immune privilege. The immune implications of tryptophan have begun to extend into the CNS as well. Tryptophan is also the sole precursor of an important neurotransmitter, serotonin, or 5-hydroxytryptophan. Serotonin is synthesized from tryptophan through hydroxylation and decarboxylation, processes that are catalyzed by tryptophan hydroxylase (Tph) and the aromatic acid decarboxylase, with Tph being the rate-limiting step in the synthesis. Of the 2 isoforms of Tph, Tph1 is expressed both in the periphery (skin, enterochromaffin cells of the gut, mast cells, and the pineal gland) and in the CNS, and Tph2 is expressed in neurons of the central, peripheral, and enteric nervous systems. Indeed, tph1-null mice have gross abnormalities such as an overall size reduction, altered morphology of the rhombencephalon regions and neopallial cortex, alterations in gait dynamics, and reduced motivation locomotion.¹⁰⁸ Tph2-null mice show alterations in developmental milestones, brain-to-body weight ratio, and substantial deficits in numerous validated tests of social interaction and communication with highly repetitive and compulsive behaviors.¹⁰⁹ There appears to be no substantial overlap in the expression of the 2 tph isoforms by adulthood. Dietary tryptophan can also regulate serotonin synthesis in the brain and can affect mood, behavior, and cognition. Serotonin synthesis is thus an important tryptophan pathway and is a topic of intense research due to its broad impact as a neuromodulator. Multiple lines of evidence support its association with numerous neuropsychiatric conditions such as Parkinson disease, schizophrenia, depression, anxiety, and, of great significance, autism.

Autism, which is characterized as both a neurodevelopmental and a neuropsychiatric disease, has also distinctly evolved into a disease of the immune system.^110–112 One or more core behavioral symptoms, such as impaired social recognition, reduced social interactions, communication deficits, increased anxiety, motor stereotypies, repetitive behaviors, insistence on sameness, and restricted interests, identify autism. The Centers for Disease Control and Prevention estimates that ~1 in 88 children is diagnosed with autism each year, more than those diagnosed annually with cancer, diabetes, and AIDS combined. Currently, approximately $35 billion in direct and indirect care costs are spent annually for autism.¹¹³ The annual cost of caring for patients with autism is believed to reach $500 billion by 2025, with outside estimates reaching $1 trillion.¹¹⁴ Therefore, it is critical to gain mechanistic insights into multiple pathways coexisting in autism that will lay the foundation for new therapeutic opportunities.

Close associations between the serotonin and kynurenic pathways occur in tryptophan metabolism that are strongly influenced by the activity of the immune system. Quinolinic acid, a downstream product of the kynurenic pathway, is the structural precursor of NAD⁺, a critical energy carrier in mitochondria. Therefore, decreased tryptophan metabolism via either serotonin or QUIN will alter brain development, neuroimmune activity, and mitochondrial function. Interestingly, decreased tryptophan metabolism affecting both serotonin and kynurenic pathways has been linked to autism. Even a short-term reduction in the levels of tryptophan exacerbates repetitive, compulsive behaviors (eg, flapping, rocking, and whirling) in drug-free adults with autism.¹¹⁵ Serotonin in the blood is stored in platelets that undergo endocytosis via the serotonin transporter. Abnormal blood levels of serotonin produce autistic-like behaviors, such as impaired social communication and avoidance of new situations.¹¹⁶ Children with autism show a diminished capacity of whole-brain or regional brain serotonin synthesis that affects language production and sensory integration.^117,118 There are reports of reductions in not only serotonin concentrations but also the kynurenic acid levels in the cerebrospinal fluid of autistic children.^119,120 Diminished levels of NAD⁺ and plasma tryptophan in parallel with increased levels of oxidative stress have been reported in children with autism.^121,122 In addition, urinary levels of tryptophan are reduced in patients with autism.¹²³

Taken together, these results illustrate the critical need for a better understanding of the detailed mechanistic actions of tryptophan and NAD⁺ from cellular, molecular, and immunologic perspectives at distinct developmental time points in the CNS, which will aid in designing novel treatment strategies and bring new hope for neuroimmunological diseases such as autism. In addition, changes in tryptophan metabolism and pathway intermediates may serve in the development of new diagnostic assays for CNS immunologic disorders.

Conclusions

Increasing evidence indicates the important role of tryptophan catabolism in immune responses via the kynurenine pathway in vivo.^51,124,125 However, the exact mechanisms remain unknown. Based on the findings shown here, NAD⁺ might be responsible for the newly found functions of tryptophan in immune responses. In particular, de novo synthesis of NAD⁺ through QUIN, one of the catabolites of the kynurenine pathway, appears to have an important role in immune regulation and tolerance (Figure 1). However, tryptophan catabolites appear to have contradictory functions, depending on where they are involved and warrant further investigation. Furthermore, mast cells, although they are not typical APCs, might play an important role in the tryptophan/QUIN/NAD⁺ pathway regulating T-cell activation. Clearly, the field of immunology shaped by tryptophan and NAD⁺ is poised for several exciting discoveries in the future.

Figure 1.

Newfound functions of tryptophan in immune responses might be influenced by NAD+. De novo synthesis of NAD+ through QUIN appears to have an important role in immune regulation and tolerance. CNS indicates central nervous system; IDO, indoleamine 2,3-dyoxygenase; KYNp, kynurenine pathway; NAD+, nicotinamide adenine dinucleotide; QUIN, quinolinic acid; TDO, tryptophan 2,3-dyoxygenase; Tph1, tryptophan hydroxylase 1; Tph2, tryptophan hydroxylase 2; Tregs, regulatory T-cells; TRP, tryptophan.