Re: 파킨슨 T cell 자가면역 염증 ... 2022 논문..

[문형철]

J Parkinsons Dis. 2022; 12(Suppl 1): S65–S74.

Published online 2022 Sep 27. Prepublished online 2022 Mar 4. doi: 10.3233/JPD-223152

PMCID: PMC9535550

PMID: 35253782

T Lymphocytes in Parkinson’s Disease

Elena Contaldi,a,b Luca Magistrelli,a,c and Cristoforo Comid,*

Monitoring Editor: Bastiaan R. Bloem, Patrik Brundin, Eng King Tan, Ashley Harms, Cecilia Lindestam Arlehamn, and Caroline Williams-Gray

Author information Article notes Copyright and License information PMC Disclaimer

Go to:

Abstract

T cells are key mediators of both humoral and cellular adaptive immune responses, and their role in Parkinson’s disease (PD) is being increasingly recognized. Several lines of evidence have highlighted how T cells are involved in both the central nervous system and the periphery, leading to a profound imbalance in the immune network in PD patients. This review discusses the involvement of T cells in both preclinical and clinical studies, their importance as feasible biomarkers of motor and non-motor progression of the disease, and recent therapeutic strategies addressing the modulation of T cell response.

T세포는 

체액성 면역 반응과 세포 적응성 면역 반응의 핵심 매개체이며, 

파킨슨병(PD)에서의 역할이 점점 더 주목받고 있습니다. 

여러 증거에 따르면 

T 세포가 중추 신경계와 말초 모두에 관여하여 

PD 환자의 면역 네트워크에 심각한 불균형을 초래하는 것으로 밝혀졌습니다. 

이 리뷰에서는 전임상 및 임상 연구에서의 

T 세포의 관여, 

질병의 운동 및 비운동 진행의 실현 가능한 바이오마커로서의 중요성, 

T 세포 반응의 조절을 다루는 최근 치료 전략에 대해 설명합니다.

Keywords: Parkinson’s disease, T cells, CD4 + T cells, CD8 + T cells, neuroinflammation, peripheral immunity

INTRODUCTION

There is growing evidence suggesting the crucial involvement of T cells in Parkinson’s disease (PD). T cells are essential mediators of humoral and cellular adaptive immune responses: highly specific receptor-mediated clonal selection and expansion of T cells allow both antigen-specific immunity and immunological memory against known pathogens [1]. It is known that the precursors of T cells migrate to the thymus and develop into two distinct subsets, CD4 + and CD8 + cells, according to their peculiar surface markers. Before their activation, T cells are in the naïve condition, and once in the circulation can interact with antigen-presenting cells displaying foreign or self-antigens. Previous studies have shown that T cells play a key role both in the central nervous system (CNS) and in the periphery, leading to a profound imbalance in the immune network of PD patients.

소개

파킨슨병(PD)에

T 세포가 결정적으로 관여한다는 증거가

점점 더 많아지고 있습니다.

T 세포는

체액성 및 세포 적응성 면역 반응의 필수 매개체로,

매우 특이적인 수용체 매개 클론 선택과

T 세포의 확장은 알려진 병원체에 대한 항원 특이 면역과 면역학적 기억을 모두 가능하게 합니다 [1].

T 세포의 전구체는

흉선으로 이동하여 독특한 표면 마커에 따라

CD4 + 및 CD8 + 세포의 두 가지 다른 하위 집합으로 발달하는 것으로 알려져 있습니다.

활성화되기 전의 T 세포는 순진한 상태이며,

일단 순환계에 들어가면

외부 항원 또는 자기 항원을 나타내는

항원 제시 세포와 상호 작용할 수 있습니다.

이전 연구에 따르면

T 세포는 중추신경계(CNS)와 말초에서 모두 중요한 역할을 하며,

이로 인해 pd 환자의 면역 네트워크에 심각한 불균형을 초래하는 것으로 나타났습니다.

EVIDENCE OF T CELL INVOLVEMENT FROM ANIMAL MODELS AND NEUROPATHOLOGY: MORE CD4 + THAN CD8+?

In α-synuclein overexpression‎ animal models, early infiltration of both CD4 + and CD8 + T cells was observed [2], and T cells enhanced the number of α-synuclein aggregates by promoting a pro-inflammatory M1 phenotype in CNS myeloid cells [3]. The crucial role of T cells was further supported by the examination of postmortem human PD brains: Brochard et al. found CD8 + and CD4 + T cells, but not B cells, either in close contact with blood vessels or near melanized dopamine-containing neurons [4]. Interestingly, T cell-mediated dopaminergic toxicity was almost exclusively arbitrated by CD4 + T cells [4], as also confirmed in a neurotoxic-driven animal model [5] and from in vitro and in vivo data [6]. Furthermore, in α-synuclein overexpression‎ models, the genetic deletion of T cell receptor (TCR)β or CD4, as well as the use of the immunosuppressive drug fingolimod, reduced the CNS myeloid major histocompatibility complex (MHC)II response to α-synuclein, whereas the authors did not observe after the knockout of CD8 + T cells any significant effect on preventing the myeloid MHCII response or dopaminergic neuronal loss [7]. The interaction between CD8 + T cells and MHCI on neurons was also assessed, reporting increased MHCI expression‎ in and around virally transduced neurons (including dopamine neurons) and in CNS myeloid cells, but not astrocytes [7].

동물 모델과 신경 병리학에서 T 세포 관여의 증거: CD8+보다 CD4+가 더 많습니까?
α-시누클레인 과발현 동물 모델에서 CD4 + 및 CD8 + T 세포의 초기 침윤이 관찰되었으며[2],

T 세포는 CNS 골수 세포에서

전염증성 M1 표현형을 촉진하여

α-시누클레인 응집체의 수를 증가시켰습니다 [3].

T 세포의 중요한 역할은 사후 인간 PD 뇌를 검사함으로써 더욱 뒷받침되었습니다: Brochard 등은 혈관과 밀접하게 접촉하거나 멜라닌화된 도파민 함유 뉴런 근처에서 CD8 + 및 CD4 + T 세포를 발견했지만 B 세포는 발견하지 못했습니다 [4]. 흥미롭게도 T 세포 매개 도파민성 독성은 거의 독점적으로 CD4 + T 세포에 의해 중재되었으며[4], 이는 신경독성 중심 동물 모델 [5]과 시험관 및 생체 내 데이터 [6]에서도 확인되었습니다. 또한 α-시누클레인 과발현 모델에서 T세포 수용체(TCR)β 또는 CD4의 유전적 결실과 면역 억제 약물인 핑골리모드의 사용은 α-시누클레인에 대한 CNS 골수성 주요 조직 적합성 복합체(MHC)II 반응을 감소시켰지만, 저자는 CD8 + T 세포의 녹아웃 후 골수성 MHCII 반응이나 도파민성 신경세포 손실 예방에 큰 효과를 관찰하지 못했습니다[7]. CD8 + T 세포와 뉴런의 MHCI 간의 상호작용도 평가하여 바이러스에 의해 형질 전환된 뉴런(도파민 뉴런 포함)과 그 주변 및 CNS 골수 세포에서 MHCI 발현이 증가했지만 성상교세포는 그렇지 않다고 보고했습니다 [7].

Go to:

α-SYNUCLEIN-SPECIFIC T CELL RESPONSES

A seminal study by Sulzer et al. explored whether T cells recognize epitopes derived from α-synuclein and found that the Y39 and S129 regions act as epitopes [8]. More in detail, epitopes derived from the Y39 region were displayed by two MHC class II beta chain alleles as well as an additional MHC class II allele and an MHC class I allele, with an immune response mostly mediated by interleukin (IL-5)-secreting CD4 + T cells and interferon (IFN)γ CD8 + cytotoxic T cells [8]. Furthermore, it was reported that α-synuclein-specific T cell activation was predominant in early-stage PD [9].

α-시누클레인 특이적 T 세포 반응
Sulzer 등의 중요한 연구에 따르면 T 세포가 α-시누클레인에서 파생된 에피토프를 인식하는지 여부를 조사한 결과 Y39 및 S129 영역이 에피토프로 작용한다는 사실이 밝혀졌습니다 [8]. 좀 더 자세히 살펴보면, Y39 영역에서 파생된 에피토프는 두 개의 MHC 클래스 II 베타 사슬 대립유전자뿐만 아니라 추가 MHC 클래스 II 대립유전자 및 MHC 클래스 I 대립유전자에 의해 표시되었으며, 면역 반응은 주로 인터루킨(IL-5)을 분비하는 CD4 + T 세포와 인터페론(IFN)γ CD8 + 세포독성 T 세포를 매개로 이루어졌습니다 [8]. 또한, α-시누클레인 특이적 T 세포 활성화가 초기 PD에서 우세한 것으로 보고되었습니다 [9].

Go to:

EVIDENCE OF T CELL INVOLVEMENT FROM ANIMAL MODELS AND NEUROPATHOLOGY: MORE CD8 + THAN CD4+?

Even though several lines of evidence point to the crucial role of CD4 + T cells in the pathogenesis of PD, the involvement of CD8 + T cells should be highlighted as well.

Firstly, it is known that dopamine neurons can express MHCI in response to IFN-γ, which makes them susceptible to cell death by cytotoxic CD8 + T cells [10]. In an experimental PINK1-/- mouse model of PD, the authors hypothesized that intestinal infection may act as the precipitating event in the establishment of a cytotoxic mitochondria-specific response both in the periphery and the brain [11]. Based on neuropathological evidence, a recent study [12] assessed T cell infiltration in human substantia nigra pars compacta (SNc) throughout different PD stages (one group with α-synuclein aggregates only in the olfactory bulb representing the earliest stage of the disease and the second group with α-synuclein aggregates in the SN). Nigral cytotoxic CD8 + T cell infiltration was robust in the earliest stage of the disease when no α-synuclein aggregation and dopaminergic neuronal death were present yet, whereas in the next stage neuronal loss was accompanied by a milder CD8 + T cell infiltration, thus suggesting that CD8 + T cell-mediated attack may trigger neuronal death and synucleinopathy.

Go to:

CHANGES OF PERIPHERAL CD4 + AND CD8 + T CELLS IN PD PATIENTS

It is conceivable that the alteration of T cells in the CNS is mirrored in the periphery, likely as a consequence of blood-brain barrier disruption in PD patients [13].

Regarding CD8 + T cells, recent research by Yan et al. suggested that naïve CD8 + T cells were significantly decreased in the peripheral blood of PD patients, whereas IFN-γ–producing CD8 + T cells were increased [14]. An increase in peripheral CD8 + T cells was similarly observed in other studies [15, 16], but conflicting evidence detecting no significant differences compared with healthy controls was reported as well [17–19]. Another group [20] showed a reduction in CD8 + terminally differentiated effector memory re-expressing CD45RA (TEMRA) cells and a lower expression‎ of the cell-aging marker p16, suggesting an attenuated shift towards CD8 + T cells senescence at the earliest stages of PD.

Furthermore, several studies found reduced levels of circulating CD3 + and CD4 + T cells [15, 16, 19, 21, 22]. A meta-analysis including 21 case-control studies and 943 PD patients confirmed that the numbers of CD3 + and CD4 + T cells were significantly decreased in PD [23]. In contrast with these results, another study found that PD patients had an increase in the percentage of CD3 + and CD4 + T s and the CD4 + /CD8 + ratio [24], whereas other groups did not find any significant difference in the percentage of both CD4 + and CD8 + between PD patients and controls [17, 18, 25]. Undoubtedly, the composition of peripheral T cells from PD patients in the reported studies was quite heterogeneous, which could be explained by the influence of ethnic variations or other relevant disease-related confounders. For example, a study by Bhatia et al. found that many factors, including age, sex, disease duration, and disease severity were associated with variations in T cell pathology, with disease severity being the most significant one [26].

Different CD4 + T cell subsets orchestrate specific immune functions

Concerning CD4 + T cells, specific subsets are known to orchestrate different immune functions [27]: T helper (Th)1 and Th17 target bacterial and viral pathogens mainly through the release of IFN-γ, IL-17A, IL-21, and other pro-inflammatory cytokines. Th2 activity is focused on parasitic and allergic responses, in particular through IL-4, IL-5, and IL-13, which act as anti-inflammatory cytokines. Regulatory T cells (Tregs) modulate T cell activation and inflammation.

Imbalance of peripheral CD4 + T cell subsets in PD: Th1 and Th17

Chen et al. [21] observed in the peripheral blood of PD patients an increased proportion of circulating Th1 and Th17 cells and a decreased number of Th2 and Tregs. Compared with the control group, the Th1/Th2 and Th17/Treg ratios were significantly increased with a shift towards Th1 and Th17 subsets. The prominent role of pro-inflammatory Th1 and Th17 was further supported in a 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) model of PD: naïve CD4 + T cells treated with α-synuclein showed a polarization towards the Th1 or Th17 phenotype, thus causing cell death of dopaminergic neurons in the SN and exacerbating MPTP-induced cell death [5].

It was shown that Th1 cells may be relevant in the altered immune network of PD. This subgroup differentiates under the influence of IFN-γ and IL-12 released by antigen-presenting cells, and the release of Th1-derived pro-inflammatory cytokines is crucial for the activation of B cells and the phagocytosis of microbes [28]. Intriguingly, in PD patients, the shift towards Th1 cells was associated with motor function scores as assessed through the Unified Parkinson’s Disease Rating Scale (UPDRS)-part III [21]. Kustrimovic et al. reported no significant correlations between circulating CD4 + T cells, dopamine receptor (DR) expression‎, transcription factors mRNA levels, and demographic and clinical features of PD patients [22]. Nonetheless, the shift towards Th1 lineage was confirmed in both drug-naïve and drug-treated patients, and was associated with profound modifications of transcription factor genes expression‎ and increased production of IFN-γ and tumor necrosis factor (TNF)-α. Modifications of the transcription factors network in CD4 + T cells occur early in PD, and the absence of correlations with patients’ characteristics suggests that the alteration of CD4 + T cell differentiation mechanisms is independent of PD progression and severity and antiparkinsonian treatment [22]. The imbalance in CD4 + T cells transcription factors could be of great interest since it represents a peculiar molecular signature shared by idiopathic REM sleep behavior disorder and PD patients [29] as well as potential biomarkers of motor complications [30].

The pro-inflammatory bias could be promoted by the Th17 subpopulation as well. This specific subset is mainly involved in host defense against extracellular pathogens and plays a central role in the pathophysiology of several autoimmune diseases through the production of IL-17, IL-17F, IL-21, IL-22, and granulocyte-macrophage colony-stimulating factor (GM-CSF) [31]. Increased levels of Th17 in early-stage PD patients were reported in several studies [14, 21, 32], even though conflicting results observing no differences or reduced levels of Th17 cells were described as well [22, 33]. A recent study also found that there were significant correlations between Th17 cells and the subscales I and II of the MDS-UPDRS [14].

Regarding in vitro evidence and animal models, the critical role of Th17-driven inflammation was further explored in a recent work [6] employing autologous co-cultures of activated T cells and induced pluripotent stem cells (iPSC)-derived midbrain neurons of 10 PD patients and 10 controls. After co-culture with T cells or the addition of IL-17, PD iPSC-derived midbrain neurons underwent increased neuronal death driven by upregulation of IL-17 receptor (IL-17R), whereas blockage of IL-17 or IL-17R prevented neuronal death. Furthermore, the co-culture of MPTP-treated neurons with Th17 cells further exacerbated neuronal cell death and increased IL-1α and TNF-α levels [34]: Liu et al. found that these effects were mediated via lymphocyte function-associated antigen 1 (LFA-1) and intracellular adhesion molecule-1 (ICAM-1), and the blocking of either LFA-1 in Th17 cells or ICAM-1 in ventral mesencephalic neurons abolished Th17-induced dopaminergic neuronal death. Taken together, these results suggest that counteracting Th17 development could represent a feasible therapeutic option in PD. The restriction of Th17 development and differentiation can be achieved through different compounds, for example, the peroxisome proliferator-activated receptor-gamma [35], or through the reduction of transcription factors RORγt and STAT3 via cytokines such as IL-4 or IL-32 [31].

Imbalance of peripheral CD4 + T cell subsets in PD: Th2 and Tregs

The preval‎ence of a pro-inflammatory phenotype in PD is also favored by an altered anti-inflammatory response promoted by Th2 and Treg cells. Th2 cells differentiate from naïve T cells under the influence of IL-4 and the activation of the GATA3 and STAT6 transcription factors. The cytokines most typically associated with Th2 cells are IL-4, IL-5, IL-9, and IL-13, and combinations of these cytokines drive B cell proliferation and immunoglobulin class-switching to immunoglobulin E (IgE), eosinophilia, mastocytosis, and macrophage polarization to an M2-like phenotype [36]. Several studies have observed lower absolute numbers and frequency of Th2 cells in PD compared with healthy controls [15, 22], with increased mRNA levels of both GATA3 and STAT6 [22]. Interestingly, increased levels of STAT6 were also reported in PD patients with motor fluctuations [30], suggesting the suitable targeting of Th2 cells in the complex stage of the disease. On the other side, Alvarez-Luquin et al. demonstrated no significant difference in Th2 cell counts in PD patients compared with controls, even though a significant increase in IL-13 levels was observed [33], and also significantly increased levels of IL-4-producing Th2 have been recently reported [14].

Regulatory T cells (Tregs) represent another T cell subset possibly involved in the disruption of immune mechanisms. Tregs are responsible for the preservation of immune tolerance and inhibition of autoimmunity. They act as negative regulators of inflammation [37] through the secretion of anti-inflammatory cytokines, in particular IL-10 and TGF-β, and express granzyme A to kill effector cells in a perforin-dependent manner [38]. It was previously reported that PD patients display an impaired ability to suppress effector T cell function [39] and reduced absolute numbers of Tregs have been found as well [15, 22, 33]. Intriguingly, dysregulation of the Treg compartment was also associated in PD patients with crucial non-motor symptoms, such as cognitive impairment [40] and constipation [41].

Concerning animal studies, Reynolds et al. demonstrated a neuroprotective role for Tregs in the MPTP mouse model of PD: the adoptive transfer of CD3-activated Tregs to MPTP-intoxicated mice protected the nigrostriatal system in a dose-dependent manner [42], probably by attenuating Th17-mediated neurodegeneration [5]. Also in the MPTP mouse model examined by Li et al., Treg transfer along with anti-TNFα antibody administration increased Tregs and reduced Th1 cells leading to an amelioration of PD severity [43].

Alterations of CD8 + and CD4 + T cells in PD are summarized in Table 1 and Fig. 1.

Table 1

Summary of peripheral T changes in PD patients

Peripheral blood alterations of T cells in PD
Finding	Population	Nation	Reference

Open in a separate window

Fig. 1

Central and peripheral involvement of T cells in PD. Naïve CD4 + and CD8 + T lymphocytes are activated in the periphery after the interaction with antigen-presenting cells. CD4 + T cells then differentiate into pro-inflammatory (Th1, Th17) or anti-inflammatory (Th2, Treg) subtypes, characterized by the release of specific patterns of cytokines. Activated T cells can reach the central nervous system by crossing an altered blood-brain barrier, thus polarizing resident cells to pro-inflammatory or anti-inflammatory phenotypes. In particular, Th1 and Th17 subsets release pro-inflammatory molecules (TNF-α, IFN-γ, IL-17, IL-21, IL-22), which, in concert with other mechanisms, lead to neuronal damage and death. Detrimental pro-inflammatory pathways are indicated with red lines. Figure created with BioRender.com.

Imbalance of peripheral CD4 + T cell subsets in PD: Role of dopaminergic treatment

Several works have also explored whether dopaminergic drugs may play a significant role in regulating lymphocyte subsets in PD. Kustrimovic et al. [22, 44] did not suggest relevant effects of antiparkinsonian treatment on the peripheral immune system of PD patients. Similarly, Chen et al. found a weak association between the percentage of CD4 + T cells and the levodopa equivalent daily dose [24]. In another study [45], the negative correlation between the levels of T cytotoxic cells 1 (CD8 + Tbet+IFN-γ+) and T cytotoxic cells 2 (CD8 + GATA3 + IL-13+) with the Hoehn and Yahr scale score was observed only in patients receiving treatment with levodopa, thus suggesting that levodopa could affect T cytotoxic cells. Furthermore, it should be noticed that human and murine lymphocytes express all the five subtypes of DR, and the DRD2 agonist sumanirole was able to inhibit the shift to the Th1 and Th17 phenotypes of CD4 + T cells obtained from MPTP-intoxicated mice [46].

Go to:

T CELL IMMUNITY AND GUT MICROBIOTA

Whether the peculiar immune profile observed in PD patients arises from the periphery, favoring subsequent neuroinflammation, or is a consequence of peripheral leakage of CNS-derived antigens, has not been fully clarified. Among peripheral sources, intestinal immune activation and dysbiosis could represent one potential driver of PD inflammatory state. There is increasing research interest in the gut-brain axis: several studies have suggested in PD an association between gastrointestinal inflammation and the accumulation of α-synuclein in the enteric nervous system [47]. Moreover, a relationship between inflammatory bowel diseases (IBD) and PD has been reported [48, 49], and a recent study showed a significant reduction in the risk of developing PD in IBD patients receiving early treatment with anti-TNF-α therapy [50].

Regarding animal models, chronic mild focal intestinal inflammation accelerated brain neuropathology and motor dysfunction in α-synuclein mutant mice [51]. Additionally, when α-synuclein overexpressing mice were colonized with microbiota from PD patients, enhanced physical impairment and neuroinflammation were observed compared with microbiota transplants from healthy human donors [52].

It was shown that PD patients display an altered composition of several gut microbiome taxa [53]. Among these, Lactobacillaceae may induce Th1-type immune responses [54], whereas Prevotellaceae abundance was associated with augmented Th17-mediated mucosal inflammation [55]. Another study eval‎uating fecal DNA samples from 69 PD patients and 244 controls reported that, among the microbiota-associated epitopes involved in inflammatory pathways, two were involved in T cell responses [56]. Based on these observations, it could be speculated that T cell-related immunity, triggered by the aggregation of α-synuclein in the gut mucosa, may promote further CNS neuroinflammation and neurodegeneration. Nonetheless, the complex interaction between intestinal mechanisms, the enteric nervous system, the immune system, the CNS, and environmental factors, is yet to be fully elucidated.

Go to:

THE CONNECTION BETWEEN PD GENETIC FACTORS AND T CELLS

Finally, in this complex scenario, genetic factors should be considered as well: the association between human leukocyte antigen genes and PD was explored in several studies [57, 58] and a large-scale meta-analysis including more than 100,000 subjects [59]. Other lines of evidence found that the knockout of the α-synuclein gene affected IL-2 production by CD4 + T cells and the frequency of Tregs in mice [60]. The role of α-synuclein deficiency in promoting a pro-inflammatory immune response was also observed in experimental autoimmune encephalomyelitis models of multiple sclerosis [61, 62]. The LRRK2 G2019S gene altered myeloid cell differentiation in transgenic rats, leading to decreased Th17 cell activity [63]. Furthermore, PINK1–/– T cells exhibited a reduced suppressive function despite normal FoxP3 expression‎ kinetics [64]. A recent study [11] reported that the intestinal infection with gram-negative bacteria in PINK1–/– mice leads to autoimmune mechanisms eliciting cytotoxic mitochondria-specific CD8 + T cells, thus highlighting the role of PINK1 as a repressor of the immune system and supporting the relevance of the gut-brain axis as a triggering event in PD. Taken together, these results provide evidence that PD-associated genetic mutations could influence the immune network and suggest that specific subsets of patients with a genetic predisposition could be more suitable for immune-targeted therapies.

Go to:

FUTURE PERSPECTIVES

A deeper understanding of the peripheral immune system in PD has widened research avenues to explore whether it is a suitable target for disease-modifying therapies. In particular, the possibility of immune escape mechanisms in PD has built the premise of re-establishing immunological tolerance as a key strategy. In this context, compounds acting on the Treg compartment, i.e., vasoactive intestinal peptide (VIP), pituitary adenylate cyclase-activating polypeptide (PACAP), and GM-CSF, have been explored in recent literature [65]. VIP-receptor 2 peptide agonist (LBT-3627) attenuated neuroinflammation by promoting the restoration of Treg activity in both 6-hydroxydopamine (6-OHDA) and α-synuclein overexpression‎ rat models [66]. Similarly, PACAP exerted a neuroprotective effect in the rotenone-induced snail and 6-OHDA-induced rat models of PD. [67]. The adoptive transfer of GM-CSF-induced Tregs to MPTP mice was able to protect nigral neurons through the activation of immune-based neuronal protection pathways linked to the upregulation of IL-27 [68]. Further evidence was provided in a study carried out by Thome et al., who found that ex vivo expansion of dysfunctional Tregs restored suppressive function by diminishing multiple pro-inflammatory pathways in myeloid cells and inhibiting responder T cell proliferation [69]. Regarding clinical trials, the subcutaneous administration of sargramostim (a human recombinant GM-CSF) at 6μg/kg/day for 56 days, increased the numbers of Tregs and determined modest improvement in the UPDRS-III after 6 and 8 weeks of treatment when compared with placebo [70]. Since some adverse events were noticed, another study [71] explored long-term sargramostim treatment at 3μg/kg/day in 5 PD patients. Reductions in adverse events, as well as an increase in peripheral blood Treg numbers, function, and hypomethylation of upstream FoxP3 DNA elements, were observed. Furthermore, there was no worsening of motor function scores for any subject during the course of treatment. An alternative approach to enhance the Treg compartment is to isolate and purify Tregs from peripheral blood, expand them in vitro, and administer autologous infusions of expanded Tregs, as reported in a recent phase I trial involving patients with amyotrophic lateral sclerosis [72]. Another feasible strategy could be represented by targeting T cells through immunosuppressant drugs, i.e., azathioprine. Azathioprine is a pro-drug of 6-mercaptopurine, a purine antagonist that inhibits leukocyte proliferation by interfering with nucleotide synthesis [73]. A phase 2 trial is currently exploring whether the suppression of the peripheral immune system using azathioprine has a disease-modifying effect in PD [74]. Additionally, glatiramer acetate, an FDA-approved treatment for multiple sclerosis which improves Th2 and Treg function, was investigated as a potential disease-modifying treatment in PD: in the MPTP murine model, this compound was able to reverse motor dysfunction, promote the recovery of tyrosine hydroxylase protein expression‎ in the striatum and the levels of brain derived neurotrophic factor, and reduce the microglial activation marker IBA1 [75].

Go to:

CONCLUSION

The present review highlighted how the dysregulation of central and peripheral T cells may play a key role in PD. Nonetheless, several unanswered questions remain: 1) Is the peripheral activation of T cells a primary event leading to neurodegeneration, or is it a secondary response caused by neuronal injury? 2) What is the exact relationship between the alteration of T cell subsets in the blood and the CNS of PD patients? 3) Which are the potential applications of T cell changes as diagnostic and therapeutic biomarkers? 4) What is the role of genetic stratification in identifying PD subjects susceptible to T cell impairment and T cell-targeted therapies? Moreover, a thorough understanding of the role of PD medication and the use of comparable methodologies (i.e., use of standardized markers for the identification of T cell subsets) are warranted to avoid contradictory findings. If these issues will be correctly tackled, the modulation of T cell response could hopefully slow or even halt neuronal damage through the restoration of immune balance, thus providing new therapeutic avenues in the management of PD patients.

Go to:

ACKNOWLEDGMENTS

This research was supported by Fondazione CARIPLO http://www.fondazionecariplo.it (Project 2011-0504), and by the AGING PROJECT—Department of Excellence—Università del Piemonte Orientale. This paper is part of the PhD program of Clinical and Experimental Medicine and Medical Humanities (University of Insubria) for L.M. and Medical Science and Biotechnology for E.C. These PhD programs and therefore this paper constitute an important part of the project Recruiting and training Physician-Scientists to empower translational research, funded by Fondazione Cariplo.

Go to:

CONFLICT OF INTEREST

The authors have no conflict of interest to report.

Go to:

REFERENCES

[1] Lee H-G, Cho M-Z, Choi J-M (2020) Bystander CD4+T cells: Crossroads between innate and adaptive immunity. Exp Mol Med 52, 1255–1263. [PMC free article] [PubMed] [Google Scholar]

[2] Sanchez-Guajardo V, Febbraro F, Kirik D, Romero-Ramos M (2010) Microglia acquire distinct activation profiles depending on the degree of alpha-synuclein neuropathology in a rAAV based model of Parkinson’s disease. PLoS One 5, e8784. [PMC free article] [PubMed] [Google Scholar]

[3] Sommer A, Fadler T, Dorfmeister E, Hoffmann A-C, Xiang W, Winner B, Prots I (2016) Infiltrating T lymphocytes reduce myeloid phagocytosis activity in synucleinopathy model. J Neuroinflammation 13, 174. [PMC free article] [PubMed] [Google Scholar]

[4] Brochard V, Combadière B, Prigent A, Laouar Y, Perrin A, Beray-Berthat V, Bonduelle O, Alvarez-Fischer D, Callebert J, Launay J-M, Duyckaerts C, Flavell RA, Hirsch EC, Hunot S (2009) Infiltration of CD4+lymphocytes into the brain contributes to neurodegeneration in a mouse model of Parkinson disease. J Clin Invest 119, 182–192. [PMC free article] [PubMed] [Google Scholar]

[5] Reynolds AD, Stone DK, Hutter JAL, Benner EJ, Mosley RL, Gendelman HE (2010) Regulatory T cells attenuate Th17 cell-mediated nigrostriatal dopaminergic neurodegeneration in a model of Parkinson’s disease. J Immunol 184, 2261–2271. [PMC free article] [PubMed] [Google Scholar]

[6] Sommer A, Marxreiter F, Krach F, Fadler T, Grosch J, Maroni M, Graef D, Eberhardt E, Riemenschneider MJ, Yeo GW, Kohl Z, Xiang W, Gage FH, Winkler J, Prots I, Winner B (2018) Th17 lymphocytes induce neuronal cell death in a human iPSC-based model of Parkinson’s disease. Cell Stem Cell 23, 123–131.e6. [PubMed] [Google Scholar]

[7] Williams GP, Schonhoff AM, Jurkuvenaite A, Gallups NJ, Standaert DG, Harms AS (2021) CD4 T cells mediate brain inflammation and neurodegeneration in a mouse model of Parkinson’s disease. Brain 144, 2047–2059. [PMC free article] [PubMed] [Google Scholar]

[8] Sulzer D, Alcalay RN, Garretti F, Cote L, Kanter E, Agin-Liebes J, Liong C, McMurtrey C, Hildebrand WH, Mao X, Dawson VL, Dawson TM, Oseroff C, Pham J, Sidney J, Dillon MB, Carpenter C, Weiskopf D, Phillips E, Mallal S, Peters B, Frazier A, Lindestam Arlehamn CS, Sette A (2017) T cells from patients with Parkinson’s disease recognize α-synuclein peptides. Nature 546, 656–661. [PMC free article] [PubMed] [Google Scholar]

[9] Lindestam Arlehamn CS, Dhanwani R, Pham J, Kuan R, Frazier A, Rezende Dutra J, Phillips E, Mallal S, Roederer M, Marder KS, Amara AW, Standaert DG, Goldman JG, Litvan I, Peters B, Sulzer D, Sette A (2020) α-Synuclein-specific T cell reactivity is associated with preclinical and early Parkinson’s disease. Nat Commun 11, 1875. [PMC free article] [PubMed] [Google Scholar]

[10] Cebrián C, Zucca FA, Mauri P, Steinbeck JA, Studer L, Scherzer CR, Kanter E, Budhu S, Mandelbaum J, Vonsattel JP, Zecca L, Loike JD, Sulzer D (2014) MHC-I expression‎ renders catecholaminergic neurons susceptible to T-cell-mediated degeneration. Nat Commun 5, 3633. [PMC free article] [PubMed] [Google Scholar]

[11] Matheoud D, Cannon T, Voisin A, Penttinen A-M, Ramet L, Fahmy AM, Ducrot C, Laplante A, Bourque M-J, Zhu L, Cayrol R, Le Campion A, McBride HM, Gruenheid S, Trudeau L-E, Desjardins M (2019) Intestinal infection triggers Parkinson’s disease-like symptoms in Pink1-/- mice. Nature 571, 565–569. [PubMed] [Google Scholar]

[12] Galiano-Landeira J, Torra A, Vila M, Bové J (2020) CD8 T cell nigral infiltration precedes synucleinopathy in early stages of Parkinson’s disease. Brain 143, 3717–3733. [PubMed] [Google Scholar]

[13] Kortekaas R, Leenders KL, van Oostrom JCH, Vaalburg W, Bart J, Willemsen ATM, Hendrikse NH (2005) Blood-brain barrier dysfunction in parkinsonian midbrain in vivo. Ann Neurol 57, 176–179. [PubMed] [Google Scholar]

[14] Yan Z, Yang W, Wei H, Dean MN, Standaert DG, Cutter GR, Benveniste EN, Qin H (2021) Dysregulation of the adaptive immune system in patients with early-stage Parkinson disease. Neurol Neuroimmunol Neuroinflamm 8, e1036. [PMC free article] [PubMed] [Google Scholar]

[15] Baba Y, Kuroiwa A, Uitti RJ, Wszolek ZK, Yamada T (2005) Alterations of T-lymphocyte populations in Parkinson disease. Parkinsonism Relat Disord 11, 493–498. [PubMed] [Google Scholar]

[16] Wang P, Yao L, Luo M, Zhou W, Jin X, Xu Z, Yan S, Li Y, Xu C, Cheng R, Huang Y, Lin X, Ma K, Cao H, Liu H, Xue G, Han F, Nie H, Jiang Q (2021) Single-cell transcriptome and TCR profiling reveal activated and expanded T cell populations in Parkinson’s disease. Cell Discov 7, 52. [PMC free article] [PubMed] [Google Scholar]

[17] Schröder JB, Pawlowski M, Meyer zu Hörste G, Gross CC, Wiendl H, Meuth SG, Ruck T, Warnecke T (2018) Immune cell activation in the cerebrospinal fluid of patients with Parkinson’s disease. Front Neurol 9, 1081. [PMC free article] [PubMed] [Google Scholar]