Viruses and neurodegeneration

HSV-1 is one of the most common viruses in the general population and can cause latent infection in neurons for life-long. It belongs to the family Herpesviridae, which is a large family of double-stranded DNA viruses [32, 33]. HSV-1 is neurotropic and neuro-invasive with high neuro-virulence and grows well in vitro in both neuronal cell lines and dorsal root ganglia. Primary sympathetic neuronal cultures support HSV-1 infections, which resemble natural latency. In vivo, HSV-1 establishes life-long latency in peripheral neurons where productive replication is suppressed. While periodic reactivation results in productive infection, the molecular, genomic and proteomic basis of neuronal latency remains poorly understood.

AD is the most common form of dementia. There are 26.6 million patients suffering AD worldwide and according to the World Health Organization, the prevalence would increase to 0.441% by 2015 and to 0.556% by 2030 (WHO). Because it can’t be cured, it is one of the most expensive diseases to manage and treat in the developed countries [34]. AD is characterized by loss of neurons and synapses in the cerebral cortex and certain subcortical regions. One of the most notable pathological features is the appearance of plaques and tangles of neurofibrils within brain nerves. AD has been identified as a protein mis-folding disease as both plaques and tangles involve the deposition and accumulation of abnormally folded A-beta and tau proteins [35, 36]. Precisely how the disturbances of production and aggregation of the beta-amyloid peptide leads to the pathology of AD is poorly understood. The amyloid hypothesis suggests the accumulation of beta-amyloid peptides as the central event triggering neuron degeneration. Accumulation of aggregated amyloid fibrils, which are believed to be the toxic form of the protein responsible for disrupting the cell’s calcium ion homeostasis, induces programmed cell death (apoptosis) [37]. It is also known that βamyloid selectively builds up in the mitochondria in the cells of Alzheimer’s-affected brains, and it also inhibits certain enzyme functions and the utilization of glucose by neurons[38]. In addition, various inflammatory processes and cytokines possibly play significant role in the pathology of Alzheimer’s disease. Inflammation is indicative of tissue damage in any disease, but it is likely that it may be a marker of an immunological response [39]. Yet, the precise cause of AD is not well understood and recently brain infections have been suggested as a possible trigger or cofactor(s) in AD. Several viruses have been linked to AD (Table 1), with HSV-1 being the most popular and well studied in relation to AD.

The presence of HSV-1 DNA in elder brain, especially for APOE gene carriers, is a risk factor for AD [40]. Its seropositivity reactivation has also been shown to significantly correlate with incident AD [41]. Furthermore, HSV-1 infection in AD brain has been detected by electron microscopy and immunohistochemistry in a rapid progressor with AD, indicating the significant role of reactivation of HSV in AD progression [42]. In addition, Wozniak et al., has further demonstrated the role of HSV-1 in AD by localizing HSV-1 DNA in amyloid plaques and detected higher association between viral DNA and Amyloid beta plaques in AD patients’ brains compared to normal ageing brains (72% versus 24%, p<0.001), suggesting HSV-1 to be a possible major cause of amyloid plaques and a possible etiological factor in AD [43]. Moreover, short contiguous amino acid stretches in proteins expressed by HSV are homologous to APOE4, clusterin, and many other gene products highly relevant to AD, also suggesting the role of HSV as a causative agent that is involved in AD development [44].

The possible mechanisms by which HSV-1 triggers AD have been studied in some detail. It has been found that isolated intracellular HSV1 particles physically associated with amyloid precursor protein (APP), through which the viruses exploit to travel to the cell surface [45, 46]. APP is an integral membrane protein highly expressed in the synapses of neurons and best known as the precursor molecule whose proteolysis generates beta amyloid (Aβ). Abnormal deposition and accumulation of Aβ and tau proteins serves as the primary cause of plaques and tangles formation, which is one of the most notable pathological features in the AD brain [35, 36]. Cheng et al., has further proven that HSV1 is specifically co-localized with APP to facilitate viral transport and also alters normal APP transport, distribution, and even microtubule networks and their stability [47]. HSV-1 infection has also been shown to promote neurotoxic Aβ accumulation [48‐50], tau phosphorylation [51] and cleavage [52]in vitro. Apart from direct interaction, HSV1 infection has also been found to interfere with post-transcriptional regulation by up regulating microRNA-146a, which is significantly involved in AD [53].

With the compelling evidence of HSV-1 association with AD, HSV-1 infection in people over 50 years of age is definitely a risk factor or co-factor at least in AD. Therefore, it remains to be seen if the administration of antiviral agents to patients with mild AD has any direct effect on improvement and general well being of patients with AD. This may provide a further confirmation of HSV-1 involvement in AD.

PD is the second most common age-related neurodegenerative disorder after AD and it influences more than 1 million people in the US and prevalence is predicted to triple over the next 50 years due to increase in lifespan. Its primary characteristic is the loss of dopamine-secreting cells in the pars compacta region of the substantia nigra[102]. The cause remains unknown for majority of PD cases although small percentage of diagnosed PD has a genetic causation. Apart for several possible biological, environmental and genetic causes linked to PD, it has also been linked to influenza virus first time after the occurrence of encephalitis lethargica, an entity displaying Parkinson’s disease (PD) signs and symptoms. Influenza A viruses are negative sense, single-stranded, segmented RNA viruses, belonging to the Orthomyxoviridae family. By yearly epidemic, it can cause up to 500,000 deaths worldwide [103]. So far, it has caused five flu pandemics. 1918 flu pandemic, caused by H1N1 subtype, is the most lethal one, which killed 20–100 million people.

Increased incidence of PD in relation to the 1918 H1N1 influenza A pandemic has been well documented [104‐106],including the incidence in years around 1918 and also the incidence of people who were born around 1918 [105, 107, 108]. Followed by the 1918 Spanish influenza pandemic, the association of PD with influenza A has become more evident, yet not completely proven [109]. It has been shown by Jang et al.[110] that certain viruses can enter the CNS and are capable of directly inducing pathological alterations reminiscent of those observed in Parkinson’s disease. These include, loss of dopaminergic neurons in the SNpc, long-lasting activation of microglia in areas infected by virus, as well as upregulation of alpha-synuclein (with aggregation) in these same regions. In addition, the possible involvement of H1N1 as an etiological factor in the development of Parkinson’s disease has been offered as an alternative hypothesis due to the presence of Parkinsonian clusters, where small groups of people in close contact with each other develop Parkinson’s disease in significantly higher incidences that would be predicted from the general population, which affirms this particular influenza virus could be the etiological cause of the Parkinsonian pathologies [110]. At least with the virus Jang et al. studied, the pattern of infection mimicked the hierarchical progression of the disease as described by Braak, with infection starting in the enteric nervous system, traveling into the CNS via the vagus nerve where it first infects that solitary and dorsal motor nucleus of X, and then spreading from the brain stem into higher regions of the CNS.

So far, several influenza A viruses have been shown to be neurotropic [111‐116], including H1N1 and H5N1. In addition, substantia nigra- the most affected brain region in PD patients, has been shown to be targeted by A/WSN/33 (H1N1) before its spread in the CNS [117]. Moreover, clear motor deficits have been shown in poultry [118] as well as humans [119, 120] following H5N1 infection. Using the C57BL/6J mouse, Jang et al., has found A/Vietnam/1203/04 H5N1 virus can enter CNS from peripheral nervous system and induce Parkinsonian symptoms (e.g. loss of dopaminergic neurons) and microglia activation as well as alpha-synuclein phosphorylation and aggregation [110]. Recently, Rohn et al.[121] have also demonstrated the presence of influenza A virus within the substantia nigra pars compacta (SNpc) from postmortem PD brain sections. They also identified co-localized influenza A and immune cells with caspase-cleaved Beclin-1 within the SNpc, which clearly indicated the role of neuro-inflammation with influenza A virus’s involvement in PD pathogenesis. However, no direct correlation between virus and PD pathology degree and clinical bragging has been made, so it is hard to conclude how much this virus contributes to the disease onset and its progression.

HAND are common neurological disorders associated with HIV infection and AIDS. According to current diagnostic criteria, there is asymptomatic neurocognitive impairment (ANI), HIV-associated mild neurocognitive disorder (MND), and HIV-associated dementia (HAD). Among them, HAD is the most severe form of HAND in terms of its functional impact. Its neuropathologic features are perivascular macrophage infiltration, multinucleated giant cells, activated microglias/microglia nodules, pronounced reactive astrocytosis, myelin pallor on microscopic sections and neuron loss. The pathogenesis of HAD is not certain yet, but the neurotoxicity of viral proteins, mononuclear phagocytes activation, cytokine/chemokine and other soluble factors all show involvement [122, 123].

Although with the advent of highly active antiretroviral therapy (HAART), the incidence has considerably dropped initially, the prevalence of HIV-associated cognitive impairment appears to be on the rise due to the increased life span of HIV+ population. So far, it is still the most devastating viral-associated neurodegenerative disease because it impacts more than 30% of HIV-infected population. Compelling evidence has been shown that productive HIV infection in the brain is essential for the occurrence and deterioration of HAD [124]. Recently, it has been shown that HIV-1 can replicate in at least macrophage and CCR5+ T cells within the CNS in relation to the development and progression of dementia [125]. Further, the evidence has also demonstrated that HIV gp120 can induce neuronal apoptosis by enhancing IA via CXCR4-PKC signaling [126] and HIV Tat protein can cause neuronal dysfunction by disrupting miRNAs expression [127].

One of the most striking features of HAD is that it shares the common anatomical substrate (hippocampus and substantia nigra) with AD and PD. In addition, it also shares dopamine deficiency and testosterone deficiency with PD. Also, there is commonality between HAD and AD in many aspects, such as insulin resistance, raised cholesterol especially in mid-life, and testosterone deficiency, the cytokines that are highly secreted, elevations in lipopolysaccharide concentrations, APOE4 [128]. Thus, the manifestation of AD and PD in ageing HIV patients is not surprising.

It has also been reported that some HAD patients have MS and ALS-like syndromes [129, 130]. Our studies further supported the similarity between HAD and classical neurodegeneration on proteomic, genomic as well as transcriptional regulation levels. We have studied the brain proteome of 9 HIV-associated dementia and 5 HIV non-dementia patients found that 31 proteins to be significantly altered in certain areas of the brain [1]. Worthy to note, over 90% of the 31 proteins characterized from the HIV-infected brains with HAD have already been identified previously in studies involving other neurological diseases such as AD, PD, schizophrenia, Lewy body dementia, etc. (Table 2). This proteomic overlap between proteins found in HAD brains and classical NDs is not only striking, but its also shows how mechanistically similar are the pathways in viral and non-viral neurodegenerative diseases. The take home lesson is that further research in this area, using viruses as models, can guide us in unraveling mechanisms underlying neurodegenerative diseases, which is vital to understand if new strategies for treatment are to be developed. In addition, they can also determine any role pathogenic etiologies play in classical NDs in humans.

We have recently examined the genome wide mRNA and microRNA profiling using HIV+ patients with and without dementia. The findings indicated the significant involvement of axon guidance and its downstream signalling pathways (e.g. MAPK pathway) in HAD pathogenesis, which concurs with AD and PD as well [155]. Several specific miRNAs we found could differentiate between HAD and HIV non-dementia group, which interestingly also coincided with the miRNA seen previously in classical neurodegeneration [156‐161]. The reason for the diversity of HAND is unknown, but it might due to host genetic factors. HIV might just play prompting role in the neurodegenerative process. This hypothesis needs to be elucidated by further studies to compare genetic differences between HAND patients with different neurodegenerative syndromes. However, there is a possibility that the viral, genetic and environmental factors might participate in as well. Nonetheless, taken together this is by far the most compelling evidence at the genomic, proteomic and gene regulation levels showing viral signatures in classical neurodegenerative diseases.

ALS is fatal neurodegenerative disease characterized by degeneration or loss of spinal cord and the cortical neurons. So far the cause for majority cases is unknown although genetic factors have been reported accounting for around 5% of all cases. Several viruses have been reported to be involved in ALS.

The involvement of retroviruses, including HIV, has been shown based on findings, which reported that ALS-like syndrome to occur in HIV and human T-cell leukemia virus type-1 (HTLV-1) infection [129, 162] and MacGowan has shown that with antiretroviral therapy, an ALS-like disorder in HIV-positive patients can abate [163]. Infection with several other retroviruses infection has also been documented to cause ALS-like syndromes [164‐167]. In addition, the reverse transcriptase (RT) has been found to be positive more frequently in ALS patients’ sera compared to that of control and the levels of the activity in ALS patients were comparable to that in HIV infected patients [168‐170]. Intriguingly, RT activity is hardly detected in CSF of ALS patients and XMRV sequence is not detectable in blood [170]. This result is consistent with another work [169]. RT is an essential retroviral enzyme product that allows viral genome to integrate into the host genome and reproduce its progeny as an active virus upon activation signal. Therefore, its frequent seropositivity and high activity in patients with ALS might signal the systemic retroviral replication. The reason for its absence in CSF is unknown. The plausible explanation would be RT is released from lysed cell and CSF is a cell-free compartment. Recently, expression of distinctive HERV-K pol-like sequences has been demonstrated preferentially in prefrontal and sensory cortex, areas adjacent to the motor cortex [171]. Intriguingly, they could only identify the RT in neurons rather than other cell types.

It is well known that many viruses can enter the CNS, but the mechanism is not well defined. There are two distinct routes: one is hematogenous dissemination and the other is neuronal retrograde dissemination. The first one is better accepted that virus enter the brain by crossing blood brain barrier via several pathways: transcytosis; transition by infected endothelial cells, passage through the blood–cerebral spinal fluid (CSF) barrier of the choroid plexus, and Trojan horse (utilizing infected microphage and microglia). This hypothesis is well documented in HAD and it has been reported in other viral neurodegenerative disease as well [172]. However, there is more evidence for the latter pathway recently. It has been shown that influenza virus (A/WSN/33 strain) can enter the CNS via olfactory epithelium [173], and possibly cranial nerves as well including the vagus and trigeminal nerves [174, 175]. Recently, Harberts et al. has shown HHV-6 entry into CNS through that pathway as well [176]. HSV and rabies virus have also been documented to take this route into CNS [177]. Other study has shown that A/Vietnam/1203/04 H5N1 virus can enter CNS from peripheral nervous system [110]. We also found in HAD patients, mid part of brain as well as spinal cords were heavily involved in HIV productive infection [124]. Our findings are consistent with their findings and we have hypothesized that HIV might transmit into the brain from the peripheral nervous system (PNS).

In modern times, we have seen a dramatic increase in mean life span, which is paralleled by an epidemic of chronic disease usually associated with ageing [178]. In spite of the immune privileged status of the CNS, it is still well known that dynamic immune and inflammatory responses result from a variety of insults in this compartment, and viral infection accounts for one of them [179]. Inflammatory responses also appear to be the prevalent triggering mechanism driving tissue damage associated with different age-related diseases. Age-dependent up-regulation of the inflammatory response is primarily a consequence of chronic antigenic stress, which in turn bombards the innate immune system throughout lifetime of an individual, and possibly triggering the onset of inflammatory disease. A considerable body of experimental and clinical evidence suggests that the immune system plays a definitive role, at variable degrees, in almost all age-related or associated diseases [180].

It is well known that viruses can prime the immune system to respond aberrantly. Immune and inflammatory response is a double-edged sword in neurodegenerative disease depending on the duration of the inflammatory response. Usually, acute neuro-inflammatory response includes an immediate and short-lived activation of the innate immune system within the CNS [181, 182]. It is beneficial to the CNS, as it minimizes injury, repairs and cleans the damaged tissue. In contrast, chronic inflammation is characterized by long-standing activation of microglia and sustained release of inflammatory mediators, which lead to increase oxidative and nitrosative stress, subsequently perpetuating inflammatory cycle [183]. Moreover, chronic neuro-inflammation also contributes to further prolonged inflammation [179, 184]. Therefore, chronic neuro-inflammation is highly detrimental to long term neuronal survival compared to major protective role of acute neuro-inflammation. Several neurodegenerative diseases have been reported to be associated with chronic neuro-inflammation, including AD, PD, MS, ALS, etc. [185‐188]. Furthermore, the dysregulated systemic immune responses have been shown to serve as a signature for early detection of AD [189] and long-term use of non-steroidal anti-inflammatory drugs (NSAIDs), in particular ibuprofen, have been proven to be effective preventing the development of AD [190]. As a key feature of chronic neuro-inflammation, microglia activation certainly plays a central role in the pathophysiology of neurodegenerative diseases. It has been reported that IL-1 positive activated microglia are co-localized with both αβ plaques and neurofibrillary tangles in AD brains and lead to excessive tau phosphorylation [188]. The activated microglia also present in the areas where degenerating motor neurons are present in both ALS patients and animal models [191, 192]. In addition, positron emission tomography (PET) studies have confirmed the correlation between the increased activated microglia in the motor cortex and upper motor neuron symptoms [193]. Significantly elevated microglia activation in the pons, basal ganglia, striatum, and frontal and temporal cortical regions of PD brains has also been shown by PET study [194]. It has been shown that several neurotropic viruses, such as HIV and HSV, can trigger long-term neuro-immune activation [195], which might be one of the underlying mechanisms of viral neurodegenerative diseases.

Neuroinflammation can be either a cause, or a consequence of chronic oxidative stress. Therefore, in this context it is important to mention that oxidative stress is one of the main features of neurodegenerative diseases and it binds all neurological and neurodegenerative diseases together. The oxidative stress causes lipid, protein, and genetic structural alterations that result in degeneration of nerves. Although the oxidative stress has variety of causes, such as environmental toxic insults in combination with genetic factors, it is also attributed to the involvement of pathogenic etiologies that cause neurodegenerative diseases. Chronic viral and pathogen-mediated proteins in the presence of excess reactive oxygen species can induce pathologic changes in neural tissue and lead to chronic inflammation of the brain, as seen in classical neurodegenerative diseases.

Innate immunity is an evolutionarily ancient system that provides organisms with immediately available defense mechanisms through recognition of pathogen-associated molecular patterns. Evidence shows that the dysregulation of innate immune system has been seen broadly in classical neurodegenerative diseases, such as AD, PD and Schizophrenia and it is an excellent indication of pathogen-related footprints on neurodegeneration. Lenhardt et al., have shown that in the CNS, specific activation of innate immunity through a Toll-like receptor 4 (TLR4)-dependent pathway leads to neurodegeneration [196]. It is important to iterate that innate immunity is a constitutive component of the central nervous system (CNS) and heavily depends on resident myeloid cells, the microglia. Recently emerging evidence suggests that the most abundant glial cell population of the CNS, the astrocyte, participates in the local innate immune response triggered as a consequence of constant insults they go through during infection or inflammation and it is important to state that they have been shown to be reservoirs of HIV-1 and play a significant role in virus-mediated neurodegeneration. Interestingly, astrocytes display an array of receptors, which are involved in innate immunity, including Toll-like receptors, nucleotide-binding oligomerization domains, etc.

Fassbender et al., have shown that the detection of CD14 overexpression in brains of APP transgenic mice points towards the key role of innate immunity receptor CD14 in significantly contributing to the neuroinflammatory responses in AD. CD14 recognizes the pattern associated with the ß-sheet fibrillar conformation of Aß, as this receptor interacts with fibrillar but not with non-fibrillar Aß. The affinity of fibrillar Aß to CD14 is ~50-fold lower than that to LPS. However, since in contrast to LPS the AD brains contain very high concentrations of Aß fibrils (in contrast to LPS) for years and decades, it is likely that even at this submaximal affinity, this interaction is sufficient to maintain a chronic neuro-inflammation. Overall, this study provides the basis for possible structural mimicry between highly hydrophobic fibrillar Aß and pathogen-associated molecular patterns contributing to neuro-inflammation in AD and opens the therapeutically relevant perspective that the enormous progress being made in the field of innate immunity could be extended to AD and other neurodegenerative disorder research [197]. Previous studies have suggested that pathogens could be involved in AD too. CD33, one of four genes found to be significantly associated with AD in a recent genome-wide association screening (Bertram et al., 2008), is involved in activating the innate immune system. But perhaps the most prominent example of a dementia associated with viral infection is HIV-associated dementia, which shows the innate immune system involvement and proteomic overlaps with AD, PD and Schizophrenia (Table 2) [1].

In the context of innate immune system involvement in classical neurodegeneration, it is important to mention that scientists in France and the US discovered that a type of immune system cell may facilitate the development of PD and it has been suggested that targeting part of the immune system with drugs could be a new way to treat the disease [198]. In their study, Brochard and colleagues used postmortem evidence of human patients to show that CD8+ and CD4+ T cells, but not B cells, had invaded their brains. They then used mice that had been given a neurotoxin to induce symptoms of Parkinson’s (the MPTP mouse model) to show that it was almost exclusively the CD4+ T cells that arbitrated the accelerated death of dopamine cells. This only happened when the FasL cell death triggering protein was expressed, and not when the IFN-γ inflammatory cytokine was expressed. This study suggests both activated microglia and T lymphocytes do make significant contribution to neurodegeneration in PD.

Elevated T cell responses to specific CNS antigen, or shift in CD4+ and CD8+ T cell population in the periphery as well as CNS has also been observed in neurodegenerative disorders [199‐201]. Both CD4 and CD8+ T cells can be detrimental and protective to the CNS. However, in that T cells do not significantly accumulate in the brain undergoing neurodegeneration and more importantly T cells directed to myelin or neuronal antigens can also be found in healthy control subjects [202, 203], therefore it is difficult to conclude any direct involvement of T cells as a causative factor in neurodegenerative diseases. Nevertheless, the alteration of CD4+ and CD8+ T cells observed in the periphery in neurodegenerative diseases indicates that there is persistent antigenic challenge and T cells are playing a role in neurodegenerative diseases. It is worthy to note that the ratio of CD8+ to CD4+ T cell or the shift to a Tc1/Th1-type immune response may contribute to the harmful brain inflammatory reaction.

Further the evidence solidifying the role of immune system in NDs, is the presence of antibodies against neuronal antigen observed in neurodegenerative diseases and some of them are pathogenic [2]. The mechanisms of how these antibodies arise remain unknown. One plausible explanation is the possible homology between some pathogen antigens and human neuronal antigens.

Overall, together these studies give further evidence that the immune system can both protect and attack the brain. Whether this is a generalized possibility across all neurodegenerative disorders is an open area of investigation. Although this study, combined with several other studies discussed in this review, cumulatively implicate pathogen and innate immune system involvement in classical neurodegeneration, which upon further studies will open the door to developing new treatments that target the immune system for treating classical neurodegenerative disorders, especially if the NDs occur at younger age because treating the ageing immune system may not yield the same effect.

In case of schizophrenia, both the unspecific and the specific arms of the immune system seem to be involved in the dysfunction of the immune system in schizophrenia. The unspecific, “innate” immune system shows signs of over-activation in un-medicated schizophrenic patients, as indicated by increased monocytes and γδ-cells. Increased levels of interleukin-6 (IL-6) and the activation of the IL-6 system in schizophrenia might be the result of the activation of monocytes/macrophages, too. On the other hand, several parameters of the specific cellular immune system are blunted, such as, for example, the decreased T helper-1 (TH-1)-related immune parameters in schizophrenic patients both in vitro and in vivo. It seems that a TH-1/TH-2 imbalance with a shift to the TH-2 system is associated with schizophrenia [204]. Three schizophrenia genetics research consortia, each funded in part by NIMH, have reported separately on their genome-wide association studies (http://​www.​genome.​gov/​20019523) online July 1, 2009, in the journal Nature. However, the SGENE, International Schizophrenia (ISC) and Molecular Genetics of Schizophrenia (MGS) consortia shared their results-making possible meta-analyses of a combined sample totaling 8,014 cases and 19,090 controls. Interestingly, all three studies implicate an area of Chromosome 6 (6p22.1), which is known to harbor genes involved in immunity and controlling how and when genes turn on and off. This hotspot of association might help to explain how environmental factors and infection by pathogens affect risk for schizophrenia. Recently, genetic data from multiple large cohorts of patients were published in ‘Nature’ showing that different gene loci located on chromosome 6p22.1 are the most probable susceptibility genes for schizophrenia [3]. This region includes several genes of interest, which are related to the immune function. The strongest evidence for association was observed in or near a cluster of histone protein genes which could be relevant through their roles in regulation of DNA transcription or repair, i.e. in epigenetics [205], or their direct role in antimicrobial defense [206]. Moreover, several genes of the HLA complex, which regulate the immune function and already earlier have been discussed to be involved in schizophrenia, are located in these regions [207].

Although an immune dysfunction and the involvement of infectious agents in the pathophysiology of schizophrenia are discussed since decades, the field never came into the mainstream of research. These genetic findings and further recent interesting observations, however, may contribute shifting research into the direction of immunological alterations and inflammation as cause for schizophrenia. Although the involvement of infectious agents has long been suspected in schizophrenia, results from animal models indicate that the immune response determines the risk for schizophrenia [208].

It is well known that the molecules participating in both innate and adaptive immune responses have been shown to be induced in a wide diversity of neurological disorders, which include AD, MS, HD, PD, and ALS all discussed in this review. The recent evidence on immune response within the brain actually points towards host immune mechanisms could be the actual culprit or in other word etiologically linked to the manifestation of neurodegenerative diseases. Further, this also suggests that the primary causes of a large majority of neurologic disorders seen in humans could originate outside the central nervous system. Some infectious agents are known to gain entry into the CNS within infected migratory macrophages, which traverse the blood brain barrier by transcytosis or by intra-neuronal transfer from peripheral nerves. In case of various viruses, especially the ones associated with NDD, the systemic nature of these pathogens is able to trigger immune responses, along with affecting the immune system and other organ systems including the brain, resulting in neurologic manifestation.

Although the underlying mechanisms of HAD are still uncertain, the cumulative evidence has pointed out that HIV might cause immune-senescence. First of all, it is evident that the age of HIV+ patients who manifest dementia and Alzheimer’s disease, which is 15 years (50–52 years) less than HIV- individuals who manifest AD (Average age 65–85). Second, apart from dementia, HIV can also lead to other aged diseases, which is closely related to immune-senescence, such as cardiovascular diseases and cancer, as HIV interferes with metabolic and oxidative phosphorylation pathways [209]. Third, it has been shown that HIV infection can induce T lymphocytes immune-senescence, which is indicated by deteriorated shortening of telomeres in CD8+ CD28- T cells while no significant change in CD4+ T cells [210, 211] and this is highly similar with what has been seen in the elderly. In addition, a marker of immunosenescence, CD57, can also be detected during initial stage of HIV infection [212]. Furthermore, HIV infection can induce similar alterations to innate immune cells, including monocytes, NK cells, dendritic cells and neutrophils, compared to that induced by ageing [213]. In this context it is important to mention that even though HIV shares anatomical, clinical and proteomic overlaps with both AD and PD, the involvement of virus or any pathogen in classical neurodegeneration has not been proven.

It is well known that metabolic pathways have an integral involvement in neurodegenerative process in humans. With ageing, there is up regulation of both oxidative stress and metabolic pathways in the human brain and more so during the manifestation of neurological disease. The significant dysregulation of both these pathways is apparent in a variety of viruses, which include, HIV, HCV, Influenza, etc. It has been shown that the impairment of energy metabolism can exacerbate synaptic dysfunction, neuronal injury, which together may lead to neurodegenerative disorders [214]. Viruses are completely reliant on their host’s cellular nucleic acids, proteins and membrane, as well as energy to enable viral synthesis. Disturbance/dysregulation of several core metabolic pathways have been reported by viral infections, including glycolysis and lipid metabolism, which all play a very important role in neurodegenerative diseases [215]. Viruses use several means to interfere with host metabolism, including manipulating host gene expression; inhibiting host cellular process (such as RNA and protein synthesis); impairing mitochondrial function and interfering ATP production [215]. Indirect evidence also comes neuro-proteomic analysis of HIV+ patients with and without dementia, which showed the first evidence that >90% of the protein candidates identified in the HAD brains, particularly in the oxidative phosphorylation (OXPHOS) and glycolysis pathways appear also to over represent in non-viral mediated neurodegenerative diseases, such as vascular dementia, AD, PD and amyotrophic lateral sclerosis (ALS) [1], a study which is highly significant as it shows the ultimate footprints of a virus on neurodegenerative disease and its overlap with classical forms of neurodegeneration has considerable potential for treatments for NDs in humans.

Viral infection also interferes with host transport machinery, whose alterations are cardinal feature of neurodegenerative diseases, eg. neurofibrillary changes in AD, Lewy bodies in PD, and different types of filamentous inclusion bodies in motor neuron disease. It has been well documented that viral proteins can modulate the structure and function of the actin cytoskeleton to initiate, sustain and spread infections [216].