Mini ReviewOpen Access

A Quantitative View on Naturally Occurring Autoantibodies in Neurodegenerative Diseases

Yannick Kronimus, Richard Dodel*, Sascha Neumann

Department of Geriatrics, University Duisburg-Essen, Germaniastrasse 1-3, 45356 Essen, Germany


Accumulation and aggregation of Beta-Amyloid (Aβ) and Alpha-Synuclein (α-Syn) are considered as central or even causative for the development of Alzheimer’s (AD) and Parkinson’s disease (PD). Therefore, the regulation of these proteins seems to be an essential aspect for prevention and is of central interest in current research aiming to find therapeutic approaches. The human immunological repertoire already contains such a regulatory system. Naturally occurring autoantibodies (nAbs) against the proteins Aβ (nAbs-Aβ) and α-Syn (nAbs-α-Syn) are part of the innate immune system and modulate the metabolism of their specific antigens including protein clearance and inhibition of aggregation. Thus, many researchers hypothesize that in the course of AD and PD, quantitative alterations of nAbs-Aβ and nAbs-α-Syn arise resulting in impaired proteastasis. Such alterations would represent promising, reliable biomarkers and indicate potential approaches for therapeutic strategies. Hence, it is not surprising that many studies dealing with nAbs-Aβ and nAbs-α-Syn titers in AD and PD patients in comparison to control participants are available in the literature. In this mini review, we summarize the current evidence. Furthermore, we critically discuss problems and future requirements for nAbs quantification when a clinical application is the overriding goal.


The human antibody repertoire can be subdivided into conventional and naturally occurring antibodies, based on their originating B cell type. While conventional antibodies derive during life from plasma and memory B cells differentiated from B2 or marginal zone B cells after antigenic activation, naturally occurring antibodies arise in fetogenetic periods and thus are present from birth1-4. They are produced from B1 cells without extrinsic stimuli and T cell assistance. A special characteristic of B1 cells is the germline-closed configuration of the recombined immunoglobulin genes resulting in less hypermutated and affinity matured antibodies with lower affinities5. Although conventional antibodies are usually the main subject in textbooks, naturally occurring antibodies account for the greatest portion in humans6. Among them, a fraction shows autoreactivity and is termed naturally occurring autoantibodies (nAbs), which are mostly from the IgM and IgA, fewer from the IgG type7. They circulate through human body fluids, maintain physiological homeostasis, support the clearance of distinct secreted proteins and apoptotic cells, and protect from pathologically altered structures like oxidatively damaged, aggregated, and non-functional lipids and proteins8,9. In the following sections we want to focus on the beneficial aspects of nAbs and their potential clinical applications, especially for therapeutics and diagnostics in neurodegenerative dis¬orders.

The two most common neurodegenerative disorders – Alzheimer’s (AD) and Parkinson’s disease (PD) – are among others histopathologically characterized by extra- and intracytoplasmic protein deposits primarily consisting of the proteins beta-amyloid (Aβ) in the case of AD or alpha-synuclein (α-Syn) in the case of PD10,11. Albeit the accurate pathomechanism has not been fully clarified, neither for AD nor for PD, it is widely accepted that the metabolic dysregulation of the proteins has etiological significance12. For Aβ, especially the isoform containing 42 amino acids (Aβ42) has been identified as minatory as it exhibits heightened hydrophobicity. The accumulation and aggregation of both, Aβ and α-Syn into small soluble oligomers and fibrils have been connected to many (in)direct neuro- and cytotoxic effects indicating their participation in disease onset and progression13-16. Furthermore, especially for α-Syn, a transmitting pathological mechanism is highly hypothesized within literature encompassing the spreading of aggregates from cell to cell17.

Although AD- and PD-associated protein deposition and the resulting detrimental effects are more obvious in the central nervous system (CNS), Aβ as well as α-Syn dysregulation also occurs in the periphery. In particular, this is indicated by vascular Aβ deposition – very common in AD – as well as α-Syn pathology detectable in erythrocytes and nerve cells of the enteric system in PD patients18-20.

Thus, since many years and considering all aspects, researchers follow the idea of an early and preventive intervention counteracting protein dysregulation, aggregation, and propagation as it is believed to modify disease progression in AD, PD, and other proteinopathies. Here, Aβ42 and/or α-Syn specific antibody treatment could represent a promising therapeutic strategy due to a targeted modulation of the metabolism of their antigen. Such approaches have already been tested in diverse in-vitro and in-vivo experi¬ments and revealed positive effects including reduced protein deposits and decreased neurodegeneration, however, failed in phase three at the latest when tested in the clinical state of AD21-25.

It is an interesting fact that antibodies that maintain tissue homeostasis and proteostasis are already present in humans26,27. In child- and adulthood as well as in health and disease, nAbs recognizing the proteins Aβ42 (nAbs-Aβ42) and α-Syn (nAbs-α-Syn) but also further proteins that become misfolded in disease cases (such as prion and tau protein) are detectable in the serum and cerebrospinal fluid (CSF) suggesting the presence of innate protective mechanisms2,27-32. Quantitative or qualitative alterations of nAbs could impair their normal functions, worsen the protection system, and thus represent causal or supporting factors for the development of AD and PD. Especially quantitative alterations, namely changed titers, may act as biomarkers in clinical applications and illustrate restoring of Aβ42 and α-Syn specific antibodies as a promising therapeutic strategy. It is not surprising that a number of studies investigating titers of nAbs-Aβ42/α-Syn have already been published in the past and will be following discussed.

A large body of literature exists harboring inconsistent, even contrasting data regarding nAbs-Aβ titers in AD patients. In a comprehensive study by Britschgi et al. (2009), nAbs-Aβ recognizing various natures of its antigen could be detected within serum and CSF samples of AD patients and nondemented control subjects of different ages33. Using ELISA technique and antigen microarrays the highest reactivity was uncovered for aggregated and posttranslationally modified Aβ40 and Aβ42 forms. Between AD patients and controls, no significant differences of nAbs-Aβ42 plasma titers against oligomeric or monomeric protein forms were identified. However, comparing mildly to moderately and severely affected AD patients, the latter group showed in one sample set significantly decreased nAbs-Aβ42 plasma titers suggesting a role in disease progression. Unchanged nAbs-Aβ titers in AD patients were also verified in further studies examining nAbs-Aβ40 and -Aβ4226,28. Marcello and coworkers (2011) revealed similar results even the experimental setup was limited to IgM autoantibodies34.

Although they were not able to detect altered nAbs-Aβ42 titers, plasma level of nAbs recognizing N-truncated Aβ consisting of the amino acid sequence three to seven and a modified pyroglutamate (pGlu3-7) was significantly decreased in patients suffering from AD. Such peptides have often been detected in the brains of AD patients and were shown to strengthen the aggregation process35. Three further studies identified significantly changed blood titers of nAbs against distinct Aβ forms using ELISA techniques. Qu et al. (2014) demonstrated reduced serum titers of nAbs recognizing Aβ1-15 but unchanged nAbs-Aβ against soluble and aggregated full-length peptides in AD patients36. Moir and colleagues (2005) found decreased nAbs levels against redox-modified Aβ40 and again unchanged nAbs-Aβ40 in AD patients37. In contrast, Gruden and coworkers (2007) detected significantly increased nAbs portions in female AD patients, namely autoantibodies against oligomeric Aβ consisting of the amino acids 25 to 3538. This peptide fragment – inter alia detectable in AD brains – is often used as a model system as it maintains the neurotoxic properties of Aβ with the simultaneous option of better controlling the aggregation process39. Elevated titers of unbound autoantibodies recognizing these eleven amino acids containing and most toxic sequence may be a hint for decreased but necessary antigen binding and thus regulation of Aβ25-35 what may result in disease onset or progression. The exclusive investigation of such antibodies has the ability to be a critical step and advantage as all further Aβ targeting nAbs with various epitopes could overlap a specific effect of the indeed crucial sequence.

As mentioned above, there are also contrary data available including studies that revealed increased or decreased nAbs portions recognizing the full-length peptide Aβ42. On the one hand, some ELISA as well as radiolabeled immuno-precipitation based experiments have uncovered lowered nAbs-Aβ42 serum titers in AD patients when compared to healthy or cognitively unremarkable subjects40,41. On the other hand, Nath and colleagues (2003) determined elevated nAbs serum titers against soluble and pre-aggregated Aβ42 in AD patients42. In the same study, CSF samples have also been investigated, however, only three of the AD patients – but interestingly the severely affected ones – and none of the controls contained detectable amounts of nAbs-Aβ42. Since CSF data are generally less frequent than serum data –it encompasses a more invasive clinical method – only a few more studies dealing with variable nAbs structures have been published. For example, Du and colleagues (2001) revealed decreased nAbs-Aβ40 titers in CSF of AD patients using ELISA43. Within a second study published by Maftei et al. (2013) the same method was applied to analyze nAbs/Aβ42 immune complexes. Here, a significantly increased portion in the CSF of people suffering from AD was detected44. Although the studies investigated nAbs targeting different antigenic structures, similar effects can underlie both observations as decreased free nAbs titers can be the result of increased Aβ bound nAbs (immune complexes).

Table 1. NAbs Serum/Plasma and CSF titers in AD patients compared to control subjects. Summary of exemplified studies investigating changed serum/plasma and CSF concentration of nAbs-Aβ. For each study and if information were available (n.a. = not available), p-value of the statistical analysis, age- (AM), gender-matching (GM), and Mini-Mental-State-Examination Score of the study participants as well as the used method are shown. *No comparison possible as nAbs-Aβ42 were only detectable in the CSF of severely affected AD patients.

 

Serum/plasma concentration CSF concentration
titer nAbs reference p-value AM/GM/MMSE method titer nAbs reference p-value AM/GM/MMSE method
            only detectable in severe cases* 42 n.a. +/+/17 vs 29 ELISA
Increased in AD nAbs-Aβ42 42 0.005 +/+/17 vs 29 ELISA            
nAbs-Aβ25-35 38 < 0.01 +/+/15 vs 27 ELISA Increased in AD bound nAbs-Aβ42 44 0.03 +/+/20 vs 29 ELISA
bound nAbs-Aβ42 44 0.03 +/+/20 vs 29 ELISA            
unchanged nAbs-Aβ42 26 0.85 +/+/n.a. ELISA            
  28 0.056 +/+/17 vs 29 ELISA            
  33 n.a. +/-/23 vs 30 ELISA            
  34 n.a. +/+/17 vs n.a. ELISA unchanged          
  36 n.a. +/+/20 vs 29 ELISA
Dot Blot
           
nAbs-Aβ40 28 0.19 +/+/17 vs 29 ELISA            
  37 n.a. +/+/n.a. ELISA            
Decreased in AD nAbs-Aβ42 40 < 0.02 +/n.a./n.a. ELISA            
  41 0.001 -/-/21 vs 29 IP            
nAbs-pGlu3-7 34 0.021 +/+/17 vs n.a. ELISA Decreased in AD nAbs-Aβ40 43 0.02 +/n.a./n.a. ELISA
nAbs-Aβ1-15 36 0.02
0.0008
+/+/20 vs 29 ELISA
Dot Blot
           
nAbs-red40 37 0.018 +/+/n.a. ELISA            
Table 2. NAbs Serum/Plasma and CSF titers in PD patients compared to control subjects. Summary of exemplified studies investigating changed serum/plasma and CSF concentration of nAbs-α-Syn. For each study and if information were available (n.a. = not available), p-value of the statistical analysis, age- (AM), gender-matching (GM), and Hoehn & Yahr Scale (H&Y; median or *mean) of the study participants as well as the used method are shown.

 

Serum/plasma concentration CSF concentration
titer nAbs reference p-value AM/GM/H&Y* method titer nAbs reference p-value AM/GM/H&Y* method
Increased in PD nAbs-α-Syn 46 < 0.05 n.a./+/2 ELISA Increased in PD          
  47 < 0.01 +/+/2.1* ELISA nAbs-α-Syn 45 0.016 +/-/3 ELISA
  48 < 0.007
< 0.001
n.a. ELISA/WB
SPR
         
  49 < 0.001 +/+/1 ELISA nAbs-α-Syn 46 < 0.05 n.a./+/2 ELISA
unchanged nAbs-α-Syn 45 0.19 +/+/3 ELISA unchanged          
  51 0.5 -/-/2 ELISA nAbs-α-Syn        
  52 0.69 +/+/1.3* ELISA          
  53 n.a. -/-/2.4 ELISA/WB          
Decreased in PD nAbs-α-Syn 30 < 0.05 +/+/2 ELISA Decreased in PD        
  50 0.005 -/-/2 ELISA nAbs-α-Syn        
bound nAbs-α-Syn 50 0.042 -/-/2 ELISA          

Conflicting results of nAbs-α-Syn titers are also available in literature about PD. Two exemplary studies using ELISA technique and dealing with serum and CSF nAbs-α-Syn demonstrate significantly elevated autoantibody titers in patients suffering from PD45,46. While Horvath and colleagues (2017) found differences between PD patients and control subjects in both, CSF and serum, Akhtar and coworkers (2018) detected only increased nAbs levels in the CSF. This is of particular interest as Horvath revealed a stronger effect size for changed serum titers and the loss of significant differences of CSF titers when separating the patient cohort into mild and moderate affected individuals. In line with these observations, Gruden et al. (2011) as well as Yanamandra et al. (2011) performed serum ELISA experiments and surface plasmon resonance spectroscopy with monomeric and aggregated α-Syn, identified increased nAbs-α-Syn titers against both protein forms in PD patients, and revealed an attenuated effect with increasing disease duration47,48. In a further publication, Shalash and colleagues (2017) expanded the comparison of nAbs-α-Syn serum levels to PD patients, controls, and AD patients and again detected an elevated portion in the PD cohort49.

These studies provide the impression of increased nAbs-α-Syn titers in especially early stages of PD suggesting disease duration as a critical factor for such findings. However, contrasting hints with both, short- and long-term affected PD patients and correspondent differences in age and disease severety exist as well. Besong-Agbo et al. (2013) as well as Brudek et al. (2017) demonstrated significantly decreased nAbs-α-Syn serum titers in the plasma and serum of PD patients30,50. Additionally, in the latter paper PD patients were also shown to exhibit lower titers of α-Syn/nAbs immune complexes resulting in a decreased total nAbs-α-Syn fraction.

As opposed to the already outlined studies, Maetzler and coworkers published in 2014 the presence of comparable nAbs-α-Syn serum levels in PD and healthy persons51. Such unchanged nAbs-α-Syn titers have also been confirmed in two further publications investigating serum or plasma samples of PD patients and healthy controls52,53. Here, especially the publication by Smith et al. (2012) is of great interest as they additionally summarize and demonstrate conflicting studies regarding α-Syn protein52.

For the development of reliable diagnostic markers but also as therapeutic targets, the determination of nAbs-Aβ and nAbs-α-Syn titers are of certain interest in AD and PD research. However, as mentioned above, in both cases many different and contrasting results have been published in the last years including increased, decreased, and unchanged nAbs levels in affected persons. Not until this drawback is eliminated, the application of nAbs titers has a chance to receive clinical significance.

A number of reasons might be responsible for the great variance and contrary data of altered nAbs titer in AD and PD. In many cases, typical parameters like incorrect diagnoses of the included participants, small sample sizes and technical limitations are cited as causes. However, it is largely impossible that the contrasting findings are a method-based effect as in almost all cases ELISA technique was applied to determine nAbs titers. Within the experimental setups, differences in the sample preparation are more likely responsible for contrary results. The utilization of different body fluids including plasma, serum, or CSF harbors also risks for fluctuations like a previous antibody purification. Additionally, a number of further variabilities may account for inconsistent data on nAbs-Aβ and nAbs-α-Syn titers. Here, two main factors represent 1) the choice of the incorporated participants and 2) the antigen that is used to determine its corresponding nAbs titer. Control probands often range from younger healthy controls to age-matched patients without disease-associated symptoms36,51. Furthermore, patient cohorts often differ in disease severity and duration. Such variabilities result in different physical and immunological conditions and may significantly influence nAbs titer analyses. Especially, the latter aspect is of utmost importance as directly age dependent and indirectly medication mediated effects on antibody titers have been identified54-56. This should not be disregarded even though authors including individuals without age-matching usually argue that their cohorts do not show positive correlation between age and antibody titers.

Different protein states can also greatly influence results of ELISA and related assays. The choice between recombinant or synthetic peptides including the expression system with its particular posttranslational modifications (PTMs), full-length or peptide fragments, and monomeric or oligomeric structures probably impact antigen binding. Regarding the last aspect, especially nAbs-Aβ analyses exhibit great potential for variability as Aβ shows a naturally high aggregation property that complicates the control of its exact state e.g. during the ELISA coating process57.

Additionally, most of the performed studies feature limitation in their experimental setup in general as their analyses are restricted to either the antigen bound or the unbound nAbs fraction. However, to draw a comprehensive picture about the immunological status in AD and PD, information about both conditions as well as the antigen concentration are important to be considered.

Overall, for the clinical application of quantitative analyses of nAbs-Aβ and nAbs-α-Syn, the primary future goal has to be the elimination of the already described major drawbacks within the experimental setups. This includes both, the possible causes of failure and variability as well as the consideration of antigen/nAbs immune complexes and free circulating nAbs. Here, a standardization of the experimental setup with the formulation of guidelines within a consortium would be helpful to decreased variabilities across studies and laboratories. A similar procedure has been applied for biomarkers in AD, called Global Biomarker Standardization Consortium (GBSC)58.

If nAbs-Aβ and nAbs-α-Syn quantification will be reliably and reproducibly executed in future studies, thresholds for concentration can be set for its application as a diagnostic biomarker provided that actual differences between healthy and diseased people are present. Furthermore, such findings would demonstrate the necessity of an antibody targeted therapy. On the other hand, quantitative differences do not represent the only possible disease-causing alteration as especially qualitative properties like avidity, immune activation, or PTMs are also crucial properties of nAbs.

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Article Notes

  • Published on: July 5, 2018

Keywords

  • Naturally occurring autoantibodies
  • Alzheimer’s disease
  • Parkinson’s disease
  • serum titers
  • CSF titers
  • Beta-Amyloid
  • Alpha-Synuclein
  • ELISA
  • Antibody
  • Antibodies

*Correspondence:

Dr. Richard Dodel, MD
Department of Geriatrics, University Duisburg-Essen, Germaniastrasse 1-3, 45356 Essen, Germany
Telephone No: +49 (0)201-89760; Fax No: +49 (0)201 8976229
Email: richard.dodel@uk-essen.de

 ©2018 Dodel R. This article is distributed under the terms of the Creative Commons Attribution 4.0 International License.